多硫化物
催化作用
硫黄
氧化还原
电化学
锂(药物)
阳极
阴极
化学
锂硫电池
电池(电)
电催化剂
无机化学
化学工程
材料科学
物理化学
电解质
电极
有机化学
内分泌学
工程类
功率(物理)
物理
医学
量子力学
作者
Qin Yang,Xijun Wei,Xuan Cao,Le Chen,Lixian Song,Long Kong,Wei Sun,Kefeng Xie,Yingze Song
标识
DOI:10.1016/j.cej.2022.139638
摘要
Lithium–sulfur batteries (LSBs) have emerged as prospective candidates for energy storage systems due to their high energy density and low cost of sulfur. However, the fast capacity degradation stemming from the fatal lithium polysulfide (LiPS) shuttle and sluggish redox reaction kinetic acts as the bottleneck for the real implementation of LSBs. Herein, we propose a well-designed nanosphere functionalized with trimetallic Fe-Co-Ni phosphides (FCNP) to host sulfur and promote the sulfur redox reactions. The well-dispersed trimetallic phosphides can not only enhance polarity and electron conductivity but also supply sufficient conversion sites and short sulfur evolution pathway. Therefore, the elaborated trimetallic phosphides on carbon nanosphere effectively inhibits LiPSs escaping from the cathode to anode. Further, the systematic electrochemical measurements and synchrotron X-ray three-dimensional nano-computed tomography (X-ray 3D nano-CT) results provide clear evidence that FCNP as a bidirectional electrocatalyst smoothly accelerates the generation and decomposition of Li2S. Accordingly, the S/FCNP cathode exhibits a remarkable discharge capacity of 1172.3 mA h g−1 at 0.2C in coin cell, 1164.0 mA h g−1 at 0.1C in pouch cell and the favorable cycling performance.
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