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Preparation of 3D g-C3N4 foam supported Cu(OH)2 nanosheets for photocatalytic CO2 reduction

Authors :
FANG Wei
SUN Zhimin
ZHAO Lei
CHEN Hui
HE Xuan
DU Xing
WANG Daheng
Source :
Cailiao gongcheng, Vol 51, Iss 4, Pp 141-150 (2023)
Publication Year :
2023
Publisher :
Journal of Materials Engineering, 2023.

Abstract

To optimize the gas transfer, adsorption and photo-generated charge separation in the process of photocatalytic CO2 reduction by g-C3N4, the photocatalytic materials were designed from the aspects of foam pore structure and heterojunction construction. The typical g-C3N4 foam was first constructed using surfactant foaming method, and then Cu(OH)2 nanosheets were loaded to prepare the Cu(OH)2/CNF composites with projects of electroless copper plating and hydrogen oxidation treatment. The structure and photocatalytic properties of the as-prepared samples were investigated. The results show that g-C3N4 foam and Cu(OH)2/CNF all demonstrate developed structures with 3D micron pore frameworks, which is conducive to improving CO2 diffusion and adsorption at dynamics during gas-solid catalytic process. The adsorption amounts of CO2 for g-C3N4 foam and Cu(OH)2/CNF are respectively 3.97 cm3/g and 3.59 cm3/g, which are 2.96 times and 2.68 times respectively higher than that of pure g-C3N4 powder. Moreover, many Cu(OH)2 nanosheets are also formed in the Cu(OH)2/CNF samples which provide a way to simultaneously broaden light absorption and form heterojunction between g-C3N4 and Cu(OH)2. This heterojunction can accelerate the separation of photo-generated e--h+ and make photo-generated electrons transfer from g-C3N4 to Cu(OH)2. As a result, the Cu(OH)2/CNF has demonstrated optimal photocatalytic activity with CO production rate at 11.041 μmol·g-1·h-1, which is 2.76 times and 6.83 times respectively higher than that of g-C3N4 foam and g-C3N4 powder.

Details

Language :
Chinese
ISSN :
10014381
Volume :
51
Issue :
4
Database :
Directory of Open Access Journals
Journal :
Cailiao gongcheng
Publication Type :
Academic Journal
Accession number :
edsdoj.8e30acb73f64f56b4ded71a13a7a21b
Document Type :
article
Full Text :
https://doi.org/10.11868/j.issn.1001-4381.2022.000120