过电位
电催化剂
表面改性
催化作用
材料科学
氧化还原
化学工程
吸附
离解(化学)
电池(电)
纳米技术
离域电子
无机化学
动力学
密度泛函理论
化学
电极
储能
电化学
氯
能量密度
过渡金属
作者
R. Y. Zhang,Peng Zhang,Xue Tian,Haonan Cui,Razium Ali Soomro,Jian Hao,Yiqing He,Tianli Wu,Bin Xu
标识
DOI:10.1021/acsenergylett.6c00453
摘要
Li-CO2 batteries hold potential due to the advantages in energy density and CO2 utilization, with their application limited by the CO2 reduction/evolution reaction kinetics (CRR/CER). Herein, Nb2CTx MXene is explored as an electrocatalyst for Li-CO2 batteries, with its surface microenvironment engineered by functionalizing with -O, -F, -Cl, -Br, and -I terminations to optimize the catalytic activity. Theoretical and experimental analyses reveal that chlorine functionalization (Nb2CClx) enhances the adsorption of Li, CO2, and Li2CO3, promotes d-orbital electron delocalization in Nb atoms, and increases electron donation capability. Moreover, Li2CO3 formed on Nb2CClx displays an elongated Li–O bond and a reduced dissociation energy. Consequently, the Nb2CClx-based Li-CO2 battery delivers a discharge capacity of 15521.2 mAh g–1, an overpotential of 1.50 V, and an extended lifetime of over 157 cycles. These findings underscore the importance of surface chemistry in designing catalytically active MXene-based electrocatalysts for reversible Li-CO2 batteries.
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