催化作用
材料科学
一氧化碳
电子效应
纳米颗粒
铟
过渡金属
电子波段
电子结构
选择性
纳米技术
光化学
化学物理
光电子学
化学
计算化学
带隙
有机化学
作者
Lei Li,Huanhuan Liu,Tianqi Li,Fang Chen,Wentao Wang,Jiqiang Ning,Yong Hu
出处
期刊:Small
[Wiley]
日期:2024-07-27
卷期号:20 (45): e2404909-e2404909
被引量:6
标识
DOI:10.1002/smll.202404909
摘要
Abstract Modulating the electronic properties of transition metal sites in photocatalysts at the atomic level is essential for achieving high‐activity carbon dioxide photoreduction (CO 2 PR). An electronic strategy is herein proposed to engineer In‐d‐band center of InVO 4 by incorporating MnO x nanoparticles and oxygen vacancies (V O ) into holey InVO 4 nanobelts (MnO x /V O ‐InVO 4 ), which synergistically modulates the In‐d‐band center to a moderate level and consequently leads to high‐efficiency CO 2 PR. The MnO x /V O ‐InVO 4 catalyst with optimized electronic property exhibits a single carbon evolution rate of up to 145.3 µmol g −1 h −1 and a carbon monoxide (CO) product selectivity of 92.6%, coming out in front of reported InVO 4 ‐based materials. It is discovered that the modulated electronic property favors the interaction between the In sites and their intermediates, which thereby improves the thermodynamics and kinetics of the CO 2 PR‐to‐CO reaction. This work not only demonstrates the effective engineering of the d orbital of the low‐coordination In atoms to promote CO 2 PR, but also paves the way for the application of tuning d‐band center to develop high‐efficiency catalysts.
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