CN110364441B - Etching method for lithium niobate material - Google Patents
Etching method for lithium niobate material Download PDFInfo
- Publication number
- CN110364441B CN110364441B CN201810320107.2A CN201810320107A CN110364441B CN 110364441 B CN110364441 B CN 110364441B CN 201810320107 A CN201810320107 A CN 201810320107A CN 110364441 B CN110364441 B CN 110364441B
- Authority
- CN
- China
- Prior art keywords
- lithium niobate
- etching
- gas
- process gas
- niobate substrate
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 238000000034 method Methods 0.000 title claims abstract description 126
- 238000005530 etching Methods 0.000 title claims abstract description 103
- GQYHUHYESMUTHG-UHFFFAOYSA-N lithium niobate Chemical compound [Li+].[O-][Nb](=O)=O GQYHUHYESMUTHG-UHFFFAOYSA-N 0.000 title claims abstract description 80
- 239000000463 material Substances 0.000 title claims abstract description 18
- 230000008569 process Effects 0.000 claims abstract description 93
- 239000000758 substrate Substances 0.000 claims abstract description 59
- 239000000460 chlorine Substances 0.000 claims abstract description 23
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 23
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 21
- 239000007789 gas Substances 0.000 claims description 93
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 33
- 229910052786 argon Inorganic materials 0.000 claims description 19
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 8
- 239000001307 helium Substances 0.000 claims description 3
- 229910052734 helium Inorganic materials 0.000 claims description 3
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 claims description 3
- FAQYAMRNWDIXMY-UHFFFAOYSA-N trichloroborane Chemical compound ClB(Cl)Cl FAQYAMRNWDIXMY-UHFFFAOYSA-N 0.000 claims description 3
- -1 fluoride ions Chemical class 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 7
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 7
- 238000005516 engineering process Methods 0.000 description 4
- 239000006227 byproduct Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 238000009616 inductively coupled plasma Methods 0.000 description 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- PQXKHYXIUOZZFA-UHFFFAOYSA-M lithium fluoride Chemical compound [Li+].[F-] PQXKHYXIUOZZFA-UHFFFAOYSA-M 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920002120 photoresistant polymer Polymers 0.000 description 2
- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000001312 dry etching Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 238000010884 ion-beam technique Methods 0.000 description 1
- 150000002500 ions Chemical group 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000001000 micrograph Methods 0.000 description 1
- 230000005693 optoelectronics Effects 0.000 description 1
- 238000001020 plasma etching Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000012495 reaction gas Substances 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 238000001039 wet etching Methods 0.000 description 1
Images
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
- H01L21/02—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
- H01L21/34—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 not provided for in groups H01L21/0405, H01L21/0445, H01L21/06, H01L21/16 and H01L21/18 with or without impurities, e.g. doping materials
- H01L21/46—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/428
- H01L21/461—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/428 to change their surface-physical characteristics or shape, e.g. etching, polishing, cutting
- H01L21/465—Chemical or electrical treatment, e.g. electrolytic etching
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)
- Drying Of Semiconductors (AREA)
Abstract
The invention provides an etching method for a lithium niobate material, which comprises the following steps: providing a lithium niobate substrate; providing a process gas, the process gas comprising a chlorine-based gas; and ionizing the process gas to obtain plasma, and etching the lithium niobate substrate. The etching method for the lithium niobate material can improve the etching rate and ensure that the etched surface is smooth and flat.
Description
Technical Field
The invention relates to the field of semiconductor equipment, in particular to an etching method for a lithium niobate material.
Background
The lithium niobate crystal is a crystal material which is relatively difficult to etch, and a general lithium niobate waveguide structure is prepared by ion beam bombardment, mechanical processing, acid solution wet etching and other methods, but the methods have great limitations on preparing a high-quality lithium niobate waveguide with a submicron size and a smooth etched surface. Inductively Coupled Plasma (ICP) etching technology in dry etching is increasingly applied to manufacturing of optoelectronic devices due to the advantages of high control precision, good large-area etching uniformity, less pollution and the like.
In the prior art, CF is adopted4Or SF6When F-based gas is used for etching, lithium fluoride (LiF) which is not easy to volatilize can be generated, the etching rate is reduced, the etched surface is rough, and meanwhile, the problem of surface photoresist pasting can be caused by the high radio frequency source power used for improving the etching rate.
Therefore, how to increase the etching rate of lithium niobate and make the etched surface smooth becomes a problem to be solved urgently.
Disclosure of Invention
In order to solve at least one of the above technical problems, the present invention provides an etching method for a lithium niobate material. The etching method for the lithium niobate material can improve the etching rate and ensure that the etched surface is smooth and flat.
