Facile in situ fabrication of Cu2O@Cu metal-semiconductor heterostructured nanorods for efficient visible-light driven CO2 reduction

被引:90
|
作者
Zhou, Jianqing [1 ]
Li, Yifei [1 ]
Yu, Luo [1 ,2 ,3 ]
Li, Zhengpeng [1 ]
Xie, Danfeng [1 ]
Zhao, Yingying [1 ]
Yu, Ying [1 ]
机构
[1] Cent China Normal Univ, Coll Phys Sci & Technol, Inst Nanosci & Nanotechnol, Wuhan 430079, Peoples R China
[2] Univ Houston, Dept Phys, Houston, TX 77204 USA
[3] Univ Houston, TcSUH, Houston, TX 77204 USA
基金
中国国家自然科学基金;
关键词
CO2; reduction; In situ fabrication; Cu2O@Cu; Heterostructured nanorods; Visible-light; DOUBLE HYDROXIDE NANOSHEETS; NANOTUBE ARRAYS; PHOTOCATALYTIC DEGRADATION; EVOLUTION REACTION; ENHANCED ACTIVITY; CUPROUS-OXIDE; CU2O; HETEROJUNCTION; PHOTOANODE; STABILITY;
D O I
10.1016/j.cej.2019.123940
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Cuprous oxide (Cu2O) is known to be a promising photocatalyst for CO2 reduction into solar fuels under visible-light irradiation. However, the issues of fast recombination of photogenerated carriers and photocorrosion severely limit its photocatalytic (PC) performance. Herein, we report a unique design of one-dimensional (1D) Cu2O@Cu metal-semiconductor heterostructured nanorods via a simple in situ reduction method for efficient CO2 reduction to hydrocarbons fuels. The well-defined 1D Cu2O nanorod arrays ensure excellent visible-light harvesting capability, and the in situ fabricated Cu2O@Cu heterostructure endows the catalyst with enhanced conductivity as well as highly improved separation and transfer efficiency of photogenerated carriers. Consequently, the optimized Cu2O@Cu heterostructure achieves an apparent quantum efficiency of 2.40% for CH4 and C2H4 and as high as 92% activity retained after four PC cycles. Furthermore, the CO2 reduction performance was further improved when applied a low external bias. This study not only provides a novel, low-cost, and efficient strategy to address the stability and activity issues of Cu2O, but also sheds light on the development of active and robust photocatalysts for energy conversion and storage.
引用
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页数:10
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