GB2115609A - Semiconductor structure manufacturing method - Google Patents
Semiconductor structure manufacturing method Download PDFInfo
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- GB2115609A GB2115609A GB08304462A GB8304462A GB2115609A GB 2115609 A GB2115609 A GB 2115609A GB 08304462 A GB08304462 A GB 08304462A GB 8304462 A GB8304462 A GB 8304462A GB 2115609 A GB2115609 A GB 2115609A
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- 239000004065 semiconductor Substances 0.000 title claims abstract description 28
- 238000004519 manufacturing process Methods 0.000 title description 8
- 238000005468 ion implantation Methods 0.000 claims abstract description 10
- 239000002245 particle Substances 0.000 claims abstract description 9
- 239000000463 material Substances 0.000 claims abstract description 6
- 230000000873 masking effect Effects 0.000 claims abstract description 5
- 239000000126 substance Substances 0.000 claims abstract description 4
- 238000000034 method Methods 0.000 claims description 36
- 230000002093 peripheral effect Effects 0.000 claims 7
- 239000011810 insulating material Substances 0.000 claims 1
- 238000002955 isolation Methods 0.000 abstract description 52
- 238000005530 etching Methods 0.000 abstract description 17
- 150000002500 ions Chemical class 0.000 abstract description 5
- 238000009413 insulation Methods 0.000 abstract 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 70
- 239000000377 silicon dioxide Substances 0.000 description 35
- 235000012239 silicon dioxide Nutrition 0.000 description 35
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 24
- 229910052710 silicon Inorganic materials 0.000 description 22
- 239000010703 silicon Substances 0.000 description 22
- 229920002120 photoresistant polymer Polymers 0.000 description 20
- 229910052796 boron Inorganic materials 0.000 description 19
- 229910052581 Si3N4 Inorganic materials 0.000 description 18
- 239000000758 substrate Substances 0.000 description 17
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 16
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 14
- 238000009792 diffusion process Methods 0.000 description 13
- 230000003647 oxidation Effects 0.000 description 11
- 238000007254 oxidation reaction Methods 0.000 description 11
- 239000002131 composite material Substances 0.000 description 9
- -1 boron ions Chemical class 0.000 description 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 6
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 6
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- 239000002019 doping agent Substances 0.000 description 4
- 238000001465 metallisation Methods 0.000 description 4
- 238000001020 plasma etching Methods 0.000 description 4
- VLJQDHDVZJXNQL-UHFFFAOYSA-N 4-methyl-n-(oxomethylidene)benzenesulfonamide Chemical compound CC1=CC=C(S(=O)(=O)N=C=O)C=C1 VLJQDHDVZJXNQL-UHFFFAOYSA-N 0.000 description 3
- FRIKWZARTBPWBN-UHFFFAOYSA-N [Si].O=[Si]=O Chemical compound [Si].O=[Si]=O FRIKWZARTBPWBN-UHFFFAOYSA-N 0.000 description 3
- 238000003486 chemical etching Methods 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 229910052697 platinum Inorganic materials 0.000 description 3
- 229910021340 platinum monosilicide Inorganic materials 0.000 description 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- 239000012300 argon atmosphere Substances 0.000 description 2
- 229910052785 arsenic Inorganic materials 0.000 description 2
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 230000015556 catabolic process Effects 0.000 description 2
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 2
- 239000007943 implant Substances 0.000 description 2
- 238000002513 implantation Methods 0.000 description 2
- 229910021421 monocrystalline silicon Inorganic materials 0.000 description 2
- 230000003071 parasitic effect Effects 0.000 description 2
- 238000000206 photolithography Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 102000004129 N-Type Calcium Channels Human genes 0.000 description 1
- 108090000699 N-Type Calcium Channels Proteins 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- QZPSXPBJTPJTSZ-UHFFFAOYSA-N aqua regia Chemical compound Cl.O[N+]([O-])=O QZPSXPBJTPJTSZ-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000005465 channeling Effects 0.000 description 1
- 238000005229 chemical vapour deposition Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000000994 depressogenic effect Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 150000004767 nitrides Chemical group 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 238000012876 topography Methods 0.000 description 1
- 238000003631 wet chemical etching Methods 0.000 description 1
- 238000001039 wet etching Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/76—Making of isolation regions between components
