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  • Yu, Caiyan  (2)
  • Physics  (2)
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  • Physics  (2)
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  • 1
    In: Advanced Materials, Wiley
    Abstract: Transition‐metal sulfides have been regarded as perspective anode candidates for high‐energy Na‐ion batteries. Their application, however, is precluded severely by either low charge storage or huge volumetric change along with sluggish reaction kinetics. Herein, an effective synergetic Sn incorporation‐Zn substitution strategy is proposed based on copper‐based sulfides. First, Na‐ion storage capability of copper sulfide is significantly improved via incorporating an alloy‐based Sn element. However, this process is accompanied by sacrifice of structural stability due to the high Na‐ion uptake. Subsequently, to maintain the high Na‐ion storage capacity, and concurrently improve cycling and rate capabilities, a Zn substitution strategy (taking partial Sn sites) is carried out, which could significantly promote Na‐ion diffusion/reaction kinetics and relieve mechanical strain–stress within the crystal framework. The synergetic Sn incorporation and Zn substitution endow copper‐based sulfides with high specific capacity (≈560 mAh g −1 at 0.5 A g −1 ), ultrastable cyclability (80 k cycles with ≈100% capacity retention), superior rate capability up to 200 A g −1 , and ultrafast charging feature (≈4 s per charging with ≈190 mAh g −1 input). This work provides in‐depth insights for developing superior anode materials via synergetic multi‐cation incorporation/substitution, aiming at solving their intrinsic issues of either low specific capacity or poor cyclability.
    Type of Medium: Online Resource
    ISSN: 0935-9648 , 1521-4095
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2023
    detail.hit.zdb_id: 1474949-X
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  • 2
    In: Applied Physics Letters, AIP Publishing, Vol. 120, No. 19 ( 2022-05-09)
    Abstract: Employing inorganic ion conductors as solid electrolytes (SEs) is one promising solution to develop advanced all- and quasi-solid-state batteries with high energy and safety advantages. Among numerous Li+ ion conductors, Li1.4Al0.4Ti1.6(PO4)3 (LATP) has attracted extensive attention due to its preponderances of air stability and superior Li+ conductivity. However, the practical application of the LATP electrolyte is still obsessed by serious side reactions at the Li-electrode/electrolyte interface. In this work, one kind of quasi-solid electrolyte (QSE) is designed combining anodic aluminum oxide (AAO), LATP, and liquid electrolyte [LE, LiPF6/ethylene carbonate-dimethyl carbonate (EC-DMC)], wherein well-ordered LATP arrays are constructed in the AAO framework to facilitate ionic transport, and a certain content of the LE is introduced to reduce the interfacial resistances. The characterization results suggest that the ionic conductivity of as-prepared AAO–LATP–QSE (ALQSE) is boosted up to ∼6.50 × 10−3 S cm−1 with a Li+ transference number of 0.66, especially the interval between the LATP compound and the Li-metal electrode can effectively restrain Ti4+→Ti3+ reduction at the Li-anode/electrolyte interface. Thus, the assembled LiFePO4|ALQSE|Li cell exhibits excellent electrochemical stability, delivering an initial discharge capacity of 153.3 mAh g−1 at 0.1C and remaining 152.4 mAh g−1 after 60 cycles with a fairly mild reduction of 0.028% per cycle. This study not only presents a facile strategy to prepare a robust QSE framework employing an AAO template but also promotes the rational interface design between titanium (Ti)-containing solid-state electrolytes and Li-metal anodes.
    Type of Medium: Online Resource
    ISSN: 0003-6951 , 1077-3118
    RVK:
    Language: English
    Publisher: AIP Publishing
    Publication Date: 2022
    detail.hit.zdb_id: 211245-0
    detail.hit.zdb_id: 1469436-0
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