Amorphous nanostructured Ni–Fe oxide as a notably active and low-cost oxygen evolution reaction electrocatalyst for anion exchange membrane water electrolysis†

Lorenzo Mirizzi, Mohsin Muhyuddin, Carmelo Lo Vecchio, Erminia Mosca, Vincenzo Baglio, Irene Gatto, Enrico Berretti, Alessandro Lavacchi, Valerio C. A. Ficca, Rosanna Viscardi, Roberto Nisticò and Carlo Santoro
{"title":"Amorphous nanostructured Ni–Fe oxide as a notably active and low-cost oxygen evolution reaction electrocatalyst for anion exchange membrane water electrolysis†","authors":"Lorenzo Mirizzi, Mohsin Muhyuddin, Carmelo Lo Vecchio, Erminia Mosca, Vincenzo Baglio, Irene Gatto, Enrico Berretti, Alessandro Lavacchi, Valerio C. A. Ficca, Rosanna Viscardi, Roberto Nisticò and Carlo Santoro","doi":"10.1039/D5IM00008D","DOIUrl":null,"url":null,"abstract":"<p>The oxygen evolution reaction (OER) is a critical bottleneck in the commercial evolution of anion exchange membrane water electrolyzers (AEMWEs). As a potential substitute for the scarce and expensive noble metal-based electrocatalysts typically used to improve the OER activity, here amorphous NiFe oxides with varying Ni/Fe ratios were synthesized using a simplistic and cost-effective sol–gel method. After carefully investigating the structural and morphological attributes of the derived electrocatalysts, their OER activities were analyzed by acquiring the half-cell measurements. First, the influence of the electrochemical ink formulation and additives on the activity of the electrocatalyst was studied, followed by elucidating the electrocatalyst loading to configure the working electrode on the rotating disk electrode (RDE). By comparing the activities of different synthesized NiFe oxides, it was observed that Ni<small><sub>0.75</sub></small>Fe<small><sub>0.25</sub></small>O delivers the peak performance with a minimum overpotential of <em>ca.</em> 290 mV. Therefore, the aforementioned sample was utilized to configure the anode electrode for a lab-scale AEMWE, achieving 3.7 A cm<small><sup>−2</sup></small> at 2 V and 80 °C while demonstrating promising stability trends.</p><p>Keywords: NiFe oxide; AEM-WE; Alkaline media; Inorganic oxides; OER; PGM-free electrocatalysts.</p>","PeriodicalId":29808,"journal":{"name":"Industrial Chemistry & Materials","volume":" 4","pages":" 485-497"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/im/d5im00008d?page=search","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Industrial Chemistry & Materials","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/im/d5im00008d","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

The oxygen evolution reaction (OER) is a critical bottleneck in the commercial evolution of anion exchange membrane water electrolyzers (AEMWEs). As a potential substitute for the scarce and expensive noble metal-based electrocatalysts typically used to improve the OER activity, here amorphous NiFe oxides with varying Ni/Fe ratios were synthesized using a simplistic and cost-effective sol–gel method. After carefully investigating the structural and morphological attributes of the derived electrocatalysts, their OER activities were analyzed by acquiring the half-cell measurements. First, the influence of the electrochemical ink formulation and additives on the activity of the electrocatalyst was studied, followed by elucidating the electrocatalyst loading to configure the working electrode on the rotating disk electrode (RDE). By comparing the activities of different synthesized NiFe oxides, it was observed that Ni0.75Fe0.25O delivers the peak performance with a minimum overpotential of ca. 290 mV. Therefore, the aforementioned sample was utilized to configure the anode electrode for a lab-scale AEMWE, achieving 3.7 A cm−2 at 2 V and 80 °C while demonstrating promising stability trends.

Keywords: NiFe oxide; AEM-WE; Alkaline media; Inorganic oxides; OER; PGM-free electrocatalysts.

Abstract Image

无定形纳米结构Ni-Fe氧化物作为阴离子交换膜电解中活性高、成本低的析氧反应电催化剂
析氧反应(OER)是阴离子交换膜水电解槽(AEMWEs)商业化发展的关键瓶颈。作为稀有和昂贵的贵金属基电催化剂的潜在替代品,通常用于提高OER活性,本研究采用简单而经济的溶胶-凝胶法合成了具有不同Ni/Fe比的非晶态nfe氧化物。在仔细研究了衍生电催化剂的结构和形态属性后,通过获得半电池测量来分析其OER活性。首先,研究了电化学油墨配方和添加剂对电催化剂活性的影响,然后阐明了在旋转圆盘电极(RDE)上配置工作电极的电催化剂负载。通过对比不同合成的NiFe氧化物的活性,发现Ni0.75Fe0.25O的过电位最低约为290 mV。因此,上述样品被用于配置实验室规模的AEMWE阳极电极,在2 V和80°C下达到3.7 a cm - 2,同时显示出有希望的稳定性趋势。关键词:NiFe氧化物;AEM-WE;碱性媒体;无机氧化物;OER;PGM-free electrocatalysts。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Industrial Chemistry & Materials
Industrial Chemistry & Materials chemistry, chemical engineering, functional materials, energy, etc.-
自引率
0.00%
发文量
0
期刊介绍: Industrial Chemistry & Materials (ICM) publishes significant innovative research and major technological breakthroughs in all aspects of industrial chemistry and materials, with a particular focus on the important innovation of low-carbon chemical industry, energy and functional materials. By bringing researchers, engineers, and policymakers into one place, research is inspired, challenges are solved and the applications of science and technology are accelerated. The global editorial and advisory board members are valued experts in the community. With their support, the rigorous editorial practices and dissemination ensures your research is accessible and discoverable on a global scale. Industrial Chemistry & Materials publishes: ● Communications ● Full papers ● Minireviews ● Reviews ● Perspectives ● Comments
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信