- H01L21/762—Dielectric regions, e.g. EPIC dielectric isolation, LOCOS; Trench refilling techniques, SOI technology, use of channel stoppers
- H01L21/76202—Dielectric regions, e.g. EPIC dielectric isolation, LOCOS; Trench refilling techniques, SOI technology, use of channel stoppers using a local oxidation of silicon, e.g. LOCOS, SWAMI, SILO
- H01L21/76213—Dielectric regions, e.g. EPIC dielectric isolation, LOCOS; Trench refilling techniques, SOI technology, use of channel stoppers using a local oxidation of silicon, e.g. LOCOS, SWAMI, SILO introducing electrical inactive or active impurities in the local oxidation region, e.g. to alter LOCOS oxide growth characteristics or for additional isolation purpose
- H01L21/76216—Dielectric regions, e.g. EPIC dielectric isolation, LOCOS; Trench refilling techniques, SOI technology, use of channel stoppers using a local oxidation of silicon, e.g. LOCOS, SWAMI, SILO introducing electrical inactive or active impurities in the local oxidation region, e.g. to alter LOCOS oxide growth characteristics or for additional isolation purpose introducing electrical active impurities in the local oxidation region for the sole purpose of creating channel stoppers
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/302—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to change their surface-physical characteristics or shape, e.g. etching, polishing, cutting
- H01L21/306—Chemical or electrical treatment, e.g. electrolytic etching
- H01L21/308—Chemical or electrical treatment, e.g. electrolytic etching using masks
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/76—Making of isolation regions between components
- H01L21/762—Dielectric regions, e.g. EPIC dielectric isolation, LOCOS; Trench refilling techniques, SOI technology, use of channel stoppers
- H01L21/76202—Dielectric regions, e.g. EPIC dielectric isolation, LOCOS; Trench refilling techniques, SOI technology, use of channel stoppers using a local oxidation of silicon, e.g. LOCOS, SWAMI, SILO
- H01L21/76205—Dielectric regions, e.g. EPIC dielectric isolation, LOCOS; Trench refilling techniques, SOI technology, use of channel stoppers using a local oxidation of silicon, e.g. LOCOS, SWAMI, SILO in a region being recessed from the surface, e.g. in a recess, groove, tub or trench region
- H01L21/7621—Dielectric regions, e.g. EPIC dielectric isolation, LOCOS; Trench refilling techniques, SOI technology, use of channel stoppers using a local oxidation of silicon, e.g. LOCOS, SWAMI, SILO in a region being recessed from the surface, e.g. in a recess, groove, tub or trench region the recessed region having a shape other than rectangular, e.g. rounded or oblique shape
Landscapes
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Manufacturing & Machinery (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Element Separation (AREA)
- Bipolar Transistors (AREA)
Abstract
A mask comprising an upper layer 20 and a lower layer 18 of different materials is provided over the surface of a semiconductor structure. A window 21 is formed in the upper layer 20 over the portions of the structure wherein isolation regions are to be provided. Using the window 21 in the upper layer 20 as a mask, a larger window 23 is formed in the lower layer 18 by bringing a chemical etchant which etches only the lower layer into contact with the portions of the lower layer 18 exposed by the window 21 in the upper layer 20. The larger window 23 is used as an etching mask to form an isolation groove 28 in the underlying semiconductor structure. The upper layer 20 is used as an ion implantation mask for implanting particles into the bottom portion of the groove 28 while masking the side portions of the groove 28 from the ions. The grooves 28 are then filled with insulation. <IMAGE>
Description
SPECIFICATION
Semiconductor structure manufacturing method
This invention relates generally to semiconductor structure manufacturing methods and more particularly to methods used for providing isolated regions within semiconductor structures.
As is known in the art, it has been suggested that bipolar and metal oxide semiconductor (MOS) monolithic integrated circuit chips, or semiconductor structures, use oxide or dielectric isolation, as distinguished from junction isolation, to provide electrical isolation between devices formed in such chips. The main advantages offered by oxide isolation, namely lower parasitic circuit capacitance and potentially greater packing density, result in faster circuits of greater computing power on a given chip size than can typically be achieved using junction isolation.
A variety of methods have been suggested to provide oxide isolation in silicon structures.
