A density functional theory-guided discovery of bimetallic transition-metal-doped cerium oxide catalysts for the reverse water gas shift reaction

• Systematic DFT screening of bimetallic TM-doped CeO 2 (111) surfaces for RWGS. • Reaction energy is used as catalyst performance descriptor via BEP relationships. • 3 representative configurational reaction pathways identify full energy landscape. • Bimetallic TM-doping tunes OV stability and CO 2 adsorption and dissociation modes. • FeCo/CeO 2-x and FeNi/CeO 2-x are the best-performing bimetallic catalysts for RWGS. Reverse water–gas shift (RWGS) reaction is a promising route for CO 2 utilization and syngas production, yet its efficiency remains limited by catalyst performance. This study performed density-functional-theory-calculations to systematically investigate bimetallic transition-metal (TM)-doped CeO 2 (111) catalysts (M 1 M 2 /CeO 2−x ; M 1 = Fe; M 2 =Cu/Ni/Co/Mn) for direct CO 2 -to-CO reduction. A comprehensive configurational search of dopant distributions, oxygen-vacancy (OV) sites, CO 2 adsorption and dissociation configurations identified representative configurational reaction pathways: PW1 (most-stable), PW2 (most-likely), and PW3 (most-reactive), collectively mapping the full reaction energy landscape. Reaction energies (E rxn ) were used as performance descriptors based on their linear Brønsted-Evans-Polanyi (BEP) relationship with activation energies. Among all bimetallic candidates, FeCo/CeO 2−x shows the best performance, exhibiting the lowest E rxn for PW1 & PW2 and the 2nd-lowest for PW3 , outperforming the benchmark 2Fe/CeO 2−x except for a minor shortfall in PW2 . FeNi/CeO 2−x catalyst is the 2nd-best, achieving the lowest E rxn in PW3 . Both catalysts display spontaneous adsorption of CO and O after CO 2 dissociation. Transition-state analysis reveals a precursor-mediated direct CO 2 -reduction pathway and confirms linear-BEP relationships. Local dopant-environment and electronic-structure analysis reveal synergistic interactions among CeO 2 , bimetallic-dopants, and OV modulate CeO 2 -reducibility and OV-stability, tailor CO 2 adsorption and dissociative-adsorption modes, thereby tuning overall surface reactivity. These findings highlight FeCo/CeO 2−x and FeNi/CeO 2−x as promising next-generation RWGS catalysts.

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Publication Details

Journal
Applied Surface Science
Published
2026-04-25
DOI
https://doi.org/10.1016/j.apsusc.2026.167030
Primary Topic
Catalysts for Methane Reforming
Type
article
Field-Weighted Citation Impact
0.00

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article

A density functional theory-guided discovery of bimetallic transition-metal-doped cerium oxide catalysts for the reverse water gas shift reaction

Hao Wang, Sriram Ganapathi Subramanian, Gustavo Sutter, Luis Ricardez‐Sandoval et al.
Applied Surface Science
Catalysts for Methane Reforming
article

A density functional theory-guided discovery of bimetallic transition-metal-doped cerium oxide catalysts for the reverse water gas shift reaction

Hao Wang, Sriram Ganapathi Subramanian, Gustavo Sutter, Luis Ricardez‐Sandoval, Pascal Poupart
article en

Abstract

• Systematic DFT screening of bimetallic TM-doped CeO 2 (111) surfaces for RWGS. • Reaction energy is used as catalyst performance descriptor via BEP relationships. • 3 representative configurational reaction pathways identify full energy landscape. • Bimetallic TM-doping tunes OV stability and CO 2 adsorption and dissociation modes. • FeCo/CeO 2-x and FeNi/CeO 2-x are the best-performing bimetallic catalysts for RWGS. Reverse water–gas shift (RWGS) reaction is a promising route for CO 2 utilization and syngas production, yet its efficiency remains limited by catalyst performance. This study performed density-functional-theory-calculations to systematically investigate bimetallic transition-metal (TM)-doped CeO 2 (111) catalysts (M 1 M 2 /CeO 2−x ; M 1 = Fe; M 2 =Cu/Ni/Co/Mn) for direct CO 2 -to-CO reduction. A comprehensive configurational search of dopant distributions, oxygen-vacancy (OV) sites, CO 2 adsorption and dissociation configurations identified representative configurational reaction pathways: PW1 (most-stable), PW2 (most-likely), and PW3 (most-reactive), collectively mapping the full reaction energy landscape. Reaction energies (E rxn ) were used as performance descriptors based on their linear Brønsted-Evans-Polanyi (BEP) relationship with activation energies. Among all bimetallic candidates, FeCo/CeO 2−x shows the best performance, exhibiting the lowest E rxn for PW1 & PW2 and the 2nd-lowest for PW3 , outperforming the benchmark 2Fe/CeO 2−x except for a minor shortfall in PW2 . FeNi/CeO 2−x catalyst is the 2nd-best, achieving the lowest E rxn in PW3 . Both catalysts display spontaneous adsorption of CO and O after CO 2 dissociation. Transition-state analysis reveals a precursor-mediated direct CO 2 -reduction pathway and confirms linear-BEP relationships. Local dopant-environment and electronic-structure analysis reveal synergistic interactions among CeO 2 , bimetallic-dopants, and OV modulate CeO 2 -reducibility and OV-stability, tailor CO 2 adsorption and dissociative-adsorption modes, thereby tuning overall surface reactivity. These findings highlight FeCo/CeO 2−x and FeNi/CeO 2−x as promising next-generation RWGS catalysts.

Applied Surface ScienceVol. 740
University of Waterloo (CA), Vector Institute (CA), Carleton University (CA)
Mitacs, Alliance de recherche numérique du Canada
Affordable and clean energy
Openalex Percentile: Top 14%
Catalysts for Methane Reforming
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