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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.
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页码:5952 / 5957
页数:6
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