催化作用
多元醇
选择性
铂金
浸出(土壤学)
化学
水溶液
氧化态
吸附
Atom(片上系统)
键裂
化学稳定性
组合化学
无机化学
有机化学
土壤水分
土壤科学
嵌入式系统
计算机科学
聚氨酯
环境科学
作者
Hao Yan,Mingyue Zhao,Xiang Feng,Siming Zhao,Xin Zhou,Shangfeng Li,Minghao Zha,Fanyu Meng,Xiaobo Chen,Yibin Liu,De Chen,Ning Yan,Chaohe Yang
标识
DOI:10.1002/anie.202116059
摘要
Achieving efficient catalytic conversion over a heterogeneous catalyst with excellent resistance against leaching is still a grand challenge for sustainable chemical synthesis in aqueous solution. Herein, we devised a single-atom Pt1 /hydroxyapatite (HAP) catalyst via a simple hydrothermal strategy. Gratifyingly, this robust Pt1 /HAP catalyst exhibits remarkable catalytic selectivity and catalyst stability for the selective oxidation of C2 -C4 polyols to corresponding primary hydroxy acids. It is found that the Pt-(O-P) linkages with strong electron-withdrawing function of PO43- (Pt1 -OPO43- pair active site) not only realize the activation of the C-H bond, but also destabilize the transition state from adsorbed hydroxy acids toward the C-C cleavage, resulting in the sharply increased selectivity of hydroxy acids. Moreover, the strong PO43- -coordination effect provides electrostatic stabilization for single-atom Pt, ensuring the highly efficient catalysis of Pt1 /HAP for over 160 hours with superior leaching resistance.
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