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 .
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and the fee set forth in 37 CFR 1.17(e) has been timely paid, the finality of the previous Office action has been withdrawn pursuant to 37 CFR 1.114.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 03/02/26 has been entered.
Status of Claims
Applicant’s amendment and arguments, filed 03/02/26, have been fully considered. Claims(s) 1, 13, and 16–18 is/are amended; claim(s) 3–12, 14, 15, and 19–25 stand(s) as originally or previously presented; and claim(s) 2 and 26–33 are canceled; no new matter has been added. Examiner affirms that the original disclosure provides adequate support for the amendment.
Upon considering said amendment and arguments, the previous 35 U.S.C. 103 rejection set forth in the Office Action mailed 08/28/25 has/have been withdrawn. Applicant’s amendment necessitated the new grounds of rejection below.
Claim Rejections - 35 USC § 103
4. The text forming the basis for the rejection under 35 U.S.C. 103 may be found in a prior Office Action.
Claim(s) 1, 3, 5–11, and 13–25 is/are rejected under 35 U.S.C. 103 as being unpatentable over Pan et al. (US 20180241032 A1) (Pan) in view of Ahn et al. (US 20150079467 A1) (Ahn)
and Zhamu et al. (US 20190088922 A1) (Zhamu).
Regarding claims 1, 3, and 19–25, Pan discloses a lithium-ion battery (e.g., Title, ¶ 0036) comprising an anode (¶ 0035, 0036), a cathode (¶ 0036), an electrolyte in ionic contact with said anode and said cathode (¶ 0036), and an ion-conducting separator (¶ 0036, where separator necessarily conducts Li+ for battery to function), the anode comprising multiple composite particulates (surface-stabilized anode particles, e.g., Abstract and ¶ 0034), a conductive additive (e.g., ¶ 0035), and a binder resin that bonds said composite particulates and said conductive additive together (¶ 0035; the skilled artisan would recognize that a binder, in being adhesive, bonds electrode components together).
Pan further discloses that the anode active particles may exhibit a diameter preferably < 10 nm (e.g., ¶ 0024), and the encapsulating polymer layer may be preferably 0.5–5 nm thick (¶ 0016), yielding a composite diameter of 10~20 nm (composite diameter ≈ anode particles’ diameter + 2*(polymer layer thickness) ≈ 10 nm minimum and 20 nm maximum).
Though Pan fails to explicitly disclose the recited diameter of 10 nm to 50 μm, considering that Pan is analogous prior art to the claimed invention because they pertain to the same field of endeavor, namely battery negative electrode materials, Pan’s 10~20 nm appears to fall within or at least overlap the recited range such that the skilled artisan could have routinely selected within the overlap with a reasonable expectation of forming a successful composite material (MPEP 2144.05 (I)).
Additionally, Pan recognizes the need for small particle sizes for high-rate capacity (¶ 0014) but acknowledges that (excessively) reducing the particle size implies a higher surface area available for potentially reacting with liquid electrolyte to form a larger SEI, which is undesirable as a source of irreversible capacity loss (¶ 0007). To balance these effects, then, it would have been obvious to arrive at the recited diameter by routinely optimizing the particles’ size, including within the apparent overlap (MPEP 2144.05 (II)).
Pan further discloses that the composite particulate comprises anode active material particles that are encapsulated by a high-elasticity polymer (¶ 0017), wherein said high-elasticity polymer has a recoverable elastic tensile strain typically 30–500% when measured without an additive or reinforcement dispersed therein (¶ 0017), which falls within no less than 5%, and a lithium ion conductivity preferably ≥ 10-3 S/cm at room temperature (¶ 0017), which falls within no less than 10-6 S/cm.
Pan further discloses that the polymer layer may comprise crosslinked, acrylate polymer chains including, e.g., ethoxylated trimethylolpropane triacrylate (ETPTA) or ethylene glycol methyl ether acrylate (¶ 0020) yet, while not appearing necessarily limited to the exemplified acrylates to achieve the desired high elasticity and Li+ conductivity (¶ 0019), fails to explicitly disclose a crosslinked polymer network of chains of poly(propylene glycol) dimethacrylate or poly(propylene glycol) diacrylate.
Ahn, in teaching anode active particles coated with a crosslinked polymer (Abstract), teaches that the polymer may be formed from acrylate monomers such as ETPTA, dipropylene glycol diacrylate, or dipropylene glycol dimethacrylate (¶ 0026). More generally, Ahn teaches that the acrylate forms from the below formula, wherein each of R3–R5 may be H or C1–C4 alkyl groups, and m—i.e., the number of glycol units— may be 1 to 20 (¶ 0024, 0025) and, thus, encompasses, e.g., poly(propylene glycol) di(meth)acrylate (if R3 and R4 were each H or –CH3, and R5 were –CH3; compare to substantially similar general formula in instant spec., p. 20, lines 15–21).