To achieve the above object, as one aspect of the present invention, there is provided an etching method for a lithium niobate material, wherein the etching method includes:
providing a lithium niobate substrate;
providing a process gas, the process gas comprising a chlorine-based gas;
and ionizing the process gas to obtain plasma, and etching the lithium niobate substrate.
Optionally, the process gas further comprises an auxiliary process gas, and in the step of providing the process gas, a flow rate of the auxiliary process gas is greater than or equal to a flow rate of the chlorine-based gas.
Optionally, the chlorine-based gas comprises chlorine gas and/or boron trichloride gas.
Optionally, the auxiliary process gas comprises argon and/or helium.
Optionally, in the step of ionizing the process gas to obtain plasma and etching the lithium niobate substrate, the pressure of the process chamber is in a range of 5mT to 20 mT.
Optionally, in the step of ionizing the process gas to obtain a plasma and etching the lithium niobate substrate, the radio frequency power applied to the coil for ionizing the process gas is in a range of 600W to 1500W; the range of the radio frequency power loaded to the lower electrode for bearing the lithium niobate substrate is 100W-500W.
Optionally, in the step of ionizing the process gas to obtain plasma and etching the lithium niobate substrate, the temperature of the lower electrode ranges from 30 ℃ to 50 ℃.
Optionally, the etching method further includes:
pre-treating the process chamber prior to the step of providing a lithium niobate substrate.
The invention has the beneficial technical effects that:
according to the etching method for the lithium niobate material, provided by the invention, the lithium niobate substrate is etched by adopting the mode of mixing chlorine-based gas with auxiliary process gas and utilizing the inductive coupling plasma etching technology, the etched lithium niobate substrate has a smooth etching surface, and the etching method greatly improves the etching rate compared with the prior art.
Drawings
The accompanying drawings, which are included to provide a further understanding of the invention and are incorporated in and constitute a part of this specification, illustrate embodiments of the invention and together with the description serve to explain the principles of the invention and not to limit the invention. In the drawings:
FIG. 1 is a scanning electron microscope image of an etching result obtained by etching the lithium niobate material by using the etching method provided by the comparative example;
fig. 2 is a scanning electron microscope picture of an etching result obtained by etching the lithium niobate material by using the etching method provided by the embodiment of the invention;
fig. 3 is a schematic flow chart of the etching method for the lithium niobate material provided by the present invention.
Detailed Description
The following describes in detail embodiments of the present invention with reference to the drawings. It should be understood that the detailed description and specific examples, while indicating the preferred embodiment of the invention, are given by way of illustration and explanation only, not limitation.
As one aspect of the present invention, as shown in fig. 3, there is provided an etching method for a lithium niobate material, wherein the etching method includes:
in step S101, a lithium niobate substrate is provided;
in step S102, providing a process gas, the process gas including a chlorine-based gas;
in step S103, the process gas is ionized to obtain a plasma, and the lithium niobate substrate is etched.
As described above, in step S101, the lithium niobate substrate to be etched is transferred into the process chamber through the carrier plate and placed on the carrying surface of the lower electrode. Wherein, a mask pattern is arranged on the lithium niobate substrate.
In step S102, the process gas is introduced into the process chamber, and the process gas includes a chlorine-based gas.
The lithium niobate substrate may be etched by the chloride ions in the chlorine-based gas. Specifically, in step S103, a radio frequency power supply loads power to an upper electrode coil, so that the upper electrode coil ionizes the chlorine-based gas in an inductively coupled manner to form a plasma of chloride ions in a plasma state, and the plasma-formed chloride ions chemically react with the lithium niobate substrate to achieve etching of the lithium niobate substrate.
Specifically, in step S103, the plasma-formed chloride ions chemically react with the lithium niobate substrate to generate chloride, whereas in the prior art, fluorine-based gas is usually used as the process gas, and then the plasma-formed fluoride ions chemically react with the lithium niobate substrate to generate fluoride, and since chloride is more volatile than fluoride, chloride is not easily deposited on the etched surface of the lithium niobate substrate during the etching process, which speeds up the etching rate compared with the prior art and makes the etched surface of the lithium niobate substrate smoother.
Therefore, compared with the prior art, the etching method provided by the invention effectively improves the etching rate and simultaneously enables the etched surface of the lithium niobate substrate to be smooth.
In the present invention, as shown in fig. 3, the process gas further includes an auxiliary process gas, and in the step S102 of providing the process gas, a flow rate of the auxiliary process gas is greater than or equal to a flow rate of the chlorine-based gas.
