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Two-dimensional-related catalytic materials for solar-driven conversion of CO x into valuable chemical feedstocks.

Authors :
Zhao Y
Waterhouse GIN
Chen G
Xiong X
Wu LZ
Tung CH
Zhang T
Source :
Chemical Society reviews [Chem Soc Rev] 2019 Apr 01; Vol. 48 (7), pp. 1972-2010.
Publication Year :
2019

Abstract

The discovery of improved chemical processes for CO and CO2 hydrogenation to valuable hydrocarbon fuels and alcohols is of paramount importance for the chemical industry. Such technologies have the potential to reduce anthropogenic CO2 emissions by adding value to a waste stream, whilst also reducing our consumption of fossil fuels. Current thermal catalytic technologies available for CO and CO2 hydrogenation are demanding in terms of energy input. Various alternative technologies are now being developed for COx hydrogenation, with solar-driven processes over two-dimensional (2D) and 2D-related composite materials being particularly attractive due to the abundance of solar energy on Earth and also the high selectivity of defect-engineered 2D materials towards specific valuable products under very mild reaction conditions. This review showcases recent advances in the solar-driven COx reduction to hydrocarbons over 2D-based materials. Optimization of 2D catalyst performance demands interdisciplinary research that embraces catalyst electronic structure manipulation and morphology control, surface/interface engineering, reactor engineering and density functional theory modelling studies. Through improved understanding of the structure-performance relationships in 2D-related catalysts which is achievable through the application of modern in situ characterization techniques, practical photo/photothermal/photoelectrochemical technologies for CO and CO2 reduction to high-valuable products such as olefins could be realized in the not-too-distant future.

Details

Language :
English
ISSN :
1460-4744
Volume :
48
Issue :
7
Database :
MEDLINE
Journal :
Chemical Society reviews
Publication Type :
Academic Journal
Accession number :
30357195
Full Text :
https://doi.org/10.1039/c8cs00607e