硫黄
材料科学
多硫化物
氧化还原
电化学
阴极
循环伏安法
氧化物
电池(电)
锂(药物)
储能
无机化学
锂硫电池
化学工程
纳米技术
冶金
电极
电解质
化学
物理化学
热力学
功率(物理)
内分泌学
工程类
物理
医学
作者
Xiao Liang,Chun Yuen Kwok,Fernanda Lodi‐Marzano,Quanquan Pang,Marine Cuisinier,He Huang,Connor J. Hart,Diane Houtarde,Kavish Kaup,Heino Sommer,Torsten Brezesinski,Jürgen Janek,Linda F. Nazar
标识
DOI:10.1002/aenm.201501636
摘要
The lithium‐sulfur battery is a compelling energy storage system because its high theoretical energy density exceeds Li‐ion batteries at much lower cost, but applications are thwarted by capacity decay caused by the polysulfide shuttle. Here, proof of concept and the critical metrics of a strategy to entrap polysulfides within the sulfur cathode by their reaction to form a surface‐bound active redox mediator are demonstrated. It is shown through a combination of surface spectroscopy and cyclic voltammetry studies that only materials with redox potentials in a targeted window react with polysulfides to form active surface‐bound polythionate species. These species are directly correlated to superior Li‐S cell performance by electrochemical studies of high surface area oxide cathodes with redox potentials below, above, and within this window. Optimized Li‐S cells yield a very low fade rate of 0.048% per cycle. The insight gained into the fundamental surface mechanism and its correlation to the stability of the electrochemical cell provides a bridge between mechanistic understanding and battery performance essential for the design of high performance Li‐S cells.
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