Issue 1, 2024

Efficient Nb2O5@g-C3N4 heterostructures for enhanced photocatalytic CO2 reduction with highly selective conversion to CH4

Abstract

Achieving the goal of carbon neutralization using photocatalytic CO2 reduction has garnered widespread attention. However, rapid photogenerated charge recombination seriously impedes the further improvement of photocatalytic properties. In response, we propose a strategy to solve this limitation by way of constructing a heterojunction. A Nb2O5@g-C3N4 type II heterojunction photocatalyst was developed by a straightforward hydrothermal method. The construction of a heterojunction greatly accelerates the separation of photoinduced charges and increases the photocatalytic activity. As a result, Nb2O5@g-C3N4 (1 : 5) possesses outstanding properties for CO2 reduction under visible light with the production of CH4 and CO of about 19.06 and 1.93 μmol g−1, respectively. The CH4 selectivity is up to 98.79%. Furthermore, the mechanism of photocatalytic CO2 reduction is revealed in detail based on in situ DRIFTS and photochemical characterization, thus providing guidance for the design of high-performance CO2 photoreduction systems.

Graphical abstract: Efficient Nb2O5@g-C3N4 heterostructures for enhanced photocatalytic CO2 reduction with highly selective conversion to CH4

Supplementary files

Article information

Article type
Research Article
Submitted
13 iyl 2023
Accepted
17 sen 2023
First published
24 noy 2023

Inorg. Chem. Front., 2024,11, 123-132

Efficient Nb2O5@g-C3N4 heterostructures for enhanced photocatalytic CO2 reduction with highly selective conversion to CH4

X. Wang, J. Jiang, L. Wang and H. Guo, Inorg. Chem. Front., 2024, 11, 123 DOI: 10.1039/D3QI01333B

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