Issue 64, 2017, Issue in Progress

Activity of IrO2 supported on tantalum-doped TiO2 electrocatalyst for solid polymer electrolyte water electrolyzer

Abstract

TiO2 doped tantalum was successfully synthesized via an evaporation-induced self-assembly method (EISA) as a support of IrO2 for a solid polymer electrolyte water electrolyzer (SPEWE). The IrO2 was synthesized on the surface of Ta-doped TiO2 support by using the Adams fusion method. The samples were characterized by BET, XRD, SEM, TEM, CV, EIS and polarization curves of single cells. The doping amount of Tantalum (5, 10, 20, 30 at%) was thoroughly investigated to evaluate the effects on structure, electric conductivity and oxygen evolution reaction (OER) activity of Ta-doped titania supported IrO2. The results indicated that a significant effect of the Ta dopant on the phase composition and conductivity. Among all the catalysts, with the optimized catalyst IrO2 loading, the terminal applied potential was 1.849 V at 1000 mA cm−2 and 80 °C in a SPE water electrolysis cell using 80IrO2/Ti0.7Ta0.3O2 as anode. IrO2 loading 80% IrO2/Ti0.7Ta0.3O2 showed better performance than that of the pristine IrO2 after normalizing the current density for IrO2 loading. The increased performance can be attributed to the better dispersion of the IrO2 on Ti0.7Ta0.3O2 resulting in smaller crystallites and large surface area. In closing, Ti0.7Ta0.3O2 showed outstanding promise as an electrocatalyst support in SPE water electrolysis.

Graphical abstract: Activity of IrO2 supported on tantalum-doped TiO2 electrocatalyst for solid polymer electrolyte water electrolyzer

Article information

Article type
Paper
Submitted
12 Jun 2017
Accepted
14 Aug 2017
First published
17 Aug 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 40427-40436

Activity of IrO2 supported on tantalum-doped TiO2 electrocatalyst for solid polymer electrolyte water electrolyzer

H. Lv, G. Zhang, C. Hao, C. Mi, W. Zhou, D. Yang, B. Li and C. Zhang, RSC Adv., 2017, 7, 40427 DOI: 10.1039/C7RA06534E

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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