Temperature dependence of oxygen reduction activity at Nafion-coated bulk Pt and Pt/carbon black catalysts

被引:88
作者
Yano, Hiroshi
Higuchi, Eiji
Uchida, Hiroyuki
Watanabe, Masahiro
机构
[1] Univ Yamanashi, Clean Energy Res Ctr, Kofu, Yamanashi 4008510, Japan
[2] Univ Yamanashi, Interdisciplinary Grad Sch Med & Engn, Kofu, Yamanashi 4008511, Japan
关键词
D O I
10.1021/jp063497t
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Oxygen reduction reaction (ORR) activity and H2O2 formation at Nafion-coated film electrodes of bulk-Pt and Pt nanoparticles dispersed on carbon black (Pt/CB) were investigated in 0.1 M HClO4 solution at 30 to 110 C by using a channel flow double electrode method. We have found that the apparent rate constants k(app) (per real Pt active surface area) for the ORR at bulk-Pt (with and without Nafion-coating) and Nafion-coated Pt/CB ( 19.3 and 46.7 wt % Pt, dPt) 2.6 to 2.7 nm) thin-film electrodes were in beautiful agreement with each other in the operation conditions of polymer electrolyte fuel cells (PEFCs), i.e., 30-110 degrees C and ca. 0.7 to 0.8 V vs RHE. The H2O2 yield was 0.6-1.0% at 0.7-0.8 V on all Nafion-coated Pt/CB and bulk-Pt and irrespective of Pt-loading level and temperature. Nafion coating was pointed out to be a major factor for the H2O2 formation on Pt catalysts modifying the surface property, because H2O2 production was not detected at the bulk-Pt electrode without Nafion coating.
引用
收藏
页码:16544 / 16549
页数:6
相关论文
共 38 条
[1]  
AGARWAL AS, 2004, 206 M EL SOC HON HAW
[2]   Study of Pt electrode/Nafion ionomer interface in HClO4 by in situ surface-enhanced FTIR spectroscopy [J].
Ayato, Y ;
Kunimatsu, K ;
Osawa, M ;
Okada, T .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2006, 153 (02) :A203-A209
[3]   Temperature and pressure dependence of O2 reduction at Pt | Nafion® 117 and Pt | BAM® 407 interfaces [J].
Beattie, PD ;
Basura, VI ;
Holdcroft, S .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1999, 468 (02) :180-192
[4]   Electrocatalysis under conditions of high mass transport rate: Oxygen reduction on single submicrometer-sized Pt particles supported on carbon [J].
Chen, SL ;
Kucernak, A .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (10) :3262-3276
[5]   EXAMINATION OF THE IONOMER ELECTRODE INTERFACE USING THE FERRIC FERROUS REDOX COUPLE [J].
CHU, D ;
TRYK, D ;
GERVASIO, D ;
YEAGER, EB .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1989, 272 (1-2) :277-284
[6]   O2 reduction at the Pt/Nafion interface in 85% concentrated H3PO4 [J].
Chu, D .
ELECTROCHIMICA ACTA, 1998, 43 (24) :3711-3718
[7]   AN ANALYSIS OF THE PH-DEPENDENCE OF ENTHALPIES AND GIBBS ENERGIES OF ACTIVATION FOR O2 REDUCTION AT PT ELECTRODES IN ACID-SOLUTIONS [J].
DAMJANOVIC, A ;
SEPA, DB .
ELECTROCHIMICA ACTA, 1990, 35 (07) :1157-1162
[8]   ACTIVATION PARAMETERS FOR OXYGEN REDUCTION KINETICS IN TRIFLUOROMETHANE SULFONIC-ACID SYSTEMS [J].
ENAYETULLAH, MA ;
DEVILBISS, TD ;
BOCKRIS, JO .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1989, 136 (11) :3369-3376
[9]   ANALYSIS OF PLATINUM PARTICLE-SIZE AND OXYGEN REDUCTION IN PHOSPHORIC-ACID [J].
GIORDANO, N ;
PASSALACQUA, E ;
PINO, L ;
ARICO, AS ;
ANTONUCCI, V ;
VIVALDI, M ;
KINOSHITA, K .
ELECTROCHIMICA ACTA, 1991, 36 (13) :1979-1984
[10]   Temperature dependent oxygen electrochemistry on platinum low index single crystal surfaces in acid solutions [J].
Grgur, BN ;
Markovic, NM ;
Ross, PN .
CANADIAN JOURNAL OF CHEMISTRY-REVUE CANADIENNE DE CHIMIE, 1997, 75 (11) :1465-1471