材料科学
离子电导率
电解质
电导率
兴奋剂
电化学
离子键合
化学工程
快离子导体
硫化物
无机化学
扩散
化学物理
离子强度
电化学窗口
离子
碲
球磨机
锂(药物)
作者
Hongda Li,Shuai Jian,L. Y. Yang,Wanting Zhang,Jiale Wang,Pengyan Li,Haixin Chang
标识
DOI:10.1021/acsami.5c20087
摘要
Sulfide solid electrolytes enable high-performance all-solid-state batteries, where Li10SnP2S12 (LSPS) offers LGPS-comparable conductivity with superior resource sustainability, yet faces challenges in balancing ionic transport and stability. This study synthesized Te-doped Li10SnP2S12-xTex (LSPST, 0 ≤ x ≤ 0.25) electrolytes via high-energy ball milling combined with gradient annealing. Structural analyses confirm uniform Te substitution at S sites. At the optimal doping level (x = 0.1), the modified electrolyte exhibits significantly improved performance, demonstrating a 45.2% enhancement in ionic conductivity (4.3 × 10-3 S cm-1) compared to pristine LSPS, along with a lower activation energy (0.259 eV) and superior electrochemical stability. Theoretical calculations reveal that Te doping facilitates Li+ transport through elongated Li-Te bonds, weakening Li+-framework interactions and anisotropic z-axis diffusion (validated by molecular dynamics). Simultaneously suppresses electronic conductivity (8.33 × 10-9 S cm-1) to inhibit dendrites, it enables superior full-cell performance in Li-In/LSPST/Li6PS5Cl/NCM811) cells, delivering 136.1 mAh g-1 initial capacity with 67.9% capacity retention after 50 cycles, outperforming undoped counterparts by 86%. This work establishes an anionic doping strategy to concurrently enhance ionic transport and stability in cost-effective sulfide electrolytes.
科研通智能强力驱动
Strongly Powered by AbleSci AI