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- Title
Superexchange-stabilized long-distance Cu sites in rock-salt-ordered double perovskite oxides for CO<sub>2</sub> electromethanation.
- Authors
Zhu, Jiawei; Zhang, Yu; Chen, Zitao; Zhang, Zhenbao; Tian, Xuezeng; Huang, Minghua; Bai, Xuedong; Wang, Xue; Zhu, Yongfa; Jiang, Heqing
- Abstract
Cu-oxide-based catalysts are promising for CO2 electroreduction (CO2RR) to CH4, but suffer from inevitable reduction (to metallic Cu) and uncontrollable structural collapse. Here we report Cu-based rock-salt-ordered double perovskite oxides with superexchange-stabilized long-distance Cu sites for efficient and stable CO2-to-CH4 conversion. For the proof-of-concept catalyst of Sr2CuWO6, its corner-linked CuO6 and WO6 octahedral motifs alternate in all three crystallographic dimensions, creating sufficiently long Cu-Cu distances (at least 5.4 Å) and introducing marked superexchange interaction mainly manifested by O-anion-mediated electron transfer (from Cu to W sites). In CO2RR, the Sr2CuWO6 exhibits significant improvements (up to 14.1 folds) in activity and selectivity for CH4, together with well boosted stability, relative to a physical-mixture counterpart of CuO/WO3. Moreover, the Sr2CuWO6 is the most effective Cu-based-perovskite catalyst for CO2 methanation, achieving a remarkable selectivity of 73.1% at 400 mA cm−2 for CH4. Our experiments and theoretical calculations highlight the long Cu-Cu distances promoting *CO hydrogenation and the superexchange interaction stabilizing Cu sites as responsible for the superb performance. Cu-oxide-based catalysts are promising for CO2 electromethanation but suffer from inevitable reduction and structural collapse. Here the authors report a Cu-based rock-salt-ordered double perovskite oxide with superexchange-stabilized long-distance Cu sites for efficient and stable CO2 methanation.
- Subjects
COPPER; PEROVSKITE; CHARGE exchange; METHANATION; OXIDES; WATER gas shift reactions
- Publication
Nature Communications, 2024, Vol 15, Issue 1, p1
- ISSN
2041-1723
- Publication type
Article
- DOI
10.1038/s41467-024-45747-5