Prosecution Insights
Last updated: April 19, 2026
Application No. 18/130,161

METAL OXIDE LITHIOPHILIC COATING ON STAINLESS STEEL CURRENT COLLECTOR

Non-Final OA §103
Filed
Apr 03, 2023
Examiner
PHAN, AN BACH
Art Unit
3763
Tech Center
3700 — Mechanical Engineering & Manufacturing
Assignee
GM Global Technology Operations LLC
OA Round
1 (Non-Final)
Grant Probability
Favorable
1-2
OA Rounds
3y 2m
To Grant

Examiner Intelligence

Grants only 0% of cases
0%
Career Allow Rate
0 granted / 0 resolved
-70.0% vs TC avg
Minimal +0% lift
Without
With
+0.0%
Interview Lift
resolved cases with interview
Typical timeline
3y 2m
Avg Prosecution
19 currently pending
Career history
19
Total Applications
across all art units

Statute-Specific Performance

§103
59.3%
+19.3% vs TC avg
§102
25.9%
-14.1% vs TC avg
§112
9.3%
-30.7% vs TC avg
Black line = Tech Center average estimate • Based on career data from 0 resolved cases

Office Action

§103
DETAILED ACTION Notice of Pre-AIA or AIA Status The present application, filed on or after March 16, 2013, is being examined under the first inventor to file provisions of the AIA . Claim Rejections - 35 USC § 103 In the event the determination of the status of the application as subject to AIA 35 U.S.C. 102 and 103 (or as subject to pre-AIA 35 U.S.C. 102 and 103) is incorrect, any correction of the statutory basis (i.e., changing from AIA to pre-AIA ) for the rejection will not be considered a new ground of rejection if the prior art relied upon, and the rationale supporting the rejection, would be the same under either status. The following is a quotation of 35 U.S.C. 103 which forms the basis for all obviousness rejections set forth in this Office action: A patent for a claimed invention may not be obtained, notwithstanding that the claimed invention is not identically disclosed as set forth in section 102, if the differences between the claimed invention and the prior art are such that the claimed invention as a whole would have been obvious before the effective filing date of the claimed invention to a person having ordinary skill in the art to which the claimed invention pertains. Patentability shall not be negated by the manner in which the invention was made. The text of those sections of Title 35, U.S. Code not included in this action can be found in a prior Office action. The factual inquiries for establishing a background for determining obviousness under 35 U.S.C. 103 are summarized as follows: 1. Determining the scope and contents of the prior art. 2. Ascertaining the differences between the prior art and the claims at issue. 3. Resolving the level of ordinary skill in the pertinent art. 4. Considering objective evidence present in the application indicating obviousness or nonobviousness. This application currently names joint inventors. In considering patentability of the claims the examiner presumes that the subject matter of the various claims was commonly owned as of the effective filing date of the claimed invention(s) absent any evidence to the contrary. Applicant is advised of the obligation under 37 CFR 1.56 to point out the inventor and effective filing dates of each claim that was not commonly owned as of the effective filing date of the later invention in order for the examiner to consider the applicability of 35 U.S.C. 102(b)(2)(C) for any potential 35 U.S.C. 102(a)(2) prior art against the later invention. Claim(s) 1-6 is/are rejected under 35 U.S.C. 103 as being unpatentable over Kobori (US 2012/0009479), Li (2020 IOP Conf. Ser.: Earth Environ. Sci. 514 042019), and Kaskel (US 2020/0099039). Regarding claim 1, Kobori teaches a method for fabricating an anode ([0048]) electrode ([0041]), comprising: providing a current collector ([0042]); forming a metal oxide layer ([0042]) on the current collector. Kobori does not teach that the current collector is stainless steel. Kobori also does not teach pouring molten lithium over the metal oxide layer. However, Li teaches stainless steel mesh as an option for current collectors having a benefit of low cost, simple process, and large-scale production (3.4.). Accordingly, it would have been obvious to one of ordinary skill in the art before the effective filing date of the claimed invention to modify the method of Kobori to use the stainless steel mesh of Li for the benefits of low cost, simple process, and large-scale production (Li: 3.4.). Additionally, Kaskel teaches applying liquefied lithium to the mediator layer by a slot die ([0034]), with perforated metals as possible substrate materials ([0043]). Accordingly, it would also have been obvious to one of ordinary skill in the art before the effective filing date of the claimed invention to modify the method of Kobori and Li to further include the step of Kaskel to apply liquefied lithium to the mediator layer by a slot die to deposit lithium on large areas while having low thickness (Kaskel: [0005]). Modified Kobori also teaches that increasing the electrode areas and having thinner electrode plates is known