Characterization of Interfacial Charge-Transfer Photoexcitation of Polychromium-Oxo-Electrodeposited TiO2 as an Earth-Abundant Photoanode for Water Oxidation Driven by Visible Light.

Polychromium-oxo-deposited TiO2 (CrIII x Oy /TiO2 ) electrodes were fabricated by a simple electrochemical technique by using different TiO2 basal electrodes (anatase, rutile, and mixed polymorphic phases P25) as earth-abundant photoanodes for visible-light-driven water oxidation. The high-resolution transmission electron microscopy (HR-TEM) observation illustrated that an CrIII x Oy layer with approximately 2-3 nm thickness was formed on the surface of the crystalline TiO2 particles. Upon visible-light irradiation of the electrodes, the photoanodic current based on water oxidation was generated at the CrIII x Oy /TiO2 electrodes. However, the wavelength (below 620 nm) for photocurrent generation at CrIII x Oy /TiO2 -rutile was longer than that (below 560 nm) at CrIII x Oy /TiO2 -P25 by 60 nm, which is in agreement with the difference (0.2 eV) in the conduction band (CB) edge energy between rutile and anatase TiO2 . This gives a quantitative account for the photocurrent generation based on interfacial charge transfer (IFCT) from Cr 3d of the deposited CrIII x Oy layer to the TiO2 CB. The photocurrent generated for CrIII x Oy /TiO2 -rutile was higher than that for CrIII x Oy /TiO2 -anatase, which is ascribed to 1) more effective CrIII x Oy deposition on the rutile particles, 2) a larger electrolyte/CrIII x Oy interface for water oxidation as a result of smaller rutile particles (ca. 30-40 nm) compared with larger P25 particles (ca. 40-80 nm), and 3) more effective use of visible light owing to the low energy IFCT transition of rutile.