Prosecution Insights
Last updated: July 17, 2026
Application No. 18/010,941

ELECTROLYTE FOR LITHIUM-SULFUR BATTERY, AND LITHIUM-SULFUR BATTERY COMPRISING SAME

Non-Final OA §103
Filed
Dec 16, 2022
Priority
Jan 07, 2021 — RE 10-2021-0001823 +1 more
Examiner
HA, STEVEN S
Art Unit
1735
Tech Center
1700 — Chemical & Materials Engineering
Assignee
LG Energy Solution Ltd.
OA Round
3 (Non-Final)
70%
Grant Probability
Favorable
3-4
OA Rounds
0m
Est. Remaining
99%
With Interview

Examiner Intelligence

Grants 70% — above average
70%
Career Allowance Rate
479 granted / 683 resolved
+5.1% vs TC avg
Strong +30% interview lift
Without
With
+30.5%
Interview Lift
resolved cases with interview
Typical timeline
2y 5m
Avg Prosecution
40 currently pending
Career history
732
Total Applications
across all art units

Statute-Specific Performance

§101
0.1%
-39.9% vs TC avg
§103
73.2%
+33.2% vs TC avg
§102
6.6%
-33.4% vs TC avg
§112
19.4%
-20.6% vs TC avg
Black line = Tech Center average estimate • Based on career data from 683 resolved cases

