4.8 Article

Double Ionic-Electronic Transfer Interface Layers for All-Solid-State Lithium Batteries

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 60, 期 34, 页码 18448-18453

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202104183

关键词

lithium-metal batteries; mixed ion-electron interface layers; polymer electrolytes; solid electrolyte interphase; solid-state batteries

资金

  1. National Natural Science Foundation of China [11972178, 51872131, 51972156]
  2. Technology Liaoning Project Grants [2019LNZD01, 2020LNQN17, 2019QN07]
  3. Talent Project of Revitalizing LiaoNing [XLYC1807114]

向作者/读者索取更多资源

This study successfully reduced the interface resistance of solid-state lithium batteries by growing double ionic-electronic transfer interface layers at the electrode-electrolyte interfaces, achieving higher cycling stability and charge-discharge efficiency.
Large-scale implementation of all-solid-state lithium batteries is impeded by the physical limitations of the interface between the electrode and solid electrolyte; specifically, high resistance and poor stability, as well as poor compatibility with Li+ migration. We report double ionic-electronic transfer interface layers grown at electrode-electrolyte interfaces by in situ polymerization of 2,2 '-bithiophene in polyethylene oxide (PEO) electrolyte. For all-solid-state LiFePO4 parallel to PT-PEO-PT parallel to Li cells, the formation of a conductive polythiophene (PT) layer at the cathode-electrolyte interface resulted in an at least sevenfold decrease in interface resistance, and realized a capacity retention of about 94 % after 1000 cycles along with a lower polarization voltage under a rate of 2 C. The mixed ionic-electronic conductive layers imparted superior interface stability and contact while keeping good compatibility with the Li anode.

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