催化作用
材料科学
钴
电化学
吸附
锂(药物)
离解(化学)
化学工程
分解
纳米技术
无机化学
物理化学
化学
电极
有机化学
工程类
内分泌学
冶金
医学
作者
Yanli Chen,Junfeng Li,Bingyi Lu,Yingqi Liu,Rui Mao,Yanze Song,Hongtai Li,Xinqian Yu,Yongzheng Gao,Qiong Peng,Xiaosi Qi,Guangmin Zhou
标识
DOI:10.1002/adma.202406856
摘要
Catalytic reactions mainly depend on the adsorption properties of reactants on the catalyst, which provides a perspective for the design of reversible lithium-carbon dioxide (Li-CO2) batteries including CO2 reduction (CO2RR) and CO2 evolution (CO2ER) reactions. However, due to the complex reaction process, the relationship between the adsorption configuration and CO2RR/CO2ER catalytic activity is still unclear in Li─CO2 batteries. Herein, taking Co3S4 as a model system, nickel (Ni substitution in the tetrahedral site to activate cobalt (Co) atom for forming multiatom catalytic domains in NiCo2S4 is utilized. Benefiting from the special geometric and electronic structures, NiCo2S4 exhibits an optimized adsorption configuration of lithium carbonate (Li2CO3), promoting its effective activation and decomposition. As a result, the Li-CO2 batteries with NiCo2S4 cathode exhibit remarkable electrochemical performance in terms of low potential gap of 0.42 V and high energy efficiency of 88.7%. This work provides a unique perspective for the development of highly efficient catalysts in Li-CO2 batteries.
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