离子电导率
电化学
电解质
电导率
离子半径
材料科学
离子键合
兴奋剂
锂(药物)
阳极
分析化学(期刊)
无机化学
化学
物理化学
离子
电极
医学
内分泌学
光电子学
有机化学
色谱法
作者
Jialü Zhang,Chenjie Lou,Lei Dong,Weiwei Ping,Hongfa Xiang,Mingxue Tang,Xuyong Feng
标识
DOI:10.1002/sstr.202300565
摘要
High ionic conductivity is the key point in the development of new solid‐state electrolytes. Herein, a combining strategy of anion (O 2− ) doping and structure distortion is applied to enhance the Li + ion conductivity in Li 15 P 4 S 16 Cl 3 , thus converting the nonionic conductor into fast ionic conductor. Solid‐state 6 Li nuclear magnetic resonance analysis shows redistribution of Li + ions in Li 15 P 4 S 16 Cl 3 with O 2− doping or local structure distortion via ball milling, indicating energy changes at different lithium sites. As a result, the activation energy is reduced from 0.50 to 0.35 eV for the ball‐milled Li 15 P 4 S 15.6 O 0.4 Cl 3 , and the ionic conductivity is enhanced from 10 −9 to 10 −4 S cm −1 . The electrochemical stability of Li 15 P 4 S 15.6 O 0.4 Cl 3 is broadened at the anode side as well. The symmetric cell Li|Li 15 P 4 S 15.6 O 0.4 Cl 3 |Li can cycle more than 1000 h with negligible voltage increase. The LiCoO 2 |Li 15 P 4 S 15.6 O 0.4 Cl 3 |Li‐Si all‐solid‐state battery demonstrates an initial capacity of 106 mA h g −1 and retains 92% capacity after 200 cycles at 0.5 C, highlighting excellent rate performance and electrochemical stability.
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