The electronic, chemical and electrocatalytic processes and intermediates on iron oxide surfaces during photoelectrochemical water splitting

被引:27
作者
Braun, Artur [1 ]
Hu, Yelin [1 ,2 ]
Boudoire, Florent [1 ,3 ]
Bora, Debajeet K. [1 ]
Sarma, D. D. [4 ]
Graetzel, Michael [2 ]
Eggleston, Carrick M. [5 ]
机构
[1] Swiss Fed Labs Mat Sci & Technol, Empa, Lab High Performance Ceram, CH-8600 Dubendorf, Switzerland
[2] Ecole Polytech Fed Lausanne, Lab Photon & Interfaces, CH-1005 Lausanne, Switzerland
[3] Univ Basel, Dept Chem, CH-4052 Basel, Switzerland
[4] Indian Inst Sci, Solid State & Struct Chem Unit, Bangalore 560012, Karnataka, India
[5] Univ Wyoming, Dept Geol & Geophys, Laramie, WY 82071 USA
基金
瑞士国家科学基金会; 美国国家科学基金会;
关键词
X-RAY-ABSORPTION; LIQUID WATER; 2ND-HARMONIC GENERATION; OK-EDGE; HEMATITE; SPECTROSCOPY; OXIDATION; ALPHA-FE2O3; FILM; TEMPERATURES;
D O I
10.1016/j.cattod.2015.07.024
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
We re-assess experimental soft X-ray absorption spectra of the oxygen K-shell which we recorded operando from iron oxide during photoelectrochemical water splitting in KOH electrolyte. In particular, we refer to recently reported transitional electron hole states which originate within the charge carrier depletion layer of the iron oxide and on the iron oxide surface. For the latter we find that an intermediate oxy-peroxo species is formed on the iron oxide with increasing bias potential, which disappears upon further polarization of the electrode, concomitantly with the evolution and disappearance of the aforementioned surface state. The oxygen spectra contain also the spectroscopic signatures of the electrolyte water, the position of which changes with increasing bias potential towards lower X-ray energies, revealing the breaking and formation of hydrogen bonds in the water during the experiment. Combined with potential dependent impedance spectroscopy data we are able to sketch the molecular structure of chemical intermediates and their charge carrier dynamics. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:72 / 81
页数:10
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