Interfacial‐Confined Oxygen Vacancy Clusters in ZrO <sub>2</sub> ‐Supported In <sub>2</sub> O <sub>3‐</sub> <i> <sub>x</sub> </i> Catalysts Boost Methanol Production From CO <sub>2</sub>
Lulu Xu, Qi Wang, Qingqing Gu, Li Shang, Yuxing Xu, Hao Chen, Hongjun Zhang, Bangjiao Ye, Jiafu Chen, Hanbao Chong, Jing Zhou, Xinyu Liu, Zhihu Sun, Shiqiang Wei, Bing Yang, Xiang‐Kui Gu, Hengwei Wang, Junling Lu
Abstract
Abstract Oxygen vacancies (V O ) play a vital role in catalytic reactions. Tuning the V O structures beyond its density is of great significance for optimizing catalytic performance, but remains challenging due to uncontrolled reduction and its poor stability under reaction conditions. Here, we report that the integration of quantum size effect for enhanced In 2 O 3 reducibility with strong In–O–Zr interfacial confinement for high stability enables the creation of stable large‐size V O clusters (e.g., trimers, tetramers, and larger) on ZrO 2 ‐supported monolayer In 2 O 3‐ x nano‐islands with high density without overreduction to metallic indium. In the CO 2 hydrogenation reaction, the ZrO 2 ‐supported monolayer In 2 O 3‐ x catalyst with V O clusters exhibits a considerably higher intrinsic activity for methanol production than that of bulk In 2 O 3 with single V O sites. Further addition of Pd onto these monolayer In 2 O 3‐ x with enriched V O clusters allows achieving an unprecedentedly high methanol space‐time yield of 46.6 mmol MeOH ·g cat −1 h −1 at 270 °C along with long‐term stability for at least 200 h, surpassing all In 2 O 3 ‐based catalysts reported to date.