US20070183920A1 - Nanoscale metal paste for interconnect and method of use - Google Patents

Nanoscale metal paste for interconnect and method of use Download PDF

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Publication number
US20070183920A1
US20070183920A1 US10/589,399 US58939905A US2007183920A1 US 20070183920 A1 US20070183920 A1 US 20070183920A1 US 58939905 A US58939905 A US 58939905A US 2007183920 A1 US2007183920 A1 US 2007183920A1
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Prior art keywords
metal
particles
metal alloy
temperature
silver
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US10/589,399
Inventor
Guo-Quan Lu
Guofeng Bai
Jesus Calata
Zhiye Zhang
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Virginia Tech Intellectual Properties Inc
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Virginia Polytechnic Institute and State University
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Application filed by Virginia Polytechnic Institute and State University filed Critical Virginia Polytechnic Institute and State University
Priority claimed from PCT/US2005/004567 external-priority patent/WO2005079353A2/en
Publication of US20070183920A1 publication Critical patent/US20070183920A1/en
Priority to US12/019,450 priority Critical patent/US8257795B2/en
Assigned to VIRGINIA POLYTECHNIC INSTITUTE AND STATE UNIVERSITY reassignment VIRGINIA POLYTECHNIC INSTITUTE AND STATE UNIVERSITY ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: ZHANG, ZHIYE, BAI, GUOFENG, CALATA, JESUS, LU, GUO-QUAN
Assigned to VIRGINIA TECH INTELLECTUAL PROPERTIES, INC. reassignment VIRGINIA TECH INTELLECTUAL PROPERTIES, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: VIRGINIA POLYTECHNIC INSTITUTE AND STATE UNIVERSITY
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F7/00Manufacture of composite layers, workpieces, or articles, comprising metallic powder, by sintering the powder, with or without compacting wherein at least one part is obtained by sintering or compression
    • B22F7/06Manufacture of composite layers, workpieces, or articles, comprising metallic powder, by sintering the powder, with or without compacting wherein at least one part is obtained by sintering or compression of composite workpieces or articles from parts, e.g. to form tipped tools
    • B22F7/062Manufacture of composite layers, workpieces, or articles, comprising metallic powder, by sintering the powder, with or without compacting wherein at least one part is obtained by sintering or compression of composite workpieces or articles from parts, e.g. to form tipped tools involving the connection or repairing of preformed parts
    • B22F7/064Manufacture of composite layers, workpieces, or articles, comprising metallic powder, by sintering the powder, with or without compacting wherein at least one part is obtained by sintering or compression of composite workpieces or articles from parts, e.g. to form tipped tools involving the connection or repairing of preformed parts using an intermediate powder layer
    • BPERFORMING OPERATIONS; TRANSPORTING
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    • B22F1/00Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
    • B22F1/10Metallic powder containing lubricating or binding agents; Metallic powder containing organic material
    • BPERFORMING OPERATIONS; TRANSPORTING
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    • B22F1/00Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
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    • B22F1/103Metallic powder containing lubricating or binding agents; Metallic powder containing organic material containing an organic binding agent comprising a mixture of, or obtained by reaction of, two or more components other than a solvent or a lubricating agent
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Definitions

  • the present invention generally relates to materials used for interconnecting electronic devices and, particularly, devices which either generate high temperatures during use or devices which are used in high temperature applications. Furthermore, the invention is generally related to a fabrication method which reduces or eliminates the need for high pressure application during fabrication of an interconnection, such as during die attach.
  • All semiconductor chips have to be fastened or attached to a substrate to function in an electronic product.
  • the state-of-the-art technology for interconnecting these chips typically uses a lead or lead-free solder alloy, or a conductive polymeric glue, such as an epoxy.
  • solder alloys or a conductive polymeric glue, such as an epoxy.
  • conductive polymeric glue such as an epoxy.
  • these materials have poor thermal properties and do not dissipate the heat generated by the chips. They also have poor electrical properties and fail to effectively reduce loss of electrical power, and poor robustness for mechanical strength and reliability.
  • these materials may not be generally suitable for allowing some chips, such as SiC or GaN chips, to function at high temperatures.
  • solder that is reflowed at temperatures low enough for the devices to withstand.
  • the advantage of low melting temperatures becomes a liability for solder alloys because they cannot meet the requirements of high temperature operation or use in high temperature applications.
  • solder materials have relatively poor electrical and thermal properties, and poor fatigue resistance, compared to other metals such as copper and silver, which detrimentally affect the performance of the whole electronic system.
  • the nanopowder of the present invention can be prepared using known techniques, or purchased directly at a price comparable to that that of micron-size powder.
  • a dispersant is preferably used for reducing agglomeration of the particles which could lead to undesirable/low silver particle loading during mixing of the paste.
  • the nanopowder of the present invention can be combined with a polymer binder that preferably has a volatilization temperature below the desired sintering temperature.
  • a binder that preferably does not volatilize until close to the sintering temperature for the metal or metal alloy powder assists in achieving denser interconnections since sintering occurs more uniformly throughout the composition (i.e., the binder is preferably chosen and formulated into the composition such that the metal or metal alloy powder on the edges closer to the source of heat does not start to fuse with neighboring particles until the bulk of the particles begins to fuse).
  • Dispersion of the metal or metal alloy powder in the binder can be facilitated by ultrasonic or mechanical or methods, or combinations of the same.
  • compositions of the present invention have a wide range of applications. For example, they can be used to bond silicon integrated circuit chips in computers, or silicon power chips in power supplies, or optoelectronic chips in telecommunications modules. Also, in the case of silver powder, and silver alloys, where the metal melts at temperatures over 700° C. or 800° C., the invention is suitable for attaching semiconductor chips that can be operated at high temperatures, e.g., SiC or GaN power chips.
  • sintering silver or silver alloy that is in the form of a nanopowder one that is less than 500 nm in size, and most preferably below 100 nm in size
  • a relatively low temperatures e.g., on the order of 300° C.
  • a dense, conductive metal interconnection is achieved that can be operated at high temperatures without risking melting of the interconnect, as would be the case with commercial lead and lead free solders as well as conductive epoxies.
  • the ability to allow these chips to operate at a high temperatures cuts down their cooling requirement, leading to savings in materials and energy in the manufacture and operations of the product.
  • the nanosilver paste of this invention due to its high melting temperature and low processing temperature, is also useful for applications other than the attachment of silicon devices and heatsinks. It may be used to attach/interconnect wide bandgap devices that need to operate at elevated temperature such as SiC, GaN and diamond. It is also useful for attaching devices that generate substantial amounts of heat such as light-emitting diodes (LED) and semiconductor lasers.
  • LED light-emitting diodes
  • FIG. 1 is a schematic view of metal particles (e.g., nanosilver particles formed as a paste utilizing dispersants to prevent agglomeration and binder to prevent paste cracking during handling and dry processing;
  • metal particles e.g., nanosilver particles formed as a paste utilizing dispersants to prevent agglomeration and binder to prevent paste cracking during handling and dry processing;
  • FIG. 2 is a schematic view showing an exemplary two step procedure for formulating a nano scale metal particle paste for use in the present invention
  • FIG. 3 is a schematic view showing the use of metal paste according to the invention for attachment of devices to a substrate;
  • FIGS. 4 a - c are graphs showing a comparison of the relative electrical conductivity, relative thermal conductivity, and elastic modulus, respectively, of a various prior art interconnect materials and the interconnect material of the present invention
  • FIGS. 5 a - b are SEM images of the nanoscale silver paste of the present invention and the commercial silver paste (Heraeus C1075) that has micrometer-sized silver, respectively after the pastes are sintered at 300° C. for ten minutes;
  • FIG. 6 is a graph showing the expansion/shrinkage curves for different particle sizes of silver that are to be sintered.
  • FIGS. 7 a and 7 b show SEM images of 100 nm silver particles formulated respectively with higher burn out temperature PVB and fatty acid dispersants, and lower burnout temperature PRV914.
