镍
催化作用
材料科学
介电谱
电解
无机化学
析氧
化学工程
电解水
制氢
阳极
电化学
化学
电极
冶金
电解质
生物化学
物理化学
工程类
作者
Emily Cossar,Alejandro Oyarce Barnett,Frode Seland,Elena A. Baranova
出处
期刊:Catalysts
[Multidisciplinary Digital Publishing Institute]
日期:2019-09-27
卷期号:9 (10): 814-814
被引量:76
摘要
Anion exchange membrane water electrolysis (AEMWE) is an efficient, cost-effective solution to renewable energy storage. The process includes oxygen and hydrogen evolution reactions (OER and HER); the OER is kinetically unfavourable. Studies have shown that nickel (Ni)- iron (Fe) catalysts enhance activity towards OER, and cerium oxide (CeO2) supports have shown positive effects on catalytic performance. This study covers the preliminary evaluation of Ni, Ni90Fe10 (at%) and Ni90Fe10/CeO2 (50 wt%) nanoparticles (NPs), synthesized by chemical reduction, as OER catalysts in AEMWE using commercial membranes. Transmission electron microscopy (TEM) images of the Ni-based NPs indicate NPs roughly 4–6 nm in size. Three-electrode cell measurements indicate that Ni90Fe10 is the most active non-noble metal catalyst in 1 and 0.1 M KOH. AEMWE measurements of the anodes show cells achieving overall cell voltages between 1.85 and 1.90 V at 2 A cm−2 in 1 M KOH at 50 °C, which is comparable to the selected iridium-black reference catalyst. In 0.1 M KOH, the AEMWE cell containing Ni90Fe10 attained the lowest voltage of 1.99 V at 2 A cm−2. Electrochemical impedance spectroscopy (EIS) of the AEMWE cells using Ni90Fe10/CeO2 showed a higher ohmic resistance than all catalysts, indicating the need for support optimization.
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