硫黄
催化作用
反键分子轨道
氧化态
氧化还原
锂(药物)
金属
固态
化学
阴极
材料科学
无机化学
化学工程
有机化学
物理化学
原子轨道
电子
物理
量子力学
工程类
医学
内分泌学
作者
Yunqi Shou,Jiayi Ou,C. Li,Jie Huang,Tianyou Zhao,Yong Fang,Yongshuai Kang,Yongjian Zhao,Murong Huang,Chenyang Zhao
出处
期刊:ACS materials letters
[American Chemical Society]
日期:2024-09-03
卷期号:6 (10): 4545-4554
标识
DOI:10.1021/acsmaterialslett.4c01416
摘要
Single-atom catalysts (SACs) are extensively utilized as sulfur cathode promoters in liquid lithium–sulfur batteries owing to their remarkable catalytic efficacy. Nonetheless, their utilization in all-solid-state lithium–sulfur batteries (ASSLSBs) is largely constrained by the unclear metal–sulfur (M–S) interactions in the solid state. Herein, we suggest that the strength of the M–S bond formed between SACs and sulfur can be an indicator to evaluate the bidirectional catalytic ability of SACs. Single atomic sites that possess fewer occupied antibonding states bond the sulfur species robustly via enhanced d–p orbital hybridization, which effectively catalyze the redox reaction. However, the excessively strong M–S bond increases the risk of catalyst poisoning, owing to the solid-state interface characteristics. Among the prepared three SACs, CoNC featuring moderate M–S interactions displays superior rate and cycling performances. An initial capacity of 1151 mAh g–1 is achieved at 2C, with a capacity retention rate of up to 94.66% after 500 cycles.
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