  • the metal powder in the nanoscale metal paste has a particle size less than 500 nm, and most preferably, the particle size is less than 100 nm (e.g., 1-100 nm or 1-60 nm, etc.).
  • the preferred metal or metal alloy within the practice of this invention is a silver or silver alloy. This is because of a combination of low cost, as compared to gold, and the amenability of being fired in ordinary atmosphere. While it is processed at temperatures comparable to that of solder reflow, it can withstand subsequent exposure to higher temperature, which solder cannot.
  • Suitable nanosilver powder (e.g., less than 500 or 100 nm in particle size) is commercially available from various suppliers in various sizes at a cost of roughly $1/gram. Exemplary commercial suppliers include Nanostructured & Amorphous Materials, Inc., Inframat Advanced Materials, Inc., Sumitomo electric U.S.A., Inc., and Kemco International Associates. Nanosilver powder has been used in a variety of applications. For example, silver can be used as an antibacterial additive to fabric products such as carpets, napkins and surgical masks. Silver has been medically proven to kill a wide range of disease causing organisms in the body and is also relatively safe. For this reason, numerous vendors tout the use of silver colloid for attacking bacterial organisms in the body.
  • Silver nanoparticles to enhance food preservation in its refrigerator product lines.
  • Silver nanopowder is also being used as an additive in consumer products such as toothpaste, toothbrush, and soap, as well as socks because of the antibacterial property.
  • silver nanopowder is being sold for use in conductive traces, resistors, electrodes, optical filters and EMI-shielding (its application to the creation of an interconnect by sintering at low temperatures for use in high temperature applications being heretofore unrecognized until the invention described herein).
  • Nanosilver particles are also used as a coloring additive in paints, glass, ink, and cosmetics.
  • Suitable nanosilver pastes having application in the present invention may also be produced using a modified Carey Lea method.
  • the Carey Lea method was first applied to making photographic emulsions.
  • a modified process can be used to synthesize nanosilver particles (see, for example, S. M. Heard, F. Grieser, C. G. Barraclough and J. V. Sanders, J. Colloid Interface Sci. 93 (2): 545-555 1983; and F. C. Meldrum, N. A. Kotov, and J. H.
  • a reducing agent is prepared by mixing solutions of sodium citrate and ferrous sulfate. This mixture is added to a solution of silver nitrate under vigorous stirring to form a blue-black precipitate which is recovered by centrifuging the solution.
  • An example for this procedure would be as follows: Preparation of reducing agent by mixing 3.5 ml of 40% Na 3 citrate.2H 2 O and 2.5 ml of freshly prepared 30% FeSO 4 .7H 2 O. This is added to 2.5 ml of 10% AgNO 3 solution to precipitate the nanosilver particles.
  • the invention can be practiced with a wide variety of metal and metal alloy powders.
  • the composition and technique are not limited to pure silver.
  • these metals are also of the precious metals type such as Au, Pt and Pd. They do have the effect of raising the firing temperature of the paste and melting point of the alloy, which could be necessary in some cases.
  • a small amount of the palladium (Pd) could be added to silver to prevent the silver migration.
  • Au can also be added to form a gold-silver alloy with still considerably high melting temperature.
  • Adhesion/bonding to the die and substrate can be enhanced with the addition of small amounts of a lower-melting temperature metal such as indium. If present in small amounts, the operating temperature will still be higher than high-temperature solder such as eutectic AuSn, yet can be processed at comparable temperature.
  • a lower-melting temperature metal such as indium. If present in small amounts, the operating temperature will still be higher than high-temperature solder such as eutectic AuSn, yet can be processed at comparable temperature.
  • Techniques that make use of the presence of indium in the bonding layer have been developed to form high-temperature joints but typically require long processing times (see, for example, R. W. Chuang and C. C. Lee, “Silver-Indium Joints Produced at Low Temperature for High Temperature Devices,” IEEE Transactions on Components and Packaging Technologies, 25 (3) (2002) pp 453-458).
  • the nanosilver particles 10 are preferably used in a paste which includes a dispersant 12 to disperse the silver particles 10 and prevent agglomeration, a binder 14 to prevent paste cracking during the handling and dry processing, and, in some instances, a thinner 16 to adjust the paste viscosity to allow for screen or stencil printing (the current practice of applying paste to substrates).
  • a dispersant 12 to disperse the silver particles 10 and prevent agglomeration
  • a binder 14 to prevent paste cracking during the handling and dry processing
  • a thinner 16 to adjust the paste viscosity to allow for screen or stencil printing (the current practice of applying paste to substrates).
  • a wide variety of dispersants 12 can be used in the practice of the invention including fatty acids, fish oils, poly(diallyldimethyl ammonium chloride)(PDDA), polyacrylic acid (PAA), polystyrene sulfonate (PSS), etc.
  • the dispersant 12 can associate a polar head group with the surface of a nanosilver particle 10 by hydrogen bonding or other means, and the hydrophobic tail serves to space adjacent particles apart from one another and prevent agglomeration. Agglomeration leads to low solid loading and ultimately interconnections of poor electrical, thermal or mechanical properties.
  • the preferred binder 14 may be a low boiling organic, such as terpineol (bp of 220° C.) that enables unhindered densification of the powder at up to 300° C.
  • suitable binders 14 include, for example, polyvinyl alcohol (PVA), polyvinyl butyral (PVB), and wax.
  • PVA polyvinyl alcohol
  • PVB polyvinyl butyral
  • the properties of the binder 14 e.g., volatilization temperature
  • the binder 14 need to match the sintering kinetics of the nanopowder (i.e., the binder must boil, vaporize, or otherwise decompose below the sintering temperature) and the temperature limitations imposed by the device being attached.
  • binder 14 can be used to assure more uniform sintering of the particles.
  • a thinner 16 such as RV 912 from Heraus, Inc. may be added.
  • terpineol may be used as the thinner 16 .
  • the choice of thinner is wide ranging, and will depend on the needs of the fabricator, the choice of materials, and other factors.
  • Suitable thinners may include Haraeus HVS 100, texanol, terpineol, Heraeus RV-372, Heraeus RV-507, etc.
  • the volatilization temperature of the thinner 16 should match the sintering kinetics of the metal particles 10 .
  • the total binder 14 and thinner 16 addition will vary depending on the application and may constitute, for example, up to 20% by weight or more (in certain embodiments, the preferred weight percentage is between 5-20%).
  • FIG. 2 shows a two step procedure for formulating a nano-scale metal paste which may be used in the present invention.
  • Commercially obtained metal particles 20 of a size less than 500 nm and most preferably less than 100 nm in diameter, are combined with a fish oil or other suitable dispersant 22 that has been dissolved in acetone 24 .
  • the powder 26 is combined with a solution 27 which includes binder 28 dispersed or dissolved in a carrier such as a thinner, which ultimately yields a paste 30 that includes the metal particles dispersed in the binder material.
  • Dispersion of the metal particles can be aided by immersion in an ultrasonic bath using a room temperature or cold water bath to prevent heating and sintering of the metal powder. Additionally, mechanical mechanisms for stirring, vibrating, etc., can be used to assist in dispersing the metal particles in the binder.
  • excess acetone can significantly aid in a fatty acid dispersant dispersing silver particles during ultrasonic treatment. Further, the nonpolar acetone is easily separated from a mixture of silver plus fatty acid without a centrifuge.
  • the process of FIG. 2 has the advantage of making control of paste quality easier since the particle dispersing step is separate from the paste quality adjustment.
  • FIG. 2 illustrates the dissolved dispersant being combined with the metal particles
  • the particles made by the Carey Lea method described above may have citrate moieties hydrogen bonded to the surface, and the citrate may serve as a dispersant.
  • the citrate moieties may be displaced by a longer chain fatty acid or fish oil dispersant in a manner similar to that shown in FIG. 2 .
  • FIG. 3 illustrates an exemplary process for attaching electronic components to substrates in the practice of the invention.
  • a nanoscale silver powder 32 is combined with polymers 34 to form a nanoscale silver paste 36 .
  • dispersing the silver powder in the binder can be enhanced or augmented by ultrasonic methods.
