Enhanced charge carrier separation to improve hydrogen production efficiency by ferroelectric spontaneous polarization electric field

被引:97
作者
Huang, Xueyan [1 ]
Wang, Kaiqiang [1 ]
Wang, Yaozhu [1 ]
Wang, Bo [1 ]
Zhang, Lulu [1 ]
Gao, Fan [1 ]
Zhao, Yan [1 ]
Feng, Wenhui [2 ]
Zhang, Shiying [2 ]
Liu, Ping [1 ]
机构
[1] Fuzhou Univ, State Key Lab Photocatalysis Energy & Environm, Res Inst Photocatalysis, Fuzhou 350002, Fujian, Peoples R China
[2] Changsha Univ, Hunan Prov Collaborat Innovat Ctr Environm & Ener, Changsha 410022, Hunan, Peoples R China
基金
国家科技攻关计划; 中国国家自然科学基金;
关键词
Ferroelectric; Internal electric field; BaTiO3-CdS; Visible light; Photocatalysis; VISIBLE-LIGHT-DRIVEN; PHOTOCHEMICAL REDUCTION; PHOTOCATALYTIC ACTIVITY; COMPOSITE PHOTOCATALYSTS; TIO2; PHOTOCATALYSIS; H-2; EVOLUTION; WATER; CDS; SURFACE; HETEROJUNCTIONS;
D O I
10.1016/j.apcatb.2018.01.036
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
Ferroelectrics with internal polar domains has been utilized to enhance photoinduced carriers separation for improving photocatalytic performance by combining them with metal-sulfide semiconductor material. Herein, we construct a new nanohybrid photocatalyst, which combines ferroelectric n anospheres (BaTiO3) and semiconductor nanoparticles (CdS). This hybrid photocatalyst exhibits remarkable hydrogen production activity. The optimum hydrogen production rate based on BaTiO3-CdS composite structure reaches 483 mu mol h(-1) g(-1), which is about 9.7 times greater than that of pristine CdS. The observations indicate that charge carriers generated in CdS, more efficiently migrate to the surface and participate in the redox reactions, influenced by dipolar fields in the ferroelectric domains of BaTiO3. These mechanistic insights will widen our fundamental understanding of charge separation and transfer processes to steer charge flow in a desired and efficient manner.
引用
收藏
页码:322 / 329
页数:8
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