钯
光催化
催化作用
氮化碳
乙苯
光化学
氢
密度泛函理论
碳纤维
化学
转移加氢
分子
解吸
材料科学
钌
物理化学
有机化学
计算化学
吸附
复合材料
复合数
作者
En Zhao,Manman Li,Beibei Xu,Xuelu Wang,Yu Jing,Ding Ma,Sharon Mitchell,Javier Pérez‐Ramírez,Zupeng Chen
标识
DOI:10.1002/anie.202207410
摘要
Solar-driven transfer hydrogenation of unsaturated bonds has received considerable attention in the research area of sustainable organic synthesis; however, water, the ultimate green source of hydrogen, has rarely been investigated due to the high barrier associated with splitting of water molecules. We report a carbon-nitride-supported palladium single-atom heterogeneous catalyst with unparalleled performance in photocatalytic water-donating transfer hydrogenation compared to its nanoparticle counterparts. Isotopic-labeling experiments and operando nuclear magnetic resonance measurements confirm the direct hydrogenation mechanism using in situ-generated protons from water splitting under visible-light irradiation. Density functional theory calculations attribute the high activity to lower barriers for hydrogenation, facilitated desorption of ethylbenzene, and facile hydrogen replenishment from water on the atomic palladium sites.
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