  • the nanoscale silver powder 32 can be converted to a paste 36 form by the addition of an organic solvent with a low boiling point (e.g., terpineol) and thinner (e.g., RV 912 from Heraeus).
  • an organic solvent with a low boiling point e.g., terpineol
  • thinner e.g., RV 912 from Heraeus
  • Electronic devices 38 such as silicon or wide bandgap devices, can be joined to substrates 40 by sintering the nanopowder paste 36 to form a solid bond layer between the devices 38 and mounting substrate 40 .
  • the process shown in FIG. 3 may be employed with silver particles, silver alloys, as well as other metals and metal alloys.
  • Gold and silver plating can be used to improve the interconnection in the practice of this invention.
  • a thin coating of gold or silver can be applied to the bonding site and/or contacts on the device (not shown) prior to screening, stenciling or printing the nanoscale silver past 36 . Utilizing a coating of silver or gold will not pose a significant deviation from current practices since the copper substrates in the current commercially available high-performance electronic packages usually are gold coated already.
  • the methodology of joining electrical devices 38 to substrates 40 is similar to conventional metal paste firing techniques such as those performed for hybrid electronic packages.
  • the firing temperature due to the size of the metal particles (nano scale (preferably less than 100 nm in diameter) as opposed to micrometer sized), is preferably comparable to solder reflow, and, if required, only a moderate applied force may be necessary to maintain intimate contact with the sintering metal powder layer.
  • the nanoscale metal paste is typically screen or stencil printed on the substrate in the form of a thick film (e.g., 20 to 100 micrometers thick) pattern onto which the device is mounted.
  • the die may be pushed down with a moderate force and held in place while sintering takes place.
  • the sintering time and temperature will vary. In many applications, the sintering temperature will be at least 250° C. and the duration will generally be 2 minutes or longer. Sintering can be carried out in a conventional belt oven in a semi-continuous operation or in a box oven/furnace in a batch type operation.
  • FIG. 3 shows the electrical devices 38 mechanically affixed to the substrate 40 in electrical contact with traces or other contacts after the low temperature sintering operation.
  • the interconnect formed by the process is a dense, conductive metal which can operate at temperatures that are much higher than those used for sintering (e.g., on the order of 600° C., 700° C. or 900° C. or more).
  • Silver compares favorably with other known interconnect materials such as solder and silver-filled conductive epoxy.
  • Eutectic Pb—Sn solder is used in the vast majority of interconnections although lead-free alternatives are gaining ground.
  • the eutectic AuSn is often recommended because they can go to higher temperatures than Pb-based or Sn-based solders.
  • LED light emitting diodes
  • Silver-filled conductive epoxies are currently used for silicon device interconnect applications.
  • conductive epoxy is used in International Rectifier's DirectFETTM to secure the silicon dice to a copper cavity. The properties of these materials are listed in Table 1 and some are also shown in FIGS.
  • Nanoscale silver as used in the practice of the present invention instead of micron-size silver is primarily to lower the sintering temperature to the processing range of most solders. This allows it to be used as a drop-in replacement for these interconnect materials.
  • the sintering temperature is sensitive to the size and morphology of the particles. Silver, which has a very high diffusion rate, is particularly attractive because it can be sintered at well below its melting temperature (962° C.) if the particle size is made small enough.
  • Current silver paste materials must be fired to above 600° C. to obtain reasonable strength and density. The prescribed firing schedule is usually to take the paste to around 900° C. to densify it.
  • the nanoscale silver paste of the present invention where the silver particle is less than 100 nm in size, it can undergo densification starting at as low as 100° C. (although this is not the desirable temperature range).
  • the onset of sintering can be delayed until such time that the preferred firing temperature is reached ( ⁇ 280 to 300° C.) to enable very fast densification rates and attain not only high density, but also good adhesion onto the device and substrate. Therefore, in addition to the reduction in particle size, an important ingredient to the usability of the paste is the selection of the dispersant and binder system that can be volatilized and burned off just below the sintering temperature. If the binder system leaves the paste too early, the silver nanoparticles will start sintering at a lower temperature, and consequently with reduced kinetics, the activation of a non-densifying mechanism, e.g.
  • a top size of 500 nm (a size that is not traditionally in the size range considered as “nanoscale”) is a practical limit for this technique because the sintering temperature will rise accordingly, which could go beyond the desired range and, of course, will no longer be suitable as a solder drop-in replacement.
  • FIGS. 4 a - b show that the nano-silver pastes of the present invention provide superior relative electrical conductivity and thermal conductivity compared to eutectic PbSn, eutectic AuSn, and conductive epoxy.
  • FIG. 4 c shows that the elastic modulus of the sinter nano-silver paste is satisfactory for interconnect applications.
  • FIGS. 5 a and 5 b are SEM images of silver pastes sintered at 300° C. for 10 minutes.
  • FIG. 5 a shows an SEM image of a sintered nanoscale silver paste according to the present invention
  • FIG. 5 b shows an SEM image of a sintered commercially available silver paste which includes micrometer sized silver (Heraeus C1075).
  • FIG. 5 a shows that a relatively high density (approximately 80%) results from sintering a nanoscale silver paste at 300° C. for ten minutes, which is about two times the green density (silver powder loading only before sintering; organics are not included).
  • FIG. 5 b shows that the commercial paste with the micrometer sized silver fired under the same condition.
  • the microstructure is very porous, and there is minimal densification.
  • the only change in the structure in FIG. 5 b is the elimination of the sharp contacts. The annealing out of these features makes the paste difficult to densify.
  • FIG. 6 presents a graph obtained from the web site of a commercial supplier of silver powder (see Ferro's web site) which presents the shrinkage of silver powder of various sizes with increasing temperature.
  • solders are currently used for high-temperature semiconductor device interconnect applications.
  • eutectic Au80Sn20 solder can be reflowed at 310-330° C. and used at a temperature below its melting point 280° C.
  • the major differences between the solder reflow and the nanoscale silver paste sintering of the present invention include:
  • solder is processed by heating the alloy above its melting temperature to form the bond.
  • the alloy undergoes melting and solidification after the completion of the procedure known as solder reflow.
  • the requirement to melt the alloy means that only those with low melting points are suitable. This restriction also limits the maximum operating temperature of the joint to below the melting point.
  • Conductive epoxy is hardened by curing above room temperature to induce the epoxy to undergo a setting reaction. While the process temperature is low and no melting is involved, the maximum working temperature is limited by the decomposition temperature of the epoxy component, which is in the range of the curing temperature.
  • the sintering temperature of silver can be drastically reduced if micrometer-size particles are replaced by nanoscale particles. It is then possible to lower the sintering temperature to that of the reflow temperature of many solder alloys.
  • silver/silver alloy pastes contain micrometer-size silver (silver particles larger than 500 nm in size and typically on the order of 10-100 ⁇ m in size). Typically, these pastes have to be fired to a high temperature approaching the melting point of the alloy to achieve high density. For example, the recommended firing profile of silver paste is to heat it to around 900° C. (although it is possible to obtain reasonably high density for mechanical strength at lower temperatures, e.g. 700° C.). They are most often used to form conductive traces/patterns (package substrates) and electrodes (capacitors) for various electronics applications. They are not typically used for forming interconnects between devices and substrates, as is proposed in the present application.
  • results for pressure-assisted sintering of commercially available silver paste are summarized in Table 2.
  • a reasonably high density (80%) can be attained only if the external pressure on the joint is dramatically increased. This is also accompanied by substantial increases on some key parameter values of the sintered Ag joint such as electrical conductivity, thermal conductivity and shear strength.
  • the nanoscale silver paste of this invention (less than 500 nm and more preferably less than 100 nm in size), it is not necessary to apply such a high pressure to induce sintering and bonding, thus making it a potential drop-in replacement for solder and/or epoxy for die attachment and electrical interconnection.
  • the pressure used before the silver sintering with the silver paste of the present invention may be used only for better initial interface contacts, and it is recommended that this pressure not exceed 0.1 Mpa so that the silver paste does not get squeezed out (this procedure is very common on solder reflow die-attaching).
