Fe2O3 hierarchical tubular structure decorated with cobalt phosphide (CoP) nanoparticles for efficient photoelectrochemical water splitting

被引:53
作者
Nguyen Duc Quang [1 ]
Hu, Weiguang [2 ]
Chang, Hyo Sik [2 ]
Phuoc Cao Van [1 ]
Duc Duong Viet [1 ]
Jeong, Jong-Ryul [1 ]
Seo, Dong-Bum [1 ]
Kim, Eui-Tae [1 ]
Kim, Chunjoong [1 ]
Kim, Dojin [1 ]
机构
[1] Chungnam Natl Univ, Dept Mat Sci & Engn, Daejeon 34134, South Korea
[2] Chungnam Natl Univ, Grad Sch Energy Sci & Technol, Daejeon 34134, South Korea
基金
新加坡国家研究基金会;
关键词
SnO2:Fe2O3; CoP; Hierarchical tubular structure; Photoelectrochemical; Water oxidation; ALPHA-FE2O3; PHOTOANODE; NANORODS; ENERGY; CELL; ELECTROCATALYST; NANOSTRUCTURES; OXIDATION;
D O I
10.1016/j.cej.2021.129278
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Severe charge recombination and poor water oxidation kinetics limit the performance of hematite-based (Fe2O3) photoanodes far from their theoretical levels and restrict their applicability for photoelectrochemical (PEC) water splitting devices. In this study, a hierarchical tubular structure (HTS) CoP/SnO2:Fe2O3 with a large surface area and well-defined crystalline structures was fabricated via a facile template-engaged redox etching method. The SnO2 nano-layer served as a dopant source to improve the bulk charge carrier transport efficiency along the Fe2O3 HTS growth axis; therefore, the achieved photocurrent could be up to 2.0 mA cm(-2) at 1.23 V-RHE (V vs. reversible hydrogen electrode). The CoP nanoparticles (NPs) were introduced as a high-speed hole collector from the light-absorber layer as well as a catalyst to enhance charge carrier injection efficiency on the photoelectrode surface. As a result, CoP/SnO2:Fe2O3 shows the highest photocurrent density of 3.50 mA cm(-2) (at 1.23 V-RHE) with a negative shift in the onset potential of 180 mV.
引用
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页数:8
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