Common to such methods is the use of a composite silicon dioxide-silicon nitride layer used as a mask for selective oxidation of the exposed surfaces of a silicon structure. The thermally grown or deposited silicon dioxide layer (400- 2500 A thick) is formed under a later deposited silicon nitride (500-2000 A) layer. The silicon dioxide layer is used as a buffer layer to absorb some of the stresses developing between the silicon nitride and the silicon substrate due to mismatch of their thermal expansion. To fabricate the oxide isolation, windows are first etched by conventional photolithography and wet or plasma etching into the composite silicon dioxide-silicon nitride layer to delineate the regions where the isolation regions are to be formed.Next, the exposed silicon substrate is etched by isotropic or anisotropic etching to a depth approximating onehalf the thickness of the desired silicon dioxide isolation (typically 3000-20,000 A) so that a nearly planar surface is obtained after the step that follows, namely thermal oxidation of the exposed silicon. The nearly planar surface results because about twice as much silicon dioxide is formed as silicon consumed in the oxidation process. One may omit the silicon etching step if a topography where about one-half of the thickness of the oxide isolation rises above the original substrate surface can be tolerated.After the oxidation, the silicon dioxide-nitride masking layer, or nitride part alone, may be stripped and devices such as transistors, resistors, and diffused interconnects may be formed in the islands that were defined by the silicon nitride mask.
While this scheme of forming lateral oxide isolation is generally satisfactory for forming oxide isolation regions in p-type silicon epitaxial layers which are formed on n-type silicon substrates, it needs to be modified for forming isolation regions
in n-type epitaxial layers formed on p-type silicon substrates due to the positive charges that always
reside in silicon dioxide on silicon, although in various amounts (depending on the processing conditions). If the substrate doping is less than 1017 atoms/cm3 as is usually the case, the positive oxide charge may lead to an electrical inversion of the surface of the p-substrate, which thus becomes n-type.This so called n-type channel electrically connects the n-regions of the circuit components with each other which otherwise would have been isolated from each other by the oxide isolation in the lateral direction, and by a reverse biased p-n junction in the vertical direction. In addition to charges in the oxide, interconnects crossing the oxide isolation can induce inversion in substrates of both n or p type polarities, depending on the sign and magnitude of their electrical potential.
In order to prevent loss of isolation by inversion, one usually enhances the substrate doping in a shallow region under the oxide isolation. This can be done using the following methods: Method (1 )~the additional doping is selectively introduced into the substrate surface by thermal diffusion or ion implantation. An epitaxial layer is then deposited in which oxide isolation regions are formed, as described above, registered with the enhanced doping pattern;
Method (2)~after forming the oxide-nitride mask for selective oxidation, the exposed substrate surface is selectively implanted, or thermally diffused with the anti-inversion layer before the isolation oxide is grown over the same regions.
The surface is etched back before the doping takes place if a nearly planar surface after oxidation is desired; Method (3)~this is a modification of method (2) and uses a self-aligned positioning of the enhanced doping under the bottom of the oxide isolation while the sidewalls of the oxide isolation are shielded against it. This is accomplished by creating a mask overhang by etching into the substrate with isotropic or a combined anisotropic-isotropic etch, and then implanting the dopant using the overhang as a shield as described in U.S. Patent 4,187,125.
Due to elimination of registration difficulties, methods (2) and (3) have particular appeal for highly integrated circuits because of their small feature sizes. However, with epitaxial layers and oxide isolation getting shallower (less than 2 micro-meters) in order to obtain faster and smaller circuits, a problem with small breakdown voltages and relatively large parasitic capacitances arises due to the narrow spacing between the heavily doped source and drain regions of MOS transistors, or base region of bipolar transistors, and the rather heavily doped anti-inversion zone. While method (3) significantly alleviates this problem, the spacing it provides may not be large enough for some applications such as PROM's, A/D converters or buffer stages where relatively large breakdown voltages (e.g. 1 5-50 volts) are often required.
In a preferred embodiment of the present invention, a method for forming isolation regions in a semiconductor structure is provided in which a mask comprising an upper layer and a lower layer of different materials is provided over the surface of the structure, and a window is formed in the upper layer over the portions of the structure wherein the isolation regions are to be provided. Using the window in the upper layer as a mask, a larger window is formed in the lower layer by bringing a chemical etchant which etches only the lower layer into contact with the portions of the lower layer exposed by the window in the upper layer. The larger window formed in the lower layer is used as an etching mask to form an isolation groove, or depression, in the underlying semiconductor structure.The upper layer having the smaller window is- used as an ion implantation mask for implanting particles into the bottom portion of the groove while masking the side portions of the grooves from the ions.
With such method, lateral oxidation regions having a self-registered anti-inversion region are located under the bottoms of the isolation regions and are spaced from the peripheries of the isolation regions by uniform, predetermined distances. When planarity is not a concern, the above method can be used without etching a groove in the underlying semiconductor.
