共 50 条
Photocatalytic CO2 conversion to methanol by Cu2O/graphene/TNA heterostructure catalyst in a visible-light-driven dual-chamber reactor
被引:122
|作者:
Li, Fei
[1
]
Zhang, Li
[1
]
Tong, Jincheng
[1
]
Liu, Yingliang
[1
]
Xu, Shengang
[1
]
Cao, Yan
[2
]
Cao, Shaokui
[1
]
机构:
[1] Zhengzhou Univ, Sch Mat Sci & Engn, Zhengzhou 450052, Peoples R China
[2] Western Kentucky Univ, Inst Combust Sci & Environm Technol, Bowling Green, KY 42101 USA
来源:
基金:
中国国家自然科学基金;
关键词:
Cu2O;
Graphene;
Heterostructure;
Dual-chamber reactor;
CO2;
photoreduction;
REDUCED GRAPHENE OXIDE;
TIO2 NANOTUBE ARRAYS;
ELECTROCHEMICAL REDUCTION;
HYDROGEN GENERATION;
WATER REDUCTION;
FILMS;
COMPOSITE;
FABRICATION;
CU2O;
HETEROJUNCTION;
D O I:
10.1016/j.nanoen.2016.06.056
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:
Efficient photocatalytic CO2 conversion to methanol under visible light irradiation (X > 400 nm) was achieved in a light-driven dual-chamber reactor using the monolithic two-side Cu2O/graphene/TiO2 nanotube array (TNA) heterostructure as separated oxidation and reduction catalyst, that was prepared with anodic TNA as the substrate following by sequential electrochemical deposition of graphene and Cu2O. The combined heterojunction in the ternary composite helps to improve the photocatalytic performance by increasing light absorption, preventing electron-hole recombination and facilitating electron transfer across the heterojunction interfaces, as revealed by photoelectrochemical measurements. Methanol generation rate of 45 pmol cm(-2) h(-1) was achieved, which is much higher than those obtained for existing TNA-based photocatalysts reported. Moreover, the quantum efficiency of 5.71% at 420 nm has been attained. The improved photocatalytic activity together with the proposed reaction mechanism demonstrated the advantage of Cu2O/graphene/TNA heterostructure and effectiveness of the reaction system, which can efficiently suppress charge recombination, improve interfacial charge transfer and inhibit the backward reaction by separating the photocatalytic reaction sites. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:320 / 329
页数:10
相关论文