Photocatalytic Conversion of Formic Acid to Syngas (CO + H2) and Methane with Homogeneous Molecular Cobaloxime Catalysts

被引:0
|
作者
Wang, Taotao [1 ,2 ]
Zhang, Li [2 ]
Wu, Jinbao [2 ]
Chen, Muqing [1 ]
Du, Pingwu [2 ]
机构
[1] Dongguan Univ Technol, Sch Environm & Civil Engn, Dongguan 523808, Guangdong, Peoples R China
[2] Univ Sci & Technol China, Dept Mat Sci & Engn, Key Lab Precis & Intelligent Chem, Anhui Lab Adv Photon Sci & Technol, Hefei 230026, Anhui, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2024年 / 128卷 / 31期
基金
中国国家自然科学基金;
关键词
HYDROGEN EVOLUTION; METAL; REDUCTION; CATALYST; CO2; SEMICONDUCTOR; PROTONS; H-2;
D O I
10.1021/acs.jpcc.4c03575
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
The catalytic conversion of formic acid is a promising method for accessing clean fuels. H-2 and CO, as products of the conversion process, have been extensively researched, but other direct conversion processes remain to be developed. Herein, for the first time, we report the use of homogeneous molecular cobaloxime catalysts combined with CdS nanorods (NRs) as a highly efficient photocatalytic system to produce syngas with CH4 from HCOOH. As a result, the highest rate of CH4 production reached 80.5 mu mol g(-1) h(-1), with H-2 and CO evolution rates of 60.5 and 24 mmol g(-1) h(-1), respectively. Moreover, the use of cobaloxime catalysts also markedly enhanced the long-term stability of the resulting material for gas evolution. The superior performance for CH4 and syngas evolution can be attributed to the promoted charge transfer and separation in the homogeneous molecular cobaloxime systems. This work provides new insights into the photocatalytic conversion of formic acid to other clean fuels.
引用
收藏
页码:12849 / 12857
页数:9
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