密度泛函理论
钙钛矿(结构)
异质结
尖晶石
材料科学
溶解
曲面重建
吸附
电子结构
电子能带结构
化学物理
化学
纳米技术
曲面(拓扑)
蚀刻(微加工)
光电子学
物理化学
结晶学
凝聚态物理
计算化学
几何学
图层(电子)
数学
物理
冶金
作者
Jingyan Zhang,Junfu Li,Chenglin Zhong,Pinxian Xi,Dongliang Chao,Daqiang Gao
出处
期刊:Nano Letters
[American Chemical Society]
日期:2021-09-23
卷期号:21 (19): 8166-8174
被引量:56
标识
DOI:10.1021/acs.nanolett.1c02623
摘要
Reconstructing the surface-electronic-structure of catalysts for efficient electrocatalytic activity is crucial but still under intense exploration. Herein, we introduce a double-cation gradient etching technique to manipulate the electronic structure of perovskite LaCoO3. With the gradient dissolution of cations, the surface was reconstructed, and the perovskite/spinel heterostructure V-LCO/Co3O4 (V-LCO refers to LaCoO3 with La and Co vacancies) can be realized. Its surface-electronic-structure is effectively regulated due to the heterogeneous interface effect and abundant vacancies, resulting in a significantly enhanced activity for oxygen evolution reaction (OER). The V-LCO/Co3O4 exhibits low electrochemical activation energy and 2 orders of magnitude higher carrier concentrations (1.36 × 1021 cm-3) compared with LCO (6.03 × 1019 cm-3). Density functional theory (DFT) calculation unveils that the directional reconstruction of surface-electronic-structure enables the d-band center of V-LCO/Co3O4 to a moderate position, endowing perfect adsorption strength for oxo groups and thus promoting the electrocatalytic activity. ©
科研通智能强力驱动
Strongly Powered by AbleSci AI