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FeOOH Modified H-TiO2 Nanorods Array (NRA) for Stable and Improved Low-Bias Photoelectrochemical Water Splitting.

Authors :
Panzeri, Gabriele
Dell'Oro, Ruben
Panzeri, Alberto
Sansotera, Maurizio
Russo, Valeria
Bianchi, Claudia L.
Magagnin, Luca
Source :
Journal of The Electrochemical Society; Aug2021, Vol. 168 Issue 8, p878-884, 7p
Publication Year :
2021

Abstract

Iron oxyhydroxide (FeOOH) was implemented as a low-cost, stable, and earth-abundant catalyst on hydrogenated titania nanorods array (H-TiO<subscript>2</subscript>/FeOOH), for photoelectrochemical water splitting applications. The hydrogenation treatment enhanced the maximum photocurrent density delivered by the titania-based photoanode (from 0.65 mA cm<superscript>-2</superscript> to 1 mA cm<superscript>-2</superscript> at +1.23 V vs RHE) while the exploitation of FeOOH resulted in a significant improvement in the photoelectrochemical activity at low bias. The optimized photoelectrode showed ~0.6 mA cm<superscript>-2</superscript> at +0.4 V vs RHE, with a saturation current density of 1.05 mA cm<superscript>-2</superscript>. Insights on the role of FeOOH were revealed by electrochemical impedance and photoluminescence measurements, suggesting a reduction of the charge transfer resistance at the electrolyte interface and a lower frequency of recombination events. The H-TiO<subscript>2</subscript>/FeOOH photoelectrode showed a maximum applied bias photon-to-current efficiency (ABPE) of 0.68% with a 0.3 V bias, while for the bare TiO<subscript>2</subscript> nanorods array the maximum value of 0.4% was found at a bias of 0.4 V. A stable photocurrent was measured in 1 M NaOH solution through a 5 h test at 1.23 V vs RHE, under illumination (1 sun), suggesting the compatibility of FeOOH in highly alkaline solutions. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00134651
Volume :
168
Issue :
8
Database :
Supplemental Index
Journal :
Journal of The Electrochemical Society
Publication Type :
Academic Journal
Accession number :
152416225
Full Text :
https://doi.org/10.1149/1945-7111/ac1b4b