The influence of oxygen vacancies on the kinetics of water photoelectrolysis at (001) n-TiO2 rutile
Author:
Publisher
Elsevier BV
Subject
Electrochemistry,General Chemical Engineering,Analytical Chemistry
Reference11 articles.
1. Kinetic Approach to the Photocurrent Transients in Water Photoelectrolysis at n ‐ TiO2 Electrodes: II . Analysis of the Photocurrent‐Time Dependence
2. Kinetic approach to the photocurrent transients in water photoelectrolysis at n-titanium dioxide electrodes. 1. Analysis of the ratio of the instantaneous to steady-state photocurrent
3. Analysis of the photocurrent transient behaviour associated with flatband potential shifts during water splitting at n-TiO2 electrodes
4. Hole diffusion length inn‐TiO2single crystals and sintered electrodes: Photoelectrochemical determination and comparative analysis
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1. Surface evolution of rutile TiO2 (100) in an oxidizing environment;Surface Science;2007-01
2. Crystal-face and illumination intensity dependences of the quantum efficiency of photoelectrochemical etching, in relation to those of water photooxidation, at n-TiO2 (rutile) semiconductor electrodes;Journal of Electroanalytical Chemistry;2003-03
3. The surface science of titanium dioxide;Surface Science Reports;2003-01
4. Organization and Reactivity of Nanoparticles at Molecular Interfaces. Part I. Photoelectrochemical Responses Involving TiO2 Nanoparticles Assembled at Polarizable Water|1,2-Dichloroethane Junctions;The Journal of Physical Chemistry B;2002-10-01
5. The interaction of water with solid surfaces: fundamental aspects revisited;Surface Science Reports;2002-05
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