Publications by authors named "Jinshuo Mi"

Poly(vinylidene fluoride) (PVDF)-based solid electrolytes with a Li salt-polymer-little residual solvent configuration are promising candidates for solid-state batteries. Herein, we clarify the microstructure of PVDF-based composite electrolyte at the atomic level and demonstrate that the Li-interaction environment determines both interfacial stability and ion-transport capability. The polymer works as a "solid diluent" and the filler realizes a uniform solvent distribution.

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The fillers in composite solid-state electrolyte are mainly responsible for the enhancement of the conduction of Li ions but barely regulate the formation of solid electrolyte interphase (SEI). Herein, a unique filler of dielectric NaNbO for the poly(vinylidene fluoride) (PVDF)-based polymer electrolyte, which is subjected to the exchange of Li and Na during cycling, is reported and the substituted Na is engaged in the construction of a fluorinated Li/Na hybrid SEI with high Young's modulus, facilitating the fast transport of Li at the interface at a high areal capacity and suppressing the Li dendrite growth. The dielectric NaNbO also induces the generation of high-dielectric β phase of PVDF to promote the dissociation of Li salt.

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Solid-state lithium batteries (SSLBs) have great development prospects in high-security new energy fields, but face major challenges such as poor charge transfer kinetics, high interface impedance, and unsatisfactory cycle stability. Defect engineering is an effective method to regulate the composition and structure of electrodes and electrolytes, which plays a crucial role in dominating physical and electrochemical performance. It is necessary to summarize the recent advances regarding defect engineering in SSLBs and analyze the mechanism, thus inspiring future work.

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Solid-state lithium metal batteries (SSLMBs) are promising candidates for high-energy-density energy storage devices. However, there still lacks an evaluation criterion to estimate real research status and compare overall performance of the developed SSLMBs. Herein, we propose a comprehensive descriptor, Li transport throughput ( ), to estimate actual conditions and output performance of the SSLMBs.

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Article Synopsis
  • Poor ion and high electron transport at grain boundaries of ceramic electrolytes lead to lithium infiltration and short-circuiting in all-solid-state lithium metal batteries (ASLMBs).
  • The study shows that Li₂CO₃ at these boundaries can be reduced to LiC, enhancing electronic conductivity and causing lithium penetration in LLZO.
  • By using sintered LiAlF₄, the ionic conductivity is improved, lithium penetration is reduced, and a stable LiFePO₄/LAO-LLZOF/Li battery can cycle effectively over 5500 cycles at 3C rate.
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Severe interfacial side reactions of polymer electrolyte with LiNi Co Mn O (NCM811) cathode and Li metal anode restrict the cycling performance of solid-state NCM811/Li batteries. Herein, we propose a chemically stable ceramic-polymer-anchored solvent composite electrolyte with high ionic conductivity of 6.0×10  S cm , which enables the solid-state NCM811/Li batteries to cycle 1500 times.

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