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Ahn is analogous prior art to the claimed invention because they pertain to the same field of endeavor, namely battery negative electrode material.
As Ahn recognizes ETPTA, dipropylene glycol diacrylate, and dipropylene glycol dimethacrylate—and, more broadly, derivatives such as poly(propylene glycol) di(meth)acrylate—as equivalent crosslinked polymers for coating anode particles, it would have been obvious to one of ordinary skill in the art, before the effective filing date of the claimed invention, to routinely substitute Pan’s polymer such as the polymerized ETPTA with Ahn’s poly(propylene glycol) di(meth)acrylate with a reasonable expectation of forming a successful polymer coating (MPEP 2143 (B.) and 2144.06 (II)).
Pan further discloses that the high-elasticity polymer may be blended with Li+-conducting polymers like polydimethylsiloxane (¶ 0033), i.e., a siloxane, but fails to explicitly disclose an embodiment of such.
Pan further discloses the ability to blend the polymer with Li+-conducting polymers like polydimethylsiloxane—which, as a siloxane, is understood to be a plasticizer/diluent, per spec.’s p. 6, lines 10–13—but Pan fails to explicitly disclose that the polymer further comprises a plasticizer or diluent selected from the recited group.
Zhamu teaches anode active material particles coated with a high-elasticity polymer (e.g., ¶ 0042, 0053), where the polymer may be blended with a Li+ conducting polymer such as polydimethylsiloxane or poly(acrylonitrile) (PAN) (¶ 0047),.
It would have been obvious to one of ordinary skill in the art, before the effective filing date of the claimed invention, to routinely blend PAN, i.e., a derivative of the instant acrylonitrile—and, thus, reasonably disperse the PAN, similar to other dispersed additives in Pan’s ¶ 0028, 0030, 0043, and working examples, as well as Zhamu’s ¶ 0047—with a reasonable expectation of forming a successful polymer coating with enhanced Li+ conductivity (MPEP 2143 (A.), 2144.06 (I)).
Thus, in incorporating PAN, although not explicitly referenced as such, modified Pan would disclose a dispersed derivative of an acrylonitrile plasticizer or diluent because, per instant claim 1, acrylonitrile is a plasticizer or diluent.
It is submitted that the above disclosure further reads on claim 3; i.e., the high-elasticity polymer contains a cross-linked network that is crosslinked by a crosslinking agent to a degree of crosslinking that imparts an elastic tensile strain from typically 30% to 500% (Pan, ¶ 0017), which falls within 5–500%.
Regarding claims 5 and 6, modified Pan discloses the composite particulate of claim 1, wherein said high-elasticity polymer contains a lithium salt of, e.g., Li2CO3 dispersed in the polymer crosslinked network (Pan, ¶ 0028 and 0030).
Regarding claim 7, modified Pan discloses the composite particulate of claim 1.
Regarding the limitation of claim 7, it is noted that such is directed to an alternative option of parent claim 1 and, thus, not positively required by the claim. Claim 1 recites “crosslinked polymer network of chains selected from the group consisting of … chemically substituted versions thereof, derivatives thereof, and combinations thereof” (emphasis added). Accordingly, claim 7’s limitation is considered an optional, alternative limitation not positively required and dependent on selecting the chemically substituted version of the crosslinked polymer in claim 1, which, in this case, is unselected because modified Pan discloses unsubstituted poly(propylene glycol) diacrylate or poly(propylene glycol) dimethacrylate, as established in claim 1.
Regarding claims 8 and 9, modified Pan discloses the composite particulate of claim 1, wherein said high-elasticity polymer further contains 0.1–10% by weight of a carbon material of, e.g., carbon nanotubes dispersed therein (Pan, ¶ 0028), which falls within 0.01–30%, and said carbon material forms a 3D network of electron-conducting pathways that are in electronic contacts with said anode active material particles (in the nanotubes’ being dispersed into the encapsulating polymer layer at a concentration falling within the instant range, such would reasonably create a conductive, three-dimensional “network” for electrons to traverse (further corroborated by the polymer’s being designed to contact the active particles in Pan, e.g., ¶ 0068), as seen in the substantially similar configuration of the instant specification, e.g., p. 11, lines 24–27).
Regarding claims 10, 11, and 18, modified Pan discloses the composite particulate of claim 1, wherein said anode active material particles are, e.g., Si, contain a prelithiated Si, and are lithiated to contain from 0.1% to 54.7% by weight of lithium (Pan, ¶ 0021 and 0022).
Regarding claim 13, modified Pan discloses the composite particulate of claim 1, wherein a plurality of said anode active material particles is coated with a layer of carbon disposed between said plurality of anode active material particles and said high-elasticity polymer (Pan, ¶ 0025).
Regarding claim 14, modified Pan discloses the composite particulate of claim 1.
