纳米片
化学
催化作用
选择性
光催化
吸附
人工光合作用
纳米技术
密度泛函理论
分子
化学工程
载流子
Atom(片上系统)
光化学
有机化学
计算化学
材料科学
光电子学
嵌入式系统
工程类
计算机科学
作者
Shan Hu,Panzhe Qiao,Zixin Liu,Xueli Zhang,Fangyuan Zhang,Jinhua Ye,Defa Wang
标识
DOI:10.1016/j.jcat.2024.115405
摘要
Artificial photosynthesis utilizing solar energy to convert carbon dioxide (CO2) and water (H2O) into fuels and high-value chemicals offers a promising technology for mitigating energy consumption and environmental pollution. However, the development of efficient photocatalysts with high product selectivity remains a big challenge due to the sluggish dynamic transfer of photogenerated charge carriers. Herein, porous C3N4 nanosheet supported Au single atoms photocatalyst (Au1@CN) with AuN4 coordination is fabricated via a facile "impregnation + freeze-drying" process. The as-synthesized Au1@CN exhibits efficient and stable CO2 photoreduction activity with a CO evolution rate of 0.58 μmol h−1 (amount of catalyst: 10 mg), CO selectivity of 94 %, and a turnover frequency (TOF) of 10.0 h−1 using H2O as the reductant, which exceed most previous works on C3N4-based single-atom photocatalysts for CO2 reduction. Experimental studies and density functional theory (DFT) calculations reveal that the unique Au—N4 coordination promotes the dynamic transfer of photogenerated charge carriers, facilitates the adsorption/activation of CO2 molecules and generation of *COOH intermediate, thereby significantly enhancing the CO2 photoreduction activity with high CO selectivity. This study demonstrates an effective strategy for the design of M—N4 coordinated single-atom catalyst toward efficient and selective photoreduction of CO2 to CO.
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