to decrease impedance (Kobori: [0011]), which would be achieved by including the method of Kaskel. This addition is appropriate because the zinc nitrate (Kobori: [0136] [0137]) applied in modified Kobori as the metal salt was thermally decomposed into zinc oxide (Kobori: [0253]), which would be appropriate as the mediator layer for reacting with liquid lithium to form a mediating interface (Kaskel: [0045]). Regarding claim 2, modified Kobori teaches the stainless steel current collector is a mesh (Li: 3.4.). Regarding claim 3, modified Kobori teaches forming the metal oxide layer comprises: spin-coating (Kobori: [0151]) a metal nitrate salt (Kobori: [0042]) onto the stainless steel current collector; and heating the stainless steel current collector to a decomposition temperature of the metal nitrate salt (Kobori: [0045]). Regarding claim 4, modified Kobori teaches the metal nitrate salt is selected from a group consisting of zinc nitrate (Zn(NO3)3) (Kobori: [0136] [0137]). Regarding claim 5, modified Kobori teaches forming the metal oxide layer comprises: spraying (Kobori: [0151]) a metal nitrate salt (Kobori: [0042]) onto the stainless steel current collector; and heating the stainless steel current collector to a decomposition temperature of the metal nitrate salt (Kobori: [0045]). Regarding claim 6, modified Kobori teaches the metal nitrate salt is selected from a group consisting of zinc nitrate (Zn(NO3)3) (Kobori: [0136] [0137]). Claim(s) 1 and 7 is/are rejected under 35 U.S.C. 103 as being unpatentable over Kawakami (US 6432585) and Kaskel (US 2020/0099039). Regarding claim 1, Kawakami teaches a method for fabricating an anode electrode (19), comprising: providing a stainless steel current collector (19); forming a metal oxide layer (23) on the current collector. Kawakami does not teach pouring molten lithium over the metal oxide layer. However, Kaskel teaches applying liquefied lithium to the mediator layer by a slot die ([0034]), with perforated metals as possible substrate materials ([0043]). Accordingly, it would also have been obvious to one of ordinary skill in the art before the effective filing date of the claimed invention to modify the method of Kawakami to further include the step of Kaskel to apply liquefied lithium to the mediator layer by a slot die to deposit lithium on large areas while having low thickness (Kaskel: [0005]) and to make metallic lithium anodes for increased energy densities (Kaskel: [0002]). Kawakami also teaches that the grained host matrix material forming the electrode material layer (22) is desired to be covered by a layer comprising a metal which is deferent from that contained in the grained host matrix material (26), which would be achieved by including the method of Kaskel. This addition is appropriate because the zinc oxide deposited on the current collector (Kawakami: 23) would be appropriate as the mediator layer for reacting with liquid lithium to form a mediating interface (Kaskel: [0045]). Additionally, Kawakami teaches that the collector can include a mesh configuration (Kawakami: 20), which would be applicable as a perforated metal substrate (Kaskel: [0043]). Regarding claim 7, modified Kawakami teaches forming the metal oxide layer comprises electroplating the stainless steel current collector with the metal oxide layer (Kawakami: 23). Claim(s) 1 and 8 is/are rejected under 35 U.S.C. 103 as being unpatentable over Li (US 2006/019168), and Kaskel (US 2020/0099039). Regarding claim 1, Li teaches a method for fabricating an anode electrode ([0017]), comprising: providing a stainless steel current collector ([0025]); forming a metal oxide layer ([0027]) on the current collector ([0025]). Kawakami does not teach pouring molten lithium over the metal oxide layer. However, Kaskel teaches applying liquefied lithium to the mediator layer by a slot die ([0034]), with perforated metals as possible substrate materials ([0043]). Accordingly, it would also have been obvious to one of ordinary skill in the art before the effective filing date of the claimed invention to modify the method of Li to further include the step of Kaskel to apply liquefied lithium to the mediator layer by a slot die to deposit lithium on large areas while having low thickness (Kaskel: [0005]) and to use metallic lithium as the anode layer for increased energy densities (Kaskel: [0002]). This addition is appropriate because the aluminum oxide deposited on the current collector (Li: [0007]) would be appropriate as the mediator layer for reacting with liquid lithium to form a mediating interface (Kaskel: [0045]). Additionally, Li teaches that the collector can include a mesh configuration (Li: [0083]), which would be applicable as a perforated metal substrate (Kaskel: [0043]). Regarding claim 8, modified Li teaches forming the metal oxide layer comprises depositing the metal oxide layer in a vacuum deposition chamber ([0058]). Claim(s) 9-13 is/are rejected under 35 U.S.C. 103 as being unpatentable over Kobori (US 2012/0009479), Li (2020 