WO2018190780A1 - Chemical mechanical planarization of gallium nitride - Google Patents
Chemical mechanical planarization of gallium nitride Download PDFInfo
- Publication number
- WO2018190780A1 WO2018190780A1 PCT/TR2017/050138 TR2017050138W WO2018190780A1 WO 2018190780 A1 WO2018190780 A1 WO 2018190780A1 TR 2017050138 W TR2017050138 W TR 2017050138W WO 2018190780 A1 WO2018190780 A1 WO 2018190780A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- slurry
- cmp
- pad
- slurry composition
- acid
- Prior art date
Links
- 239000000126 substance Substances 0.000 title claims abstract description 28
- JMASRVWKEDWRBT-UHFFFAOYSA-N Gallium nitride Chemical compound [Ga]#N JMASRVWKEDWRBT-UHFFFAOYSA-N 0.000 title claims description 69
- 229910002601 GaN Inorganic materials 0.000 title claims description 62
- 239000002002 slurry Substances 0.000 claims abstract description 146
- 238000000034 method Methods 0.000 claims abstract description 61
- 238000005498 polishing Methods 0.000 claims description 47
- 239000000203 mixture Substances 0.000 claims description 34
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 19
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 17
- 239000002253 acid Substances 0.000 claims description 15
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 14
- 239000002245 particle Substances 0.000 claims description 14
- 239000000758 substrate Substances 0.000 claims description 10
- 239000007787 solid Substances 0.000 claims description 7
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 6
- 239000003002 pH adjusting agent Substances 0.000 claims description 6
- 239000000377 silicon dioxide Substances 0.000 claims description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical group [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 5
- 239000012736 aqueous medium Substances 0.000 claims description 5
- 229910021529 ammonia Inorganic materials 0.000 claims description 4
- 238000011176 pooling Methods 0.000 claims description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims 3
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 claims 2
- 239000005639 Lauric acid Substances 0.000 claims 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims 1
- 239000011976 maleic acid Substances 0.000 claims 1
- 235000006408 oxalic acid Nutrition 0.000 claims 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims 1
- 239000000463 material Substances 0.000 abstract description 42
- 230000008569 process Effects 0.000 abstract description 33
- 230000001965 increasing effect Effects 0.000 abstract description 12
- 230000000694 effects Effects 0.000 abstract description 8
- 238000012512 characterization method Methods 0.000 abstract description 5
- 238000005457 optimization Methods 0.000 abstract description 4
- 238000013461 design Methods 0.000 abstract description 3
- 230000003993 interaction Effects 0.000 abstract description 3
- 238000011161 development Methods 0.000 abstract description 2
- 235000012431 wafers Nutrition 0.000 description 19
- 238000006243 chemical reaction Methods 0.000 description 12
- 230000003750 conditioning effect Effects 0.000 description 9
- 230000004044 response Effects 0.000 description 8
- 238000002474 experimental method Methods 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 230000003746 surface roughness Effects 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000000523 sample Substances 0.000 description 5
- 239000008119 colloidal silica Substances 0.000 description 4
- 230000007547 defect Effects 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 238000004377 microelectronic Methods 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 238000012216 screening Methods 0.000 description 4
- 239000004065 semiconductor Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 210000000078 claw Anatomy 0.000 description 3
- 238000004090 dissolution Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000007517 polishing process Methods 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- 230000006978 adaptation Effects 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 230000003247 decreasing effect Effects 0.000 description 2
- 239000004053 dental implant Substances 0.000 description 2
- 229910003460 diamond Inorganic materials 0.000 description 2
- 239000010432 diamond Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- -1 hydroxide ions Chemical class 0.000 description 2
- 239000007943 implant Substances 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 238000009434 installation Methods 0.000 description 2
- 230000000670 limiting effect Effects 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000002105 nanoparticle Substances 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 238000004439 roughness measurement Methods 0.000 description 2
- 238000005488 sandblasting Methods 0.000 description 2
- 238000012876 topography Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 238000002048 anodisation reaction Methods 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 239000012776 electronic material Substances 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000005669 field effect Effects 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000010191 image analysis Methods 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 238000005468 ion implantation Methods 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000001459 lithography Methods 0.000 description 1
- 238000003913 materials processing Methods 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 238000007521 mechanical polishing technique Methods 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000001465 metallisation Methods 0.000 description 1
- 238000005329 nanolithography Methods 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 238000000206 photolithography Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000007788 roughening Methods 0.000 description 1
- 229910052594 sapphire Inorganic materials 0.000 description 1
- 239000010980 sapphire Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000009897 systematic effect Effects 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
- H01L21/02—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
- H01L21/30625—With simultaneous mechanical treatment, e.g. mechanico-chemical polishing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B24—GRINDING; POLISHING
- B24B—MACHINES, DEVICES, OR PROCESSES FOR GRINDING OR POLISHING; DRESSING OR CONDITIONING OF ABRADING SURFACES; FEEDING OF GRINDING, POLISHING, OR LAPPING AGENTS
- B24B37/00—Lapping machines or devices; Accessories
- B24B37/04—Lapping machines or devices; Accessories designed for working plane surfaces
- B24B37/042—Lapping machines or devices; Accessories designed for working plane surfaces operating processes therefor
- B24B37/044—Lapping machines or devices; Accessories designed for working plane surfaces operating processes therefor characterised by the composition of the lapping agent
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09G—POLISHING COMPOSITIONS; SKI WAXES
- C09G1/00—Polishing compositions
- C09G1/02—Polishing compositions containing abrasives or grinding agents
Definitions
- the CMP material removal rate of Ga depends on the crystallographic orientation of the GaN surface and hence it is beneficial to determine the specific crystallographic orientation of the GaN surface prior to CMP.
