金属有机骨架
磷光
多金属氧酸盐
光催化
催化作用
化学
电子转移
电化学
猝灭(荧光)
材料科学
镍
纳米技术
光化学
组合化学
荧光
有机化学
物理化学
电极
吸附
物理
量子力学
作者
Xiang‐Jian Kong,Zekai Lin,Zhiming Zhang,Teng Zhang,Wenbin Lin
标识
DOI:10.1002/anie.201600431
摘要
Metal-organic frameworks (MOFs) provide a tunable platform for hierarchically integrating multiple components to effect synergistic functions that cannot be achieved in solution. Here we report the encapsulation of a Ni-containing polyoxometalate (POM) [Ni4 (H2 O)2 (PW9 O34 )2 ](10-) (Ni4 P2 ) into two highly stable and porous phosphorescent MOFs. The proximity of Ni4 P2 to multiple photosensitizers in Ni4 P2 @MOF allows for facile multi-electron transfer to enable efficient visible-light-driven hydrogen evolution reaction (HER) with turnover numbers as high as 1476. Photophysical and electrochemical studies established the oxidative quenching of the excited photosensitizer by Ni4 P2 as the initiating step of HER and explained the drastic catalytic activity difference of the two POM@MOFs. Our work shows that POM@MOF assemblies not only provide a tunable platform for designing highly effective photocatalytic HER catalysts but also facilitate detailed mechanistic understanding of HER processes.
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