多硫化物
材料科学
阴极
双功能
硫黄
化学工程
纳米线
基质(水族馆)
电化学
催化作用
碳化硼
碳纳米纤维
锂(药物)
电极
纳米技术
电解质
复合材料
有机化学
化学
冶金
碳纳米管
医学
物理化学
内分泌学
工程类
地质学
海洋学
作者
Luo Liu,Sheng‐Heng Chung,Hooman Yaghoobnejad Asl,Arumugam Manthiram
标识
DOI:10.1002/adma.201804149
摘要
Developing high-energy-density lithium-sulfur (Li-S) batteries relies on the design of electrode substrates that can host a high sulfur loading and still attain high electrochemical utilization. Herein, a new bifunctional cathode substrate configured with boron-carbide nanowires in situ grown on carbon nanofibers (B4 C@CNF) is established through a facile catalyst-assisted process. The B4 C nanowires acting as chemical-anchoring centers provide strong polysulfide adsorptivity, as validated by experimental data and first-principle calculations. Meanwhile, the catalytic effect of B4 C also accelerates the redox kinetics of polysulfide conversion, contributing to enhanced rate capability. As a result, a remarkable capacity retention of 80% after 500 cycles as well as stable cyclability at 4C rate is accomplished with the cells employing B4 C@CNF as a cathode substrate for sulfur. Moreover, the B4 C@CNF substrate enables the cathode to achieve both high sulfur content (70 wt%) and sulfur loading (10.3 mg cm-2 ), delivering a superb areal capacity of 9 mAh cm-2 . Additionally, Li-S pouch cells fabricated with the B4 C@CNF substrate are able to host a high sulfur mass of 200 mg per cathode and deliver a high discharge capacity of 125 mAh after 50 cycles.
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