  • TABLE 2 Effect of pressure on the properties of sintered silver paste with micrometer-size silver. The pastes were fired at 240° C. for 5 min. Applied pressure Properties 10 MPa 40 MPa Relative Density 57% 80% Electrical conductivity 2.6 ⁇ 10 5 4.2 ⁇ 10 5 ( ⁇ ⁇ cm) ⁇ 1 Thermal conductivity 30 78 W/K-m Shear Strength 15 50 MPa
  • Regulation of the densification temperature/rate of the metal particles in the paste of this invention can be achieved by adjusting the type of components that go into the binder system.
  • this can be achieved by substituting the binder system components with alternatives that burn out at higher temperatures to closely match the desired or target peak processing temperature (e.g., the binder system might be chosen to vaporize or otherwise decompose at a temperature that is the same as or slightly below (e.g., within 50° C. or 30° C. or 10° C.) the sintering temperature for the metal or metal alloy particles.
  • the peak processing temperature need not be limited to 300° C. or below.
  • silicon carbide may be attached at temperatures as high as 600° C. using gold or its alloy(s) but with contact pad problems when fired in air.
  • the present technique can be used to make a paste that can be fired at a higher temperature to attain higher density and stronger bonding (but still lower than 600° C. since it is desired to retain the nanosilver particles until the sintering temperature).
  • An illustrative example of this technique is shown in FIGS. 7 a - 7 b where a nanosilver paste containing 100 nm particles and fatty acids of different carbon chain lengths (hence different burnout temperatures) was sintered at 450° C.

Abstract

A paste including metal or metal alloy particles (which are preferably silver or silver alloy), a dispersant material, and a binder is used to form an electrical, mechanical or thermal interconnect between a device and a substrate. By using nanoscale particles (i.e., those which are less than 500 nm in size and most preferably less than 100 nm in size), the metal or metal alloy particles can be sintered at a low temperature to form a metal or metal alloy layer which is desired to allow good electrical, thermal and mechanical bonding, yet the metal or metal alloy layer can enable usage at a high temperature such as would be desired for SiC, GaN, or diamond (e.g., wide bandgap devices). Furthermore, significant application of pressure to form the densified layers is not required, as would be the case with micrometer sized particles. In addition, the binder can be varied so as to insulate the metal particles until a desired sintering temperature is reached; thereby permitting fast and complete sintering to be achieved.

Description

    BACKGROUND OF THE INVENTION
  • 1. Field of the Invention
  • The present invention generally relates to materials used for interconnecting electronic devices and, particularly, devices which either generate high temperatures during use or devices which are used in high temperature applications. Furthermore, the invention is generally related to a fabrication method which reduces or eliminates the need for high pressure application during fabrication of an interconnection, such as during die attach.
  • 2. Background Description
  • All semiconductor chips have to be fastened or attached to a substrate to function in an electronic product. The state-of-the-art technology for interconnecting these chips typically uses a lead or lead-free solder alloy, or a conductive polymeric glue, such as an epoxy. However, these materials have poor thermal properties and do not dissipate the heat generated by the chips. They also have poor electrical properties and fail to effectively reduce loss of electrical power, and poor robustness for mechanical strength and reliability. Furthermore, because of the low melting temperatures of solder alloys and low decomposition temperatures of epoxies, these materials may not be generally suitable for allowing some chips, such as SiC or GaN chips, to function at high temperatures.
  • Sintering of microscale metal powder paste is commonly used in hybrid electronic packages for producing electrical circuit patterns. However, the high processing temperatures (>600° C.) prevents its use in joining electronic components to substrates. The current practice is to use solder that is reflowed at temperatures low enough for the devices to withstand. The advantage of low melting temperatures becomes a liability for solder alloys because they cannot meet the requirements of high temperature operation or use in high temperature applications. Furthermore, solder materials have relatively poor electrical and thermal properties, and poor fatigue resistance, compared to other metals such as copper and silver, which detrimentally affect the performance of the whole electronic system.
  • Pressure-assisted sintering using commercial silver metal paste to attach electronic components was discussed in Zhang et al., “Pressure-Assisted Low-Temperature Sintering of Silver Paste as an Alternative Die-Attach Solution to Solder Reflow”, IEEE Transactions on Electronics Packaging Manufacturing, vol. 25, no. 4, October, 2002 (pp 279-283); and Zhang et al., “Pressure-Assisted Low Temperature Sintering of Silver Paste as an Alternative Die-Attach Solution to Reflow”, The Fifth International IEEE Symposium on High Density Packaging and Component Failure Analysis in Electronics Manufacturing (HDP 2002) The metal powder in commercial silver metal paste typically has a particle size in the micrometer range. Because of the large particle size, a high sintering temperature is required (600° C. and up) under normal firing conditions. At reduced firing temperature, a large pressure is applied on the assembly to assist the sintering process. However, the application of pressure can be undesirable because of increased difficulty in manufacturing with a corresponding increase in the production cost. Applying pressure also increases the likelihood of damage to the device during processing.
  • SUMMARY OF THE INVENTION
  • It has been discovered that by using very fine conductive metal and metal alloy particles on the order of 500 nm or less, and most preferably on the order of 100 nm or less (e.g., 1-100 nm), densified metallic interconnections can be established by relatively low temperature sintering with reduced or no pressure application being required. The materials of this invention can be applied and processed like a solder paste or epoxy (e.g., dispensing, stencil/screen printing, etc.). However, the thermal, electrical and mechanical properties of the joint formed with the fine powders and compositions thereof are far superior to those of traditional lead or lead free solders, epoxy materials, and even micron sized powders (sintered at low temperature).
  • By using metal particles in the nanoscale range, it is possible to both reduce the bonding temperature (i.e., the sintering temperature in the context of the present invention), and to eliminate or reduce the need for high applied pressure. Without the need for high applied pressure, it is thus possible to make use of existing hybrid microelectronics processing techniques and fabrication equipment and, therefore, enable mass manufacturing of such components. The nanopowder of the present invention can be prepared using known techniques, or purchased directly at a price comparable to that that of micron-size powder. A dispersant is preferably used for reducing agglomeration of the particles which could lead to undesirable/low silver particle loading during mixing of the paste. The nanopowder of the present invention, preferably together with the dispersant, can be combined with a polymer binder that preferably has a volatilization temperature below the desired sintering temperature. Using a binder that preferably does not volatilize until close to the sintering temperature for the metal or metal alloy powder, assists in achieving denser interconnections since sintering occurs more uniformly throughout the composition (i.e., the binder is preferably chosen and formulated into the composition such that the metal or metal alloy powder on the edges closer to the source of heat does not start to fuse with neighboring particles until the bulk of the particles begins to fuse). Dispersion of the metal or metal alloy powder in the binder can be facilitated by ultrasonic or mechanical or methods, or combinations of the same.
  • The compositions of the present invention have a wide range of applications. For example, they can be used to bond silicon integrated circuit chips in computers, or silicon power chips in power supplies, or optoelectronic chips in telecommunications modules. Also, in the case of silver powder, and silver alloys, where the metal melts at temperatures over 700° C. or 800° C., the invention is suitable for attaching semiconductor chips that can be operated at high temperatures, e.g., SiC or GaN power chips. That is, by sintering silver or silver alloy that is in the form of a nanopowder (one that is less than 500 nm in size, and most preferably below 100 nm in size) at a relatively low temperatures (e.g., on the order of 300° C., a dense, conductive metal interconnection is achieved that can be operated at high temperatures without risking melting of the interconnect, as would be the case with commercial lead and lead free solders as well as conductive epoxies. The ability to allow these chips to operate at a high temperatures cuts down their cooling requirement, leading to savings in materials and energy in the manufacture and operations of the product.
