| Literature DB >> 27094346 |
Xiang-Jian Kong1,2, Zekai Lin1, Zhi-Ming Zhang1,2, Teng Zhang1, Wenbin Lin3,4.
Abstract
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.Entities:
Keywords: hydrogen evolution reaction; metal-organic frameworks; photocatalysis; polyoxometalate
Year: 2016 PMID: 27094346 DOI: 10.1002/anie.201600431
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336