YFeO3 Photocathodes for Hydrogen Evolution

被引:33
作者
Diez-Garcia, Maria Isabel [1 ,2 ]
Celorrio, Veronica [3 ]
Calvillo, Laura [4 ]
Tiwari, Devendra [3 ]
Gomez, Roberto [1 ,2 ]
Fermin, David J. [3 ]
机构
[1] Univ Alacant, Dept Quim Fis, Apartat 99, E-03080 Alacant, Spain
[2] Univ Alacant, Inst Univ Electroquim, Apartat 99, E-03080 Alacant, Spain
[3] Univ Bristol, Sch Chem, Bristol BS8 1TS, Avon, England
[4] Univ Padua, Dipartimento Sci Chim, Via Marzolo 1, I-35131 Padua, Italy
基金
英国工程与自然科学研究理事会;
关键词
YFeO3; perovskite; nanoparticles; photocurrent; band tails; WATER REDUCTION; VISIBLE-LIGHT; PHOTOELECTROCHEMICAL PROPERTIES; NANOCRYSTALLINE YFEO3; SURFACE MODIFICATION; THIN-FILMS; OXIDE; SEMICONDUCTORS; PHOTOACTIVITY; GENERATION;
D O I
10.1016/j.electacta.2017.06.025
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The behavior of YFeO3 thin-film electrodes under illumination is investigated for the first time. YFeO3 thin films on F-doped SnO2 (FTO) electrodes were prepared by two different methods ( A) deposition of nanoparticles synthesized by the so-called ionic liquid route at 1000 degrees C followed by sintering at 400 degrees C and (B) spin coating of a sol-gel precursor followed by a heat treatment at 640 degrees C. Method A provides highly texture films with exquisite orthorhombic phase purity and a direct band gap transition at 2.45 eV. On the other hand, method B results in very compact and amorphous films. XPS confirmed a Fe3+ oxidation state in both films, with a surface composition ratio of 70: 30 Y:Fe. Both materials exhibit cathodic photocurrent responses arising from hydrogen evolution in alkaline solutions with an onset potential of 1.05 V vs. RHE. The complex behavior of the photoresponses is rationalized in terms of recombination losses, band edge energy tails and hindered transport across the oxide thin film. (C) 2017 The Authors. Published by Elsevier Ltd.
引用
收藏
页码:365 / 371
页数:7
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