Photothermal catalytic CO2 hydrogenation to methanol

Abstract

Utilization of waste CO2 to replace traditional fossil-based resources for the production of valuable fuels or chemicals is an ideal strategy to release the pressure on energy and environment. As a platform molecule with both energy carrier and chemical feedstock attributes, methanol (CH3OH)'s synthesis has attracted increasing attention, especially with CO2 feedstock. Different from the traditional syngas pathway requiring high temperature and pressure, high energy input and expensive H2, the photothermal technology for CH3OH synthesis from CO2 has milder reaction conditions, and utilizes renewable solar energy and green H2O as the hydrogen source by coupling light energy capture with the thermocatalytic process. Although many encouraging results have been reported in photothermal CO2 hydrogenation to CH3OH, a systematic summary on the recent development of photothermal CO2 hydrogenation to CH3OH is lacking. In this review, we first introduce the significance of CO2 valoration and CH3OH as well as the thermodynamic property of CO2 hydrogenation to CH3OH, then discuss the advantages and nature of photothermal catalysis, summarize the development and common design strategies of photothermal catalysts for CO2 hydrogenation to CH3OH, and finally elucidate the nature of three reaction mechanisms, namely photo-driven thermocatalysis, photo-assisted thermocatalysis and thermal-assisted photocatalysis, and give several examples how to distinguish them. This review will be helpful to stimulate the design of active catalysts and deepen the understanding of reaction mechanisms, thus advancing the development of this technology.

Graphical abstract: Photothermal catalytic CO2 hydrogenation to methanol

Article information

Article type
Tutorial Review
Submitted
02 Feb 2026
Accepted
02 Apr 2026
First published
08 Apr 2026

Green Chem., 2026, Advance Article

Photothermal catalytic CO2 hydrogenation to methanol

J. Lin, C. Jiao, Z. Wang, H. Yin and X. Dai, Green Chem., 2026, Advance Article , DOI: 10.1039/D6GC00690F

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