- a simple and accurate method of surface crystalline structure determination is desirable prior to CM] 3 process setup.
- the type of surface crystalline structure can be determined by wettability (contact angle) measurements in accordance with embodiments of the present disclosure.
- Figure 7 is an enlarged view of the CMP device and the distal end of the robotic arm of Figure 6 in accordance with embodiments of the present disclosure.
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (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)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Mechanical Treatment Of Semiconductor (AREA)
- Finish Polishing, Edge Sharpening, And Grinding By Specific Grinding Devices (AREA)
Abstract
The present invention provides for the characterization of the surface chemical nature of GaN samples and optimization of the CMP process in terms of material removal rates and surface quality by slurry chemistry and tool design development. It was observed that GaN CMP is preliminarily driven by the chemical impact from the slurry chemical interactions based on the observation of increasing material removal rates and better surface quality when the mechanical components of the CMP process are kept less aggressive while the chemical components are promoted. The effect of the CMP process set-up variables such as applied downforce, pad type, and slurry flow rate and temperature are also evaluated to optimize the CMP performance.
Description
The present invention is related to chemical mechanical pianarization (CMP) of hard and difficult materials to polish such as gallium nitride (GaN) and alternative I07V, II/VI semiconductors, and in particular to chemical modification of CMP slurries, adaptation of processes, and tool setup to the particular design and chemistry requirements for these specific slurry modifications used in microelectronics and photonics semiconductor device manufacturing.
GaN has become a material of choice for semiconductor applications that require direct and wide band-gap energy and high power applications. It is highly utilized for light-emitting diodes (LEDs), and high-power, high-frequency field effect transistor (FET) devices. Particularly, the utilization of GaN in LED applications requires a very smooth and defect free surface finish, and hence CMP is needed after its deposition. Epitaxial layers of GaN are most commonly grown on sapphire substrates, although other substrates such as silicon substrates may be implemented as well. However, large lattice mismatch and difference in thermal expansion between the GaN layer or film and the substrate often results in defects in the epitaxial GaN film, thereby limiting the performance of the manufactured device. GaN is also known to be a difficult material to polish due to its hardness. Thus, introducing CMP on a film that is poorly grown due to epitaxial challenges, in addition to GaN being a very hard film, makes the use of GaN a challenging task.
The preliminary studies on CMP of GaN in the literature using colloidal silica based slurries focused on modulating the CMP performance mainly by increasing the applied downforce or pre-polishing the GaN surface by using a diamond-based abrasive slurry that enhanced the mechanical abrasions. Although the diamond-based slurries were able to remove GaN, the surface finish was very rough. The colloidal silica based slurries were able to improve surface quality by enabling polishing on the Ga reach face of GaN (Face-β), but the nitrogen reach face (Face-cc) showed an extremely low polishing rate due to chemical inertness. However, it served as important evidence that softer silica particles were able to remove the hard GaN material without inducing sub-surface damage. Prior research has also proposed a basic chemical interaction mechanism explaining the reaction on the -face of GaN in the colloidal silica based
slurry. The mechanism suggests that along the [1 1 2 0] direction for N-polar Ga selective etching takes place through: (i) formation of a nitrogen terminated layer with one negatively- charged dangling bond on each nitrogen atom; (ii) adsorption of hydroxide ions; (iii) formation of oxides; and (iv) dissolution of the oxides. While there are conventional techniques available for the application of planarization on materials surfaces, such as sandblasting, nano-lithography, anodic oxidization, ion implantation, and the like, most of these techniques have some disadvantages such as: (i) the tendency of particles used in sandblasting to stick on the metal surfaces creating points of anodization; (ii) lithography techniques being very expensive; and furthermore the fact that neither of these techniques can help prevent corrosion,
GaN is a difficult material to polish and mechanical polishing techniques typically result in poor surface quality. It is therefore highly desirable to improve the post-CMP surface quality and removal rates of GaN in order to improve various applications, such as in the manufacture of LED and microelectronics devices, SUMMARY
Gallium Nitride (GaN) is a key electronic material for light emitting diode (LED) applications based on its direct band gap and high power adoptability. Manufacturing LEDs made of GaN requires enhanced smoothness and wafer planarity that necessitates the application of a chemical mechanical planarization (CMP) process. GaN is a difficult material to polish and planarize due to its hardness. Mechanical polishing applications result in limited removal rates and unacceptable surface quality and hence a chemical component is required to enable smooth surface finish and optimal material removal rates. The present invention provides for the characterization of the surface chemical nature of GaN samples and optimization of the CMP process in terms of material removal rates and surface quality by slurry chemistry and tool design development. It was observed that GaN CMP is preliminarily driven by the chemical impact from the slurry chemical interactions based on the observation of increasing material removal rates and better surface quality when the mechanical components of the CMP process are kept less aggressive while the chemical components are promoted. The effect of the CMP process set-up variables such as applied downforce, pad type, and slurry flow rate and temperature were also evaluated to optimize the CMP performance.
The present disclosure provides optimized CMP setup procedures for GaN through characterization of the surface nature of GaN samples and then correlating the results to the
surface energy, surface wettability, and CMP. The effect of the CMP process setup variables such as slurry/platen rotational speed, slurry temperature, pad conditioning, applied down-force and slurry flow rate are outlined to obtain optimal CMP results through increased material removal rate response, reduced surface roughness and defects for LED applications as well as integrated microelectronics device fabrication where GaN is used.
The CMP material removal rate of Ga depends on the crystallographic orientation of the GaN surface and hence it is beneficial to determine the specific crystallographic orientation of the GaN surface prior to CMP. A simple and accurate method of surface crystalline structure determination is desirable prior to CM]3 process setup. The type of surface crystalline structure can be determined by wettability (contact angle) measurements in accordance with embodiments of the present disclosure.