  • The nanosilver paste of this invention, due to its high melting temperature and low processing temperature, is also useful for applications other than the attachment of silicon devices and heatsinks. It may be used to attach/interconnect wide bandgap devices that need to operate at elevated temperature such as SiC, GaN and diamond. It is also useful for attaching devices that generate substantial amounts of heat such as light-emitting diodes (LED) and semiconductor lasers.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • The foregoing and other objects, aspects and advantages will be better understood from the following detailed description of a preferred embodiment of the invention with reference to the drawings, in which:
  • FIG. 1 is a schematic view of metal particles (e.g., nanosilver particles formed as a paste utilizing dispersants to prevent agglomeration and binder to prevent paste cracking during handling and dry processing;
  • FIG. 2 is a schematic view showing an exemplary two step procedure for formulating a nano scale metal particle paste for use in the present invention;
  • FIG. 3 is a schematic view showing the use of metal paste according to the invention for attachment of devices to a substrate;
  • FIGS. 4 a-c are graphs showing a comparison of the relative electrical conductivity, relative thermal conductivity, and elastic modulus, respectively, of a various prior art interconnect materials and the interconnect material of the present invention;
  • FIGS. 5 a-b are SEM images of the nanoscale silver paste of the present invention and the commercial silver paste (Heraeus C1075) that has micrometer-sized silver, respectively after the pastes are sintered at 300° C. for ten minutes;
  • FIG. 6 is a graph showing the expansion/shrinkage curves for different particle sizes of silver that are to be sintered; and
  • FIGS. 7 a and 7 b show SEM images of 100 nm silver particles formulated respectively with higher burn out temperature PVB and fatty acid dispersants, and lower burnout temperature PRV914.
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS OF THE INVENTION
  • It has been discovered that sintering a nanoscale metal paste is a viable solution to forming electrical interconnect because it enables circumventing the requirements of a high processing temperature and high processing pressure which are required with micrometer sized metal powder. Preferably, the metal powder in the nanoscale metal paste has a particle size less than 500 nm, and most preferably, the particle size is less than 100 nm (e.g., 1-100 nm or 1-60 nm, etc.).
  • The preferred metal or metal alloy within the practice of this invention is a silver or silver alloy. This is because of a combination of low cost, as compared to gold, and the amenability of being fired in ordinary atmosphere. While it is processed at temperatures comparable to that of solder reflow, it can withstand subsequent exposure to higher temperature, which solder cannot.
  • Suitable nanosilver powder (e.g., less than 500 or 100 nm in particle size) is commercially available from various suppliers in various sizes at a cost of roughly $1/gram. Exemplary commercial suppliers include Nanostructured & Amorphous Materials, Inc., Inframat Advanced Materials, Inc., Sumitomo electric U.S.A., Inc., and Kemco International Associates. Nanosilver powder has been used in a variety of applications. For example, silver can be used as an antibacterial additive to fabric products such as carpets, napkins and surgical masks. Silver has been medically proven to kill a wide range of disease causing organisms in the body and is also relatively safe. For this reason, numerous vendors tout the use of silver colloid for attacking bacterial organisms in the body. Samsung also uses silver nanoparticles to enhance food preservation in its refrigerator product lines. Silver nanopowder is also being used as an additive in consumer products such as toothpaste, toothbrush, and soap, as well as socks because of the antibacterial property. In electronic applications, silver nanopowder is being sold for use in conductive traces, resistors, electrodes, optical filters and EMI-shielding (its application to the creation of an interconnect by sintering at low temperatures for use in high temperature applications being heretofore unrecognized until the invention described herein). Nanosilver particles are also used as a coloring additive in paints, glass, ink, and cosmetics.
  • Suitable nanosilver pastes having application in the present invention may also be produced using a modified Carey Lea method. The Carey Lea method was first applied to making photographic emulsions. However, a modified process can be used to synthesize nanosilver particles (see, for example, S. M. Heard, F. Grieser, C. G. Barraclough and J. V. Sanders, J. Colloid Interface Sci. 93 (2): 545-555 1983; and F. C. Meldrum, N. A. Kotov, and J. H. Fendler, “Utilization of surfactant-stabilized colloidal silver nanocraystallites in the constructruction of mono- and multiparticulate Langmuir-Boldgett films”, Langmuir 10(7): 2035-2040, 1994). In this technique, a reducing agent is prepared by mixing solutions of sodium citrate and ferrous sulfate. This mixture is added to a solution of silver nitrate under vigorous stirring to form a blue-black precipitate which is recovered by centrifuging the solution. An example for this procedure would be as follows: Preparation of reducing agent by mixing 3.5 ml of 40% Na3citrate.2H2O and 2.5 ml of freshly prepared 30% FeSO4.7H2O. This is added to 2.5 ml of 10% AgNO3 solution to precipitate the nanosilver particles.
  • It will be apparent to those of skill in the art that the invention can be practiced with a wide variety of metal and metal alloy powders. And, in particular, in the case of the preferred silver powder, the composition and technique are not limited to pure silver. In fact, it is common practice to modify the alloy composition and paste components to make them suitable for a wide variety of applications. Often these metals are also of the precious metals type such as Au, Pt and Pd. They do have the effect of raising the firing temperature of the paste and melting point of the alloy, which could be necessary in some cases. A small amount of the palladium (Pd) could be added to silver to prevent the silver migration. Au can also be added to form a gold-silver alloy with still considerably high melting temperature. Adhesion/bonding to the die and substrate can be enhanced with the addition of small amounts of a lower-melting temperature metal such as indium. If present in small amounts, the operating temperature will still be higher than high-temperature solder such as eutectic AuSn, yet can be processed at comparable temperature. Techniques that make use of the presence of indium in the bonding layer have been developed to form high-temperature joints but typically require long processing times (see, for example, R. W. Chuang and C. C. Lee, “Silver-Indium Joints Produced at Low Temperature for High Temperature Devices,” IEEE Transactions on Components and Packaging Technologies, 25 (3) (2002) pp 453-458).
  • With reference to FIG. 1, the nanosilver particles 10 are preferably used in a paste which includes a dispersant 12 to disperse the silver particles 10 and prevent agglomeration, a binder 14 to prevent paste cracking during the handling and dry processing, and, in some instances, a thinner 16 to adjust the paste viscosity to allow for screen or stencil printing (the current practice of applying paste to substrates). A wide variety of dispersants 12 can be used in the practice of the invention including fatty acids, fish oils, poly(diallyldimethyl ammonium chloride)(PDDA), polyacrylic acid (PAA), polystyrene sulfonate (PSS), etc.
  • As shown in FIG. 1, in the case of a fatty acid or fish oil, the dispersant 12 can associate a polar head group with the surface of a nanosilver particle 10 by hydrogen bonding or other means, and the hydrophobic tail serves to space adjacent particles apart from one another and prevent agglomeration. Agglomeration leads to low solid loading and ultimately interconnections of poor electrical, thermal or mechanical properties.
  • The preferred binder 14 may be a low boiling organic, such as terpineol (bp of 220° C.) that enables unhindered densification of the powder at up to 300° C. Examples of other suitable binders 14 include, for example, polyvinyl alcohol (PVA), polyvinyl butyral (PVB), and wax. The properties of the binder 14 (e.g., volatilization temperature) need to match the sintering kinetics of the nanopowder (i.e., the binder must boil, vaporize, or otherwise decompose below the sintering temperature) and the temperature limitations imposed by the device being attached. As will be discussed in more detail below (see for example, Comparative Example 1 and Example 1), judicious selection of or formulation of binder 14 can be used to assure more uniform sintering of the particles. To reduce viscosity of the paste, which may be required for enabling stenciling and other operations to be performed, a thinner 16, such as RV 912 from Heraus, Inc. may be added. Depending on the choice of binder 14, terpineol may be used as the thinner 16. The choice of thinner is wide ranging, and will depend on the needs of the fabricator, the choice of materials, and other factors. Suitable thinners may include Haraeus HVS 100, texanol, terpineol, Heraeus RV-372, Heraeus RV-507, etc. As with the binder 14, the volatilization temperature of the thinner 16 should match the sintering kinetics of the metal particles 10. The total binder 14 and thinner 16 addition will vary depending on the application and may constitute, for example, up to 20% by weight or more (in certain embodiments, the preferred weight percentage is between 5-20%).