Office Action

§103
DETAILED ACTION Status of the Claims Applicant’s amendment filed 13 March 2026 is acknowledged. Claims 1 and 12 have been amended, claims 8-10 have been canceled, and claims 1-3 and 5-13 remain pending. 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 . Continued Examination Under 37 CFR 1.114 A request for continued examination under 37 CFR 1.114, including the fee set forth in 37 CFR 1.17(e), was filed in this application after final rejection. Since this application is eligible for continued examination under 37 CFR 1.114, and the fee set forth in 37 CFR 1.17(e) has been timely paid, the finality of the previous Office action has been withdrawn pursuant to 37 CFR 1.114. Applicant's submission filed on 13 March 2026 has been entered. 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. 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, 2, and 5-13 is/are rejected under 35 U.S.C. 103 as being unpatentable over Chen et al. (US 2021/0218015, hereinafter “Chen”), in view of Jung et al. (US 2002/0045102, hereinafter “Jung”; listed in the IDS filed 16 December 2022) and Park et al. (US 2019/0051940, hereinafter “Park”; listed in the IDS filed 26 December 2023), with evidence by NIH (National Center for Biotechnology Information. "PubChem Compound Summary for CID 8071, 1,2-Dimethoxyethane" PubChem, https://pubchem.ncbi.nlm.nih.gov/compound/1_2-Dimethoxyethane. Accessed 5 April, 2026, NPL). Regarding claim 1, Chen teaches an electrolyte solution for a lithium-sulfur battery, comprising: a lithium nitrate (lithium nitrate (LiNO3), see [0057]); a borate-based lithium salt (lithium tetrafluoroborate (LiBF4), see [0057]); and a lithium salt different from the lithium nitrate and the borate-based lithium salt (see [0057]). Chen teaches one or more solvents (see [0013]), but is silent to a first solvent comprising a heterocyclic compound containing one or more double bonds and any one of an oxygen atom and a sulfur atom, a second solvent comprising at least one of an ether-based compound, an ester-based compound, an amide-based compound, and a carbonate-based compound, wherein volume ratio of the first solvent to the second solvent is 1:2.5 to 1:6, and wherein the first solvent comprises 2-methylfuran, and the second solvent comprises 1,2-dimethoxyethane. Jung teaches a lithium electrolyte solution which includes at least two groups selected from a weak polar solvent group, a strong polar solvent group, and a lithium protection solvent group (see abstract). The lithium protection solvent can be represented by 2-methyl furan (equated to the claimed first solvent; see [0029]). The weak polar solvent can be represented by 1,2-dimethoxyethane (dimethoxyethane, equated to the claimed second solvent; see [0027]; also see evidence by NIH in section 2.4.2 which cites “1,2-dimethoxyethane as a synonym for “dimethoxyethane”). The lithium protection solvent in combination with a weak polar solvent forms a protective layer providing a stable solid electrolyte interface on the lithium surface resulting in good cyclic efficiency (see [0026]). In view of Jung’s teachings, it would have been obvious to one of ordinary skill in the art at the time the invention was filed to modify the solution of Chen to include a first solvent comprising a heterocyclic compound containing one or more double bonds and any one of an oxygen atom and a sulfur atom, equated to 2-methylfuran (see [0029]), and a second solvent comprising at least one of an ether-based compound, an ester-based compound, an amide-based compound, and a carbonate-based compound, equated to 1,2-dimethoxyethane (dimethoxyethane, see [0027]; also see evidence by NIH in section 2.4.2 which cites “1,2-dimethoxyethane as a synonym for “dimethoxyethane”), as taught by Jung, because it helps to form a protective layer providing a stable solid electrolyte interface on the lithium surface resulting in good cyclic efficiency. The combination of Chen and Jung is silent to wherein volume ratio of the first solvent to the second solvent is 1:2.5 to 1:6. Park teaches an electrolyte for a secondary battery that can comprise a mixed solvent (see [0012]-[0015]), comprising a linear ether (see [0039] for examples) and a cyclic ether (see [0040] for examples) mixed in a volume ratio of 5:95 to 95:5 (see [0012]-[0015] and [0042]). The lithium secondary battery provided with the electrolyte according to the disclosure has an excellent cycle-dependent capacity retention rate, and accordingly, is effective in improving a battery lifespan property (see abstract). In view of Park’s teachings, it would have been obvious to one of ordinary skill in the art at the time the invention was filed to modify the invention of the combination of Chen and Jung to include wherein volume ratio of the first solvent to the second solvent is 1:2.5 to 1:6, as taught by Park, because it helps produce a battery with an excellent cycle-dependent capacity retention rate and is effective in improving a battery lifespan property. Regarding claim 2, the combination of Chen, Jung, and