IOP Conf. Ser.: Earth Environ. Sci. 514 042019), Kaskel (US 2020/0099039), and Parsian (US 2006/0115718). Regarding claim 9, Kobori teaches a method for fabricating a battery cell, comprising: forming an anode ([0048]) electrode ([0041]) by: providing a current collector ([0042]); and forming a metal oxide layer ([0042]) on the current collector. Kobori does not teach that the current collector is stainless. Kobori also does not teach pouring molten lithium over the metal oxide layer. Kobori is also silent to arranging the plurality of the anode electrode, a plurality of cathode electrodes, and separators in a predetermined sequence in an enclosure of a battery cell. However, Li teaches stainless steel mesh as an option for current collectors having a benefit of low cost, simple process, and large-scale production (3.4.). Accordingly, it would have been obvious to one of ordinary skill in the art before the effective filing date of the claimed invention to modify the method of Kobori to use the stainless steel mesh of Li for the benefits of low cost, simple process, and large-scale production (Li: 3.4.). Additionally, Kaskel teaches applying liquefied lithium to the mediator layer by a slot die ([0034]), with perforated metals as possible substrate materials ([0043]). Accordingly, it would also have been obvious to one of ordinary skill in the art before the effective filing date of the claimed invention to modify the method of Kobori and Li to further include the step of Kaskel to apply liquefied lithium to the mediator layer by a slot die to deposit lithium on large areas while having low thickness (Kaskel: [0005]). Modified Kobori also teaches that increasing the electrode areas and having thinner electrode plates is known to decrease impedance (Kobori: [0011]), which would be achieved by including the method of Kaskel. This addition is appropriate because the zinc nitrate (Kobori: [0136] [0137]) applied in modified Kobori as the metal salt was thermally decomposed into zinc oxide (Kobori: [0253]), which would be appropriate as the mediator layer for reacting with liquid lithium to form a mediating interface (Kaskel: [0044]). Moreover, Parsian teaches positioning, in sequence, a negative electrode current collector, a negative electrode, a first porous separator, a positive electrode, and a positive electrode current collector to form a single cell unit ([0038]). A plurality of the single cell units is then positioned adjacent one another in sequence, and a second porous separator is positioned between adjacent single cell units ([0038]). A number of cells may then be adhered and bundled together to form a battery or multi-cell ([0006]). Accordingly, it would have been obvious to one of ordinary skill in the art before the effective filing date of the claimed invention to modify the method of further modified Kobori to position the negative electrode current collector and negative electrode according to the multi-cell method of Parsian as described above ([0038]) to achieve high discharge rate and high power capability. Regarding claim 10, modified Kobori teaches forming the metal oxide layer comprises: spin-coating (Kobori: [0151]) a metal nitrate salt (Kobori: [0042]) onto the stainless steel current collector; and heating the stainless steel current collector to a decomposition temperature of the metal nitrate salt (Kobori: [0045]). Regarding claim 11, modified Kobori teaches the metal nitrate salt is selected from a group consisting of zinc nitrate (Zn(NO3)3) (Kobori: [0136] [0137]). Regarding claim 12, modified Kobori teaches forming the metal oxide layer comprises: spraying (Kobori: [0151]) a metal nitrate salt (Kobori: [0042]) onto the stainless steel current collector; and heating the stainless steel current collector to a decomposition temperature of the metal nitrate salt (Kobori: [0045]). Regarding claim 13, modified Kobori teaches the metal nitrate salt is selected from a group consisting of zinc nitrate (Zn(NO3)3) (Kobori: [0136] [0137]). Claim(s) 9 and 14 is/are rejected under 35 U.S.C. 103 as being unpatentable over Kawakami (US 6432585), Kaskel (US 2020/0099039), and Parsian (US 2006/0115718). Regarding claim 9, Kawakami teaches a method for fabricating a battery cell, comprising: fabricating an anode electrode (19), comprising: providing a stainless steel current collector (19) mesh (20); forming a metal oxide layer (23) on the current collector. Kawakami does not teach pouring molten lithium over the metal oxide layer. Kawakami also does not teach arranging the plurality of the anode electrode, a plurality of cathode electrodes, and separators in a predetermined sequence in an enclosure of a battery cell. However, Kaskel teaches applying liquefied lithium to the mediator layer by a slot die ([0034]). Accordingly, it would also have been obvious to one of ordinary skill in the art before the effective filing date of the claimed invention to modify the method of Kawakami to further include the step of Kaskel to apply liquefied