催化作用
选择性
X射线光电子能谱
漫反射红外傅里叶变换
格式化
水煤气变换反应
纳米颗粒
光化学
辐照
化学
傅里叶变换红外光谱
材料科学
漫反射
化学工程
光催化
纳米技术
有机化学
工程类
物理
光学
核物理学
作者
Yunxiang Tang,Simeng Wu,Yanxiang Wang,Lixiang Song,Zhengyi Yang,Chan Guo,Jiurong Liu,Fenglong Wang
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2022-12-16
卷期号:37 (1): 539-546
被引量:10
标识
DOI:10.1021/acs.energyfuels.2c03604
摘要
Photo-assisted catalytic CO2 hydrogenation represents a promising route to convert CO2 into value-added chemicals under mild conditions, but challenges remain in the design and development of highly active and selective catalysts. Herein, we synthesized highly efficient catalysts comprising Rh nanoparticles supported on TiO2 nanosheets for photo-assisted catalytic CO2 hydrogenation, which achieved a high CO production rate of 20.6 mmol gcat–1 h–1 (5.15 mol gRh–1 h–1) with nearly 100 % selectivity and excellent stability at 250 °C under light irradiation, outperforming most reported metal-based catalysts. X-ray photoelectron spectroscopy revealed that the electrons transfer from Rh nanoparticles to TiO2, hinting a strong interaction between Rh and the TiO2 support. Under illumination, the accumulated hot electrons on TiO2 surfaces could effectively promote the activation of CO2 molecules. In situ diffuse reflectance infrared Fourier transform spectroscopy results revealed that formate was the critical intermediate in the reverse water–gas shift reaction process, and light irradiation could effectively facilitate the activation and conversion of reactants and intermediate species, thereby improving CO production. This work provides a new strategy for the integration of solar and thermal energy for an efficient RWGS reaction under mild conditions.
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