As described above, in step S102, the process gas is introduced into the process chamber, the process gas includes a chlorine-based gas and the auxiliary process gas, and the flow rate of the auxiliary process gas is ensured to be greater than or equal to the flow rate of the chlorine-based process gas, so as to ensure the smooth proceeding of the etching process, and the specific principle will be described in detail below.
In the present invention, the chlorine-based gas includes chlorine gas and/or boron trichloride gas; the auxiliary process gas comprises argon and/or helium.
As described above, as a preferred embodiment of the present invention, the chlorine-based gas is selected as chlorine gas, the auxiliary process gas is selected as argon gas, and in step S102, the chlorine gas and the argon gas are introduced into the process chamber at a flow ratio of less than or equal to 1:1, so as to ensure that the etching is performed smoothly.
In a preferred embodiment of the present invention, the chlorine gas has a flow rate of 30sccm (standard-state cubic centrifuge per minute, volume flow rate unit, the same applies hereinafter), and the argon gas has a flow rate of 50 sccm.
Specifically, by performing step S103, as described above, power is applied to the upper electrode coil by the rf power source, so that the upper electrode coil ionizes the chlorine and the argon gas in an inductively coupled manner, forming plasma-formed chlorine ions and plasma-formed argon ions, and at the same time, power is applied to the lower electrode by the rf power source, so that a self-bias voltage is formed on the lower electrode, so as to attract the lithium niobate substrate located on the lower electrode carrying surface to be etched, including the plasma-formed chlorine ions and the plasma-formed argon ions. The self-bias voltage is formed by loading power on the lower electrode, so that the etching rate can be increased.
In addition, as described above, in step S102, argon gas is introduced into the process chamber, coupling discharge is performed after the upper electrode coil is powered on, the argon gas is ionized to form a plasma argon ion, and lithium chloride (LiCl), which is a reaction byproduct on the etched surface of the lithium niobate substrate, is formed by bombardment of the plasma argon ion to further accelerate the volatilization process of the lithium chloride, so that the lithium chloride, which is a reaction byproduct, is separated from the etched surface of the lithium niobate substrate and dissociated in the process chamber in an ion form, so as to be easily absorbed by a vacuum system, thereby ensuring smooth proceeding of the etching process, accelerating the reaction rate, smoothing the etched surface of the lithium niobate substrate, and improving the yield of products.
Further, compared with the prior art which adopts CF4Or SF6And when F-based gas is used for etching to generate lithium fluoride (LiF) which is not easy to volatilize, the generated by-product LiCl is easier to volatilize because chlorine-based gas is used as reaction gas in the etching method provided by the invention, so that the etching rate is ensured not to be influenced, and the problem of photoresist pasting on the surface of the lithium niobate substrate caused by high radio frequency power used for improving the etching rate is avoided.
It should be noted that the plasma including the argon ions may also physically bombard the etched surface of the lithium niobate substrate, so as to further increase the etching rate.
In the present invention, in step S103 of ionizing the process gas to obtain plasma and etching the lithium niobate substrate, the pressure of the process chamber is in a range of 5mT to 20mT (millitorr, pressure unit, the same applies below).
As described above, during the execution of the etching process, the gas pressure in the process chamber is kept relatively stable, and specifically, in step S102, the process gas is introduced into the process chamber, and meanwhile, the gas including impurity particles generated by etching in the process chamber is sucked away by the vacuum system, so as to keep the dynamic balance between the gas inflow and the gas outflow, thereby ensuring that the gas pressure in the process chamber is relatively stable.
Optionally, as an embodiment of the present invention, the pressure in the process chamber is in a range of 5mT to 20mT, and in order to further optimize the etching result of the lithium niobate substrate, the pressure in the process chamber is preferably 10 mT.
In the invention, in the steps of ionizing the process gas to obtain plasma and etching the lithium niobate substrate, the radio frequency power loaded to a coil for ionizing the process gas is 600W-1500W; the radio frequency power loaded to the lower electrode for bearing the lithium niobate substrate ranges from 100W to 500W.
As described above, as an optional embodiment of the present invention, when step S103 is executed, the rf power range loaded to the upper electrode coil is 600W to 1500W; the range of the radio frequency power loaded to the lower electrode is 100W-500W.
It should be noted that, in order to further optimize the etching result of the lithium niobate substrate, in the present invention, preferably, the radio frequency power loaded to the upper electrode coil is 800W; the RF power applied to the bottom electrode was 200W.
In the present invention, in step S103 of ionizing the process gas to obtain a plasma, and etching the lithium niobate substrate, the temperature of the lower electrode is 30 to 50 ℃.
