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Enhanced photocatalytic CO2 reduction using a trimetallic organic framework as the catalyst under visible light.

Authors :
Li, Chunxia
Yu, Huimin
Guo, Shaohong
Jia, Jingchun
Chang, Ying
Jia, Meilin
Wang, Jiang
Source :
New Journal of Chemistry; 2/28/2024, Vol. 48 Issue 8, p3364-3369, 6p
Publication Year :
2024

Abstract

The photocatalytic reduction of carbon dioxide into high value-added chemical feedstock is significant for mitigation of the energy crisis and the greenhouse effect. Metal–organic frameworks (MOFs) possess broad application prospects in photocatalytic CO<subscript>2</subscript> conversion due to the ability to adjust the metal types in metal cluster nodes. Herein, the CO<subscript>2</subscript> photocatalytic performance of trimetallic Fe<subscript>0.02</subscript>Ni<subscript>0.10</subscript>–Co<subscript>x</subscript>–PCN-250 (x = 0.05, 0.10, 0.15, 0.20 mol) was investigated by adjusting the content of Co. Notably, the photocatalytic yields of Fe<subscript>0.02</subscript>Ni<subscript>0.10</subscript>–Co<subscript>x</subscript>–PCN-250 (x = 0.05, 0.10, 0.15, 0.20 mol) were higher than those of bimetallic Fe<subscript>0.02</subscript>Ni<subscript>0.10</subscript>–PCN-250 and Fe<subscript>0.02</subscript>Co<subscript>0.10</subscript>–PCN-250 irradiated by visible light. The optimum yield of CO was obtained by trimetallic Fe<subscript>0.02</subscript>Ni<subscript>0.10</subscript>–Co<subscript>0.15</subscript>–PCN-250, up to 299 μmol g<superscript>−1</superscript> h<superscript>−1</superscript>. The enhanced yield of CO might be ascribed to the high CO<subscript>2</subscript> adsorption capacity and photogenerated electron transfer after addition of a suitable amount of the third ion, Co. This study provides new insights by designing trimetallic catalysts to increase the efficiency of photocatalytic CO<subscript>2</subscript> reduction. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
11440546
Volume :
48
Issue :
8
Database :
Complementary Index
Journal :
New Journal of Chemistry
Publication Type :
Academic Journal
Accession number :
175525047
Full Text :
https://doi.org/10.1039/d3nj05781j