PTB7:PC61BM Bulk Heterojunction-Based Photocathodes for Efficient Hydrogen Production in Aqueous Solution

被引:25
作者
Shi, Wenwen [1 ,2 ]
Yu, Wei [1 ]
Li, Deng [1 ,2 ]
Zhang, Doudou [1 ]
Fan, Wenjun [1 ]
Shi, Jingying [1 ]
Li, Can [1 ,3 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, State Key Lab Catalysis, Dalian 116023, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Collaborat Innovat Ctr Chem Energy Mat iChEM, Dalian 116023, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
POLYMER SOLAR-CELLS; LAYER; TIO2; ENERGY; DEGRADATION; STABILITY; CONTACT; FILMS; OXIDE; SI;
D O I
10.1021/acs.chemmater.8b04629
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
Because of excellent light absorption and charge separation properties, a polymer bulk heterojunction (BHJ) composed of electron-donor and electron-acceptor is very promising to be used for photoelectrode preparation. In this work, a PTB7:PC61BM BHJ-based photocathode is fabricated for photoelectrochemical (PEC) hydrogen evolution reaction (HER) in aqueous solution. With CuOx and TiOx thin films as interfacial modification layers, the photocathode with full structure (fluorine-doped tin oxide/CuOx/PTB7:PC61BM/TiOx/Pt) generates a maximum photocurrent density up to -7.27 mA cm(-2) and an onset potential as positive as 0.63 V. The half-cell solar-to-hydrogen efficiency is up to 1.5%, outperforming all of the previous BHJ-based photocathodes for HER CuOx is identified to play a role of facilitating charge separation, whereas TiOx improves the charge injection as well as blocks the back migration of holes during the PEC process. The factors including permeation of water and oxygen molecules, incident light spectrum, and current flowing that affect the PEC stability are investigated and discussed.
引用
收藏
页码:1928 / 1935
页数:8
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