As described above, in performing the step S103, the temperature of the process chamber is required to be 30-50 ℃ to obtain a fast etching rate, and in order to maximize the etching rate, as a preferred embodiment of the present invention, the temperature of the process chamber is 40 ℃.
It should be noted that the parameters provided in the etching method provided by the present invention are particularly suitable for the case of using chlorine and argon as the process gases.
In the present invention, the process chamber is pretreated before the step S101 of providing a lithium niobate substrate.
As described above, before the lithium niobate substrate is transferred into the process chamber, the process chamber needs to be pre-cleaned, so as to avoid negative effects of impurity particles on the etching process in the subsequent etching process.
It should be noted that the precleaning is to perform plasma bombardment on the inner wall of the process chamber, the bottom electrode trench and other parts by using an inductively coupled plasma etching technology to remove impurities adhered in the process chamber.
Examples
In step S101, the lithium niobate substrate provided with the strip mask pattern is disposed in a process chamber of an etching apparatus;
in step S102, a process gas is introduced into the process chamber, wherein the process gas includes chlorine gas and argon gas, the flow rate of the chlorine gas is 30sccm, the flow rate of the argon gas is 50sccm,
in step S103, ionizing the process gas to obtain a plasma, and etching the lithium niobate substrate;
the pressure in the process chamber is 10mT, the radio-frequency power loaded to the upper electrode coil is 800W, the radio-frequency power loaded to the lower electrode is 200W, the temperature of the lower electrode is 40 ℃, the etching time of the lithium niobate substrate is 10min, the etching depth is 754nm, and the etching rate is 75.4 nm/min.
Comparative example
In step S101, the lithium niobate substrate provided with the strip mask pattern is disposed in a process chamber of an etching apparatus;
in step S102, a process gas is introduced into the process chamber, wherein the process gas includes carbon tetrafluoride gas and argon gas, the flow rate of the carbon tetrafluoride gas is 10sccm, the flow rate of the argon gas is 50sccm,
in step S103, ionizing the process gas to obtain a plasma, and etching the lithium niobate substrate;
the pressure in the process chamber is 5mT, the radio-frequency power loaded to the upper electrode coil is 800W, the radio-frequency power loaded to the lower electrode is 150W, the temperature of the lower electrode is 40 ℃, the etching time of the lithium niobate substrate is 24min, the etching depth is 948nm, and the etching rate is 40 nm/min.
FIG. 1 is a scanning electron microscope picture obtained by scanning an etched lithium niobate substrate by using an SU 8010 scanning electron microscope with the parameters of the above comparative example by using an etching method for a lithium niobate material provided by the prior art;
fig. 2 is a scanning electron microscope picture obtained by scanning the etched lithium niobate substrate with the SU 8010 scanning electron microscope with the parameters of the above embodiment by using the etching method for lithium niobate materials provided by the present invention;
as can be seen from comparison between fig. 1 and fig. 2, the etching surface of the lithium niobate substrate obtained by etching the lithium niobate substrate by using the etching method provided by the present invention is smoother, and in addition, the etching time of the lithium niobate substrate sample shown in fig. 2 is 10min, and the etching depth is 754nm, and the etching rate is 75.4 nm/min. In the preferred embodiment of the prior art, the etching time of the lithium niobate substrate sample shown in fig. 1 is 24min, the etching depth is 948nm, and the etching rate is 40nm/min, that is, the maximum value of the etching rate which can be realized by the prior art is 40nm/min, so that the etching rate of the etching method provided by the present invention is obviously improved compared with the prior art.
In summary, the etching method for the lithium niobate material provided by the invention adopts a mode of chlorine-based gas mixed auxiliary process gas and utilizes an inductively coupled plasma etching technology to etch the lithium niobate substrate, the etched lithium niobate substrate has a smooth etching surface, and the etching method greatly improves the etching rate compared with the prior art.
It will be understood that the above embodiments are merely exemplary embodiments adopted to illustrate the principles of the present invention, and the present invention is not limited thereto. It will be apparent to those skilled in the art that various modifications and improvements can be made without departing from the spirit and scope of the invention, and such modifications and improvements are also considered to be within the scope of the invention.