  • FIG. 2 shows a two step procedure for formulating a nano-scale metal paste which may be used in the present invention. Commercially obtained metal particles 20, of a size less than 500 nm and most preferably less than 100 nm in diameter, are combined with a fish oil or other suitable dispersant 22 that has been dissolved in acetone 24. This yields a free flowing powder (non-agglomerated) 26 of particles that have dispersant associated on their surfaces. The powder 26 is combined with a solution 27 which includes binder 28 dispersed or dissolved in a carrier such as a thinner, which ultimately yields a paste 30 that includes the metal particles dispersed in the binder material. Dispersion of the metal particles can be aided by immersion in an ultrasonic bath using a room temperature or cold water bath to prevent heating and sintering of the metal powder. Additionally, mechanical mechanisms for stirring, vibrating, etc., can be used to assist in dispersing the metal particles in the binder. In the process shown in FIG. 2, excess acetone can significantly aid in a fatty acid dispersant dispersing silver particles during ultrasonic treatment. Further, the nonpolar acetone is easily separated from a mixture of silver plus fatty acid without a centrifuge. The process of FIG. 2 has the advantage of making control of paste quality easier since the particle dispersing step is separate from the paste quality adjustment.
  • While FIG. 2 illustrates the dissolved dispersant being combined with the metal particles, it should be understood that the particles made by the Carey Lea method described above may have citrate moieties hydrogen bonded to the surface, and the citrate may serve as a dispersant. Alternatively, the citrate moieties may be displaced by a longer chain fatty acid or fish oil dispersant in a manner similar to that shown in FIG. 2.
  • FIG. 3 illustrates an exemplary process for attaching electronic components to substrates in the practice of the invention. Initially, a nanoscale silver powder 32 is combined with polymers 34 to form a nanoscale silver paste 36. As discussed in conjunction with FIGS. 1 and 2, dispersing the silver powder in the binder can be enhanced or augmented by ultrasonic methods. The nanoscale silver powder 32 can be converted to a paste 36 form by the addition of an organic solvent with a low boiling point (e.g., terpineol) and thinner (e.g., RV 912 from Heraeus). Electronic devices 38, such as silicon or wide bandgap devices, can be joined to substrates 40 by sintering the nanopowder paste 36 to form a solid bond layer between the devices 38 and mounting substrate 40. The process shown in FIG. 3 may be employed with silver particles, silver alloys, as well as other metals and metal alloys.
  • Gold and silver plating can be used to improve the interconnection in the practice of this invention. For example, to prevent copper oxidation, since copper oxide cannot form a good bond with silver by interdiffusion, a thin coating of gold or silver can be applied to the bonding site and/or contacts on the device (not shown) prior to screening, stenciling or printing the nanoscale silver past 36. Utilizing a coating of silver or gold will not pose a significant deviation from current practices since the copper substrates in the current commercially available high-performance electronic packages usually are gold coated already.
  • Except for the low temperature preferably used in the practice of this invention, the methodology of joining electrical devices 38 to substrates 40 is similar to conventional metal paste firing techniques such as those performed for hybrid electronic packages. The firing temperature, due to the size of the metal particles (nano scale (preferably less than 100 nm in diameter) as opposed to micrometer sized), is preferably comparable to solder reflow, and, if required, only a moderate applied force may be necessary to maintain intimate contact with the sintering metal powder layer. As shown in FIG. 3, the nanoscale metal paste is typically screen or stencil printed on the substrate in the form of a thick film (e.g., 20 to 100 micrometers thick) pattern onto which the device is mounted. After device placement, the die may be pushed down with a moderate force and held in place while sintering takes place. Depending on the thickness of the film, the size of the particles, and the material of the particles (e.g., silver or silver alloy) the sintering time and temperature will vary. In many applications, the sintering temperature will be at least 250° C. and the duration will generally be 2 minutes or longer. Sintering can be carried out in a conventional belt oven in a semi-continuous operation or in a box oven/furnace in a batch type operation. FIG. 3 shows the electrical devices 38 mechanically affixed to the substrate 40 in electrical contact with traces or other contacts after the low temperature sintering operation. As will be discussed in more detail below, the interconnect formed by the process is a dense, conductive metal which can operate at temperatures that are much higher than those used for sintering (e.g., on the order of 600° C., 700° C. or 900° C. or more).
  • COMPARATIVE EXAMPLE 1
  • Nanoscale Silver Paste Versus Micrometer-Size Silver Paste
  • Silver compares favorably with other known interconnect materials such as solder and silver-filled conductive epoxy. Eutectic Pb—Sn solder is used in the vast majority of interconnections although lead-free alternatives are gaining ground. For higher-temperature applications such as bonding of light emitting diodes (LED) and semiconductor lasers, the eutectic AuSn is often recommended because they can go to higher temperatures than Pb-based or Sn-based solders. However, it is a far more expensive solution. Silver-filled conductive epoxies are currently used for silicon device interconnect applications. For example, conductive epoxy is used in International Rectifier's DirectFET™ to secure the silicon dice to a copper cavity. The properties of these materials are listed in Table 1 and some are also shown in FIGS. 4 a-c.
    TABLE 1
    Property comparison of some common interconnect materials with
    the sintered nanosilver paste of the present invention.
    Reflowed Reflowed Silver filled Sintered
    eutectic PbSn eutectic AuSn conductive nanosilver
    solder solder epoxy paste
    Composition (wt %) 37Pb63Sn 80Au20Sn Silver filler and Pure Ag
    resin and
    hardener
    Density 8.47 g/cm3 14.7 g/cm3 ˜3 g/cm3 8.58 g/cm3
    (˜80% of bulk
    Ag due to
    porosity)
    Bonding mechanism Liquidus reflow Liquidus reflow Epoxy curing Sintering/solidus
    interdiffusion
    Peak processing  210° C.  310° C. ˜150° C.  280° C.
    temperatures
    Application <180° C. <280° C. <150° C. <900° C.
    temperature range
    Electrical conductivity 0.69 × 105 (Ω-cm)−1 0.62 × 105 (Ω-cm)−1 ˜0.1 × 105 (Ω-cm)−1 2.6 × 105 (Ω-cm)−1
    Thermal conductivity 51 (W/K-m) 58 (W/K-m) 0.1 (W/K-m) 240 (W/K-m)
    Young's modulus 16 GPa (hard) 68 GPa (hard) <1 GPa (soft) 7 GPa
    Joint Strength N/A 50 Mpa 5-40 MPa >20 MPa
    CTE 25 (PPM/° C.) 16 (PPM/° C.) ˜25 (PPM/° C.) 19 (PPM/° C.)
    Tensile/shear >27 Mpa 275/275 Mpa ˜10/10 MPa 43 MPa
    strength
    Price estimate $0.1/gram $40/gram $4/gram $4/gram
  • Nanoscale silver as used in the practice of the present invention instead of micron-size silver is primarily to lower the sintering temperature to the processing range of most solders. This allows it to be used as a drop-in replacement for these interconnect materials. The sintering temperature is sensitive to the size and morphology of the particles. Silver, which has a very high diffusion rate, is particularly attractive because it can be sintered at well below its melting temperature (962° C.) if the particle size is made small enough. Current silver paste materials must be fired to above 600° C. to obtain reasonable strength and density. The prescribed firing schedule is usually to take the paste to around 900° C. to densify it. However, in the case of the nanoscale silver paste of the present invention where the silver particle is less than 100 nm in size, it can undergo densification starting at as low as 100° C. (although this is not the desirable temperature range).
