One-step construction of buried a-Si/c-Si junction photocathodes for boosting photoelectrochemical hydrogen production

被引:9
|
作者
Li, Sijie [1 ,2 ]
Lin, Huiwen [2 ,4 ]
Yang, Gaoliang [5 ]
Ren, Xiaohui [2 ]
Luo, Shunqin [2 ]
Ye, Jinhua [1 ,2 ,3 ]
机构
[1] Hokkaido Univ, Grad Sch Chem Sci & Engn, Sapporo, Hokkaido 0600814, Japan
[2] Natl Inst Mat Sci NIMS, Int Ctr Mat Nanoarchitecton WPI MANA, 1-1 Namiki, Tsukuba, Ibaraki 3050044, Japan
[3] Tianjin Univ, Sch Mat Sci & Engn, TJU NIMS Int Collaborat Lab, Tianjin 300072, Peoples R China
[4] Southeast Univ, Sch Mat Sci & Engn, Nanjing 211189, Peoples R China
[5] ASTAR, Inst Mat Res & Engn, 2 Fusionopolis Way, Singapore 138634, Singapore
基金
中国国家自然科学基金;
关键词
Buried a-Si; c-Si junction; Surface; interface engineering; Planar Si photocathode; Photoelectrochemical hydrogen evolution; PLATINUM ELECTROLESS DEPOSITION; FLUORIDE SOLUTIONS; SILICON; SOLAR; PERFORMANCE; EVOLUTION; EFFICIENT; OXIDATION; DEVICE;
D O I
10.1016/j.cej.2022.140898
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The activity of Si-based photocathode for photoelectrochemical hydrogen production is mainly restricted by inadequate photovoltage and easy (photo)-corrosion, requiring complex doping or deposition techniques for improvement. Herein, a mild and feasible strategy is proposed to fabricate an amorphous Si/crystal Si (a-Si/c-Si) junction photocathode with co-deposited Pt cocatalyst. The a-Si layer acts as an electron transfer mediator to form an a-Si/c-Si buried junction with large energy band shift, thereby ensuring facile charge transfer. Meanwhile, the a-Si layer serves as a growth substrate to obtain controllable Pt nanoparticles. The Pt/a-Si/c-Si photocathode shows an onset potential of 0.42 V vs reversible hydrogen electrode (VRHE). A photocurrent up to - 35.0 mA cm-2 at 0 VRHE is obtained on Pt/a-Si/c-Si, which is much higher than that without a-Si layer. This study provides a practical manner for improving the photoresponse of planar Si-based photocathodes based on the construction of Si junction.
引用
收藏
页数:7
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