Under the context of energy shortages and global warming, the photocatalytic reduction of carbon dioxide (CO2) to carbon monoxide (CO) using simulated sunlight has attracted considerable research attention. Herein, three-dimensional (3D) Z-scheme cobalt-alumina-layered double hydroxide/bismuth oxybromide (CoAl-layered double hydroxide (LDH)/BiOBr) heterojunction photocatalysts with oxygen vacancies were constructed by intercalating two-dimensional CoAl-LDH between BiOBr layers in the mechanical mixing. The conversion of CO2 in the water phase was greatly improved compared to CoAl-LDH/BiOBr under 300-W xenon light. The transformation efficiency of 23.62 μmol⋅g-1⋅h-1 for CoAl-LDH/BiOBr-10 (CBO-10) is 2.96 and 8.34 times that of pure BiOBr and CoAl-LDH, respectively, with CO selectivity in the obtained products reaching as high as 95 %. Furthermore, CBO-10 catalysts exhibited outstanding stability in terms of structure and catalytic performance. The construction of Z-scheme heterojunctions and oxygen vacancies enlarges the photoresponse range of the BiOBr catalyst while reducing the photoelectron-hole recombination efficiency. The unique 3D structure offers more Z-scheme heterojunction interfaces for the separation and transfer of electrons between CoAl-LDH and BiOBr during photoreaction. This study is expected to guide the development of new high-performance photocatalysts and the selective regulation of reduction products.
Keywords: BiOBr; CoAl-LDH; High selectivity; Photocatalytic CO(2) reduction; Z-scheme heterojunction.
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