  • With the addition of the proper types of dispersant, binder, and solvent, the onset of sintering can be delayed until such time that the preferred firing temperature is reached (˜280 to 300° C.) to enable very fast densification rates and attain not only high density, but also good adhesion onto the device and substrate. Therefore, in addition to the reduction in particle size, an important ingredient to the usability of the paste is the selection of the dispersant and binder system that can be volatilized and burned off just below the sintering temperature. If the binder system leaves the paste too early, the silver nanoparticles will start sintering at a lower temperature, and consequently with reduced kinetics, the activation of a non-densifying mechanism, e.g. surface diffusion, occurs resulting in a microstructure that is difficult to densify even at the higher targeted sintering temperature. If the binder system components burn off at a temperature higher than the desired firing temperature, the silver particles will not sinter properly because the polymer components will prevent the widespread contact between particles. A top size of 500 nm (a size that is not traditionally in the size range considered as “nanoscale”) is a practical limit for this technique because the sintering temperature will rise accordingly, which could go beyond the desired range and, of course, will no longer be suitable as a solder drop-in replacement. Most of the experimental work performed to date and reported herein, other than commercial Ag paste, has been performed on powder 100 nm or smaller.
  • FIGS. 4 a-b show that the nano-silver pastes of the present invention provide superior relative electrical conductivity and thermal conductivity compared to eutectic PbSn, eutectic AuSn, and conductive epoxy. FIG. 4 c shows that the elastic modulus of the sinter nano-silver paste is satisfactory for interconnect applications.
  • FIGS. 5 a and 5 b are SEM images of silver pastes sintered at 300° C. for 10 minutes. FIG. 5 a shows an SEM image of a sintered nanoscale silver paste according to the present invention, while FIG. 5 b shows an SEM image of a sintered commercially available silver paste which includes micrometer sized silver (Heraeus C1075). FIG. 5 a shows that a relatively high density (approximately 80%) results from sintering a nanoscale silver paste at 300° C. for ten minutes, which is about two times the green density (silver powder loading only before sintering; organics are not included). FIG. 5 b shows that the commercial paste with the micrometer sized silver fired under the same condition. However, the microstructure is very porous, and there is minimal densification. Specifically, the only change in the structure in FIG. 5 b is the elimination of the sharp contacts. The annealing out of these features makes the paste difficult to densify.
  • FIG. 6 presents a graph obtained from the web site of a commercial supplier of silver powder (see Ferro's web site) which presents the shrinkage of silver powder of various sizes with increasing temperature. The data in this graph, along with the experiments presented herein, demonstrate that the nanoscale silver paste of the present invention can be sintered at lower temperatures with decreasing size.
  • COMPARATIVE EXAMPLE 2
  • Comparison of Process for Different Types of Interconnect Materials
  • Some high-temperature-melting solders are currently used for high-temperature semiconductor device interconnect applications. For example, eutectic Au80Sn20 solder can be reflowed at 310-330° C. and used at a temperature below its melting point 280° C. The major differences between the solder reflow and the nanoscale silver paste sintering of the present invention include:
  • 1) Solder is processed by heating the alloy above its melting temperature to form the bond. The alloy undergoes melting and solidification after the completion of the procedure known as solder reflow. The requirement to melt the alloy means that only those with low melting points are suitable. This restriction also limits the maximum operating temperature of the joint to below the melting point.
  • 2) Conductive epoxy is hardened by curing above room temperature to induce the epoxy to undergo a setting reaction. While the process temperature is low and no melting is involved, the maximum working temperature is limited by the decomposition temperature of the epoxy component, which is in the range of the curing temperature.
  • 3) Attachment/interconnection by nanosilver paste, according to the present invention, is achieved through a sintering process wherein the silver nanoparticles undergo consolidation through diffusion processes rather than by melting. By doing so, high processing temperature is avoided. On the other hand, because the melting point of bulk silver is much higher than the sintering temperature of nanosilver particles, the interconnections can be operated at temperatures higher than the processing temperature. In sum, the nanopowder sintering technique of this invention is a low-temperature bonding solution for high-temperature applications. The sintering temperature can be reduced significantly by making the particle size of the powder smaller. As shown above and as is discussed in comparative example 3, the sintering temperature of silver can be drastically reduced if micrometer-size particles are replaced by nanoscale particles. It is then possible to lower the sintering temperature to that of the reflow temperature of many solder alloys.
  • COMPARATIVE EXAMPLE 3
  • Prior Art on the use of Silver Paste Containing Micrometer Sized Silver
  • Currently available commercial silver/silver alloy pastes contain micrometer-size silver (silver particles larger than 500 nm in size and typically on the order of 10-100 μm in size). Typically, these pastes have to be fired to a high temperature approaching the melting point of the alloy to achieve high density. For example, the recommended firing profile of silver paste is to heat it to around 900° C. (although it is possible to obtain reasonably high density for mechanical strength at lower temperatures, e.g. 700° C.). They are most often used to form conductive traces/patterns (package substrates) and electrodes (capacitors) for various electronics applications. They are not typically used for forming interconnects between devices and substrates, as is proposed in the present application. There are numerous vendors for these products such as DuPont, Heraeus, and Ferro. Silver paste has also been considered as a die-attach and interconnect material. To make it work, an external pressure is applied to the assembly (about 40 MPa) to lower the sintering temperature to 300° C. or lower (see, for example, H. Schwarzbauer, “Method of securing electronic components to a substrate,” U.S. Pat. No. 4,810,672; H. Schwarzbauer and R. Kuhnert, “Novel large Area jointing technique for improved power device performance”, IEEE Trans. Ind. Appl. 27 (1): 93-95, 1991; and Z. Zhang and G. Q. Lu, “Pressure-assisted low-temperature sintering of silver paste as an alternative die-attach solution to solder reflow”, IEEE Trans. Electron. Pack. Manu., 25 (4): 279-283, 2002), which is basically the maximum temperature a semiconductor device can be exposed to without destroying it. However, high applied pressure is not the norm in the packaging industry and could pose serious complications to the attachment/interconnection process, which in turn could lead to more failures (e.g., cracked die) and higher manufacturing costs. It may require major modifications to existing production lines, thus it may not be considered as a drop-in replacement for solder. The higher cost alone may discourage industry from adopting it.
  • Results for pressure-assisted sintering of commercially available silver paste (micrometer sized) are summarized in Table 2. A reasonably high density (80%) can be attained only if the external pressure on the joint is dramatically increased. This is also accompanied by substantial increases on some key parameter values of the sintered Ag joint such as electrical conductivity, thermal conductivity and shear strength. In contrast, with the nanoscale silver paste of this invention (less than 500 nm and more preferably less than 100 nm in size), it is not necessary to apply such a high pressure to induce sintering and bonding, thus making it a potential drop-in replacement for solder and/or epoxy for die attachment and electrical interconnection. In practice, the pressure used before the silver sintering with the silver paste of the present invention may be used only for better initial interface contacts, and it is recommended that this pressure not exceed 0.1 Mpa so that the silver paste does not get squeezed out (this procedure is very common on solder reflow die-attaching).
    TABLE 2
    Effect of pressure on the properties of sintered
    silver paste with micrometer-size silver. The pastes
    were fired at 240° C. for 5 min.
    Applied pressure
    Properties
    10 MPa 40 MPa
    Relative Density 57% 80%
    Electrical conductivity 2.6 × 105 4.2 × 105
    (Ω · cm)−1
    Thermal conductivity 30 78
    W/K-m
    Shear Strength 15 50
    MPa
  • EXAMPLE 1
  • Method for Regulating the Densification of Silver by Binder System Composition
  • Regulation of the densification temperature/rate of the metal particles in the paste of this invention can be achieved by adjusting the type of components that go into the binder system. In particular, it is possible to increase or reduce the firing temperature for any given particle size of the silver (or other metal or metal alloy). For example, if it is desired to increase the effective onset of densification of, for example, a nanosilver paste as discussed above, this can be achieved by substituting the binder system components with alternatives that burn out at higher temperatures to closely match the desired or target peak processing temperature (e.g., the binder system might be chosen to vaporize or otherwise decompose at a temperature that is the same as or slightly below (e.g., within 50° C. or 30° C. or 10° C.) the sintering temperature for the metal or metal alloy particles. This has the added benefit of retaining the nanoscale silver that will quickly densify when the temperature is reached, thus keeping the processing time short.
