4.8 Article

Unveiling the critical role of interfacial ionic conductivity in all-solid-state lithium batteries

期刊

NANO ENERGY
卷 72, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.nanoen.2020.104686

关键词

Interfacial ionic conductivity; Ion transport kinetics; Li+ diffusivity; All-solid-state batteries

资金

  1. Natural Sciences and Engineering Research Council of Canada (NSERC)
  2. Canada Research Chair Program (CRC)
  3. Canada Foundation for Innovation (CFI)
  4. Ontario Research Fund (ORF)
  5. China Automotive Battery Research Institute Co., Ltd.
  6. Glabat Solid-State Battery Inc.
  7. Canada Light Source (CLS) at University of Saskatchewan
  8. Interdisciplinary Development Initiatives (IDI) by Western University
  9. University of Western Ontario
  10. Mitacs Elevate Postdoctoral Fellowships
  11. Center for Functional Nanomaterials, U.S. DOE Office of Science Facility, at Brookhaven National Laboratory [DE-SC0012704]

向作者/读者索取更多资源

Advancement of all-solid-state lithium-ion (Li+) batteries (ASSLIBs) has been hindered by the large interfacial resistance mainly originating from interfacial reactions between oxide cathodes and solid-state sulfide electrolytes (SEs). To suppress the interfacial reactions, an interfacial coating layer between cathodes and SEs is indispensable. However, the kinetics of interfacial Li+ transport across the coating layer has not been well understood yet. Herein, we tune the interfacial ionic conductivity of the coating layer LiNb0.5Ta0.5O3 (LNTO) by manipulating post-annealing temperature. It is found that the interfacial ionic conductivity determines interfacial Li+ transport kinetics and enhancing the interfacial ionic conductivity can significantly boost the electrochemical performance of SE-based ASSLIBs. A representative cathode LiNi0.5Mn0.3Co0.2O2 coated by LNTO with the highest interfacial ionic conductivity exhibits a high initial capacity of 152 mAh.g(-1) at 0.1 C and 107.5 mAh. g(-1) at 1 C. This work highlights the importance of increasing interfacial ionic conductivity for high-performance SE-based ASSLIBs.

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