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.
引用
收藏
页码:41313 / 41320
页数:8
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