| Literature DB >> 25959077 |
R Latsuzbaia1, E Negro1, G J M Koper2.
Abstract
The dissolution of noble-metal catalysts under mild and carbon-preserving conditions offers the possibility of in situ regeneration of the catalyst nanoparticles in fuel cells or other applications. Here, we report on the complete dissolution of the fuel cell catalyst, platinum nanoparticles, under very mild conditions at room temperature in 0.1 M HClO4 and 0.1 M HCl by electrochemical potential cycling between 0.5-1.1 V at a scan rate of 50 mV s(-1) . Dissolution rates as high as 22.5 μg cm(-2) per cycle were achieved, which ensured a relatively short dissolution timescale of 3-5 h for a Pt loading of 0.35 mg cm(-2) on carbon. The influence of chloride ions and oxygen in the electrolyte on the dissolution was investigated, and a dissolution mechanism is proposed on the basis of the experimental observations and available literature results. During the dissolution process, the corrosion of the carbon support was minimal, as observed by X-ray photoelectron spectroscopy (XPS).Entities:
Keywords: electrochemistry; fuel cells; nanoparticles; platinum; supported catalysts
Mesh:
Substances:
Year: 2015 PMID: 25959077 DOI: 10.1002/cssc.201500019
Source DB: PubMed Journal: ChemSusChem ISSN: 1864-5631 Impact factor: 8.928