多硫化物
材料科学
硒化物
锂(药物)
铋
电解质
硫黄
无机化学
催化作用
阴极
化学工程
氧化还原
兴奋剂
纳米技术
电极
硒
化学
有机化学
物理化学
内分泌学
冶金
工程类
医学
光电子学
作者
Mengyao Li,Dawei Yang,Jordi Jacas Biendicho,Xu Han,Chaoqi Zhang,Kun Liu,Jiefeng Diao,Junshan Li,Jing Wang,Marc Heggen,Rafal E. Dunin‐Borkowski,Jiaao Wang,Graeme Henkelman,J.R. Morante,Jordi Arbiol,Shulei Chou,Andreu Cabot
标识
DOI:10.1002/adfm.202200529
摘要
Abstract The shuttling behavior and sluggish conversion kinetics of intermediate lithium polysulfides (LiPS) represent the main obstacles to the practical application of lithium–sulfur batteries (LSBs). Herein, an innovative sulfur host is proposed, based on an iodine‐doped bismuth selenide (I‐Bi 2 Se 3 ), able to solve these limitations by immobilizing the LiPS and catalytically activating the redox conversion at the cathode. The synthesis of I‐Bi 2 Se 3 nanosheets is detailed here and their morphology, crystal structure, and composition are thoroughly. Density‐functional theory and experimental tools are used to demonstrate that I‐Bi 2 Se 3 nanosheets are characterized by a proper composition and micro‐ and nano‐structure to facilitate Li + diffusion and fast electron transportation, and to provide numerous surface sites with strong LiPS adsorbability and extraordinary catalytic activity. Overall, I‐Bi 2 Se 3 /S electrodes exhibit outstanding initial capacities up to 1500 mAh g −1 at 0.1 C and cycling stability over 1000 cycles, with an average capacity decay rate of only 0.012% per cycle at 1 C. Besides, at a sulfur loading of 5.2 mg cm −2 , a high areal capacity of 5.70 mAh cm −2 at 0.1 C is obtained with an electrolyte/sulfur ratio of 12 µL mg −1 . This work demonstrated that doping is an effective way to optimize the metal selenide catalysts in LSBs.
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