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Transport effects in the electrooxidation of methanol studied on nanostructured Pt/glassy carbon electrodes

Y.E. Seidel ; A. Schneider ; Z. Jusys ; Björn Wickman (Institutionen för teknisk fysik, Kemisk fysik ; Kompetenscentrum katalys (KCK)) ; Bengt Kasemo (Institutionen för teknisk fysik, Kemisk fysik ; Kompetenscentrum katalys (KCK)) ; R.J. Behm
Langmuir (0743-7463). Vol. 26 (2010), 5, p. 3569-3578.
[Artikel, refereegranskad vetenskaplig]

Transport effects in the methanol oxidation reaction (MOR) were investigated using nanostructured Pt/glassy carbon (GC) electrodes and, for comparison, a polycrystalline Pt electrode. The nanostructured Pt/GC electrodes, consisting of a regular array of catalytically active cylindrical Pt nanostructures with 55 +/- 10 nm in diameter and different densities supported on a planar GC substrate, were fabricated employing hole-mask colloidal lithography (HCL). The MOR measurements were performed under controlled transport conditions in a thin-layer flow cell interfaced to a differential electrochemical mass spectrometry (DEMS) setup. The measurements reveal a distinct variation in the MOR activity and selectivity (product distribution) with Pt nanostructure density and with electrolyte rate, showing an increasing overall activity, reflected by a higher Faradaic reaction current, as well as a pronounced increase of the turnover frequency for CO(2) formation and of the CO(2) current efficiency with decreasing flow rate and increasing Pt coverage. These findings are discussed in terms of the "desorption-readorption-reaction" model introduced recently (Seidel et al. Faraday Discuss 2008, 140, 67). Finally, consequences for applications in direct methanol fuel cells are outlined.

Available online 7 December 2009

Denna post skapades 2010-02-05. Senast ändrad 2015-07-01.
CPL Pubid: 111559


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Institutioner (Chalmers)

Institutionen för teknisk fysik, Kemisk fysik (1900-2015)
Kompetenscentrum katalys (KCK)


Kemisk fysik

Chalmers infrastruktur