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The Pt3Sn/C catalyst with high electrochemical activity was synthesized under optimizing preparation conditions. The surface of carbon support pretreated by strong acid contains many O-H and C=O groups, which will increase the active sites of PtSn/C catalysts. The catalyst structure was characterized by X-ray diffraction (XRD), transmission electron microscope (TEM) and temperature programmed reduction (TPR). The co-reduction of Pt4+ and Sn2+ ions causes Sn to enter Pt crystal lattice to form PtSn alloy whose surface, however, contains tin oxides with Sn4+ and Sn2+ valences, which can promote the ethanol oxidation. The crystallinity of PtSn decreases with the reduction of the atomic ratio of Pt:Sn. By prolonging the reaction time of formic acid, the forward anodic peak current of ethanol oxidation reaches 16.2 mA on the Pt3Sn/C catalyst with 0.025 mg Pt loading. (C) 2007 Elsevier Ltd. All rights reserved.
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ELECTROCHIMICA ACTA
ISSN: 0013-4686
Year: 2008
Issue: 7
Volume: 53
Page: 3102-3108
3 . 0 7 8
JCR@2008
5 . 5 0 0
JCR@2023
ESI Discipline: CHEMISTRY;
JCR Journal Grade:1
Cited Count:
WoS CC Cited Count: 72
SCOPUS Cited Count: 75
ESI Highly Cited Papers on the List: 0 Unfold All
WanFang Cited Count:
Chinese Cited Count:
30 Days PV: 2
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