Claims (5)
1. An etching method for a lithium niobate material, characterized by comprising:
providing a lithium niobate substrate;
providing a process gas, wherein the process gas comprises a chlorine-based gas and an auxiliary process gas, and the flow rate of the auxiliary process gas is greater than or equal to that of the chlorine-based gas;
ionizing the process gas to obtain plasma, and etching the lithium niobate substrate to ensure that the etched lithium niobate substrate has a smooth etching surface and improve the etching rate; wherein:
in the steps of ionizing the process gas to obtain plasma and etching the lithium niobate substrate, the radio frequency power loaded to a coil for ionizing the process gas is 600W-1500W; the range of the radio frequency power loaded to the lower electrode for bearing the lithium niobate substrate is 100W-500W;
in the step of ionizing the process gas to obtain plasma and etching the lithium niobate substrate, the temperature range of the lower electrode is 30-50 ℃.
2. The etching method according to claim 1, wherein the chlorine-based gas includes chlorine gas and/or boron trichloride gas.
3. The etching method according to claim 1, wherein the auxiliary process gas comprises argon and/or helium.
4. The etching method according to any one of claims 1 to 3, wherein in the step of ionizing the process gas to obtain plasma and etching the lithium niobate substrate, a pressure of a process chamber is in a range of 5mT to 20 mT.
5. The etching method according to claim 4, further comprising:
pre-treating the process chamber prior to the step of providing a lithium niobate substrate.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201810320107.2A CN110364441B (en) | 2018-04-11 | 2018-04-11 | Etching method for lithium niobate material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201810320107.2A CN110364441B (en) | 2018-04-11 | 2018-04-11 | Etching method for lithium niobate material |
Publications (2)
Publication Number | Publication Date |
---|---|
CN110364441A CN110364441A (en) | 2019-10-22 |
CN110364441B true CN110364441B (en) | 2022-07-22 |
Family
ID=68214363
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201810320107.2A Active CN110364441B (en) | 2018-04-11 | 2018-04-11 | Etching method for lithium niobate material |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN110364441B (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111740009B (en) * | 2020-06-17 | 2022-05-24 | 上海新硅聚合半导体有限公司 | Piezoelectric wafer surface treatment method based on ion beam enhanced corrosion |
CN115506032A (en) * | 2021-06-23 | 2022-12-23 | 江苏鲁汶仪器有限公司 | Method for dry etching lithium niobate |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0727911A (en) * | 1993-07-12 | 1995-01-31 | Sumitomo Electric Ind Ltd | Microfabrication method for dielectric optical material |
CN102738339A (en) * | 2012-07-04 | 2012-10-17 | 杭州士兰明芯科技有限公司 | Lithium niobate substrate provided with pattern structure and manufacturing method thereof |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9525398B1 (en) * | 2014-05-27 | 2016-12-20 | Sandia Corporation | Single crystal micromechanical resonator and fabrication methods thereof |
-
2018
- 2018-04-11 CN CN201810320107.2A patent/CN110364441B/en active Active
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0727911A (en) * | 1993-07-12 | 1995-01-31 | Sumitomo Electric Ind Ltd | Microfabrication method for dielectric optical material |
CN102738339A (en) * | 2012-07-04 | 2012-10-17 | 杭州士兰明芯科技有限公司 | Lithium niobate substrate provided with pattern structure and manufacturing method thereof |
Also Published As
Publication number | Publication date |
---|---|
CN110364441A (en) | 2019-10-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US10541147B2 (en) | Etching method | |
JP2008085288A (en) | Plasma processing apparatus of substrate, and plasma processing method thereof | |
US9570312B2 (en) | Plasma etching method | |
US20220181162A1 (en) | Etching apparatus | |
US9805945B2 (en) | Etching method | |
US10580655B2 (en) | Plasma etching method for selectively etching silicon oxide with respect to silicon nitride | |
CN110364441B (en) | Etching method for lithium niobate material | |
CN107644812B (en) | Substrate etching method | |
CN117334574A (en) | Post-treatment of indium-containing compound semiconductors | |
CN106504982B (en) | Substrate etching method | |
JPH06122983A (en) | Plasma treatment and plasma device | |
US9754797B2 (en) | Etching method for selectively etching silicon oxide with respect to silicon nitride | |
JP2014216331A (en) | Plasma etching method | |
JP7190988B2 (en) | Etching method and substrate processing apparatus | |
WO2014206296A1 (en) | Substrate etching method | |
US11658040B2 (en) | Plasma processing method | |
JP5154013B2 (en) | Dry etching method | |
EP3046137A1 (en) | Etching method | |
JP2012227334A (en) | Plasma processing method | |
US20240203751A1 (en) | Plasma processing method | |
CN114944331A (en) | Semiconductor process and semiconductor device | |
CN113906829A (en) | Plasma etching method | |
CN115172153A (en) | Method for improving uniformity in silicon groove etching | |
WO2011115008A1 (en) | Etching method and etching device | |
CN111106005A (en) | Pattern trimming method and plasma processing device |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |