In-situ anchoring Ag through organic polymer for configuring efficient plasmonic BiVO4 photoanode

被引:95
作者
Guan, Peng [1 ]
Bai, Hongye [1 ]
Wang, Fagen [1 ]
Yu, Hao [2 ]
Xu, Dongbo [1 ]
Fan, Weiqiang [1 ]
Shi, Weidong [1 ]
机构
[1] Jiangsu Univ, Sch Chem & Chem Engn, Zhenjiang 212013, Peoples R China
[2] Shandong Univ Sci & Technol, Coll Chem & Environm Engn, Qingdao 266590, Peoples R China
基金
中国国家自然科学基金;
关键词
BiVO4; N-doped carbon; Plasmonic photoanode; Photoelectrochemical water splitting; PHOTOELECTROCHEMICAL WATER OXIDATION; LIGHT PHOTOCATALYTIC ACTIVITY; LAYERED DOUBLE HYDROXIDE; CARBON QUANTUM DOTS; SPLITTING PERFORMANCE; HYDROGEN-PRODUCTION; OXYGEN VACANCIES; INVERSE OPAL; THIN-FILM; PHOTOANODES;
D O I
10.1016/j.cej.2018.10.066
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Photoelectrochemical (PEC) water splitting is a promising method for converting solar energy into hydrogen fuel, but how to further improve the efficiency of solar energy conversion is still a large challenge. Here, it is the first time to decorate BiVO4 with Ag and N-doped carbon (BiVO4-C/N-Ag) for efficient solar-to-chemical energy conversion, and we in-depth demonstrated the superiorly of BiVO4-C/N-Ag heterostructure in PEC water splitting system. Polydopamine (PDA) as medium material realized the in-situ anchor of both Ag and N-doped carbon on BiVO4, which significantly boosted the charge injection efficiency (eta(inj)) and charge separation efficiency (eta(sep)) to 88.59% and 29.75% (1.23 V vs. RHE), respectively. The effective function of Ag and N-doped carbon exhibited an obvious influence on the enhancement of PEC performance. The photocurrent density of BiVO4-C/N-Ag increased up to 2.42 mA/cm(2) at 1.23 V vs. RHE, and 7.5-fold IPCE value (30%, 400 nm, 1.23 V vs. RHE) over bare BiVO4 has been achieved, indicating the successful configuration of a promising photoanode in the field of PEC water splitting.
引用
收藏
页码:658 / 665
页数:8
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