多硫化物
电化学
材料科学
催化作用
成核
密度泛函理论
硫黄
阴极
锂(药物)
氧化还原
纳米技术
化学工程
电催化剂
氮化物
锂硫电池
阳极
过渡金属
碳纤维
化学反应
介电谱
氮化碳
电化学能量转换
有机自由基电池
无机化学
储能
化学过程
电化学储能
化学能
电极
作者
Jing Yu,Oleg Usoltsev,Irina Martynova,Chen Huang,Zhifu Liang,Ivan Pinto‐Huguet,Canhuang Li,Liqiang Lu,Chaoqi Zhang,Xuan Lu,Kapil Gupta,Marc Botifoll,Laura Simonelli,François Fauth,Jinyuan Zhou,Jordi Llorca,Yan Lü,Chaoyue Zhang,Jordi Arbiol,Andreu Cabot
标识
DOI:10.1002/adma.202511345
摘要
S nucleation over competing chemical reactions, enabling high charge-discharge rates while preventing active material loss and enhancing stability. Electrochemical analysis, density functional theory, and operando spectroscopy reveal that TM-Bi pairing shifts d-band states closer to the Fermi level and modulates HOMO-LUMO levels, promoting lithium polysulfide (LiPS) interaction and facilitating efficient charge transfer. These findings offer valuable insights for designing advanced catalysts for LSBs and broader electrocatalytic applications.
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