多硫化物
硫黄
材料科学
阴极
铜
水溶液
化学工程
集电器
金属
电化学
储能
纳米技术
无机化学
电极
电解质
冶金
化学
有机化学
物理化学
工程类
功率(物理)
物理
量子力学
作者
Pei‐Rong Li,Lu Ma,Tianpin Wu,Hualin Ye,Junhua Zhou,Feipeng Zhao,Na Han,Yeyun Wang,Yunling Wu,Yanguang Li,Jun Lü
标识
DOI:10.1002/aenm.201800624
摘要
Abstract Room‐temperature Li/Na‐S batteries are promising energy storage solutions, but unfortunately suffer from serious cycling problems rooted in their polysulfide intermediates. The conventional strategy to tackle this issue is to design host materials for trapping polysulfides via weak physical confinement and interfacial chemical interactions. Even though beneficial, their capability for the polysulfide immobilization is still limited. Herein, the unique sulfiphilic nature of metallic Cu is revisited. Upon the exposure to polysulfide in aqueous or aprotic solution, the surface sulfidization rapidly takes place, resulting in the formation of Cu 2 S nanoflake arrays with tunable texture. When the sulfidized Cu current collector is directly used as the sulfur‐equivalent cathode, it enables high‐performance Li/Na‐S batteries at room temperature with reasonable high sulfur loading. Specific capacities up to ≈1200 mAh g −1 for Li‐S and ≈400 mAh g −1 for Na‐S are measured when normalized to the amount of equivalent sulfur, and can be readily sustained for >1000 cycles.
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