The system and process of the present disclosure each helps improve the GaN removal rate by 6 to 10 times as compared to the conventional CMP implementations. The system and process of the present disclosure al so improve surface roughness by 2 to 3 times. The process setup is optimized in terms of slurry flow rate, solids concentration, pH, temperature, and applied down force.
The present disclosure also introduces a procedure of adding an acid, such as hydrochloric acid (HC1), citric acid or similar acid, at the pad surface in conjunction with a high pH slurry formulation to neutralize the ammonia generated as a product of the GaN dissolution reaction. Hence, the present disclosure stimulates the reaction towards the products side, thereby- improving material removal rates.
The present disclosure also introduces a tool setup with a slurry pool designed on top of the platen and the polishing pad that helps minimize the slurry consumption in combination with the neutralization process of the ammonia (N¾) that is a product of the GaN dissolution reaction.
The present disclosure may be utilized with a two-dimensional (2D) CMP process and processing tool, a three-dimensional (3D) configured CMP processing tool with the integration of a robotic arm and a force/torque sensor sample holder, and the like, to enable improved CMP of GaN layers and also nano-structuring of multidimensional objects.
CMP is a process that is used to planarize the wafer surfaces in microelectronics manufacturing to enable multi-layer metallization. A CMP process employs slurries that involve an aggressive chemistry to alter the properties of the layer or film to be polished and this film is removed by the mechanical actions of the particulates in the suspension. In one example particularly applied
to metallic layers the formation of a metal oxide film may be self-limiting and once formed, it can protect the underlying metal from further attack of the slurry chemicals. This allows the polishing of the higher level metal while protecting the lower levels; in other words, to achieve topographic selectivity and hence provide planarization. In another example, the polishing and material removal of the oxide type layers is achieved by formation of a hydrated gel-like layer on the surface of the material through mainly a pH adjustment.
It is possible to induce roughness on the surfaces of the metallic materials at variable root mean square (RMS) values by changing the polishing pads as well as slurry formulations (both chemicals and the sizes and solids loading of the slurry nano-particles) used during the CMP process, which affect the surface roughness both chemically and mechanically.
Through utilization of a CMP system and/or process in a controlled manner, it is plausible to induce improved material removal rates and also improved polished surface quality with nano- scale smoothness as well as nano-scale roughness for GaN layers in various applications, such as in materials science and engineering fields where processes are frequently required to improve the surfaces of the materials.
The present disclosure provides systems, tools, and methods that improve efficient smoothening or roughening of the materials surface, both mechanically and chemically, to provide highly efficient material removal rates and surface quality while providing efficient usage of slurry raw materials, and in some cases nano-structuring. Thus, another aspect of the present disclosure is to provide a process, which can perform nano-structuring by employing CMP techniques.
Furthermore, the present disclosure may be easily adoptable to the other fields of materials processing with adjustments and process configurations. Hence, it will be possible to apply the innovation on three dimensional materials in a number of sectors where surface structure (roughness or smoothness) is important besides the semiconductor and photonics industries, such as in automotives, biomateriais, aircrafts, resistors, implants, and the like.
In accordance with embodiments of the present disclosure, a slurry composition for chemical mechanical polishing of a gallium nitride layer is comprised of: a silica particle based slurry; wherein the slurry has a particle size between 0,04 μη - 0.2 μηι; wherein the slurry has a temperature between 2 °C - 25 °C; wherein the slurry has a pH between 3 - 12; a pH adjusting agent, and an aqueous medium, wherein the slurry composition is comprised of 5 - 25 wt% solids, and wherein the slurry composition is combined with an acid prior to chemical mechanical poll shing.
In accordance with other embodiments, a method for chemical mechanical polishing of a gallium nitride layer is provided. The method comprises providing a slurry composition as described above. The method further includes applying an acid to a polishing pad; and applying the slurry composition onto the substrate with the polishing pad.
In accordance with yet other embodiments, a system for chemical mechanical polishing (CMP) of a gallium nitride layer is comprised of: a carrier/chuck for holding a gallium nitride wafer to be polished; a CMP device (B) including: a rotatable pad (D) for CMP including a a slurry retainer, the slurry retainer having a base coupled to the pad (D), a retaining cylinder coupled to the base, and a cover coupled to the retaining cylinder; and a slurry pump system for providing a slurry composition as described above to the pad (D), the slurry composition pooled within the slurry retainer, and an acid applied to the pad (D) prior to CMP. DESCRIPTION OF THE FIGURES
Systems and methods according to the invention and some particular embodiments thereof will be described with reference to the following figures. These and other features, aspects, and advantages of the present invention will become better understood when the following detailed description is read with reference to the accompanying drawings in which like characters represent like parts throughout the drawings. Some embodiments are illustrated by way of example and not limitation in the figures of the accompanying drawings. Unless noted, the drawings may not be drawn to scale.
Figures 1 A and I B illustrate a top view and a sectional view, respectively, of a 2D CMP system in accordance with embodiments of the present disclosure. Figures 2A, 2B, and 2C illustrate a perspective view, a side view, and a top view, respectively, of an assembly of the slurry retainer parts in accordance with embodiments of the present disclosure.
Figures 3 A-3E illustrate different views of a cover component of a slurry retainer for a rotatable CMP pad in accordance with embodiments of the present disclosure, Figures 4 A-4E illustrate different views of a retaining cylinder component of slurry retainer for a rotatable CMP pad in accordance with embodiments of the present disclosure.
Figures 5A-5E illustrate different views of a base component of a slurry retainer for a rotatable CMP pad in accordance with embodiments of the present disclosure.
Figure 6 shows a configuration of a CMP device and a robotic arm that is used to hold the work piece against the CMP device for 3D CMP in accordance with embodiments of the present disclosure.
