Surface engineering of nanotubular ferric oxyhydroxide “goethite” on platinum anodes for durable formic acid fuel cells

Funding Sponsor

Faculty of Science, Cairo University

Author's Department

Energy Materials Laboratory

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https://doi.org/10.1016/j.ijhydene.2021.10.037

All Authors

Bilquis Ali Al-Qodami, Hafsa H. Alalawy, Islam M. Al-Akraa, Sayed Youssef Sayed, Nageh K. Allam, Ahmad M. Mohammad

Document Type

Research Article

Publication Title

International Journal of Hydrogen Energy

Publication Date

1-1-2021

doi

10.1016/j.ijhydene.2021.10.037

Abstract

A peerless inexpensive electrochemical engineering of spherical Pt nanoparticles (nano-Pt: ca. 100 nm in average diameter) was achieved with intersected ferric oxyhydroxide nanotubes (α-FeOOH (goethite): ca. 20 nm in average diameter). The FeOOH@Pt catalyst exhibited ca. 2.5 and 1.94-times increases in the catalytic activity and poisoning tolerance, respectively, of the formic acid electro−oxidation (FAO) – the anodic reaction in the direct formic acid fuel cells (DFAFCs). Surprisingly, with a post-activation of the FeOOH@Pt catalyst at 0.48 V vs. reversible hydrogen electrode (RHE) in 0.2 mol L−1 NaOH, a favorable Fe2+/Fe3+ transformation succeeded to eliminate the permanent CO poisoning of Pt that impaired the catalytic performance of DFAFCs. This was synchronized (relatively to nano-Pt) with a four-fold increase in the catalytic efficiency, ca. −174 mV shift in the onset potential, and eightfold enhancement in the catalyst's durability for FAO. The activated FeOOH@Pt catalyst also showed a mass activity of 296 mA mg−1Pt (at 0.8 V), which was ca. nine times higher than that (34 mA mg−1Pt) of the commercial Pt/C catalyst. The ascertained improvement in the electron transfer at the FeOOH@Pt surface foresees quick industrialization for DFAFCs.

First Page

264

Last Page

275

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