催化作用
光化学
制氢
钌
光催化
超快激光光谱学
分解水
电子转移
材料科学
氢
人工光合作用
电化学
吸收光谱法
光谱学
光催化分解水
钯
化学
电极
物理化学
物理
有机化学
量子力学
生物化学
作者
Sha Chen,Kang Li,Fang Zhao,Lei Zhang,Mei Pan,Yan‐Zhong Fan,Jing Guo,Jianying Shi,Cheng‐Yong Su
摘要
Photocatalytic water splitting is a natural but challenging chemical way of harnessing renewable solar power to generate clean hydrogen energy. Here we report a potential hydrogen-evolving photochemical molecular device based on a self-assembled ruthenium-palladium heterometallic coordination cage, incorporating multiple photo- and catalytic metal centres. The photophysical properties are investigated by absorption/emission spectroscopy, electrochemical measurements and preliminary DFT calculations and the stepwise electron transfer processes from ruthenium-photocentres to catalytic palladium-centres is probed by ultrafast transient absorption spectroscopy. The photocatalytic hydrogen production assessments reveal an initial reaction rate of 380 μmol h-1 and a turnover number of 635 after 48 h. The efficient hydrogen production may derive from the directional electron transfers through multiple channels owing to proper organization of the photo- and catalytic multi-units within the octahedral cage, which may open a new door to design photochemical molecular devices with well-organized metallosupramolecules for homogenous photocatalytic applications.
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