Enhancing the Reaction of CO<sub>2</sub> and H<sub>2</sub>O Using Catalysts within a Nonthermal Plasma

The direct conversion of emitted and captured carbon dioxide into usable fuels remains a significant challenge and is a key element in the transition to net zero. Herein, we examine the reaction of CO<sub>2</sub> and H<sub>2</sub>O over Ni- and Cu-based catalysts combined with nonthermal plasma (NTP) technology. The catalysis under NTP conditions enabled significantly higher CO<sub>2</sub> conversion and product yield, which was almost six times higher than that of the plasma-only system. A maximum H<sub>2</sub> concentration of ∼2500 ppm was achieved for the Cu/ZSM5 catalyst at 17% CO<sub>2</sub> conversion. Comprehensive catalyst characterization together with the reaction performances reveals that Cu in a reduced state promotes both the CO<sub>2</sub> and H<sub>2</sub>O conversion leading to H<sub>2</sub> formation. <i>In situ</i> diffuse reflectance infrared spectroscopy (DRIFTS) coupled with mass spectrometry (MS) analysis of the gas phase products confirms that CO is the major active species to drive the water gas shift reaction to form H<sub>2</sub> in addition to the direct CO<sub>2</sub> and H<sub>2</sub>O interaction. It also explains how the different metal support interactions influence the CO adsorption and its interaction with water. Among the catalysts studied, ZSM5-supported Cu catalysts were found to be the most effective in facilitating the CO<sub>2</sub> and H<sub>2</sub>O reaction to produce H<sub>2</sub>.

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Publication Details

Journal
ACS Catalysis
Published
2025-04-16
DOI
https://doi.org/10.1021/acscatal.5c00747
Citations
5
Primary Topic
Catalytic Processes in Materials Science
Type
article
Field-Weighted Citation Impact
2.59

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article

Enhancing the Reaction of CO2 and H2O Using Catalysts within a Nonthermal Plasma

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5 citations
ACS Catalysis
Catalytic Processes in Materials Science
2.59
article

Enhancing the Reaction of CO2 and H2O Using Catalysts within a Nonthermal Plasma

Matthew Conway, Cory A. Hawkins, M. W. Lindley, Sorin V. Filip, Peter Hinde, Cristina Stere, Piu Chawdhury, Stephen Poulston, Meenakshisundaram Sankar, Christopher Hardacre, Sarah J. Haigh, J. Parker, Ben Dennis-Smither
article en
5 citations

Abstract

The direct conversion of emitted and captured carbon dioxide into usable fuels remains a significant challenge and is a key element in the transition to net zero. Herein, we examine the reaction of CO<sub>2</sub> and H<sub>2</sub>O over Ni- and Cu-based catalysts combined with nonthermal plasma (NTP) technology. The catalysis under NTP conditions enabled significantly higher CO<sub>2</sub> conversion and product yield, which was almost six times higher than that of the plasma-only system. A maximum H<sub>2</sub> concentration of ∼2500 ppm was achieved for the Cu/ZSM5 catalyst at 17% CO<sub>2</sub> conversion. Comprehensive catalyst characterization together with the reaction performances reveals that Cu in a reduced state promotes both the CO<sub>2</sub> and H<sub>2</sub>O conversion leading to H<sub>2</sub> formation. <i>In situ</i> diffuse reflectance infrared spectroscopy (DRIFTS) coupled with mass spectrometry (MS) analysis of the gas phase products confirms that CO is the major active species to drive the water gas shift reaction to form H<sub>2</sub> in addition to the direct CO<sub>2</sub> and H<sub>2</sub>O interaction. It also explains how the different metal support interactions influence the CO adsorption and its interaction with water. Among the catalysts studied, ZSM5-supported Cu catalysts were found to be the most effective in facilitating the CO<sub>2</sub> and H<sub>2</sub>O reaction to produce H<sub>2</sub>.

ACS CatalysisVol. 15(9)
Whitchurch Hospital (GB), University of Manchester (GB), Johnson Matthey (United Kingdom) (GB), Nano Carbon (Poland) (PL), Cardiff University (GB)
University of Manchester, Cardiff University, Engineering and Physical Sciences Research Council
Openalex Percentile: Top 11%
Catalytic Processes in Materials Science
2.59
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