lithium to the mediator layer by a slot die to deposit lithium on large areas while having low thickness (Kaskel: [0005]) and form a rechargeable lithium battery. Kawakami also teaches that the grained host matrix material forming the electrode material layer (22) is desired to be covered by a layer comprising a metal which is deferent from that contained in the grained host matrix material (26), which would be achieved by including the method of Kaskel. This addition is appropriate because the zinc oxide deposited on the current collector (Kawakami: 23) would be appropriate as the mediator layer for reacting with liquid lithium to form a mediating interface (Kaskel: [0045]). Additionally, Kawakami teaches that the collector can include a mesh configuration (Kawakami: 20), which would be applicable as a perforated metal substrate (Kaskel: [0043]). Additionally, Parsian teaches positioning, in sequence, a negative electrode current collector, a negative electrode, a first porous separator, a positive electrode, and a positive electrode current collector to form a single cell unit ([0038]). A plurality of the single cell units is then positioned adjacent one another in sequence, and a second porous separator is positioned between adjacent single cell units ([0038]). A number of cells may then be adhered and bundled together to form a battery or multi-cell ([0006]). Accordingly, it would have been obvious to one of ordinary skill in the art before the effective filing date of the claimed invention to modify the method of modified Kawakami to position the negative electrode current collector and negative electrode according to the multi-cell method of Parsian as described above (Parsian: [0038]) to achieve high discharge rate and high power capability. Regarding claim 14, modified Kawakami teaches forming the metal oxide layer comprises electroplating the stainless steel current collector with the metal oxide layer (Kawakami: 23). Claim(s) 9 and 15 is/are rejected under 35 U.S.C. 103 as being unpatentable over Li (US 2006/019168), Kaskel (US 2020/0099039), and Parsian (US 2006/0115718). Regarding claim 1, Li teaches a method for fabricating a battery cell, comprising: fabricating an anode electrode ([0017]), comprising: providing a stainless steel current collector ([0025]) mesh ([0083]); forming a metal oxide layer ([0027]) on the current collector ([0025]). Li does not teach pouring molten lithium over the metal oxide layer. Li also does not teach arranging the plurality of the anode electrode, a plurality of cathode electrodes, and separators in a predetermined sequence in an enclosure of a battery cell. However, Kaskel teaches applying liquefied lithium to the mediator layer by a slot die ([0034]), with perforated metals as possible substrate materials ([0043]). Accordingly, it would also have been obvious to one of ordinary skill in the art before the effective filing date of the claimed invention to modify the method of Li to further include the step of Kaskel to apply liquefied lithium to the mediator layer by a slot die to deposit lithium on large areas while having low thickness (Kaskel: [0005]) and to use metallic lithium as the anode layer for increased energy densities (Kaskel: [0002]). This addition is appropriate because the aluminum oxide deposited on the current collector (Li: [0007]) would be appropriate as the mediator layer for reacting with liquid lithium to form a mediating interface (Kaskel: [0045]). Additionally, Li teaches that the collector can include a mesh configuration (Li: [0083]), which would be applicable as a perforated metal substrate (Kaskel: [0043]). Additionally, Parsian teaches positioning, in sequence, a negative electrode current collector, a negative electrode, a first porous separator, a positive electrode, and a positive electrode current collector to form a single cell unit ([0038]). A plurality of the single cell units is then positioned adjacent one another in sequence, and a second porous separator is positioned between adjacent single cell units ([0038]). A number of cells may then be adhered and bundled together to form a battery or multi-cell ([0006]). Accordingly, it would have been obvious to one of ordinary skill in the art before the effective filing date of the claimed invention to modify the method of modified Li to position the negative electrode current collector and negative electrode according to the multi-cell method of Parsian as described above (Parsian: [0038]) to achieve high discharge rate and high power capability. Regarding claim 15, modified Li teaches forming the metal oxide layer comprises depositing the metal oxide layer in a vacuum deposition chamber ([0058]). Claim(s) 16 is/are rejected under 35 U.S.C. 103 as being unpatentable over Kobori (US 2012/0009479), Li (2020 IOP Conf. Ser.: Earth Environ. Sci. 514 042019), Kaskel (US 2020/0099039), and Parsian (US 2006/0115718). Regarding claim 16, Kobori teaches a method for fabricating a battery cell, comprising: forming an anode ([0048]) electrode ([0041]) by: providing a current collector ([0042]); forming a metal oxide layer ([0042]) on the current collector by: spin-coating ([0151]) a metal nitrate salt ([0042]) onto the current collector, wherein the metal nitrate salt is zinc nitrate (Zn(NO3)3) ([0136] [0137]); and heating the stainless steel current collector to a decomposition temperature of the metal nitrate salt ([0045]). Kobori does not teach that the current collector is a stainless steel mesh, foil, or expanded metal. Kobori also does not teach pouring molten lithium over the metal oxide layer. Kobori is also silent to arranging the plurality of the anode electrode, a plurality of cathode electrodes, and separators in a predetermined sequence in an enclosure of a battery cell. However, Li teaches stainless steel mesh as an option for current collectors having a benefit of low cost, simple process, and large-scale production (3.4.). Accordingly, it would have been obvious to one of ordinary skill in the art before the effective filing date of the claimed invention to modify the method of Kobori to use the stainless steel mesh of Li for the benefits of low cost, simple process, and large-scale production (Li: 3.4.). Additionally, Kaskel teaches applying liquefied lithium to the mediator layer by a slot die ([0034]), with perforated metals as possible substrate materials ([0043]). Accordingly, it would also have been obvious to one of ordinary skill in the art before the effective filing date of the claimed invention to modify the method of Kobori and Li to further include the step of Kaskel to apply liquefied lithium to the mediator layer by a slot die to deposit lithium on large areas while having low thickness (Kaskel: [0005]). Modified Kobori also teaches that increasing the electrode areas and having thinner electrode plates is known to decrease impedance (Kobori: [0011]), which would be achieved by including the method of Kaskel. This addition is appropriate because the zinc nitrate (Kobori: [0136] [0137]) applied in modified Kobori as the metal salt was thermally decomposed into zinc oxide (Kobori: [0253]), which would be appropriate as the mediator layer for reacting with liquid lithium to form a mediating interface (Kaskel: [0044]). Moreover, Parsian teaches positioning, in sequence, a negative electrode current collector, a negative electrode, a first porous separator, a positive electrode, and a positive electrode current collector to form a single cell unit ([0038]). A plurality of the single cell units is then positioned adjacent one another in sequence, and a second porous separator is positioned between adjacent single cell units ([0038]). A number of cells may then be adhered and bundled together to form a battery or multi-cell ([0006]). Accordingly, it would have been obvious to one of ordinary skill in the art before the effective filing date of the claimed invention to modify the method of further modified Kobori to position the negative electrode current collector and negative electrode according to the multi-cell method of Parsian as described above (Parsian: [0038]) to achieve high discharge rate and high power capability. Conclusion Any inquiry concerning this communication or earlier communications from the examiner should be directed to An Bach Phan whose telephone number is (571)272-7244. The examiner can normally be reached M-F, 9-5 ET. Examiner interviews are available via telephone, in-person, and video conferencing using a USPTO supplied web-based collaboration tool. To schedule an interview, applicant is encouraged to use the USPTO Automated Interview Request (AIR) at http://www.uspto.gov/interviewpractice. If attempts to reach the examiner by telephone are unsuccessful, the examiner’s supervisor, Miriam Stagg can be reached at (571) 270-5256. The fax phone number for the organization where this application or proceeding is assigned is 571-273-8300. Information regarding the status of published or unpublished applications may be obtained from Patent Center. Unpublished application information in Patent Center is available to registered users. To file and manage patent submissions in Patent Center, visit: https://patentcenter.uspto.gov. Visit https://www.uspto.gov/patents/apply/patent-center for more information about Patent Center and https://www.uspto.gov/patents/docx for information about filing in DOCX format. For additional questions, contact the Electronic Business Center (EBC) at 866-217-9197 (toll-free). If you would like assistance from a USPTO Customer Service Representative, call 800-786-9199 (IN USA OR CANADA) or 571-272-1000. /A.B.P./Examiner, Art Unit 1724 /MIRIAM STAGG/Supervisory Patent Examiner, Art Unit 1724
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Prosecution Timeline

Apr 03, 2023
Application Filed
Dec 30, 2025
Non-Final Rejection — §103
Mar 26, 2026
Interview Requested
Apr 01, 2026
Applicant Interview (Telephonic)
Apr 01, 2026
Examiner Interview Summary

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