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Supported Vanadium Carbide Catalysts for Reverse Water Gas Shift and Methanol Steam Reforming: Activity, Stability, and Coking Pathways

Abstract:
A series of supported vanadium carbide (VC x ) catalysts were prepared, characterized, and tested for the carbon dioxide and methanol activation via the Reverse Water Gas Shift (RWGS) and Methanol Steam Reforming (MSR) reactions, respectively. Crystallite sizes of VC x ranging from 9 to 36 nm were obtained depending on the support used (γ-Al2O3, SiO2, CeO2, ZrO2 and TiO2). In both reactions, the supported catalysts exhibited superior performance compared to the bulk VC x sample. In the RWGS reaction, all catalysts showed high CO selectivity, with VC x /Al2O3 demonstrating the best performance and no significant deactivation after 100 h at 873 K. Under MSR conditions, VC x /ZrO2 achieved the highest methanol conversion. However, all catalysts suffered from significant deactivation due to coke formation, with CH4 as the main product instead of the desired H2 and CO2 from full steam reforming. Density Functional Theory (DFT) calculations revealed that methanol decomposition is more facile than CO2 decomposition on both stoichiometric VC and carbon-deficient V8C7 surfaces, particularly in the presence of carbon vacancies, leading to coke formation in the form of partially hydrogenated C x H y * species. These findings indicate that VC x catalysts are more susceptible to coking under MSR than RWGS conditions, in line with experimental observations, and highlight the critical role of the carbide surface structure and vacancy concentration in coke formation.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1021/acsami.5c16601

Authors

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Role:
Author
ORCID:
0000-0002-0160-2770
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Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry
Role:
Author
ORCID:
0000-0003-4991-253X
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry
Role:
Author
ORCID:
0000-0001-8338-8706


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Funder identifier:
https://ror.org/003x0zc53
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Funder identifier:
https://ror.org/021018s57
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Funder identifier:
https://ror.org/012mzw131


Publisher:
American Chemical Society
Journal:
ACS Applied Materials & Interfaces More from this journal
Volume:
17
Issue:
49
Pages:
66595-66607
Publication date:
2025-11-21
Acceptance date:
2025-11-10
DOI:
EISSN:
1944-8252
ISSN:
1944-8244


Language:
English
Keywords:
Pubs id:
2334775
UUID:
uuid_f476af15-e274-4a51-9b59-359dfd54d874
Local pid:
pubs:2334775
Source identifiers:
3636633
Deposit date:
2026-01-06
ARK identifier:
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