The invention will now be described in more detail, solely by way of example, with reference to the accompanying drawings, in which:
Figs. 1 to 12, and 14 to 17 are cross-sectional elevation views of a portion of a bipolar transistor according to the invention at various steps in the manufacture thereof;
Fig. 2A is a plan view of the bipolar transistor at one step in the fabrication thereof, Fig. 2 being a a cross-sectional elevation view taken along line 2-2 of Fig. 2A;
Figs. 9A and 9B are plan and isometric views, respectively, of the bipolar transistor at one step
in the fabrication thereof, Fig. 9 being a crosssectional elevation view taken along line 9-9 of
Fig. 9A;;
Figs. 1 OA and 1 OB are plan and isometric views, respectively, of the bipolar transistor at one
step in the fabrication thereof, Fig. 10 being a
cross-sectional elevation view taken along line 10~10 of Fig. 1 OA; and
Fig. 13 is a plan view of the bipolar transistor
at one step in the fabrication thereof, Fig. 12
being a cross-sectional elevation view taken
along line 12-12 of Fig. 13.
Referring now to Fig. 1, a substrate 10, here ptype silicon, having a surface in the < 100 > crystallographic plane and a resistivity of 10 to 40 ohm-cm is shown having an n-type conductivity subcollector region 12 formed therein using any conventional process, here ion implanting arsenic
(or antimony) through a silicon dioxide or photoresist mask (not shown). Alternatively, such subcollector region 12 may be formed by diffusion. After stripping the silicon dioxide or
photoresist mask by conventional techniques, an
epitaxial layer 14 of n-type conductivity silicon is
grown. Such epitaxial layer 14 is here grown to a thickness of 1.5 to 3 micrometers.
Referring to Figs. 2 and 2A, a composite layer 1 6 is formed over the surface of the epitaxial layer 14. In particular, such composite layer 16 includes: a layer 18 of silicon dioxide, here thermally grown or chemically vapor deposited over the surface of the epitaxial layer 14 to a thickness of 500 to 3000 Angstroms (A); and, a silicon nitride layer 20 deposited, here chemically vapor deposited over the surface of the silicon dioxide layer 18, here to a thickness of 1500 A. A layer 24 of photoresist is deposited over the composite layer 16 and is patterned into an isolation mask using conventional photolithographic-chemical etching techniques to form windows 26, as shown. Preferably, the widths of such isolation windows 26 are as small as practical, here in the order of 2 micrometers.
Using the patterned photoresist layer 20 as a mask, the composite layer 16 is selectively etched away as shown. For example, here the exposed portions of the silicon nitride layer 20 are removed using conventional plasma etching forming windows 21 (Fig.3) and then exposed portions of the silicon dioxide layer 18 are removed by using a suitable chemical etchant, here a hydrofluoric acid solution or also by plasma etching forming larger sized windows 23. In any event, it is noted that the etchant used to etch the silicon dioxide layer 18 is selective; that is, such etchant is selectively etching silicon dioxide layer 18 without attacking either silicon, silicon nitride, or photoresist. The silicon dioxide etching process continues so that the silicon dioxide layer 18 undercuts the etched silicon nitride layer as shown in Fig. 3.The amount of undercutting is controlled by controlling the length of time of the silicon dioxide chemical etching process. Here the amount of undercutting is about 1 micrometer.
The photoresist layer 24 is then removed in any conventional manner.
The remaining portions of the etched composite layer 16 are used to provide a mask for etching a depression, or an isolation groove 28 in the epitaxial layer 14, as shown in Fig. 4, here with an anisotropic etchant. If a nearly planar structure is desired and the epitaxial layer 14 is no more than 3 micrometers thick, the isolation grooves 28 are etched to a depth of 5000 A to 10,000 using a conventional anisotropic etchant such as a potassium hydroxide solution.
For a thicker epitaxial layer 14, i.e. 3.5 to 4 micrometers, the etching is carried to a depth of 1.6 to 2 micrometers using a combination etching technique. That is, first 0.3 micrometers to 0.5 micrometers of the silicon epitaxial layer 14 is etched using an anisotropic etchant and the remaining 1.3 to 1.7 micrometers of the epitaxial layer 14 are selectively removed using an isotropic etchant. This latter method yields isolation grooves with sloped side walls if it is not practical to backfill the entire isolation groove with thermally grown silicon dioxide upon which metallization will be formed as described in my
U.S. Patent4,187,125.
Since the anisotropic etch preferably attacks along the < 100 > crystallographic axis, a silicon substrate 10 (Fig. 1) having a surface in the < 100 > crystallographic plane is required in such method with the isolation groove patterns to be etched aligned along the < 110 > crystallographic axes.
