Trilayer CdS/carbon nanofiber (CNF) mat/Pt-TiO2 composite structures for solar hydrogen production: Effects of CNF mat thickness

被引:35
作者
Kim, Young Kwang [1 ]
Lim, Sang Kyoo [1 ]
Park, Hyunwoong [2 ]
Hoffmann, Michael R. [3 ]
Kim, Soonhyun [1 ]
机构
[1] Daegu Gyeongbuk Inst Sci & Technol, Div Nano & Energy Convergence Res, Daegu 42988, South Korea
[2] Kyungpook Natl Univ, Sch Energy Engn, Daegu 41566, South Korea
[3] CALTECH, Linde Robinson Labs, Pasadena, CA 91125 USA
关键词
Photocatalytic water splitting; Carbon nanomaterial; Composite catalyst; Electron-transfer mediation; TIO2-EMBEDDED CARBON NANOFIBERS; GRAPHENE OXIDE; PHOTOCATALYTIC ACTIVITY; HYBRID PHOTOCATALYST; VISIBLE-LIGHT; GENERATION; NANOTUBES; CONVERSION; WATER;
D O I
10.1016/j.apcatb.2016.05.045
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
Solar H-2 production by photocatalytic water splitting is a promising technology that permits direct H-2 production from the clean and abundant resources of water and solar light. We successfully fabricated trilayer heterostructures of CdS/carbon nanofiber (CNF) mat/Pt-deposited TiO2 (Pt-TiO2) for solar H-2 production. The CNF mat was prepared by electrospinning and carbonization. CdS and Pt-TiO2 were coated on the front and back of the CNF mat by doctor blading. Under visible-light irradiation on the CdS side, the addition of the Pt-TiO2 coating improved the H-2 production by a factor of 3.4. This suggests that the H-2 production reaction could occur on Pt-TiO2, which is not active under visible irradiation; therefore, the CNF mat could act as an efficient photogenerated electron-transfer mediator from CdS to Pt-TiO2. The H-2 production rates of the trilayer CdS/CNF/Pt-TiO2 heterostructures were strongly affected by the thickness of the CNF mat and the carbonization temperatures used in production, which affect the resistance of the CNF mat between the CdS and Pt-TiO2 sides. The results clearly demonstrated that the CNF acted as an efficient electron-transfer mediator as well as a support material. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:216 / 222
页数:7
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