材料科学
硫化物
相间
电化学
快离子导体
相容性(地球化学)
电极
化学工程
锂(药物)
电解质
固态
纳米技术
物理化学
化学
复合材料
内分泌学
冶金
工程类
生物
医学
遗传学
作者
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
标识
DOI:10.1002/aenm.202100881
摘要
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 Li x Zr 2 (PO 4 ) 3 surprisingly exhibit great compatibility with both 4.5 V LiCoO 2 and Li 6 PS 5 Cl, 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.
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