Park teaches wherein the borate-based lithium salt is at least one selected from the group consisting of lithium tetrafluoroborate (LiBF4) and lithium bis(oxalate)borate (LiBOB) (Chen: see [0057]). Regarding claim 5, the combination of Chen, Jung, and Park teaches the borate-based lithium salt (Chen: lithium tetrafluoroborate (LiBF4), see [0057]) and the lithium nitrate (Chen: lithium nitrate (LiNO3), see [0057]). Though the combination of Chen, Jung, and Park is silent to wherein a weight ratio of the borate-based lithium salt and to the lithium nitrate is 1:1 to 1:30, based on general disclosure of Chen regarding the combination of lithium salts, it would be obvious to one of ordinary skill in the art to at least start with a 1:1 ratio for the two salts and vary the ratio based on the characteristics each salt adds to the performance of the battery. Furthermore, the Applicant is reminded that where the general conditions of a claim are disclosed in the prior art, it is not inventive to discover the optimum or workable ranges by routine experimentation. See MPEP 2144.05(II)(A). Regarding claim 6, the combination of Chen, Jung, and Park teaches wherein the lithium salt is LiBr, LiI, LiClO4, LiBF4, LiCF3SO3, LiAsF6, LiAlCl4, CF3SO3Li, (SO2F)2NLi (Chen: see [0057]). Regarding claim 7, the combination of Chen, Jung, and Park teaches wherein a concentration of lithium salt is 0.2 to 2.0 M (Chen: see [0058]). Regarding claim 11, the combination of Chen, Jung, and Park teaches the electrolyte solution further comprising at least one selected from the group consisting of lanthanum nitrate, potassium nitrate (Park: see [0057]), cesium nitrate (Park: see [0057]), magnesium nitrate, barium nitrate (Park: see [0057]), lithium nitrite (Park: see [0057]), potassium nitrite (Park: see [0057]), and cesium nitrite (Park: see [0057]). Regarding claim 12, the combination of Chen, Jung, and Park teaches the battery, comprising: 2-methylfuran as the first solvent (Jung: lithium protection solvent, see [0029]), 1,2-dimethoxyethane as the second solvent (Jung: weak polar solvent, see [0027]; also see evidence by NIH in section 2.4.2 which cites “1,2-dimethoxyethane as a synonym for “dimethoxyethane”), LiFSI ((SO2F)2NLi) as the lithium salt (Chen: see [0057]), lithium difluoro(oxlato)borate (LiFOB) as the borate-based lithium salt (Chen: see [0057]), and the lithium nitrate (Chen: see [0057]). Regarding claim 13, the combination of Chen, Jung, and Park teaches a lithium-sulfur battery comprising, a positive electrode (Chen: cathode 24, see [0049]); a negative electrode (Chen: anode 22, see [0049]); a separator between the positive electrode and the negative electrode (Chen: separator 26 disposed between the electrodes 22, 24; [0050]); and the electrolyte solution according to claim 1 (see rejection for claim 1 above). Claim(s) 3 is rejected under 35 U.S.C. 103 as being unpatentable over the combination of Chen, Jung, and Park as applied to claim 1 above, and further in view of Kim et al. (WO 2020/009340 A1, hereinafter “Kim”; using US PGPub 2021/0265662 for the English translation and citations; listed in the IDS filed 16 December 2022). Regarding claim 3, the combination of Chen, Jung, and Park is silent to wherein the content of the borate-based lithium salt is 0.01 wt. % to 5.0 wt. % relative to the total weight of the electrolyte solution for the lithium-sulfur battery. Kim teaches a borate-based lithium salt may be included in an amount of 0.1 wt% to 10 wt% based on a total amount of the electrolyte (see [0046]). Kim teaches that when borate-based lithium salt is used in an amount of less than 0.05wt%, the effect of suppressing the interface resistance may be insignificant, but when the boroate-based lithium salt is used in an amount greater than 20 wt%, viscosity and interface resistance may be increased, and accordingly, there may be a problem of not securing capacity and battery performance such as a cycle-life and the like (see [0048]). Therefore, the amount of borate-based lithium salt relative to the total weight of the electrolyte is a result effective variable. In view of Kim’s teachings, it would have been obvious to one of ordinary skill in the art at the time the invention was filed to modify the invention of the combination of Chen, Jung, and Park to include wherein the content of the borate-based lithium salt is 0.01 wt. % to 5.0 wt. % relative to the total weight of the electrolyte solution for the lithium-sulfur battery, as taught by Kim, because it is a result effective variable (Kim: see [0048]), and it would not be inventive to discover its optimum range through routine experimentation. See MPEP §2144.05(II)(A). Response to Arguments Applicant's arguments filed 13 March 20206 have been fully considered but they are not persuasive. On pages 5-9 of the remarks, Applicant argues, with respect to claim 1, that the prior art, either taken alone or in combination, fails to teach or suggest the five-component combination of the claimed invention. The claimed invention requires (1) a first solvent