电极
电解质
催化作用
阴极
锂(药物)
硫黄
材料科学
纳米技术
化学工程
氧化还原
带隙
电池(电)
化学
无机化学
冶金
光电子学
工程类
物理化学
有机化学
物理
功率(物理)
量子力学
内分泌学
医学
作者
Meng Guo,Shaonan Gu,Rong Zhou,Zheng Zhang,Shuzheng Xu,Yinan Wang,Guowei Zhou
标识
DOI:10.1016/j.cej.2024.149500
摘要
The practical usage of lithium sulfur (Li–S) batteries has been hampered by the severely sluggish conversion kinetics of lithium polysulfides (LiPSs) and the overused of binders and electrolyte, resulting in energy density decreased dramatically. In this work, as a catalyst for LiPSs conversion of great potential, the poor catalytic performance of MoTe2 is revealed to be the wide gap of d-p band center, which hinders the electron exchange of interfacial redox dynamics. Accordingly, the binder-free cathodes are fabricated by recrystallizing sulfur on phosphorus-doped MoTe2 decorated carbon cloth (P-MoTe2/CC) to boost Li–S battery performance. The electron deficient P in MoTe2 lifts the d-band center of P-MoTe2 to Fermi level and narrows the gap of d-p band center when it interacts with LiPSs, which significantly increases the catalytic activity of MoTe2 towards both LiPSs oxidation and reduction. With these features, the P-MoTe2/CC cathodes therefore offers a high initial discharge capacity of 1480.55 mAh g−1 and a low capacity decay of 0.42 % per cycle. Even at high sulfur loading and lean electrolyte of 4.3 (E/S ratio), the Li–S pouch cell can also perform an outstanding cycling stability and reach a high energy density of about 400 Wh kg−1.
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