Effect of temperature on the activities and stabilities of hydrothermally prepared IrOx nanocatalyst layers for the oxygen evolution reaction

被引:91
作者
da Silva, Gabriel C. [1 ]
Perini, Nickson [1 ]
Ticianelli, Edson A. [1 ]
机构
[1] Univ Sao Paulo, Inst Quim Sao Carlos, CP 780, BR-13560970 Sao Carlos, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Iridium oxide; Oxygen evolution reaction; Stability; Identical location transmission electron microscopy; TRANSMISSION ELECTRON-MICROSCOPY; X-RAY-ABSORPTION; IRIDIUM OXIDE; ELECTROCATALYTIC ACTIVITIES; WATER OXIDATION; PARTICLE-SIZE; PURE IRIDIUM; REACTION OER; CATALYST; RUO2;
D O I
10.1016/j.apcatb.2017.06.044
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
Iridium oxide nanoparticles are prepared via a hydrothermal method, treated at different calcination temperatures, and their activities and stabilities for the oxygen evolution reaction (OER) evaluated. The catalysts are physicochemically characterized using several techniques including X-ray diffraction, energy dispersive X-ray spectroscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, and X-ray absorption spectroscopy. Voltammetric profiles obtained for the catalysts calcined up to 300 degrees C are similar to that of electrochemically prepared hydrous iridium oxide, while the CV profiles are characteristic of thermally prepared iridium oxide after calcination at higher temperatures. Performance as an OER catalyst decreases with increasing IrOx calcination temperature, while the opposite trend in stability is observed for these materials. Catalysts calcined between 400 and 500 degrees C exhibit better balances between activity and stability. However, despite higher performance losses, the non-calcined IrOx material still exhibits higher mass activity at the end of the aging experiments at electrode potentials up to 1.6 V vs. RHE. The causes of electrode activity degradation are investigated using identical location transmission electron microscopy, which reveal that III). electrode instability is due to the degradation of the thin IrOx layer, in addition to iridium oxide dissolution. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:287 / 297
页数:11
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