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Pyrene-functionalized polymeric carbon nitride with promoted aqueous-organic biphasic photocatalytic CO2 reduction
被引:41
|作者:
Gong, Xuezhong
[1
]
Yu, Sijia
[1
]
Guan, Meili
[2
]
Zhu, Xianglin
[1
]
Xue, Can
[1
]
机构:
[1] Nanyang Technol Univ, Sch Mat Sci & Engn, 50 Nanyang Ave, Singapore 639798, Singapore
[2] Jiangsu Univ, Inst Energy Res, 301 Xuefu Rd, Jingkou 212013, Zhejiang, Peoples R China
基金:
中国博士后科学基金;
中国国家自然科学基金;
关键词:
HYDROGEN GENERATION;
MICROSPHERES;
OXIDATION;
TIO2;
SEMICONDUCTORS;
FORMATE;
D O I:
10.1039/c8ta09801h
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:
We have demonstrated a simple copolymerization process to covalently graft pyrene-functional groups on the polymeric carbon nitride (PCN) surface. The resulting pyrene functionalized carbon nitride (Py-PCN) exhibits unique biphasic photocatalytic activities, which enable efficient CO2 photoreduction in aqueous solution with simultaneous alkene (C=C) oxidation in the organic phase. The great biphasic activities are attributed to the increased lipophilicity from surface pyrene-functional groups, which allows the hydrophobic alkene molecules to readily approach the PCN surface and react with the hydroxyl radicals created from -OH oxidation by photogenerated holes. In this way, the alkene compounds indirectly consume the photo-holes from excited Py-PCN, promoting the overall photocatalytic process. Our study provides a new strategy for solar fuel production with simultaneous organic synthesis by the oxidation power of photo-holes on amphiphilic metal-free semiconductors.
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页码:7373 / 7379
页数:7
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