Rational construction of S-doped FeOOH onto Fe2O3 nanorods for enhanced water oxidation

被引:41
|
作者
Quang, Nguyen Duc [1 ,2 ]
Van, Phuoc Cao [1 ]
Majumder, Sutripto [1 ]
Jeong, Jong-Ryul [1 ]
Kim, Dojin [1 ]
Kim, Chunjoong [1 ,2 ]
机构
[1] Chungnam Natl Univ, Dept Mat Sci & Engn, Daejeon 34134, South Korea
[2] Chungnam Natl Univ, Daejeon 34134, South Korea
基金
新加坡国家研究基金会;
关键词
Fe2O3; S-doped FeOOH; Photocatalyst; Photoelectrochemical; Water oxidation; SPLITTING PERFORMANCE; BIVO4; PHOTOANODES; HEMATITE; GRAPHENE; LAYER; OXIDE;
D O I
10.1016/j.jcis.2022.02.117
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
Hematite-based photoanode (alpha-Fe2O3) is considered the promising candidate for photoelectrochemical (PEC) water splitting due to its relatively small optical bandgap. However, severe charge recombination in the bulk and poor surface water oxidation kinetics have limited the PEC performance of Fe2O3 photo electrodes, which is far below the theoretical value. Herein, a new catalyst, S-doped FeOOH (S-FeOOH), has been immobilized onto the surface of the Fe2O3 nanorod (NR) array by a facile chemical bath deposition incorporated thermal sulfuration process. The grown S-FeOOH layer acts not only as an efficient catalyst layer to accelerate the water oxidation on the surface of photoelectrode but also constructs a heterojunction with the light absorption layer to facilitate the interface charge carrier separation and transfer. As expected, the modified S-FeOOH@Fe2O3 photoanode achieves a remarkable increase in PEC performance of 2.30 mA cm(-2) at 1.23 V versus the reversible hydrogen electrode (VRHE) and an apparent negative shifted onset potential of 250 mV in comparison with pristine Fe2O3 (0.95 mA cm(-2) at 1.23 VRHE). These results provide a simple and effective strategy to coupling oxygen evolution catalysts with photoanodes for practically high-performance PEC applications. (C)& nbsp;2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:749 / 758
页数:10
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