Gallium Cluster-Promoted In2O3 Catalyst for CO2 Hydrogenation to Methanol

被引:8
|
作者
Yang, Yuxiang [1 ,2 ]
Wu, Linlin [1 ]
Yao, Bingqing [3 ]
Zhang, Lei [2 ]
Jung, Munam [2 ]
He, Qian [3 ]
Yan, Ning [2 ]
Liu, Chang-Jun [1 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Tianjin 300350, Peoples R China
[2] Natl Univ Singapore, Dept Chem & Biomol Engn, Singapore 117585, Singapore
[3] Natl Univ Singapore, Dept Mat Sci & Engn, Singapore 117575, Singapore
来源
ACS CATALYSIS | 2024年 / 14卷 / 18期
关键词
gallium; CO2; hydrogenation; methanol; indium oxide; interface site; FINDING SADDLE-POINTS; SELECTIVE HYDROGENATION; INFRARED-SPECTRUM; INDIUM OXIDE; MECHANISM; SITE;
D O I
10.1021/acscatal.4c03045
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this work, highly dispersed gallium clusters are constructed on In2O3 (denoted as Ga/In2O3) to promote hydrogenation of CO2 to methanol. Compared to pristine In2O3, the Ga/In2O3 catalysts show markedly improved CO2 conversion and methanol space-time yield (STY), as well as enhanced stability over 60 h on stream. A strong electronic interaction between the loaded gallium and In2O3 support, as confirmed by multiple techniques, results in well-dispersed, stable gallium clusters on In2O3, which is beneficial to long-term performance. The interface between gallium clusters and the defective In2O3 support serves as active sites to facilitate the activation of H-2 and CO2. This interfacial synergy not only enhances the adsorption and dissociation of H-2 but also effectively inhibits the strong adsorption of CO2 as carbonate. The activated CO2 at the interface sites can be dissociated readily into adsorbed CO for further hydrogenation into methanol.
引用
收藏
页码:13958 / 13972
页数:15
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