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  • Royal Society of Chemistry (RSC)  (3)
  • Cheng, Shijie  (3)
  • 2020-2024  (3)
Material
Publisher
  • Royal Society of Chemistry (RSC)  (3)
Language
Years
  • 2020-2024  (3)
Year
  • 1
    In: Journal of Materials Chemistry A, Royal Society of Chemistry (RSC)
    Abstract: Sulfurized polyacrylonitrile (SPAN), featuring uniform dispersion of short-chain sulfur in organic skeleton, shows great promise in lithium-sulfur (Li-S) batteries since the inhibited polysulfide dissolution and hence improved electrochemical performance. However, the practical property of SPAN is significantly limited by its relatively poor ionic and electronic conductivity, as well as sulfur content ( 〈 50%). Herein, Triallyl Isocyanurate (TI) is incorporated to fabricate SPAN fiber with robust chemical structure and high sulfur loading. The fine-tuned organosulfur cathode (Se0.05S0.95PAN-TI11, 1F) demonstrates hoisted S & Se content of 54.2% and excellent electrochemical performance in Li/Na-S batteries. As a result, 1F exhibits an ultrahigh composite capacity of 671 mAh g−1 at 0.1C (capacity retention up to 100%) and remarkable rate capability of 405 mAh g−1 at 8C in Li-S batteries. Additionally, 1F shows prolonged cycle ability over 300 cycles at 0.5C when applied in RT-S battery. Notably, under harsh conditions (loading of 10.0 mg cm−2 and E/S= 5µL/mg), Li-1F battery displays a brilliant initial areal capacity of 8.0 mAh cm−2 at 0.1C (reversible capacity of 6.3 mAh cm−2) and retains capacity of 5.3 mAh cm−2 at the 200th cycle (capacity retention of 84%). Consequently, 1F is promising for practical applications in high-performance Metal-S batteries.
    Type of Medium: Online Resource
    ISSN: 2050-7488 , 2050-7496
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2023
    detail.hit.zdb_id: 2702232-8
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  • 2
    In: Chemical Science, Royal Society of Chemistry (RSC), Vol. 14, No. 10 ( 2023), p. 2745-2754
    Abstract: “Solvent-in-salt” electrolytes (high-concentration electrolytes (HCEs)) and diluted high-concentration electrolytes (DHCEs) show great promise for reviving secondary lithium metal batteries (LMBs). However, the inherently sluggish Li + transport of such electrolytes limits the high-rate capability of LMBs for practical conditions. Here, we discovered a “tug-of-war” effect in a multilayer solvation sheath that promoted the rate capability of LMBs; the pulling force of solvent–nonsolvent interactions competed with the compressive force of Li + -nonsolvent interactions. By elaborately manipulating the pulling and compressive effects, the interaction between Li + and the solvent was weakened, leading to a loosened solvation sheath. Thereby, the developed electrolytes enabled a high Li + transference number (0.65) and a Li (50 μm)‖NCM712 (4 mA h cm −2 ) full cell exhibited long-term cycling stability (160 cycles; 80% capacity retention) at a high rate of 0.33C (1.32 mA cm −2 ). Notably, Li (50 μm)‖LiFePO 4 (LFP; 17.4 mg cm −2 ) cells with a designed electrolyte reached a capacity retention of 80% after 1450 cycles at a rate of 0.66C. An 6 Ah Li‖LFP pouch cell (over 250 W h kg −1 ) showed excellent cycling stability (130 cycles, 96% capacity retention) under practical conditions. This design concept for an electrolyte provides a promising path to build high-energy-density and high-rate LMBs.
    Type of Medium: Online Resource
    ISSN: 2041-6520 , 2041-6539
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2023
    detail.hit.zdb_id: 2559110-1
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  • 3
    In: Energy & Environmental Science, Royal Society of Chemistry (RSC), Vol. 16, No. 2 ( 2023), p. 546-556
    Abstract: Developing advanced electrolytes is indispensable for next-generation lithium-ion batteries (LIBs). Yet the strong solvating interaction between Li + and various solvents often leads to sluggish desolvation and solvent co-intercalation into graphite electrodes, thus limiting the scope of electrolyte design. Here, we present a mechanism of dipole–dipole interactions to facilitate desolvation and inhibit co-intercalation through deliberately tuning the interactions among Li + , solvents and non-coordinating molecules (non-solvents). Specifically, the non-solvents counteract electrostatic attractions to tame the affinity between Li + and solvents without altering the primary solvation structure at medium Li salt concentration. Consequently, the weakened Li + -solvent strength enables facile desolvation and thus superior electrochemical compatibility with graphite anodes for various solvents including DME (1,2-dimethoxyethane), DMSO (dimethyl sulfoxide), TMP (trimethyl phosphate), PC (propylene carbonate) and DEC (diethyl carbonate). We believe that the strategy of dipole–dipole interactions can extend the horizon of electrolyte design towards achieving advanced LIBs.
    Type of Medium: Online Resource
    ISSN: 1754-5692 , 1754-5706
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2023
    detail.hit.zdb_id: 2439879-2
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