氧化还原
硫黄
多硫化物
材料科学
锂(药物)
有机自由基电池
快离子导体
无机化学
电极
化学工程
电解质
化学
物理化学
医学
工程类
冶金
内分泌学
作者
Hong Yuan,Hong‐Jie Peng,Jia‐Qi Huang,Qiang Zhang
标识
DOI:10.1002/admi.201802046
摘要
Abstract Lithium–sulfur (Li–S) batteries have been strongly considered as one of the most promising future energy storage systems because of ultrahigh theoretical energy density of 2600 Wh kg −1 . The natural abundance, affordable cost, and environmental benignity of elemental sulfur constitute additional advantages. However, complicated reaction behaviors at working electrode/electrolyte interfaces that involve multiphase conversion and multistep ion/electron diffusion during sulfur redox reactions have impeded the thorough understanding of Li–S chemistry and its practical applications. This perspective article highlights the influence of the ion/electron transport and reaction regulation through electrocatalysis or redox mediation at electrode/electrolyte interfaces on various interfacial sulfur redox reactions (liquid–liquid–solid interconversion between soluble lithium polysulfide with different chain lengths and insoluble lithium sulfides in liquid‐electrolyte Li–S batteries and direct solid–solid conversion between sulfur and Li 2 S in all‐solid‐state Li–S batteries). The current status, existing challenges, and future directions are discussed and prospected, aiming at shedding fresh light on fundamental understanding of interfacial sulfur redox reactions and guiding the rational design of electrode/electrolyte interfaces for next‐generation Li–S batteries with high energy density and long cycle life.
科研通智能强力驱动
Strongly Powered by AbleSci AI