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Peer-reviewedCC BYThe journal of physical chemistry letters

Plasma-Driven Carbon Mobilization Creates a Transient Near-Surface Carbonaceous Interphase for Selective CO2 Conversion into CO.

4 affiliations
  1. 1Department of Materials Chemistry, Adsorption and Catalysis, Faculty of Chemistry, Nicolaus Copernicus University in Toruń, Gagarina 7, 87-100Toruń, Poland.
  2. 2Institute of Advanced Studies, Nicolaus Copernicus University in Toruń, Wileńska 4, 87-100Toruń, Poland.
  3. 3Institute for Catalysis and Energy Solutions, University of South Africa, Christiaan de Wet and Pioneer, Florida1709, Roodepoort, Gauteng, South Africa.
  4. 4Institute of Future Technology, Zhejiang University of Technology, Hangzhou310014, China.

Abstract

Carbon beds enhance plasma-assisted CO2 conversion into resources, but are commonly treated as stationary reactant surfaces. Here, we show that nonthermal plasma (NTP) continuously mobilizes and reconstructs carbon, generating a transient near-surface carbonaceous interphase. In this study, we test these properties of carbon beds as enabling selective CO production during CO2 decomposition under low-temperature plasma conditions. Graphene oxide/chitosan-derived carbons, amorphous carbon, and graphite were examined under CO2 and Ar using gas-phase FTIR, time-resolved SEM, and Raman spectroscopy. GO@CHT-650 displayed the highest CO2 conversion into CO as well as oxygen-scavenging selectivity. Carbonaceous nanodeposits formed under NTP, developed continuously with exposure time, remained confined to the C-surface, and exhibited morphologies and dimensions dependent on the parent carbon structure. Raman analysis showed that the reconstructed phase remained predominantly disordered. These observations link plasma-driven carbon mobility with reactor performance and reveal a catalyst-reactant duality: individual carbon species are consumed stoichiometrically, whereas the dynamically reconstructed interphase persists as the reaction medium. Efficient plasma-assisted CO2 conversion into CO, therefore, requires a transient near-surface carbonaceous interphase created and sustained by the plasma itself.

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BibTeX
@article{moszczynska2026plasmadriven,
  title = {{Plasma-Driven Carbon Mobilization Creates a Transient Near-Surface Carbonaceous Interphase for Selective CO2 Conversion into CO.}},
  author = {Julia Moszczynska and Xinying Liu and Marek Wiśniewski},
  journal = {The journal of physical chemistry letters},
  year = {2026},
  month = oct,
  doi = {10.1021/acs.jpclett.6c02597},
  url = {https://europepmc.org/article/MED/42917158},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Plasma-Driven Carbon Mobilization Creates a Transient Near-Surface Carbonaceous Interphase for Selective CO2 Conversion into CO.
AU  - Julia Moszczynska
AU  - Xinying Liu
AU  - Marek Wiśniewski
PY  - 2026
DA  - 2026/10/01
JO  - The journal of physical chemistry letters
DO  - 10.1021/acs.jpclett.6c02597
UR  - https://europepmc.org/article/MED/42917158
AB  - Carbon beds enhance plasma-assisted CO2 conversion into resources, but are commonly treated as stationary reactant surfaces. Here, we show that nonthermal plasma (NTP) continuously mobilizes and reconstructs carbon, generating a transient near-surface carbonaceous interphase. In this study, we test these properties of carbon beds as enabling selective CO production during CO2 decomposition under low-temperature plasma conditions. Graphene oxide/chitosan-derived carbons, amorphous carbon, and graphite were examined under CO2 and Ar using gas-phase FTIR, time-resolved SEM, and Raman spectroscopy. GO@CHT-650 displayed the highest CO2 conversion into CO as well as oxygen-scavenging selectivity. Carbonaceous nanodeposits formed under NTP, developed continuously with exposure time, remained confined to the C-surface, and exhibited morphologies and dimensions dependent on the parent carbon structure. Raman analysis showed that the reconstructed phase remained predominantly disordered. These observations link plasma-driven carbon mobility with reactor performance and reveal a catalyst-reactant duality: individual carbon species are consumed stoichiometrically, whereas the dynamically reconstructed interphase persists as the reaction medium. Efficient plasma-assisted CO2 conversion into CO, therefore, requires a transient near-surface carbonaceous interphase created and sustained by the plasma itself.
SN  - 1948-7185
ER  -