Deciphering electronic metal-support interaction in Ce1/ZnO single-atom catalysts for boosting CO2 electroreduction
Year: 2025
Type: article
Abstract: Single-atom catalysts (SACs) have triggered great interest in the field of catalysis due to their high atom utilization and unique structures. Tailoring the electronic metal-support interaction (EMSI) of SACs is crucial to enhancing the catalytic performance. Herein, a novel Ce 1 /ZnO SAC has been precisely constructed by a facile one-pot hydrothermal strategy, and the modulation of EMSI with different d-orbital electrons (Ce, Fe, and Zr) is for the first time proposed for electrochemical CO 2 reduction (CO 2 RR). The Ce 1 /ZnO catalyst exhibits an excellent performance with a Faradaic efficiency of 84% for CO production and a record-high turnover frequency of 10658 h -1 at -1.1 V vs. RHE, exceeding Zr 1 /ZnO and Fe 1 /ZnO counterparts. Detailed characterizations and theoretical calculations reveal that the EMSI effect induces charge redistribution via the asymmetric metal-O-Zn moieties, while the unique Ce 3+ /Ce 4+ redox feature can exert a more pronounced electronic communication with the substrate. The strong electronic interaction between single-atom Ce and ZnO alters the d-band center structure of Ce sites, facilitating the adsorption of CO 2 and lowering the energy barrier of *COOH formation, thus accelerating CO production. This work elucidates the pivotal role of the electronic metal-support communication effect in engineering SACs toward boosted catalysis. The electronic metal-support interaction (EMSI) of single-atom catalysts is demonstrated. The novel and low-cost Ce 1 /ZnO catalyst exhibits excellent performance, outperforming the Zr 1 /ZnO, Fe 1 /ZnO, and most of the reported SACs. The ZnO donates partial electrons to Ce via asymmetrical Ce-O-Zn moieties, significantly promoting the activation of CO 2 and the formation of *COOH, thus boosting the performance. • The novel and low-cost Ce 1 /ZnO single-atom catalyst is developed. • Electronic metal-support interaction (EMSI) in SACs is revealed. • Strong interaction between Ce 1 and ZnO alters the d-orbital center structure of Ce sites, achieving excellent CO 2 reduction performance. • The asymmetrical Ce-O-Zn moieties lower the energy barrier for *COOH formation, thus boosting CO 2 electroreduction.
Authors: Yang Chen, ShuoShuo Jiang, Xu Liu, Boxue Pang, Mingyu Jia, Hui Li, Yang Wu, Tianyi Ma
Language: English
Field: Energy
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $5,950
Awards: Rechargeable lithium carbon dioxide battery - catalyst design to prototype , Engineering vanadium oxide-based cathode for aqueous ammonium ion batteries, G4377272621, Monolithic Solar Thermal Photocatalytic Membrane for Hydrogen Production, G5568209302, G6391818764, Sustainable Electrolysis via Functional Hybrids for Ammonia Production, ARC Research Hub for Intelligent Energy Efficiency in Future Protected Cropping, G74262681, G7765776526, Perovskite-Based Ferroelectrics for Solar Fuel Production
OpenAlex ID: W4416040473