comprising 2-methylfuran, (2) a second solvent comprising 1,2-dimethoxyethane, (3) a lithium nitrate, (4) a borate-based lithium salt, and (5) a lithium salt different from the lithium nitrate and the borate-based lithium salt. Applicant argues that neither Chen nor Jung teaches or suggests the claimed ratio of 1:2.5 to 1:6, and Park’s volume ratio range partially overlaps with the claimed range but is approximately 8,020% broader than the claimed range. Park’s broad disclosure cannot reasonably direct one of ordinary skill in the art to the narrow claimed range. Applicant alleges that the claimed invention exhibits unexpected and superior results attributable to the combination of elements (1)-(5) and the claimed ratio range of 1:2.5 to 1.6. As shown in TABLES 1-3, the claimed electrolyte formulations (Examples 1-8) provide dramatically improved lifetime characteristics and lithium cycle efficiency compared to Comparative Example 2, which differs only by using a slightly different (outside) volume ratio (1:2) and a first solvent having saturated cyclic structures. Example 8 demonstrates more than a 2.75-times increase in 80% capacity retention compared with Comparative Examples 2, and TABLEs 1 and 2 show consistent improvement throughout the claimed ratio range (1:2.5 to 1.6). These results demonstrate that the claimed ratio is critical and not the product of routine optimization. The Examiner finds these arguments unpersuasive. The combination of Chen, Jung, and Park teaches the five-component combination as claimed. Chen teaches (3) a lithium nitrate (lithium nitrate (LiNO3), see [0057]), (4) a borate-based lithium salt (lithium tetrafluoroborate (LiBF4), see [0057]), and (5) a lithium salt different from the lithium nitrate and the borate-based lithium salt (see [0057]). Jung teaches (1) a first solvent comprising 2-methylfuran (see [0029]) and (2) a second solvent comprising 1,2-dimethoxyethane (Jung: see [0027] which teaches dimethoxyethane; also see evidence by NIH in section 2.4.2 which cites “1,2-dimethoxyethane as a synonym for “dimethoxyethane”). With regard to the alleged unexpected results of the narrow claimed range as compared to the broader range of the prior art of Park, Applicant only provides a single Comparative Example data point (“Comparative Example 2”) outside of the claimed range. In order to support unexpected results for the range of 1:2.5-1:6, Applicant should provide enough data points to support said range, both inside and outside of this range. The current singular data point is not a showing commensurate in scope that the volume ratio outside of the claimed range shows poor results. See MPEP §716.02(d). To establish unexpected results over a claimed range, applicants should compare a sufficient number of tests both inside and outside the claimed range to show the criticality of the claimed range. In re Hill, 284 F.2d 955, 128 USPQ 197 (CCPA 1960). Park teaches that the lithium secondary battery provided with the electrolyte mixed with the volume ratio according to the disclosure has an excellent cycle-dependent capacity retention rate, and accordingly, is effective in improving a battery lifespan property (see abstract). Therefore, as Applicant has not successfully demonstrated unexpected results that are commensurate with the claimed range, the Examiner maintains that regarding the overlap of the claimed range, in the case where the claimed ranges "overlap or lie inside ranges disclosed by the prior art" a prima facie case of obviousness exists. See MPEP §2144.05(I). Furthermore, as the combination of the prior art teaches an electrolyte solution that is identical to that of the claimed invention, any unexpected and/or superior result which is given to the Applicant’s invention must also be given to the invention of the combination of the prior art. Conclusion Any inquiry concerning this communication or earlier communications from the examiner should be directed to STEVEN HA whose telephone number is (571)270-5934. The examiner can normally be reached M-F 8:00-5:00 EST. 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, Keith Walker can be reached at 571-272-3458 . 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. /S.S.H/Examiner, Art Unit 1735 4 April 2026 /KEITH WALKER/Supervisory Patent Examiner, Art Unit 1735
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Prosecution Timeline

Dec 16, 2022
Application Filed
Aug 27, 2025
Non-Final Rejection mailed — §103
Nov 04, 2025
Response Filed
Dec 15, 2025
Final Rejection mailed — §103
Mar 13, 2026
Request for Continued Examination
Mar 17, 2026
Response after Non-Final Action
Apr 15, 2026
Non-Final Rejection mailed — §103
Jul 09, 2026
Response Filed

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Prosecution Projections

3-4
Expected OA Rounds
70%
Grant Probability
99%
With Interview (+30.5%)
2y 5m (~0m remaining)
Median Time to Grant
High
PTA Risk
Based on 683 resolved cases by this examiner. Grant probability derived from career allowance rate.

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