Authors
Qimeng Sun, Xinyu Liu, Yang Liu, Shichen Dong, Yan Xu, Wen Wen, Hengwei Wang, Rui Jin, Yuxing Xu, Lulu Xu, Zuwei Luo, Fuyang Li, Yue Lin, Yong Yang, Junling Lu
Published in
Angewandte Chemie (International ed. in English). Pages e1906096. Jul 16, 2026. Epub Jul 16, 2026.
Abstract
Reactive metal-support interactions (RMSIs) frequently occur under high-temperature reaction conditions, leading to intricate reconstructions of metal-oxide interfaces and alloy formation. Such uncontrollable features severely impede the optimization of catalytic performance. In this study, we demonstrate precise control over RMSIs by leveraging the high mobility of InOx on CeO2 support under hydrogen reducing conditions-directly visualized by in situ environmental electron microscopy-in combination with the quantitative tuning of InOx content via atomic layer deposition. The resulting optimized catalyst delivers an exceptional space-time yield of 1.67 gMeOH·gcat -1·h-1 at 280°C in the CO2 hydrogenation reaction, surpassing previously reported Ni-based catalysts and even Pd-based noble metal catalysts in the literature. In situ spectroscopic characterization reveals that the controlled RMSIs enables the optimization of InOx/NiIn interface, which promotes the selective conversion of HCOO* to CH3O* and subsequently to methanol, thereby significantly enhancing the methanol production. These findings highlight the critical role of precisely regulated RMSIs in the rational design of high-performance catalysts.
PMID:
42464490
Bibliographic data and abstract were imported from PubMed on 17 Jul 2026.
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