Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/70308
標題: Synthesis of highly dispersed platinum/carbon catalyst using cetyltrimethyl ammonium bromide as a dispersant for proton exchange membrane fuel cells
作者: Huang, R.H.
Chao, W.K.
Yu, R.S.
Hsueh, K.L.
Shieu, F.S.
關鍵字: Platinum nanocatalyst
Proton exchange membrane fuel cells
Cetyltrimethyl ammonium bromide
Electrochemically active surface area
carbon-supported platinum
oxygen reduction reaction
mesoporous carbon
cathode catalyst
nanoparticles
size
nanocatalysts
pemfc
layer
期刊/報告no:: Journal of Power Sources, Volume 205, Page(s) 93-99.
摘要: The highly dispersed platinum/carbon (Pt/C) catalysts with excellent activity were synthesized using an impregnation method with cetyltrimethyl ammonium bromide (CTAB) as a dispersant. The catalysts were then calcined at 300 degrees C under high vacuum to remove CTAB. The calcination temperature used was lower than the high temperatures (>= 500 degrees C) typically used for removing surfactants in nitrogen or argon. The high vacuum pressure prevents the aggregation and oxidation of Pt nanoparticles. Transmission electron microscopy results showed that the Pt nanoparticles, which had average sizes of 2.0, 2.3, and 2.7 nm at CTAB concentrations of 1.37 x 10(-2), 2.75 x 10(-2), and 4.12 x 10(-2) M. respectively, were well dispersed on carbon black. Thermogravimetric analyses indicated that the Pt/C catalysts content increased with increasing CTAB concentration. Cyclic voltammetry analyses confirmed that the electrochemically active surface area and long-term stability of the Pt/C catalysts were better than those of commercial 20 wt.% Pt/C catalyst. The Pt/C-4.12 catalyst performed exceptionally well; the power density of a single cell was 40.9% and 45.4% higher than that of a commercial one at operating cell temperatures of 25 and 75 degrees C, respectively. The results show that Pt/C catalysts synthesized from this method have promising applications in proton exchange membrane fuel cells. (C) 2012 Elsevier B.V. All rights reserved.
URI: http://hdl.handle.net/11455/70308
ISSN: 0378-7753
文章連結: http://dx.doi.org/10.1016/j.jpowsour.2012.01.026
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