Referring again to Fig. 4, here an anisotropic etchant is used to form the isolation groove 28, as shown. During the etching with the anisotropic etchant portions of the silicon epitaxial layer 14 under the composite layer 1 6 are removed, such composite layer 16 providing the etch resistant mask for the anisotropic etchant, as shown. That is, during the anisotropic etching process, the silicon nitride layer 20 overhangs the side walls 29 of the isolation groove 28 formed in the epitaxial layer 14. It should be noted that the etching mask is here provided by the silicon dioxide layer 18. The surface of the structure thus formed and shown in Fig. 4 is next subjected to an ion implantation process.In particular, the surface of the structure thus formed is exposed to boron ions 17 (or other particles capable of providing a p-type conductivity region in the n-type conductivity epitaxial layer 14). Here the ion implantation dosage is: 1.5 xl 014/cm2 at 30 Kev so that the range of peak concentration of the implantation is at a depth from the surface of the exposed epitaxial layer 14 in the order of 1000 A.
It is noted that the overhang portion of the silicon nitride 20 shields the side walls 29 of the isolation grooves 28 from the boron ions and thus provides the ion implantation mask and the boron ions 17 are implanted only in the bottom portion 27 of the groove 28. As noted above, the chemical etching mask used to form the isolation grooves 28 was provided by silicon dioxide layer 18. Further, it is noted that the aperture or window formed in layer 1 8 was larger than that formed in layer 20. Thus, the resulting side wall portions of groove 28 have a wider span than that which would have resulted if the window in layer 18 was the same as the window in layer 20. In this way, the self-registered anti-inversion region to be formed from the implanted ions 17 has adequate separation from the side wall portions of the grooves 28.It is also noted that the isolation grooves 28 will be thermally oxidized to fill such grooves in a manner to be described to provide a substantially planar surface for metallization which passes over the surface of the structure, and over the filled grooves to electrically interconnect devices formed in the structure and that a significant portion of the boron implantation will diffuse into the epitaxial layer. In this way, the oxidation of the silicon of epitaxial layer 14, in the manner to be described, does not remove substantial amounts of the boron dopant and the final structure has a proper boron, p-type conductivity, in the region of the epitaxial layer 14 beneath the bottom portion of the groove 28 to provide a structure with minimum inversion possibility.
After an anneal at 1 0000C for 20 minutes in an argon atmosphere, the structure thus formed is placed in an oxidizing atmosphere so that a layer 30 of silicon dioxide is thermally grown selectively over the exposed portions of the silicon epitaxial layer 14, as shown in Fig. 5. In particular, the isolation grooves 28 (Fig. 4) are selectively oxidized in a clean, wet 02 atmosphere (with HCI added) to grow a layer 30 (Fig. 5) of silicon dioxide 1.2 micrometers to 1.5 micrometers thick.
Typically, the oxidation cycle lasts for 8 hours at 1 0000 C. During this oxidation (and later heating cycles to be described) portions of the implanted boron particles diffuse through the silicon epitaxial layer 14 into the substrates 10 to form a doped region 31, as shown in Fig. 5. With an initial isolation groove depth of 8000 A and growing a 1.5 micrometer thick silicon dioxide layer 30, for example, the boron region 31 cuts through the remainder of a 3 micrometer thick epitaxial layer 14 into the substrate 10 to provide the desired isolation region, as shown. For a thicker epitaxial layer 14, one may use additional up-diffusion of boron placed into selected regions of the substrate prior to the formation of the epitaxial layer 14. This up-diffusion will then meet with the down-diffusion of the implanted boron resulting in an increased depth of isolation.For a transistor structure, it is important that the lateral diffusion of the boron implanted into the isolation grooves is small so that the boron remains well separated from the base region of the transistor to be formed later. The lateral diffusion occurs at a substantially lower rate than the downward diffusion thereby inherently facilitating the separation of the isolation boron from the base region of the transistor to be formed. This condition is achieved by the phenomenon of oxidation enhancement of diffusivity which, up to a temperature of about 1 0000C, causes the boron to diffuse sufficiently faster under an area where the oxide is grown, particularly in the < 100 > crystallographic direction.The silicon nitride layer 20 (Fig. 4) is then stripped using any conventional technique and is replaced with a 2000 thick layer 38 of silicon dioxide, here such layer being grown in steam at 1 0000C for approximately 35 minutes. The resulting structure with a layer 38 of silicon dioxide formed thereon is now in the order of 2500 A thick, as shown in Fig. 5.