Figure 7 is an enlarged view of the CMP device and the distal end of the robotic arm of Figure 6 in accordance with embodiments of the present disclosure.
Figure 8 illustrates an assembly perspective view of the robotic arm configuration employed in the method used for 3D CMP configuration in accordance with embodiments of the present disclosure.
Description of Part References
A. Robotic arm configuration
1. Industrial robotic arm
2. Flange
3. Connection plate
5, Force-torque sensor
9. Retainer base
10. Retainer head
1 1. Fastener
B. CMP device
1 10. Slurry retainer
1 12. Cover
1 14. Retaining cylinder
1 16. Base
120. Slurry pump system
130. C arri er/chu ck
140. Wafer
150. Pad conditioner
160. Platen
C. Work piece
D. Pad
DETAILED DESCRIPTION
A systematic experimental approach was followed to determine the conditions to promote material removal rate while controlling surface defects for GaN CMP. Initially, surface characterization of a 2" GaN wafer was conducted through FTIR and the results were compared to the surface energy and wettability responses enabling an easy approach to predict the material removal rates of GaN. Furthermore, CMP tests were performed as a function of applied downforce, slurry flow rate, slurry pH, and temperature adjustment, as well as with and without conditioning by using a mono-sized commercial silica slurry. The optimal polishing conditions were implemented to screen for the polishing pad selection that can enable high removal rates while protecting the surface quality in terms of minimum surface roughness.
Materials
2" diameter n-type GaN wafers with 350±25 micrometer of GaN deposited on a silicon substrate or bulk GaN coupons with a and β sides exposed at the front and backside, respectively.
Polishing slurry was chosen as a baseline silica slurry. Slurry pH was consistently kept at pH 9 for all the experiments other than the study conducted on evaluating the effect of pH on material removal rate (MRR). The polishing slurry was detected to be 0.109 micrometer based on differential volume percent. A standard IC 1000/Suba IV stacked polishing pad with K-grove was used for the preliminary experiments conducted to study the effects of applied downforce, slurry pH, flow rate and pad conditioning. The effect of pad aging by extensive conditioning (up to 100 wafers) and pad type were also evaluated on the MRR response of the GaN wafers.
Methods
Wettability and surface energy analyses: The wettability and surface energy calculations of the GaN wafer was based on the contact angle measurements performed by sessile-drop contact angle measurement technique by KSV ATTENSION Theta Lite Optic Contact Angle Goniometer, Three bubbles were measured on each sample and the results were averaged. The bubble image stored by a camera and an image analysis system was used to calculate the contact angle (Θ) based on the shape of the bubble. In order to measure the surface energy and determine the work of adhesion of the GaN surfaces as a function of the temperature, an acid-base technique was adopted. Polar and apolar probe liquids were selected following standard procedures including ethylene glycol, formamide, glycerol, and deionized water.
CMP experiments: CMP experiments were conducted on a desktop Tegrapol-31 polisher by using a standard IC 1000/Suba IV pad for the preliminary screening analyses. The down force was set to 100 N after optimization on the 2" diameter wafer coupons with 100 rpm rotational velocity and 25 mi/min slurry flow rate. Ail the CMP tests were performed for at least 5 minutes. CMP responses were obtained in terms of M R (A/min) and surface roughness measurements. The material removal rates were determined from the difference in the weights of the wafers before and after polishing measured by using a PRECISA 360 ES scientific balance with 0.01 mg accuracy.
Surface topography analyses: Surface roughness measurements were conducted by Nanomagnetics Instruments Atomic Force Microscope (AFM) on 2.5-μηι by 2.5-μιη scans using contact mode. The averages of minimum measurements were reported including the standard deviations to verify the statistical significance of the observed values.
Table 1 below includes ranges for various CMP settings or variables used for analysis.
Table 1
Optimization of operational CMP variables and consumables to maximize MRR response:
CMP tests were conducted on a desktop Tegrapol-31 polisher by using a standard SUBAIV- IC1000 stacked K-grove polishing pad. 2" GaN wafers were polished with an aged IC 1000/Suba IV stacked polishing pad (with in-situ conditioning) at room temperature (~23°C) and 30 N downforce. The MRR value of -10 A/min was obtained. When a fresh set of consumables were adopted, the new IC 1000/Suba IV stacked pad was only able to remove ~6 A/min of GaN. Hence, for the preliminary screening, the aged IC 1000 pad was used.
In order to improve the MRR responses of the GaN wafers, experimental evaluations were started by screening the operational variables of the CMP process, namely the applied downforce and slurry flow rate. The effect of downforce was studied first by varying the values between 30 N to 200 N and retaining the platen and head rotational speeds at 100 rpm and the slurry flow rate at 20-25 ml/min. All polishing experiments were conducted for 5 minutes. Material removal rates as a function of the applied downforce using the standard colloidal silica slurry were determined. It was observed that the MRR values increased with increasing downforce up to 100 N (7, 15 psi) but decreased above the 100 N setting. Although not limited to this theory, it is suspected the decrease in the MRR can be explained by the limited slurry flow between the pad surface and the wafer surface at this high pressure setting. Furthermore, the very high pressure settings also resulted in elevated friction and heating of the pad at the 200 N downforce. Therefore, the optimal downforce was set to 100 N for the following experiments. In order to verify the impact of efficient slurry flow, the CMP tests were also conducted at 100 N with and without using in-situ conditioning and it was observed that the MRR values decreased from 40 A/min (with conditioning) to 36 A/min. These results also verified the tendency of increasing removal rates with more efficient slurry feeding between the pad and the wafer surface by use of conditioning. As another standard CMP setup variable, the effect of slurry flow rate on MRR responses was evaluated under the same experimental conditions by setting the downforce to 100N. MRR values were observed to tend to increase with increasing slurry flow up to 25 ml/min and then reach a plateau. Hence, as the second process variable the slurry flow rates were set to 25 ml/min.
