Enhancing the reaction of CO2 and H2O using catalysts within a non-thermal plasma

Piu Chawdhury, Sarayute Chansai, Matthew Conway, Joseph Parker, Matthew Lindley, Cristina Stere, Meenakshisundaram Sankar, Sarah Haigh, Benjamin Dennis-Smither, Sorin V. Filip, Stephen Poulston, Peter Hinde, Chris Hardacre, Christopher Hawkins

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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 CO2 and H2O over Ni and Cu based catalysts combined with non-thermal plasma (NTP) technology. The catalysis under NTP condition enabled significantly higher CO2 conversion and products yield, which was almost 6 times higher than that of the plasma-only system. A maximum H2 concentration of ~ 2500 ppm was achieved for Cu/ZSM5 catalyst at 17% CO2 conversion. Comprehensive catalyst characterization together with the reaction performances reveals that Cu in a reduced state promotes both the CO2 and H2O conversion leading to H2 formation. In-situ diffuse reflectance infra-red 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 H2 in addition to the direct CO2 and H2O interaction. It also explains how the different metal support interaction influences 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 CO2 and H2O reaction to produce H2.
Original languageEnglish
JournalACS Catalysis
Publication statusAccepted/In press - 3 Apr 2025

Keywords

  • Non-thermal plasma (NTP) catalysis
  • CO2 and H2O conversion
  • H2 production
  • Cu catalysts
  • metal-support interaction
  • in-situ DRIFT-MS

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