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Effects of the Substitution of Β-Site Ion on Oxygen Reduction Electrode Properties of Pb2Ru2O7- δ in Aqueous Solutions

Journal Key Engineering Materials (Volume 350)
Volume Electroceramics in Japan X
Edited by K. Katayama, K. Kato, T. Takenaka, M. Takata and K. Shinozaki
Pages 171-174
DOI 10.4028/www.scientific.net/KEM.350.171
Citation Kenji Yoshihara et al., 2007, Key Engineering Materials, 350, 171
Online since October, 2007
Authors Kenji Yoshihara, Yoshinobu Saito, Morihiro Saito, Jun Kuwano, Hidenobu Shiroishi
Keywords Acid Solution, Alkaline Solution, Oxygen Reduction, Pyrochlore, Substitution
Abstract

The activities of the pyrochlores Pb2Ru2-xMxO7-δ (M=Mn,Fe,Co,Ni)[PRM(0x)] toward electrochemical oxygen reduction (EOR) were examined in 0.1 M KOH and 0.05 M H2SO4 aqueous solutions. The onset voltage (Vo) and the efficiency (E4) of 4-electron reduction of oxygen for PRM(0x) were evaluated by semi-steady state voltammetry with rotating ring-disk electrodes. In PRM01, the order of the EOR activities was PRMn01 > PRCo01 > PRNi01 > PRFe01 in both solutions. This was consistent with the variation of the lattice parameters, i.e. PRM01 with a smaller lattice parameter showed higher EOR activity. In addition, PRMn05 showed higher EOR activity than PRMn01. The onset voltages Vo were 0.95 and 0.50 V vs. reversible hydrogen electrode in 0.1 M KOH and 0.05 M H2SO4, respectively, while E4 was almost 100 % in both solutions. These results indicate that the EOR activity of PRM(0x) depends on the incorporated metal ions on the B-sites and their contents.

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