After the mechanical factors of the CMP process were set, the impact of slurry chemistry on removal rates was studied. The correlation between pH and MRR response was observed to be a direct correlation and the MRR values increased with increasing pH. Based on the through screening of the process settings, slurry properties and surface characterization, Table 2 below summarizes the optimal CMP conditions for GaN planarization in accordance with embodiments of the present disclosure. Although the removal rates are still limited, they can be modulated by setting the pressure values to -7-15 psi with 20-25 ml/min slurry flow rates and 100 rpm of platen and head rotational velocity at slurry pH of 9 for 2" GaN wafers.
Material Removal Rate Analyses with 0.1 M Nth as a Function of HC1 Addition during CMP:
GaN has two crystallographic faces, alpha and beta. Between these faces, the Alpha phase is typically harder to polish yet preferred for LED applications.
The differences in etch characteristics of the Ga-reach beta-face and the N-reach alpha-face have been examined in a number of studies. As an example, Palacois et al . demonstrated that the nitrogen polar GaN epiiayers (alpha-face) were etched in aqueous KOH between 26 and 80°C. The hydroxide ions (OFF) are first adsorbed on the GaN sample surface and subsequently react with Ga atoms following reaction [1] below:
KOH
2GaN + 3H20 + Ga203 + 2NH3 [1]
According to this reaction, in a basic environment (after adding the KOFI), the reaction shifts to the right side resulting in more effective removal of N as NH3. Hence, in order to promote the removal of the N layer, the reaction needs to be shifted to the products side. This action can be accomplished through (i) increasing the GaN as a reactant or (ii) removal of the NH3 that forms
as a reaction product. Since the GaN surface area cannot be changed on a given wafer size, the more practical method is to promote the formation of H3 by removing it from the reaction products through addition of an acidic component. Therefore, HQ addition to the CMP pad surface was analyzed during the polishing application. Experiments and observations were carried out to increase MRR values of GaN in a silica based polishing slurry with 0.1 M NH3 as a function of HCl concentration at pH 9-1 1 at room temperature. The maximum MRR was observed with the same concentration of NH3 and HCl usage by using a SUBAIV-IC1000 stacked polishing pad. It was observed that the additional flow of HCl into the polishing environment at the same molar concentration as the NH3 promoted removal rates (increased MRR value). If the HCl concentration was higher than the NH3 concentration, the removal rates tended to decrease, which is expected due to the shift of the reaction towards the reactants side. Likewise, if an acidic slurry is used and an NH based flow is supplied to the pad surface, removal rates are negligible. In addition, the same process application on the pure silicon wafer also resulted in no material removal rate change. Hence, the addition of the same concentration of HCl or a weak acid to a H3 based slurry during the polishing operation promoted material removal, particularly at low temperatures. Hence, an aspect of the present invention promotes GaN removal by adding the same molarity of HCl or similar acidic media during the CMP process.
Adaptation of the proposed process on a new too! setup A new tool set up is introduced in combination with the proposed process improvements in which the slurry is deposited on the polishing platen where a modification is made to collect the slurry in a pool. Since the reaction continuously produces ammonia during the polishing process the introduction of a small amount of HCl or similar acid would help push the reaction towards the products side and hence enable material removal on the GaN sample. This confi guration helps prevent excessive slurry consumption during the polishing of bulk GaN films while enabling faster material removal rates. A following buffing step can be introduced on a secondary polishing platen to further control the surface quality of the GaN wafers.
Example robotic arm configurations with a new tool set up are now explained in further detail.
First Alternative Configuration Referring now to Figures 1A and IB, a top view and a sectional view of a 2D CMP system 100 are respectively illustrated in accordance with embodiments of the present disclosure.
System 100, for 2D chemical mechanical polishing (CMP), includes a rotatable pad D on a platen 160, a slurry retainer 110, a slurry pump system 120 for providing a slurry composition to the pad D, and a carrier/chuck 130 for holding a wafer 140 to be polished. System 100 may further include a conditioner 150 for conditioning pad D. In one example, the slurry composition may comprise a silica particle based slurry; wherein the slum' has a particle size between 0,04 μτη - 0,2 μτη; wherein the slurry has a temperature between 2 °C - 25 °C; wherein the slurry has a pH between 3 - 12; a pH adjusting agent; an aqueous medium, wherein the slurry composition is comprised of 5 - 25 wt% solids; and an acid applied to the pad (D) prior to CMP. Pad D and wafer 140 are pressed together by dynamic carrier/chuck 130, which may be rotated with different axes of rotation (e.g., non-concentric). This removes material and tends to even out any irregular topography, making the wafer flat or planar. For example, CMP can bring the entire surface within the depth of field of a photolithography system, or selectively remove material based on its position, As noted above, slurry retainer 1 10 provides for collecting the slurry in a pool, which then allows for the introduction of a small amount of HC1 or similar acid to push the reaction towards the products side and hence enables improved material removal on the GaN wafer. This configuration helps prevent excessive slurry consumption during the polishing of bulk GaN films while enabling faster material removal rates. Figures 2A-2C illustrate a perspective view, a side view, and a top view, respectively, of an assembly of components of the slurry retainer 1 10 in accordance with embodiments of the present disclosure. Slurry retainer 110 includes a base 116 for mounting to pad D and/or platen 160, a retaining cylinder 114 mounted on base 116 and/or pad D along an outer lip region 1 4a, and a cover 112 mounted on retaining cylinder 1 14 along the outer lip region 114a. In other words, pad D is positioned between retaining cylinder 14 and base 1 16.
