Kinetics versus Charge Separation: Improving the Activity of Stoichiometric and Non-Stoichiometric Hematite Photoanodes Using a Molecular Iridium Water Oxidation Catalyst

详细信息    查看全文

• 作者：Jonathon W. Moir ; Emma V. Sackville ; Ulrich Hintermair ; Geoffrey A. Ozin
• 刊名：Journal of Physical Chemistry C
• 出版年：2016
• 出版时间：June 23, 2016
• 年：2016
• 卷：120
• 期：24
• 页码：12999-13012
• 全文大小：703K
• 年卷期：0
• ISSN：1932-7455

文摘

Oxygen-deficient iron oxide thin films, which have recently been shown to be highly active for photoelectrochemical water oxidation, were surface-functionalized with a monolayer of a molecular iridium water oxidation cocatalyst. The iridium catalyst was found to dramatically improve the kinetics of the water oxidation reaction at both stoichiometric and nonstoichiometric α-Fe₂O_3-x surfaces. This was found to be the case in both the dark and in the light as evidenced by cyclic voltammetry, Tafel analysis, and electrochemical impedance spectroscopy (EIS). Oxygen evolution measurements under working conditions confirmed high Faradaic efficiencies of 69–100% and good stability over 22 h of operation for the functionalized electrodes. The resulting ∼200–300 mV shift in onset potential for the iridium-functionalized sample was attributed to improved interfacial charge transfer and oxygen evolution kinetics. Mott–Schottky plots revealed that there was no shift in flat-band potential or change in donor density following functionalization with the catalyst. The effect of the catalyst on thermodynamics and Fermi level pinning was also found to be negligible, as evidenced by open-circuit potential measurements. Finally, transient photocurrent measurements revealed that the tethered molecular catalyst did improve charge separation and increase charge density at the surface of the photoanodes, but only at high applied biases and only for the nonstoichiometric oxygen-deficient iron oxide films. These results demonstrate how molecular catalysts can be integrated with semiconductors to yield cooperative effects for photoelectrochemical water oxidation.