Bidirectionally Compatible Buffering Layer Enables Highly Stable and Conductive Interface for 4.5 V Sulfide-Based All-Solid-State Lithium Batteries

Longlong Wang, Xingwei Sun, Jun Ma, Bingbing Chen, Chao Li, Jiedong Li, Liang Chang, Xinrun Yu, Ting Shan Chan, Zhiwei Hu, Malachi Noked, Guanglei Cui

Research output: Contribution to journalArticlepeer-review

39 Scopus citations

Abstract

High-voltage all-solid-state lithium batteries (HVASSLBs) are considered attractive systems for portable electronics and electric vehicles, due to their theoretically high energy density and safety. However, realization of HVASSLBs with sulfide solid electrolytes (SEs) is hindered by their limited electrochemical stability, resulting in sluggish interphase dynamics. Here, a bidirectionally compatible buffering layer design scheme is proposed to overcome the interfacial challenges of sulfide-based HVASSLBs. As a proof of concept, it is found that NASICON-type LixZr2(PO4)3 surprisingly exhibit great compatibility with both 4.5 V LiCoO2 and Li6PS5Cl, based on the results of first-principles calculations and various in situ/ex situ characterizations. This compatibility significantly restrains the interface reactivity and boosts interfacial Li-ion transport. Therefore, 4.5 V sulfide-based HVASSLBs can exhibit remarkably enhanced initial discharge capacity (143.3 vs 125.9 mAh·g−1 at 0.2C), capacity retention (95.53% vs 74.74% after 100 cycles), and rate performance (97 vs 45 mAh·g−1 at 2C). This work sheds light on the great prospects of sulfide-based HVASSLBs with high-rate characteristics, and constitutes a crucial step toward the rational design of interface and interphase chemistry for high-performance sulfide-based HVASSLBs.

Original languageEnglish
Article number2100881
JournalAdvanced Energy Materials
Volume11
Issue number32
DOIs
StatePublished - 26 Aug 2021

Bibliographical note

Funding Information:
L.W. and X.S. contributed equally to this work. This work was supported by the National Key R&D Program of China (2017YFE0127600), the National Natural Science Foundation of China (No. 21975274, U1706229), the Strategic Priority Research Program of the Chinese Academy of Sciences (XDA22010600), Shandong Provincial Natural Science Foundation (ZR2020KE032), the National Natural Science Foundation for Distinguished Young Scholars of China (51625204), the Taishan Scholars of Shandong Province (ts201511063), and Youth Innovation Promotion Association CAS (2021210). The authors acknowledge the support from the Max Planck‐POSTECH‐Hsinchu Center for Complex Phase Materials.

Funding Information:
L.W. and X.S. contributed equally to this work. This work was supported by the National Key R&D Program of China (2017YFE0127600), the National Natural Science Foundation of China (No. 21975274, U1706229), the Strategic Priority Research Program of the Chinese Academy of Sciences (XDA22010600), Shandong Provincial Natural Science Foundation (ZR2020KE032), the National Natural Science Foundation for Distinguished Young Scholars of China (51625204), the Taishan Scholars of Shandong Province (ts201511063), and Youth Innovation Promotion Association CAS (2021210). The authors acknowledge the support from the Max Planck-POSTECH-Hsinchu Center for Complex Phase Materials.

Publisher Copyright:
© 2021 Wiley-VCH GmbH

Keywords

  • all-solid-state lithium batteries
  • buffering layers
  • cathode interfaces
  • high voltage
  • sulfide electrolytes

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