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Research Article | Open Access

Photocatalytic benzylic and aliphatic sp3 C–H activation and CO2 carboxylation over Z-scheme CdS@g-C3N4

Heyan Jiang1,§ ( )Denghong Zhao1,§Long Qin1,§Jia Zeng1 ( )Hang Liu1Mingwei Yang1Rui Wang2Bin Sun1
Key Laboratory of Catalysis Science and Technology of Chongqing Education Commission, Chongqing Key Laboratory of Environmental Catalysis, Chongqing Technology and Business University, Chongqing 400067, China
School of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing 400054, China

§ Heyan Jiang, Denghong Zhao, and Long Qin contributed equally to this work.

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Abstract

Achieving heterogeneous photocatalytic activation of sp3 C–H bonds and carboxylation of CO2 to produce arylacetic acids and alkyl carboxylic acids with increased carbon chains is a highly significant and demanding research endeavor. In this work, a new method for synthesizing redox centers spatially separated Z-scheme CdS@graphitic carbon nitride (g-C3N4) was developed, aiming to achieve photocatalytic benzylic and aliphatic sp3 C–H activation as well as CO2 carboxylation without sacrificial agent. Notably, both benzylic and aliphatic sp3 C–H activation together with CO2 carboxylation were achieved in heterogeneous photocatalytic system, resulting in the production of carboxylic acids with increased carbon chains under mild conditions. Various methylbenzene derivatives and cycloalkanes were employed to synthesize carbon-chain increased acids via a process involving K3PO4-assisted photogenerated holes activation for benzyl radical generation, photoinduced CO2 reduction, as well as solvent-assisted chemoselective carboxylation. Various characterizations and density functional theory (DFT) results revealed that Z-scheme CdS@g-C3N4 not just significantly enhanced separation of charges and accumulation of photoinduced electrons on g-C3N4 but also facilitated adsorption along with activation of CO2. This research provided novel heterogeneous photocatalytic approach to produce carbon chains increased carboxylic acids via sp3 C–H activation and CO2 carboxylation.

Graphical Abstract

Benzylic/aliphatic sp3 C–H activation and CO2 carboxylation were achieved in heterogeneous photocatalysis over CdS@C3N4. The Z-scheme mechanism and its interaction with CO2 were analyzed using density functional theory (DFT) calculations. Spatially separated redox centers in CdS@graphitic carbon nitride (g-C3N4) were favorable for radical generation and CO2 carboxylation. This research provided novel heterogeneous catalytic method to attain the carbon-neutral goal.

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Nano Research
Article number: 94907941

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Cite this article:
Jiang H, Zhao D, Qin L, et al. Photocatalytic benzylic and aliphatic sp3 C–H activation and CO2 carboxylation over Z-scheme CdS@g-C3N4. Nano Research, 2026, 19(1): 94907941. https://doi.org/10.26599/NR.2025.94907941
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Received: 08 April 2025
Revised: 08 August 2025
Accepted: 18 August 2025
Published: 09 December 2025
© The Author(s) 2026. Published by Tsinghua University Press.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, https://creativecommons.org/licenses/by/4.0/).