Figures 3A-3E illustrate different views of cover 1 12 of slurry retainer 1 0 for a rotatable CMP pad in accordance with embodiments of the present disclosure. Figure 3B is a sectional view of cover 1 12 along line B-B in Figure 3A. Figure 3C is a top view and Figure 3E is a bottom perspective view of cover 1 12. Figure 3D is an upright side view of cover 1 12. Figures A-4E illustrate different views of retaining cylinder 114 of slurry retainer 110 for a rotatable CMP pad in accordance with embodiments of the present disclosure. Figure 4B is a sectional view of retaining cylinder 114 along line C-C in Figure 4A. Figure 4C is a top view and
Figure 4E is a top perspective view of retaining cylinder 1 14. Figure 4D is an upright side view of retaining cylinder 1 14. Retaining cylinder 114 includes outer lip region 114a used for mounting to the base and the cover, and a retaining wall 1 14b for pooling the slurry.
Figures 5A-5E illustrate different views of base 116 of slurry retainer 1 10 for a rotatable CMP pad in accordance with embodiments of the present disclosure. Figure 5B is a sectional view of base 116 along line D-D in Figure 5 A. Figure 5C is a top view and Figure 5E is a top perspective view of base 16. Figure 5D is an upright side view of base 1 16.
When slurry retainer 110 is mounted onto pad D and/or platen 160, the slurry composition from slurry pumping system 150 may be collected within retaining wall 114b to pool the slurry for addition of acid and CMP processing. Advantageously, this configuration helps prevent excessive slurry consumption during the polishing process (e.g., of bulk GaN films) while enabling faster material removal rates.
Second Alternative Configuration
Referring now to Figure 6, a system 200 is illustrated including a CM3 device and a robotic arm that is used to hold the work piece against the CMP device for 3D CMP in accordance with embodiments of the present disclosure.
Figure 7 is an enlarged view of the CMP device and the distal end of the robotic arm of Figure 6 in accordance with embodiments of the present disclosure.
Figure 8 illustrates an assembly perspective view of the robotic arm configuration employed in the method used for 3D CMP configuration in accordance with embodiments of the present disclosure.
Referring now to Figures 6-8, a robotic arm configuration (A) is comprised of an industrial robot arm (1), a flange (2), connection plates (3), a force-torque sensor (5), a retainer base (9), a retainer head (10), and a fastener (1 1). In the robotic arm configuration (A), industrial robot arm (1) has industrial serial kinematics configuration with 6 degrees of freedom. The aforementioned industrial robot arm (1 ) ensures access to any point from any angle in 3 dimensional space, based on these features. Flange (2) connects the connection plates (3) and industrial robotic arm (1) together. Robotic arm configuration (A) contains two connection plates (3). The function of connection plates (3) is to connect force-torque sensor (5) to the flange (2). Function of force-torque sensor (5) is to measure the force between the surface of the work piece (C) and the pad (D ), Retainer base (9) is
the part where retainer head (10) is placed inside. Retainer head (10) is the component, which retains the work piece (C). Fastener (11) is preferably a nut and used as an apparatus for tightening the retainer head ( 10) to the retainer base (9), Retainer is composed of retainer base (9), retainer head (10) and fastener (11). A configuration, which is similar to a claw, can be used as a retainer instead of these components.
Installation of the robotic arm configuration may be realized as follows. Firstly, the work piece (C) which is preferably a dental implant is placed inside the retainer head (10). Then, by tightening the fastener (1 1) work piece (C) as an example an implant, is tightened inside the retainer head (10). In a configuration where a claw is used as retainer, this installation steps can be omitted and the work-piece can be retained by the help of a claw. Force-torque sensor (5) is located between retainer and industrial robotic arm (1). Two connection plates (3) are used to fix the force-torque sensor (5) to the industrial robotic arm (1). One of the connection plates (3) is screwed to connect force-torque sensor (5) and the second one to the flange (2). Two connection plates (3) are screwed together to fix force-torque sensor (5) to the industrial robot arm (1). Pad (D) is contacted to the surface of the work piece (C) to ensure structuring or smoothing the aforementioned surface. Different types of pads (D) can be used in the robotic arm configuration
(A) . A slurry retainer (110) as described above is again mounted to pad (D) to enable pooling of the slurry for receiving acid, improving slurry consumption efficiency, and improving material removal rates. A robotic arm configuration may function as follows. First of all, the work piece (C) is held by the retainer and the pad (D), which will be used in the process is positioned inside the CMP device (B) according to the shape of the surface and location of the work piece by the help of the industrial robotic arm (1). The work piece (C) is pressed against the pad (D) by the help of the industrial robotic arm (!) and a contact surface is established between the pad (D) and the work piece (C). The force created on the aforementioned contact surface is measured by a force-torque sensor (5), retainer is positioned again to the force values determined beforehand and it is ensured that the work piece (e.g., a dental implant) is kept still by the industrial robotic arm (1). With the pad (D) installed, the pad table of the CMP device (B) originates rotation at a predefined speed to ensure mechanical abrasion on the contact surface. Meanwhile, chemical is fed to the work piece (C) at the required quantity by the slurry pump system of the CMP device
(B) throughout the predefined process and mechanical removal is performed on the surface of the work piece as a result of the friction occurring on the contact surface between the pad (D) and the work piece. Also, by the help of the slurry chemicals, a non-porous and protective oxide
layer may be formed on the surface of the work piece and the hence the processed surface is protected. The retainer is positioned at different positions by the industrial robotic arm (1) to ensure that the overall surface of the work piece (C) is exposed during polishing uniformly. Upon performing positioning, aforementioned processes, which are listed below, are performed in a cycle until the entire surface of the work piece (C) is treated:
- measurement of the force created on the contact surface by force-torque sensor (5),
- repositioning of the retainer to the predefined force values;
- rotation of the pad table of CMP device (B) which is installed with the pad (D) at a defined speed; slurry flow on the work piece (C);
- positioning of the retainer at different positions during polishing process by the industrial robotic arm (1).
