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Fully Conjugated Covalent Organic Polymer with Carbon-Encapsulated Ni2P for Highly Sustained Photocatalytic H2 Production from Seawater
被引:86
|作者:
Liu, Yaoyao
[1
]
Xiang, Zhonghua
[1
]
机构:
[1] Beijing Univ Chem Technol, Coll Chem Engn, State Key Lab Organ Inorgan Composites, Beijing 100029, Peoples R China
基金:
北京市自然科学基金;
关键词:
seawater spitting;
Pt-free cocatalyst;
organic photocatalyst;
carbon-encapsulated Ni2P;
visible-light-driven hydrogen production;
EFFICIENT Z-SCHEME;
HYDROGEN EVOLUTION;
NITRIDE SEMICONDUCTORS;
G-C3N4;
NANOSHEETS;
WATER;
METAL;
FRAMEWORKS;
CATALYSTS;
SURFACE;
HETEROJUNCTION;
D O I:
10.1021/acsami.9b13540
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
Organic photocatalysts are widely used to mimic artificial photosynthesis for sustainable solar-driven hydrogen production from water splitting. However, few photocatalytic H-2 production is reported using seawater, which is a significantly important parameter for practical application, and most organic photocatalysts employed precious and scarce Pt as a cocatalyst. Herein, we report an organic hybridized photocatalyst (termed COP-TF@CNi2P), carbon-encapsulated nickel phosphide, as a cocatalyst loaded on a fully conjugated organic polymer, which is applied for stable and efficient H-2 generation from seawater splitting. Both experiments and theory calculations suggest that the carbon layers covered around nickel phosphide not only can strengthen pi-pi interactions with the polymers but also can attract the photoinduced electrons from COP-TF to the surface of CNi2P, which contributes to expedite exciton dissociation. As a result, the as-synthesized COP-TF@CNi2P achieves a remarkable photocatalytic H-2 production efficiency up to 2500 mu mol g(-1) h(-1) (lambda >= 400 nm) from seawater and even maintains 92% of initial efficiency after 16 intermittent cycles, which lasts for half a month.
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页码:41313 / 41320
页数:8
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