Direct Observation of Two Electron Holes in a Hematite Photoanode during Photoelectrochemical Water Splitting

被引:129
作者
Braun, Artur [1 ]
Sivula, Kevin [2 ]
Bora, Debajeet K. [1 ,3 ,5 ]
Zhu, Junfa [4 ]
Zhang, Liang [4 ,5 ]
Graetzel, Michael [2 ]
Guo, Jinghua [5 ]
Constable, Edwin C. [3 ]
机构
[1] Empa Swiss Fed Labs Mat Sci & Technol, Lab High Performance Ceram, CH-8600 Dubendorf, Switzerland
[2] Ecole Polytech Fed Lausanne, Lab Photon & Interfaces, CH-1015 Lausanne, Switzerland
[3] Univ Basel, Dept Chem, CH-4056 Basel, Switzerland
[4] Univ Sci & Technol China, Natl Synchrotron Radiat Lab, Hefei 230029, Peoples R China
[5] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Adv Light Source, Berkeley, CA 94720 USA
基金
欧洲研究理事会; 瑞士国家科学基金会;
关键词
X-RAY-ABSORPTION; OXYGEN K-EDGE; ALPHA-FE2O3; PHOTOELECTRODES; OXIDE; SPECTROSCOPY; PERFORMANCE; CELLS; PHOTOCATALYST; IMPEDANCE; OXIDATION;
D O I
10.1021/jp304254k
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
Visible light active photoelectrodes for hydrogen generation by solar photoelectrochemical water splitting have been under scrutiny for many decades. In particular, the role of electron holes and charge transfer remains controversial. We have investigated the oxygen evolution of hematite in alkaline aqueous electrolyte under a bias potential during visible light illumination in a photoelectrochemical cell operando with soft X-ray (O 1s) spectroscopy. Only under these conditions, two new spectral signatures evolve in the valence band, which we identify as an O 2p hole transition into the charge transfer band and an Fe 3d type hole into the upper Hubbard band. Quantitative analysis of their spectral weight and comparison with the photocurrent reveals that both types of holes, contrary to earlier speculations and common perception, contribute to the photocurrent.
引用
收藏
页码:16870 / 16875
页数:6
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