Referring now to Fig. 6, a photoresist mask from a layer 42 of photoresist is formed over the surface of the structure using conventional photolithography to provide a window 44 to expose the base region. Using this mask, boron particles 45 are ion implanted through the silicon dioxide layer 38 into the base region using a dosage, here as follows: 8x 10'3/cm2 at 100 Kev.
The photoresist layer 42 is then removed, using any conventional process. The structure is then annealed in argon at 11 000C for 10 minutes so that the base region spreads because of diffusion of the boron dopant to a depth in the order of 3000 A to form the inactive base region 43 (i.e.
the base region used to electrically interconnect the active base region to the base electrode, as will be discussed).
Referring now to Fig. 7, a layer 50 of photoresist is again applied to the surface of the structure and formed into a mask, as shown, using conventional photolithographic techniques.
The photoresist mask is formed to expose all contact openings (emitter, base and collector) simultaneously. Using this photoresist mask, portions of the silicon dioxide layer 38 (and a similar upper layer portion of the silicon dioxide in the isolation grooves) are removed to a thickness in the order of 500 to 1000 A, as shown.
Alternatively, the silicon dioxide layer 38 may be etched through to the epitaxial layer in the contact areas unmasked by the photoresist and replaced with a freshly grown silicon dioxide layer in the order of 500 A thick. (This thin silicon dioxide layer acts as a stress absorbing pad as well as an etch stop if a silicon nitride layer, to be deposited in the next step, is subsequently etched in a plasma etcher).
Referring now to Fig. 8, the photoresist layer 50 is removed and a layer 52 of silicon nitride is here chemically vapor deposited to a thickness of
1000 to 1500 A. A photoresist layer 54 is then deposited over the silicon nitride layer 52 and formed into a mask, as shown, using conventional photolithographic techniques. This noncritical oversized mask is used to selectively remove the exposed portions of the silicon nitride layer 52 by conventional plasma etching and the then exposed underlying thin silicon dioxide layer 38 from the emitter area using conventional wet chemical etching processes, as shown in Fig. 8, to form the structure shown in Figs 9, 9A and 9B after the photoresist layer 54 is removed.
The surface of the structure is brought into contact with a suitable anisotropic etch, here potassium hydroxide solution, to selectively remove the exposed portions of the silicon epitaxial layer 14 as shown in Figs.10,1 OA and 1 OB. In particular, it should be noted that the
anisotropic etch is brought into contact with the
< 100 > surface of the epitaxial layer 14 along the < 110 > direction so that the side walls 39 of the depression 56 are converging and are parallel to the < 111 > crystallographic plane of the silicon
epitaxial layer 14 and such anisotropic etch does
not undercut the emitter contact opening but
leaves a generally triangularly-shaped region 58,
as shown, between the depression 56 and the
isolation groove 30.It is also noted that the
anisotropic etch removes the portions of the
inactive doped base region 43 of the epitaxial
layer 14, as shown. As a result, the triangularly
shaped portion 58 of the inactive base region 43
is retained between the emitter opening, i.e.,
depression or groove 56, and the silicon dioxide
filled isolation groove 30, as shown. Region 58
prevents inversion from electrically short
circuiting between the emitter and collector
regions of the transistor to be formed. Without
the boron doped region 58, positive charges
residing in the silicon dioxide isolation groove 30
(or charges induced in the silicon by subsequent
metallization formed over such silicon dioxide in a
manner to be described hereinafter) can cause
inversion at the silicon-silicon dioxide interface
and thus cause an emitter-collector electrical
short circuit by channeling.After the anisotropic
etching, the structure is heated in argon to 11 000C for about 20 minutes in order to drive the
inactive base region 43 deeper by in the order of
3000 A so that it extends to a level slightly below
the bottom 61 of the etched depression 56 as
shown in Fig.11, i.e. the bottom of the depressed
emitter contact opening.
Next, the active base region is formed by
implanting boron ions through the emitter contact
opening (i.e. depression 56) with a dosage
ranging from 7 xl 012/cm2 to 1 xl 013/cm2, depending on the beta of the transistor desired, as
shown in Figs. 12 and 13. The implant is made in
two steps, namely at 40 Kev and 100 Kev. If
desired, a thin oxide layer (not shown) in the order
of 300 to 500 A thick may be grown or deposited
on the emitter contact opening before the implant
to act as a shield for undesired impurities.The
structure is then heated in an argon atmosphere
at 1 0000C for 20 minutes to anneal and activate
the boron ions and thereby form the active base
region 45 (Fig. 14). Further, the base region 43 is
driven slightly further into, the epitaxial layer 14
during this step.