Chemical agents administered by the pump system of the CMP device (B) may vary dependent on the work piece (C) and may contain nano-particles of varying structures, water-based chemicals, surfactants etc.
The foregoing examples have been provided merely for the purpose of explanation and are in no way to be construed as limiting of the present invention. While the present invention has been disclosed with reference to embodiments, the words used herein are intended to be words of description and illustration, rather than words of limitation, W e the present invention has been described with reference to particular materials and embodiments, the present invention is not intended to be limited to the particulars disclosed herein. Rather, the present invention extends to all functionally equivalent structures, materials, and uses, such as are within the scope of the appended claims. Changes may be made, within the purview of the appended claims, as presently stated and as may be amended, without departing from the scope and spirit of the present invention. All terms used in this disclosure should be interpreted in the broadest possible manner consistent with the context.
Claims
1. A slurry composition for chemical mechanical polishing of a gallium nitride layer, the slurry composition comprising:
a silica particle based slurry;
wherein the slurry has a particle size between 0,04 μηι - 0.2 μη ; wherein the slurry has a temperature between 2 °C - 25 °C;
wherein the slurry has a pH between 3 - 12;
a pH adjusting agent; and
an aqueous medium,
wherein the slurry composition is comprised of 5 - 25 wt% solids, and
wherein the slurry composition is combined with an acid prior to chemical mechanical polishing, 2. The slurry composition according to claim 1, wherein the particle size of the slurry is between 0.04 μιη - 0,08 μηι.
3. The slurry composition according to claim 1, wherein the temperature of the slurry is between about 2 °C and 4 °C.
4. The slurry composition according to claim 1 , wherein the pH of the slurry is about 9.
5. The slurry composition according to claim 1, wherein the pH adjusting agent is potassium hydroxide or ammonia,
6. A method for chemical mechanical polishing of a gallium nitride layer, the method comprising:
providing a slurry composition comprising:
a silica particle based slum';
wherein the slurry has a particle size between 0.04 μιη - 0.2 μηι;
wherein the slurry has a temperature between 2 °C - 25 °C;
wherein the slurry has a pH between 3 - 12;
a pH adjusting agent; and
an aqueous medium,
wherein the slurry composition is comprised of 5 - 25 wt% solids; applying an acid to a polishing pad; and
applying the slurry composition onto the substrate with the polishing pad. 7. The method according to claim 6, wherein the particle size of the slurry is between 0.04 μτη - 0.08 μιη.
8. The method according to claim 6, wherein the temperature of the slurry is between about 2 °C and about 4 °C.
9. The method according to claim 6, wherein the pH of the slurry is about 9,
10. The method according to claim 6, wherein the slurry composition is applied onto the substrate with the polishing pad at a force between 3 psi and 15 psi and at a rotational speed between 100 rpm and 150 rpm.
1 1. The method according to claim 6, wherein the slurry composition is applied onto the substrate with the polishing pad at a force between 7 psi and 8 psi and at a rotational speed between 100 rpm and 150 rpm.
12. The method according to claim 6, wherein the slurry composition is supplied to the polishing pad at a flowrate between 10 ml/minute and 200 ml/minute.
13. The method according to claim 6, wherein the slurry composition is supplied to the polishing pad at a flowrate between about 50 ml/minute and about 70 ml/minute.
14. The method according to claim 6, wherein the acid applied to the polishing pad is selected from the group consisting of acetic acid, citric acid, maleic acid, oxalic acid, lauric acid, hydrochloric acid, and a combination thereof. 5. The method according to claim 6,
wherein the slurry has a particle size between 0.04 μηι - 0.08 μηι;
wherein the slurry has a temperature between 3 °C - 4 °C;
wherein the slurry has a pH of about 9; and
further comprising:
supplying the slurry composition to the polishing pad at a flow rate of about 20-25 ml/minute; and
applying the slurry composition onto the substrate with the polishing pad at a force of about 7-15 psi and at a rotational speed of about 100 rpm.
16. A system, for chemical mechanical polishing (CMP) of a gallium nitride layer, the system comprising:
a carrier/chuck for holding a gallium nitride wafer to be polished;
a CMP device (B) including:
a rotatable pad (D) for CMP including a a slurry retainer, the slurry retainer having a base coupled to the pad (D), a retaining cylinder coupled to the base, and a cover coupled to the retaining cylinder;
a slurry pump system for providing a slurry composition to the pad (D), the slurry composition comprising:
a silica particle based slurry;
wherein the slurry has a particle size between 0.04 μηι - 0.2 μηι;
wherein the slurry has a temperature between 2 °C - 25 °C;
wherein the slurry has a pH between 3 - 12;
a pH adjusting agent; and
an aqueous medium,
wherein the slurry composition is comprised of 5 - 25 wt% solids; and an acid applied to the pad (D) prior to CMP.
17, The system according to claim 16, further comprising a robotic arm configuration (A) including:
a robotic arm (1) having serial kinematics configuration with 6 degrees of freedom,
a force-torque sensor (5) operably coupled to a distal end of the robotic arm (1), and
a work piece retainer operably coupled to a distal end of the force-torque sensor (5), the work piece retainer for holding a work piece (C) including a gallium nitride layer,
18, The system according to claim 16, wherein the carrier/chuck applies a force between 3 psi and 15 psi to the wafer and wherein the pad provides a rotational speed between 100 rpm and 150 rpm.
19, The system according to claim 16, wherein the slurry pump system supplies the slurry composition to the polishing pad at a fiowrate between 10 ml/minute and 200 ml/minute.
