材料科学
硫黄
催化作用
无定形固体
阴极
电解质
化学工程
硼化物
无机化学
无定形碳
物理化学
电极
结晶学
有机化学
化学
冶金
工程类
作者
Feng Tao,Teng Zhao,Nanxiang Zhang,Yuzhen Duan,Li Li,Feng Wu,Renjie Chen
标识
DOI:10.1002/adfm.202202766
摘要
Abstract The amorphous metal boride materials are attractive catalyst for advanced lithium sulfur batteries, but their catalytic mechanism remains unclear. Herein, 2D amorphous Mo‐doped cobalt boride (Co 7 Mo 3 B) is designed for the first time as bidirectional sulfur catalysis by rapid chemical reduction. The atom cluster structure of Co 7 Mo 3 B is revealed by theoretical calculation. Electron paramagnetic resonance test further confirms that Co 7 Mo 3 B has interstitial compound structure characteristics. Experimental results show that the porous 2D nanosheets structure and the interaction of Mo, B, Co atoms contribute to enhanced conductivity, high long‐chain lithium polysulfides affinity, and reversible Li 2 S nucleation and dissociation, thus accelerating LiPSs reduction and Li 2 S oxidation kinetics. In addition, the interstitial Co 7 Mo 3 B enables intercalation of Li and B during charging–discharging while keeping the structure stable. As a result, the S cathode with Co 7 Mo 3 B catalyst delivers good life (1000 cycles at 5 C), superior rate performance (10 C). Even at high sulfur areal loading of 6.79 mg cm –2 and electrolyte/sulfur ratio of 5 μL mg –1 , the Co 7 Mo 3 B/S composite cathode still exhibits good areal capacity and capacity retention rate.
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