Electronic structure vs. electrocatalytic activity of iridium oxide

被引:37
作者
Lervik, Ingrid Anne [1 ,2 ]
Tsypkin, Mikhail [1 ]
Owe, Lars-Erik [1 ]
Sunde, Svein [1 ]
机构
[1] Norwegian Univ Sci & Technol NTNU, Dept Mat Sci & Engn, NO-7491 Trondheim, Norway
[2] Axess AS, N-6402 Molde, Norway
关键词
Water electrolysis; Iridium oxide; Hydrolysis; Colloid; Electronic structure; Electrocatalysis; OXYGEN EVOLUTION REACTION; WATER ELECTROLYSIS; ANODIC EVOLUTION; BULK PROCESSES; POLYMER; SURFACE; FILMS; ELECTROCHROMISM; COUPLE; RUO2;
D O I
10.1016/j.jelechem.2010.04.024
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The electrochemical oxidation and reduction of hexacyanoferrate redox couples at anodically formed iridium oxide (AIROF) and nanostructured iridium oxide produced by hydrolysis, hIrO(2), are compared. Whereas AIROF displays the characteristics of a semiconducting electrode in its reduced state, hlrO(2) is similar to a metal electrode. In view of also significant differences between the two oxides' optical and intercalation properties, this strongly indicates that hIrO(2) has a different bulk electronic structure. Yet, the charge-normalised electrocatalytic activity for the oxygen-evolution reaction at AIROF and hIrO(2) is the same. This indicates that the electrocatalytic properties of iridium oxide are a function of the local structure at the oxide surface and not uniquely related to the bulk electronic structure. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:135 / 142
页数:8
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