20, The system according to claim 16, wherein the retaining cylinder includes an outer lip for mounting and an interior retaining wall for pooling the slurry.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/TR2017/050138 WO2018190780A1 (en) | 2017-04-12 | 2017-04-12 | Chemical mechanical planarization of gallium nitride |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/TR2017/050138 WO2018190780A1 (en) | 2017-04-12 | 2017-04-12 | Chemical mechanical planarization of gallium nitride |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2018190780A1 true WO2018190780A1 (en) | 2018-10-18 |
Family
ID=63792796
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/TR2017/050138 WO2018190780A1 (en) | 2017-04-12 | 2017-04-12 | Chemical mechanical planarization of gallium nitride |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2018190780A1 (en) |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6129613A (en) * | 1998-01-30 | 2000-10-10 | Philips Electronics North America Corp. | Semiconductor manufacturing apparatus and method for measuring in-situ pressure across a wafer |
US20020185054A1 (en) * | 2001-06-08 | 2002-12-12 | Advanced Technology Materials Inc. | High surface quality gan wafer and method of fabricating same |
EP2025468A2 (en) * | 2007-08-09 | 2009-02-18 | Fujitsu Limited | Polishing method, substrate manufacturing method, and electronic apparatus manufacturing method |
WO2010105240A2 (en) * | 2009-03-13 | 2010-09-16 | Saint-Gobain Ceramics & Plastics, Inc. | Chemical mechanical planarization using nanodiamond |
EP2514858A1 (en) * | 2009-12-18 | 2012-10-24 | Sumitomo Electric Industries, Ltd. | Group iii nitride crystal substrate, group iii nitride crystal substrate having epitaxial layer, and semiconductor device and method for producing the same |
KR101431633B1 (en) * | 2012-09-15 | 2014-09-23 | 김건우 | Retainer ring for Chemical Mechanical polishing |
CN104745095A (en) * | 2015-04-03 | 2015-07-01 | 清华大学 | GaN thick membrane CMP composition and preparation method thereof |
-
2017
- 2017-04-12 WO PCT/TR2017/050138 patent/WO2018190780A1/en active Application Filing
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6129613A (en) * | 1998-01-30 | 2000-10-10 | Philips Electronics North America Corp. | Semiconductor manufacturing apparatus and method for measuring in-situ pressure across a wafer |
US20020185054A1 (en) * | 2001-06-08 | 2002-12-12 | Advanced Technology Materials Inc. | High surface quality gan wafer and method of fabricating same |
EP2025468A2 (en) * | 2007-08-09 | 2009-02-18 | Fujitsu Limited | Polishing method, substrate manufacturing method, and electronic apparatus manufacturing method |
WO2010105240A2 (en) * | 2009-03-13 | 2010-09-16 | Saint-Gobain Ceramics & Plastics, Inc. | Chemical mechanical planarization using nanodiamond |
EP2514858A1 (en) * | 2009-12-18 | 2012-10-24 | Sumitomo Electric Industries, Ltd. | Group iii nitride crystal substrate, group iii nitride crystal substrate having epitaxial layer, and semiconductor device and method for producing the same |
KR101431633B1 (en) * | 2012-09-15 | 2014-09-23 | 김건우 | Retainer ring for Chemical Mechanical polishing |
CN104745095A (en) * | 2015-04-03 | 2015-07-01 | 清华大学 | GaN thick membrane CMP composition and preparation method thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US8398878B2 (en) | Methods for producing and processing semiconductor wafers | |
US11781244B2 (en) | Seed crystal for single crystal 4H—SiC growth and method for processing the same | |
US7815489B2 (en) | Method for the simultaneous double-side grinding of a plurality of semiconductor wafers | |
KR101110682B1 (en) | Water-based polishing slurry for polishing silicon carbide single crystal substrate, and polishing method for the same | |
TWI421934B (en) | Method for polishing a semiconductor wafer | |
US10189142B2 (en) | Method for polishing a semiconductor wafer | |
CN1204600C (en) | Method for cutting material on two-sided of semiconductor piece | |
JP2005510072A (en) | Method for polishing a substrate surface | |
US9224613B2 (en) | Method for polishing both sides of a semiconductor wafer | |
US20130331006A1 (en) | Method and apparatus for conformable polishing | |
EP3128536A1 (en) | Method for polishing gan single crystal material | |
CN104064455B (en) | The polishing method of wafers of semiconductor material | |
US8389409B2 (en) | Method for producing a semiconductor wafer | |
JP2009283964A (en) | Edge removal of silicon-on-insulator transfer wafer | |
WO2002015247A2 (en) | Method and apparatus for processing a semiconductor wafer using novel final polishing method | |
US20230219188A1 (en) | Mega-sonic vibration assisted chemical mechanical planarization | |
ZHANG | Method of surface treatment on sapphire substrate | |
US7198549B2 (en) | Continuous contour polishing of a multi-material surface | |
WO2018190780A1 (en) | Chemical mechanical planarization of gallium nitride | |
US11117239B2 (en) | Chemical mechanical polishing composition and method | |
Kubota | Surface finishing of single-crystal SiC and GaN wafers using a magnetic tool in H2O2 solution | |
Karagoz et al. | Chemical mechanical planarization studies on gallium nitride for improved performance | |
Karagoz et al. | Surface characterization driven CMP optimization for gallium nitride | |
Shi et al. | Realization of atomic-level smooth surface of sapphire (0001) by chemical-mechanical planarization with nano colloidal silica abrasives | |
JP2003170351A (en) | Polishing tool plate |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 17905404 Country of ref document: EP Kind code of ref document: A1 |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 17905404 Country of ref document: EP Kind code of ref document: A1 |