过电位
对偶(语法数字)
电池(电)
材料科学
催化作用
分解
工作(物理)
吸附
接口(物质)
离子
数码产品
纳米技术
中心(范畴论)
光电子学
动力学
动能
电子结构
金属
化学
科技与社会
化学工程
国家(计算机科学)
作者
Xue Tian,Huan Liu,Bin Cao,Haonan Cui,Bin Xu
摘要
ABSTRACT The cyclability of Li–CO 2 batteries is fundamentally limited by the sluggish kinetics of Li 2 CO 3 formation and decomposition. In this work, we develop a Ru‑N 4 single‑atom catalyst anchored on MXene (MX‑Ru SA ), in which the atomic interface establishes a synergistic dual d ‑band center to overcome this kinetic constraint. The N coordination modifies the electronic state of Ru, upshifting its d ‐band center to strengthen intermediate adsorption and steer the growth of vertically aligned Li 2 CO 3 nanosheets that facilitate efficient electron and ion transport. Meanwhile, the presence of Ru‐N 4 sites modulates the electronic structure of the MXene support, optimizing the d ‐band center of Ti, which weakens the Li─O bonds in Li 2 CO 3 and significantly reduces its decomposition barrier. As a result, the Li–CO 2 battery with MX‑Ru SA delivers a high discharge capacity of 14757 mA h g −1 , along with an ultralow charging overpotential of 0.56 V and a long cycle life over 3000 h at 100 mA g −1 . This work demonstrates interfacial dual d ‑band synergy as a promising design principle toward high‑performance catalysts for metal‐gas battery systems.
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