  • There are applications where the peak processing temperature need not be limited to 300° C. or below. For example, silicon carbide may be attached at temperatures as high as 600° C. using gold or its alloy(s) but with contact pad problems when fired in air. The present technique can be used to make a paste that can be fired at a higher temperature to attain higher density and stronger bonding (but still lower than 600° C. since it is desired to retain the nanosilver particles until the sintering temperature). An illustrative example of this technique is shown in FIGS. 7 a-7 b where a nanosilver paste containing 100 nm particles and fatty acids of different carbon chain lengths (hence different burnout temperatures) was sintered at 450° C. The fired paste in FIG. 7 a had a significantly denser microstructure than that of the paste in FIG. 7 b. The higher burn-out temperature of the PVB and longer-chain fatty acid (C-24) in the paste in FIG. 7 a prevented the aggregation and sintering reaction of 100 nm particles while still at low temperatures during heating, thus enhancing the densification rate at the sintering temperature. Being able to retain the original particle size (or most of it) while heating to the sintering temperature (thus preventing the annealing out of the energy needed by the sintering process) helped achieve the result.
  • While the invention has been described in terms of its preferred embodiments, those skilled in the art will recognize that the invention can be practiced with modification within the spirit and scope of the appended claims.

Claims (20)

1. A composition for forming electrical interconnect, comprising:
a metal or metal alloy powder composed of a plurality of particles of a particle size of 500 nm or less;
a dispersant associated with particles of the metal or metal alloy powder, said dispersant being present in sufficient quantity to reduce or prevent agglomeration of said particles of the metal or metal alloy powder; and
a binder having a temperature of volatilization below the sintering temperature of said metal or metal alloy powder.
2. The composition of claim 1 wherein said particle size is 100 nm or less.
3. The composition of claim 1 wherein said metal or metal alloy is silver or a silver alloy.
4. The composition of claim 1 wherein the dispersant is a fatty acid or a fish oil.
5. The composition of claim 1 wherein said binder is a polymeric material.
6. The composition of claim 1 further comprising a viscosity adjusting component.
7. A method for forming an interconnect which performs at least one of mechanically, thermally or electrically connecting a device to a substrate, comprising the step of:
sintering metal or metal alloy particles that have a size of 500 nm or less which are positioned on contacts on the device and the substrate and sandwiched therebetween, said sintering step forming a metal or metal alloy layer from said metal or metal alloy particles which performs one or more of mechanically, thermally, or electrically interconnecting the device and the substrate.
8. The method of claim 7 further comprising the step of depositing on at least one electrical contact of at least one of the device and the substrate said metal or metal alloy particles.
9. The method of claim 8 wherein said step of depositing is performed by screening, printing or stenciling.
10. The method of claim 7 wherein said metal or metal alloy particles are of a size of 100 nm or less.
11. The method of claim 7 further comprising the step of holding the device and the substrate together during the step of sintering.
12. The method of claim 7 wherein said metal or metal alloy is silver or silver alloy.
13. The method of claim 7 wherein said metal or metal alloy, prior to said step of sintering, is present in the form of a paste which comprises a dispersant associated with the metal or metal alloy particles, said dispersant being present in sufficient quantity to reduce or prevent agglomeration of said metal or metal alloy particles, and a binder having a temperature of volatilization below the sintering temperature of said metal or metal alloy particles.
14. A method for connecting a substrate and a device, comprising:
positioning a paste between contacts of said substrate and said device which comprises a metal or metal alloy powder composed of a plurality of particles of a particle size of 500 nm or less, a dispersant associated with particles of the metal or metal alloy powder, said dispersant being present in sufficient quantity to reduce or prevent agglomeration of said particles of the metal or metal alloy powder, and a binder having a temperature of volatilization below the sintering temperature of said metal or metal alloy powder; and
heating said paste to a temperature and for a time sufficient to remove said binder and said dispersant, and to sinter metal particles of said metal or metal alloy powder together to form a metal or metal alloy layer from said metal or metal alloy particles which performs at least one of mechanically, thermally, or electrically interconnecting the device and the substrate.
15. The method of claim 14 wherein said metal or metal alloy is silver or silver alloy.
16. The method of claim 14 wherein said particles are 100 nm or less in size.
17. The method of claim 14 wherein said positioning step is performed by stenciling, printing, or screening.
18. The method of claim 14 further comprising the step of selecting said binder in said paste based on a desired temperature of volatilization.
19. The method of claim 14 further comprising the step of isolating said metal or metal alloy particles with said binder until a preset temperature during said heating step, wherein said preset temperature is determined based on said binder and a sintering temperature for said metal or metal alloy particles.
20. The method of claim 19 wherein said preset temperature is the same as or slightly below a sintering temperature for said metal or metal alloy particles.
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EP3725432A1 (en) 2019-04-18 2020-10-21 ISP System Method and device for manufacturing preforms intended for the brazing of electronic , photonic, thermal or mechanical components
US20200373269A1 (en) * 2017-12-01 2020-11-26 Panasonic Intellectual Property Management Co., Ltd. Joined structure, joining method, and joining material
EP3666429A4 (en) * 2017-09-15 2021-01-27 LINTEC Corporation Film-shaped firing material and support-sheet-equipped film-shaped firing material
US20220062990A1 (en) * 2020-09-03 2022-03-03 Commissariat A L'energie Atomique Et Aux Energies Alternatives Method for interconnecting components of an electronic system by sintering

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US20120070920A1 (en) * 2010-09-21 2012-03-22 Toyoda Gosei Co., Ltd. Method for mounting luminescent device
US8852970B2 (en) * 2010-09-21 2014-10-07 Toyoda Gosei Co., Ltd. Method for mounting luminescent device
US20160254146A1 (en) * 2010-12-24 2016-09-01 Ananda H. Kumar Methods and structures for preparing single crystal silicon wafers for use as substrates for epitaxial growth of crack-free gallium nitride films and devices
US20130193580A1 (en) * 2012-01-30 2013-08-01 Toyoda Gosei Co., Ltd. Method of manufacturing semiconductor device and semiconductor device
US8853006B2 (en) * 2012-01-30 2014-10-07 Toyoda Gosei Co., Ltd. Method of manufacturing semiconductor device and semiconductor device
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US9888568B2 (en) 2012-02-08 2018-02-06 Crane Electronics, Inc. Multilayer electronics assembly and method for embedding electrical circuit components within a three dimensional module
US11172572B2 (en) 2012-02-08 2021-11-09 Crane Electronics, Inc. Multilayer electronics assembly and method for embedding electrical circuit components within a three dimensional module
DE102012204159A1 (en) 2012-03-16 2013-03-14 Continental Automotive Gmbh Power semiconductor module for controlling electric machine in e.g. motor mode, has punching lattice provided with metal strips, where covers of lattice comprise connection between surfaces of electrode with terminal surfaces
CN102637598A (en) * 2012-04-18 2012-08-15 润奥电子(扬州)制造有限公司 Method for manufacturing high-power semiconductor device die
US20150236183A1 (en) * 2014-02-19 2015-08-20 Tsmc Solar Ltd. Solar cell and method of fabricating same
US9230726B1 (en) 2015-02-20 2016-01-05 Crane Electronics, Inc. Transformer-based power converters with 3D printed microchannel heat sink
EP3666429A4 (en) * 2017-09-15 2021-01-27 LINTEC Corporation Film-shaped firing material and support-sheet-equipped film-shaped firing material
US11420255B2 (en) 2017-09-15 2022-08-23 Lintec Corporation Film-shaped firing material and film-shaped firing material with a support sheet
US20200373269A1 (en) * 2017-12-01 2020-11-26 Panasonic Intellectual Property Management Co., Ltd. Joined structure, joining method, and joining material
EP3725432A1 (en) 2019-04-18 2020-10-21 ISP System Method and device for manufacturing preforms intended for the brazing of electronic , photonic, thermal or mechanical components
FR3095142A1 (en) 2019-04-18 2020-10-23 Isp System Method and device for manufacturing preforms intended for soldering electronic, photonic, thermal or mechanical components.
US20220062990A1 (en) * 2020-09-03 2022-03-03 Commissariat A L'energie Atomique Et Aux Energies Alternatives Method for interconnecting components of an electronic system by sintering
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