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© 2025 Elsevier B.V.The conversion of carbon dioxide into valuable C₁ resources not only enhances its economic value but also represents a promising strategy for mitigating climate change. Non-thermal plasma technology has been demonstrated as an effective approach for the transformation of this molecule into high-value compounds. In this study, nanostructured In2O3 catalysts rich in oxygen vacancies and high surface area were synthesized through a novel method integrating chemical precipitation with dielectric barrier discharge (DBD) treatment. The synergistic effects on carbon dioxide conversion were explored through the combined application of DBD plasma and the In2O3 catalyst. The results demonstrate that oxygen vacancies in the catalyst play a crucial role in promoting this process. Notably, when laboratory-prepared catalyst was loaded into the reactor, the CO2 conversion efficiency can reach 29.7 % under optimal conditions, which is a 50.7 % increase compared to the CO2 conversion rate of the empty DBD plasma. Meanwhile, the CO selectivity can also be maintained at a high level of over 90 %. The commercial and home-made In2O3 catalyst samples were analyzed using XRD, SEM, XPS, EPR, and BET techniques. Furthermore, a mechanism for DBD plasma-enhanced CO2 conversion using the In2O3 catalyst was proposed, informed by both experimental outcomes and DFT calculations. The integration of these experimental and theoretical insights has refined the understanding of the microscopic reaction mechanisms involved in decomposing CO2 to CO and O2 on In2O3 catalyst facilitated by dielectric barrier discharge plasmas. This work not only bridges a gap in theoretical research but also provides important implications for future studies on plasma-mediated CO₂ conversion.
Author(s): Li S, Wang Y, Zhang K, Zhu H, Liao G, Li Q, Jia S, Feng Q, Pan J, Tan R, Feng Z, Yang D
Publication type: Article
Publication status: Published
Journal: Journal of Alloys and Compounds
Year: 2025
Volume: 1039
Print publication date: 10/09/2025
Online publication date: 28/08/2025
Acceptance date: 25/08/2025
ISSN (print): 0925-8388
ISSN (electronic): 1873-4669
Publisher: Elsevier Ltd
URL: https://doi.org/10.1016/j.jallcom.2025.183304
DOI: 10.1016/j.jallcom.2025.183304
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