Abstract
Photocatalytic CO2 reduction to CH4 has attracted notable focus because of its capacity to convert CO2 into high-value hydrocarbon fuels. Among the different photocatalysts, g-C3N4 (graphitic carbon nitride) has emerged as an attractive candidate due to its stability, nontoxicity, and facile synthesis. However, its poor crystallinity and inefficient charge separation severely limit its photocatalytic efficiency. Herein, K+ ions were introduced into the g-C3N4 framework to improve its crystallinity, which was followed by coupling with CuO to form a CuO/K-g-C3N4 heterostructure to improve charge separation. The CuO/K-g-C3N4 photocatalysts achieved excellent CO2 photoreduction performance, yielding 41.21 μmol/g/h CH4 with 93.03% selectivity upon visible-light illumination. The augmented conversion ability was mainly due to the synergistic effects of better crystallinity, light arrestation, exciton dissociation, charge separation, and CO2 adsorption. This work discloses a g-C3N4-derived photocatalyst design as well as stresses the capability of CuO/K-g-C3N4 as a photoactive catalyst for elevated CH4 selectivity, contributing to renewable energy and environmental protection.
| Original language | English |
|---|---|
| Journal | Electron |
| DOIs | |
| State | Accepted/In press - 2026 |
Bibliographical note
Publisher Copyright:© 2026 The Author(s). Electron published by Harbin Institute of Technology and John Wiley & Sons Australia, Ltd.
Keywords
- CH selectivity
- CO photoreduction
- charge separation
- g-CN
- solar fuels
ASJC Scopus subject areas
- General
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