Referring to Fig. 14, a photoresist layer 62 is
deposited over the surface of the structure to
form a relatively non-critical, oversized mask, as
shown, to enable a selected portion of the silicon
nitride layer 52 and thinned silicon dioxide layer
38 to be removed from the collector contact area,
as shown, using any conventional etching
technique.
Referring now to Fig.15, a layer 66 of
polycrystalline silicon is deposited, here by
chemical vapor deposition (using cracking of SiH4
at 600 to 7000C), onto the surface of the
structure to a thickness in the order of 2000 to
3000 A. The deposited polycrystalline silicon
layer 66 is then doped with a suitable dopant,
here phosphorous, by conventional diffusion at
900 to 9500C. (Alternatively, the deposited polycrystalline silicon layer 66 may be doped by
ion implantation of phosphorous or arsenic).The
temperature cycle involved in the diffusion is no
longer than 20 to,25 minutes so that the diffusion
into the single crystal epitaxial layer will be very shallow (less than 1000 A), especially because
the diffusion in the polycrystalline silicon layer 66
is much more rapid than in single crystal silicon.
Using an oversized photoresist mask (not shown),
the doped polycrystalline layer 66 is etched into
emitter and collector contacts 68, 70, respectively, as shown in Fig.15. An emitter-base
junction is thus formed between the emitter
contact 68 and the lightly doped, active base
region 45. Note that it is desirable that the doped polycrystalline silicon emitter contact 68 extends
slightly beyond the periphery of the emitter
opening in order to protect the emitter-base
junction.
Referring now to Fig. 16, a layer 72 of
photoresist is patterned, as shown, to form a mask which exposes the region where the base contact is to be formed. The exposed portions of the silicon nitride layer 52 and thinned silicon dioxide layer 38 are etched, using any conventional technique. Next, a layer of platinum is deposited by sputtering and selectively lifted off by dissolving photoresist layer 72, except from the base contact area as shown in Fig.17. The remaining platinum is then sintered in the base contact area to form a region 74 of PtSi as shown in Fig.17 and the excess platinum is then removed by etching in aqua regia. Alternatively, the PtSi may be omitted if such is not needed for the base contact.The process described may be easily modified to form PtSi simultaneously on the base contact and on portions of the collector region, as by extending the base contact window to expose portions of the adjacent collector regions to obtain a Schottky contact.
A A metallization layer 76, preferably aluminum, 5000 to 7000 A thick, is deposited over the surface of the structure and patterned into conductors (i.e. emitter, base and collector contacts 80, 82, 84, respectively), as shown in Fig. 1 7. Note that the oversized polycrystalline silicon emitter 68 protects the emitter junction from being shorted by the aluminum and from alloying spikes which can form in single crystal silicon in specific crystallographic orientations. It is also noted that the active base region 45 is electrically coupled to the base contact 82 through the more heavily doped inactive base region 43. It follows then that the term "active base region" refers to the p-type conductivity region which interacts with the emitter contact 68 and the term "inactive base region" refers to the p-type conductivity region which is used to electrically interconnect the active base region to the base contact 82.
Having described preferred embodiments of this invention it is now evident that other embodiments incorporating these concepts may be used. For example, while the invention has been described for forming isolation regions for bipolar transistors, such method may be used to provide isolated regions for other devices, such as
MOS transistors. It is felt, therefore, that this invention should not be restricted to the disclosed embodiments, but rather should be limited only by the scope of the appended claims.
Claims (6)
1. A method for forming a semiconductor structure comprising the steps of:
(a) forming a mask comprising upper and lower layers of different materials over a surface of a semiconductor with a first window in such lower layer and a second smaller window in the upper layer;
(b) forming a depression in the portion of the I semiconductor disposed beneath the first window
with side wall portions masked by peripheral
portions of the second window; and
(c) ion implantation particles into the position
of the depression exposed by the second window
and unmasked by the peripheral portion of the
second window.
2. A method for forming a semiconductor
structure comprising the steps of:
(a) forming a mask comprising upper and lower
layers of different material over a surface of a
semiconductor with a first window in such lower
layer exposing a portion of the surface of the
semiconductor and a smaller, second window in
the upper layer having peripheral portions
masking peripheral portions of the exposed
surface portion of the semiconductor;
(b) bringing an etchant into contact with the
exposed surface portion of the semiconductor
forming a depression in such semiconductor with
side wall portions masked by the peripheral
portions of the second window; and
(c) ion implanting particles into the portion of
the depression exposed by the second window
and unmasked by the peripheral portions of the
second window.
