材料科学
石墨烯
阴极
阳极
多硫化物
气凝胶
化学工程
锂(药物)
涂层
兴奋剂
容量损失
电解质
纳米技术
光电子学
电极
化学
内分泌学
工程类
医学
物理化学
作者
Guangmin Zhou,Eunsu Paek,Gyeong S. Hwang,Arumugam Manthiram
标识
DOI:10.1002/aenm.201501355
摘要
Lithium‐sulfur (Li‐S) batteries are being considered as the next‐generation high‐energy‐storage system due to their high theoretical energy density. However, the use of a lithium‐metal anode poses serious safety concerns due to lithium dendrite formation, which causes short‐circuiting, and possible explosions of the cell. One feasible way to address this issue is to pair a fully lithiated lithium sulfide (Li 2 S) cathode with lithium metal‐free anodes. However, bulk Li 2 S particles face the challenges of having a large activation barrier during the initial charge, low active‐material utilization, poor electrical conductivity, and fast capacity fade, preventing their practical utility. Here, the development of a self‐supported, high capacity, long‐life cathode material is presented for Li‐S batteries by coating Li 2 S onto doped graphene aerogels via a simple liquid infiltration–evaporation coating method. The resultant cathodes are able to lower the initial charge voltage barrier and attain a high specific capacity, good rate capability, and excellent cycling stability. The improved performance can be attributed to the (i) cross‐linked, porous graphene network enabling fast electron/ion transfer, (ii) coated Li 2 S on graphene with high utilization and a reduced energy barrier, and (iii) doped heteroatoms with a strong binding affinity toward Li 2 S/lithium polysulfides with reduced polysulfide dissolution based on first‐principles calculations.
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