2020
DOI: 10.1039/d0cp03233f
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Anisotropy of Pt nanoparticles on carbon- and oxide-support and their structural response to electrochemical oxidation probed by in situ techniques

Abstract: Identifying the structural response of nanoparticle-support ensembles to the reaction conditions is essential to determine their structure in the catalytically-active state as well as to unravel possible degradation pathways. In...

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Cited by 10 publications
(8 citation statements)
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“…The peak of CoSe oxidation was observed at ca. 0.9 V versus saturated calomel electrode (SCE), which was lower than the potential of Pt oxidation (above 1.2 V), , indicating the more facile adsorption and formation of oxygen-containing species. The methanol oxidation performance was evaluated by the cyclic voltammetry (CV) technique in the electrolyte of 0.5 M H 2 SO 4 and 1.0 M CH 3 OH at a scan rate of 50 mV s –1 (Figure a).…”
Section: Resultsmentioning
confidence: 90%
“…The peak of CoSe oxidation was observed at ca. 0.9 V versus saturated calomel electrode (SCE), which was lower than the potential of Pt oxidation (above 1.2 V), , indicating the more facile adsorption and formation of oxygen-containing species. The methanol oxidation performance was evaluated by the cyclic voltammetry (CV) technique in the electrolyte of 0.5 M H 2 SO 4 and 1.0 M CH 3 OH at a scan rate of 50 mV s –1 (Figure a).…”
Section: Resultsmentioning
confidence: 90%
“…Schmies et al used this approach to better describe the anisotropic ellipsoidal shape of Pt nanocrystallites synthesized on various carbon or oxide support materials, and could correlate in situ the shape of the particles with their resistance to oxidation and dissolution. 458 A more versatile description of the particle shape is possible with SAXS. Using a model of hollow nanoparticles to fit SAXS data, Asset et al could monitor in situ the shape evolution of hollow PtNi/C nanoparticles during mild and harsh accelerated stress tests.…”
Section: Platinum Group Metal Based Single Crystalsmentioning
confidence: 99%
“…Due to the signal-to-noise ratio, it is difficult to inspect the nucleation/coalescence phase (few nanometers) using traditional XRD. To analyze small crystalline grains, two strategies can be followed, one is to use a high-energy (HE)-XRD, [122,123] and another is to extend the dwell time during data collection. However, the latter approach is not desired as it makes in situ analysis difficult to perform.…”
Section: Morphologymentioning
confidence: 99%