Self-assembly of polyoxometalates, Pt nanoparticles and metal-organic frameworks into a hybrid material for synergistic hydrogen evolution

被引:84
|
作者
Guo, Weiwei [1 ]
Lv, Hongjin [1 ]
Chen, Zheyuan [1 ]
Sullivan, Kevin P. [1 ]
Lauinger, Sarah M. [1 ]
Chi, Yingnan [1 ]
Sumliner, Jordan M. [1 ]
Lian, Tianquan [1 ]
Hill, Craig L. [1 ]
机构
[1] Emory Univ, Dept Chem, 1515 Dickey Dr, Atlanta, GA 30322 USA
关键词
VISIBLE-LIGHT; ARTIFICIAL PHOTOSYNTHESIS; WATER OXIDATION; CATALYTIC-PROPERTIES; CO2; REDUCTION; SIZE; PHOTOCATALYSIS; DESIGN; OXYGEN; TIO2;
D O I
10.1039/c6ta00011h
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A polyoxometalate (POM), Pt nanoparticles (NPs) and a metal-organic framework (MOF, NH2-MIL-53) self-assemble into a hybrid material, PNPMOF, that displays synergistic activity for visible-light-driven catalytic hydrogen evolution (the PNPMOF is far more active than any of the three functional components alone). The POM has four targeted functions in this hybrid material: it reduces H2PtCl6 to Pt NPs, stabilizes the Pt NPs, induces a strong electrostatic association of the negatively charged Pt NPs with the protonated NH2-MIL-53 sites on the particle surfaces, and facilitates the catalytic reduction reaction itself. The NH2-MIL-53 in this work protects the light sensitive 2-aminoterephthalate groups in the pores from oxidation by the POMs, while the surface protonated NH2 units on the MOF particle surfaces strongly bind the negatively charged POM-stabilized Pt NPs.
引用
收藏
页码:5952 / 5957
页数:6
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