阴离子交换膜电解槽碱性水电解用氧化镍铁钴催化剂的性能评估和耐久性分析

Catalysts Pub Date : 2024-05-14 DOI:10.3390/catal14050322
K. W. Ahmed, Michael Fowler
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引用次数: 0

摘要

本研究探讨了用于阴离子交换膜(AEM)水电解的 NiFeCoOx 催化剂的催化活性。催化剂的镍钴比为 2:1,铁含量为 2.5 至 12.5 wt%。使用扫描电子显微镜(SEM)和 X 射线衍射(XRD)技术对催化剂进行了表征。通过线性扫频伏安法(LSV)和氧进化反应(OER)的计时安培计(CA)实验评估了 NiFeCoOx 催化剂的催化活性。铁含量为 5%的催化剂表现出最高的催化活性,在电流密度为 10 mA cm-2 时,过电位为 228 mV。催化剂在 AEM 水电解槽中进行了进一步的单电池测试分析,阳极含 5%铁的 NiFeCoOx 催化剂在 2.1 V、55 ℃ 和 70 ℃ 的条件下分别表现出 1516 mA cm-2 和 1620 mA cm-2 的最高电流密度。在 2.2 V 和 70 °C 时,最大电流密度为 1880 mA cm-2。55 °C电解的奈奎斯特图分析表明,与其他铁负载相比,含 5%铁的镍铁钴氧体催化剂的活化电阻较低,表明其性能有所提高。进行了 8 小时的耐久性测试,结果表明 AEM 水电解效果稳定,降解程度最低。在 0.8 A cm-2 的较高电流密度下运行时,电池总效率达到 70.5%。
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Performance Evaluation and Durability Analysis of NiFeCoOx Catalysts for Alkaline Water Electrolysis in Anion Exchange Membrane Electrolyzers
This study examines the catalytic activity of NiFeCoOx catalysts for anion exchange membrane (AEM) water electrolysis. The catalysts were synthesized with a Ni to Co ratio of 2:1 and Fe content ranges from 2.5 to 12.5 wt%. The catalysts were characterized using scanning electron microscopy (SEM) and X-ray diffraction (XRD) techniques. The catalytic activity of the NiFeCoOx catalysts was evaluated through linear sweep voltammetry (LSV) and chronoamperometry (CA) experiments for the oxygen evolution reaction (OER). The catalyst with 5% Fe content exhibited the highest catalytic activity, achieving an overpotential of 228 mV at a current density of 10 mA cm−2. Long-term catalyst testing for the OER at 50 mA cm−2 showed stable electrolysis operation for 100 h. The catalyst was further analyzed in an AEM water electrolyzer in a single-cell test, and the NiFeCoOx catalyst with 5% Fe at the anode demonstrated the highest current densities of 1516 mA cm−2 and 1620 mA cm−2 at 55 °C and 70 °C at 2.1 V. The maximum current density of 1880 mA cm−2 was achieved at 2.2 V and 70 °C. The Nyquist plot analysis of electrolysis at 55 °C showed that the NiFeCoOx catalyst with 5% Fe had lower activation resistance compared with the other Fe loadings, indicating enhanced performance. The durability test was performed for 8 h, showing stable AEM water electrolysis with minimum degradation. An overall cell efficiency of 70.5% was achieved for the operation carried out at a higher current density of 0.8 A cm−2.
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