Modified Pan further discloses that the high-elasticity polymer preferably has a lithium-ion conductivity ≥ 10-3 S/cm (Pan, ¶ 0017), which, considering that there appears to be no criticality to 10-6–10-2 S/cm in the specification, is deemed to overlap with sufficient specificity so as to read on the recited range.
Assuming, arguendo, that modified Pan’s disclosure were not sufficiently specific to read on the recited range, the polymer’s Li+ conductivity of ≥ 10-3 S/cm overlaps the recited 10-6–10-2 S/cm such that the skilled artisan could have routinely selected within the overlap with the reasonable expectation of forming a successful polymer shell with suitable Li+ conductivity (MPEP 2144.05 (I)).
Regarding claim 15, modified Pan discloses the composite particulate of claim 1, wherein said high-elasticity polymer forms a mixture with an elastomer of, e.g., natural polyisoprene (Pan, ¶ 0029).
Regarding claim 16, modified Pan discloses the composite particulate of claim 1, wherein said high-elasticity polymer is mixed with an electron-conducting polymer of, e.g., polyaniline (Pan, ¶ 0032).
Regarding claim 17, modified Pan discloses the composite particulate of claim 1, wherein the high-elasticity polymer forms a mixture or blend with a lithium-ion conducting polymer of, e.g., PEO (Pan, ¶ 0033).
Claim(s) 4 is/are rejected under 35 U.S.C. 103 as being unpatentable over Pan et al. (US 20180241032 A1) (Pan) in view of Ahn et al. (US 20150079467 A1) (Ahn) and Zhamu et al. (US 20190088922 A1) (Zhamu), as applied to claim 3, further in view of Fujimoto et al. (US 20080319149 A1) (Fujimoto).
Regarding claim 4, modified Pan discloses the composite particulate of claim 3.
Pan further discloses that the polymer’s elasticity is adjustable by using different crosslinking agents (¶ 0088), but modified Pan, in appearing unconcerned with the specific crosslinker, fails to specify such and, thus, a crosslinking agent selected from the recited group.
Fujimoto, in teaching a battery electrode with a crosslinked (meth)acrylic polymer (¶ 0006), teaches that, from the viewpoint of high reactivity, ethylene glycol dimethacrylate is a preferred crosslinking agent (¶ 0033).
Fujimoto is analogous prior art to the claimed invention because they pertain to the same field of endeavor, namely acrylic polymers for use in battery electrodes.
It would have been obvious to one of ordinary skill in the art, before the claimed invention's effective filing date, that modified Pan's polymer network must necessarily be crosslinked by some medium, and, as demonstrated by Fujimoto, the skilled artisan would find it obvious to crosslink the polymer with ethylene glycol dimethacrylate from the viewpoint of high reactivity. Moreover, per MPEP 2144.07, selecting a known material based on its suitability for its intended use is prima facie obvious.
Claim(s) 12 is/are rejected under 35 U.S.C. 103 as being unpatentable over Pan et al. (US 20180241032 A1) (Pan) in view of Ahn et al. (US 20150079467 A1) (Ahn) and Zhamu et al. (US 20190088922 A1) (Zhamu), as applied to claim 1, further in view of Laicer et al. (US 20160049656 A1) (Laicer).
Regarding claim 12, modified Pan discloses the composite particulate of claim 1.
Pan further desires to regulate anode active material expansion and contraction to improve (dis)charge cycle life (¶ 0006) but fails to explicitly disclose that the anode active material particles are porous.
Laicer, in teaching porous Li-battery anode active particles (Abstract), teaches that such materials have the capacity for higher energy density and greater mechanical rigidity, as the voids provide for expansion and contraction without the anode material’s breaking apart or delaminating (¶ 0069).
Laicer is analogous prior art to the claimed invention because they pertain to the same field of endeavor, namely battery anode material.
It would have been obvious to one of ordinary skill in the art, before the effective filing date of the claimed invention, to make Pan’s anode active particles porous, as taught by Laicer, with the reasonable expectation of providing higher energy density and greater mechanical rigidity by allowing for the anode materials’ expansion and contraction without the anode material’s breaking apart or delaminating, as taught by Laicer.
Response to Arguments
Applicant’s arguments with respect to claim(s) 1 have been considered. Applicant’s amendment, in omitting the previous siloxane from the plasticizer/diluent Markush group, overcame the previous 35 U.S.C. 103 rejection—which, as noted above, has been withdrawn—and necessitated the new grounds of rejection citing Zhamu, as established above.
Conclusion
The cited art made of record but not relied upon is considered pertinent to Applicant’s disclosure:
US 20230317953 A1: anode active particles coated with layer including (meth)acrylic polymer and plasticizer such as tetrahydrothiophene 1,1-dioxide, i.e., sulfolane/sulfone.
US 20220069337 A1: anode active particles coated with layer including thermoplastic polymer and that may include plasticizers such as nitriles.
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/J.S.M./Examiner, Art Unit 1751 /Haroon S. Sheikh/Primary Examiner, Art Unit 1751