纳米片
催化作用
化学
密度泛函理论
Atom(片上系统)
选择性
X射线光电子能谱
醋酸
傅里叶变换红外光谱
光化学
谱线
红外光谱学
电子转移
原位
活动站点
光谱学
电荷密度
吸收光谱法
咔咯
材料科学
红外线的
物理化学
无机化学
结晶学
作者
Qinyuan Hu,Jiawei Xie,Fangming Zhao,Zhixing Zhang,Yanglu Yu,Xiaodong Li,Wensheng Yan,J. Hu,Junfa Zhu,Y. Pan,Meng Zhou,Yuming Dong,Xingchen Jiao
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2025-12-26
卷期号:16 (2): 1556-1564
被引量:2
标识
DOI:10.1021/acscatal.5c07765
摘要
The photoreduction of carbon dioxide (CO2) into C2 products faces a significant C–C coupling challenge. Charge asymmetry active sites constructed through loading engineering can effectively promote C–C coupling. Herein, we propose that the Au atom pairs with an asymmetric charge distribution in the ZnNb2O6 nanosheets trigger the formation of acetic acid (CH3COOH) for the photoreduction of air-concentration CO2. Density functional theory calculations indicate that the Au-ZnNb2O6 nanosheet slab has the potential to tailor CO2-to-CH3COOH pathway owing to the presence of Au atom pairs. In situ Fourier transform infrared spectra detect the *COCOH intermediate, confirming the occurrence of C–C coupling, while quasi in situ X-ray photoelectron spectroscopy verifies that the Au atoms functioned as the active sites. The TA spectra revealed the electron transfer process from ZnNb2O6 nanosheets to Au particles. Accordingly, the Au-ZnNb2O6 nanosheets achieve a CH3COOH formation rate of 2.19 μmol g–1 h–1 and a selectivity of 50.5%, whereas pristine ZnNb2O6 nanosheets produce only CO products.
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