3. A method for forming a semiconductor
structure comprising the steps of:
(a) forming a first layer of a first material over a
surface of a semiconductor;
(b) forming a second layer of a second,
different material over the first layer;
(c) forming a first window in a portion of the
second layer and exposing edge portions of the
first layer;
(d) bringing a chemical etchant into contact
with the exposed edge portions of the first layer to
selectively etch the exposed edge portions of the
first layer providing a second window in the first
layer larger than the first window with the second
window exposing a portion of the surface of the
semiconductor and with edge portions of the first
window overhanging peripheral portions of the
exposed portion of the semiconductor;;
(e) bringing an etchant into contact with the
portion of the semiconductor exposed by the
second window forming a depression in the
semiconductor with side wall portions and a
bottom portion, the edge portions of the first
window overhanging such side wall portions to
mask such side wall portions;
(f) ion implanting particles, into the bottom
portion of the depression with the edge portions
of the first window masking the side wall portions
of such depression preventing ion implantation of
such particles into the side wall portions of such
depression.
4. The method recited in claim 3 including the
step of forming an insulating material in the
formed depression subsequent to the ion
implantation step.
5. A method for forming a semiconductor structure, substantially as described hereinbefore with reference to the accompanying drawings.
6. A semiconductor structure formed by a method according to any one of the preceding claims.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US35243982A | 1982-02-25 | 1982-02-25 |
Publications (3)
Publication Number | Publication Date |
---|---|
GB8304462D0 GB8304462D0 (en) | 1983-03-23 |
GB2115609A true GB2115609A (en) | 1983-09-07 |
GB2115609B GB2115609B (en) | 1986-04-30 |
Family
ID=23385144
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB08304462A Expired GB2115609B (en) | 1982-02-25 | 1983-02-17 | Semiconductor structure manufacturing method |
Country Status (3)
Country | Link |
---|---|
JP (1) | JPS58158943A (en) |
DE (1) | DE3306702A1 (en) |
GB (1) | GB2115609B (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2206994A (en) * | 1987-06-08 | 1989-01-18 | Philips Electronic Associated | Semiconductor device |
GB2323706A (en) * | 1997-03-13 | 1998-09-30 | United Microelectronics Corp | Method to inhibit the formation of ion implantation induced edge defects |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL173110C (en) * | 1971-03-17 | 1983-12-01 | Philips Nv | METHOD FOR MANUFACTURING A SEMI-CONDUCTOR DEVICE APPLICATING ON A SURFACE OF A SEMI-CONDUCTOR BODY AT LEAST TWO PART-LAYERS OF DIFFERENT MATERIAL COATING. |
JPS5361285A (en) * | 1976-11-15 | 1978-06-01 | Hitachi Ltd | Production of semiconductor device |
CA1090006A (en) * | 1976-12-27 | 1980-11-18 | Wolfgang M. Feist | Semiconductor structures and methods for manufacturing such structures |
US4187125A (en) * | 1976-12-27 | 1980-02-05 | Raytheon Company | Method for manufacturing semiconductor structures by anisotropic and isotropic etching |
JPS5731153A (en) * | 1980-08-01 | 1982-02-19 | Nec Corp | Manufacture of semiconductor device |
-
1983
- 1983-02-17 GB GB08304462A patent/GB2115609B/en not_active Expired
- 1983-02-25 JP JP3068083A patent/JPS58158943A/en active Pending
- 1983-02-25 DE DE19833306702 patent/DE3306702A1/en not_active Ceased
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2206994A (en) * | 1987-06-08 | 1989-01-18 | Philips Electronic Associated | Semiconductor device |
GB2323706A (en) * | 1997-03-13 | 1998-09-30 | United Microelectronics Corp | Method to inhibit the formation of ion implantation induced edge defects |
GB2323706B (en) * | 1997-03-13 | 2002-02-13 | United Microelectronics Corp | Method to inhibit the formation of ion implantation induced edge defects |
Also Published As
Publication number | Publication date |
---|---|
GB2115609B (en) | 1986-04-30 |
GB8304462D0 (en) | 1983-03-23 |
JPS58158943A (en) | 1983-09-21 |
DE3306702A1 (en) | 1983-09-01 |
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PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19940217 |