催化作用
材料科学
溶解
硫黄
阴极
碳纤维
导电体
化学工程
多孔性
吉布斯自由能
氧化还原
分解
纳米技术
无机化学
化学
热力学
物理化学
复合材料
冶金
有机化学
工程类
物理
复合数
作者
Zejing Lin,Minglei Mao,Lv Tianshi,Shuwei Li,Yong‐Sheng Hu,Hong Li,Xuejie Huang,Liquan Chen,Liumin Suo
标识
DOI:10.1016/j.ensm.2022.06.055
摘要
Rechargeable aluminum‒sulfur batteries (RASBs), despite the great advantage of high energy density and low cost, are suffering from insulative solid sulfur species and sluggish reaction kinetics. The routine solution of introducing an excessive amount of inactive carbon will cause the low active material's proportion and thus high electrode porosity, dramatically compromising the energy densities. More importantly, the high Gibbs free energy of the Al2S3 decomposition remains unsolved. Herein, an Al3+-intercalative and catalytic electronic conductive framework (ECF) is constructed by Mo6S8 to replace conventional inactive carbon, in which Mo6S8 will build an efficient conductive network, provide high Al-ion storage capability, have a strong affinity to polysulfides to restrain their dissolution, and show superior catalytic activity on the decomposition of Al2S3. Consequently, the Mo6S8/S cathode achieves a highly competitive specific energy of 371 Wh/kgcathode (ca), with the voltage hysteresis of sulfur redox markedly decreased by 569 mV. Our Al3+-intercalative and catalytic ECF notably enhances the specific energy and energy efficiency of RASBs, which will push multivalent metal-sulfur batteries forward to practical application.
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