Wakabayashi Noriaki, Takeichi Masayuki, Uchida Hiroyuki, Watanabe Masahiro
Clean Energy Research Center, University of Yamanashi, Takeda 4, Kofu 400-8510, Japan.
J Phys Chem B. 2005 Mar 31;109(12):5836-41. doi: 10.1021/jp046204+.
Oxygen reduction reaction (ORR) activity and H(2)O(2) formation at Pt(54)Fe(46), Pt(68)Co(32), and Pt(63)Ni(37) electrodes in 0.1 M HClO(4) solution at 20 to 90 degrees C were investigated by using a channel flow double electrode method. In the temperature range of 20-50 degrees C, the apparent rate constants k(app) for ORR at these electrodes were found to be 2.4-4.0 times larger than that at a pure Pt electrode, whereas their apparent activation energies of 41 kJ mol(-1) at -0.525 V vs E degrees (0.760 V vs RHE at 30 degrees C) were comparable to that at the Pt electrode. H(2)O(2) yield was ca. 1.0% at Pt(54)Fe(46) and ca. 0.16% at Pt(68)Co(32) and Pt(63)Ni(37) between 0.3 and 1.0 V vs RHE. The k(app) values at the alloy electrodes decreased with elevating temperature above 60 degrees C, and settled to almost the same values at the Pt electrode. The H(2)O(2) production was not detected at the alloy electrodes once heated at the high temperature in the solution, probably due to the thickening of the Pt skin-layer by a considerable dissolution of nonprecious metal components (Fe, Co, Ni) from the alloys.
采用通道流双电极法研究了Pt(54)Fe(46)、Pt(68)Co(32)和Pt(63)Ni(37)电极在20至90摄氏度的0.1 M HClO₄溶液中的氧还原反应(ORR)活性和H₂O₂生成情况。在20 - 50摄氏度的温度范围内,发现这些电极上ORR的表观速率常数k(app)比纯Pt电极上的大2.4 - 4.0倍,而在相对于标准电极电势为-0.525 V(30摄氏度时相对于可逆氢电极的电势为0.760 V)时,它们的表观活化能为41 kJ mol⁻¹,与Pt电极相当。相对于可逆氢电极,在0.3至1.0 V之间,Pt(54)Fe(46)上的H₂O₂产率约为1.0%,Pt(68)Co(32)和Pt(63)Ni(37)上的约为0.16%。合金电极上的k(app)值在温度高于60摄氏度时随温度升高而降低,并趋于与Pt电极上几乎相同的值。一旦在溶液中高温加热,合金电极上未检测到H₂O₂生成,这可能是由于合金中非贵金属成分(Fe、Co、Ni)大量溶解导致Pt表层增厚所致。