Lanthanum‐Nickel‐Based Mixed‐Oxide‐Coated Nickel Electrodes for the OER Electrocatalysis

IF 2.6 4区 工程技术 Q3 ELECTROCHEMISTRY
Fuel Cells Pub Date : 2024-07-09 DOI:10.1002/fuce.202300239
Nikolas Mao Kubo, Rim Mhamdi, Regina Palkovits
{"title":"Lanthanum‐Nickel‐Based Mixed‐Oxide‐Coated Nickel Electrodes for the OER Electrocatalysis","authors":"Nikolas Mao Kubo, Rim Mhamdi, Regina Palkovits","doi":"10.1002/fuce.202300239","DOIUrl":null,"url":null,"abstract":"The anodic oxygen evolution reaction (OER) remains a bottleneck for electrocatalytic water splitting due to its sluggish kinetics and, thus, high overpotentials. This limits water electrolysis as a key technology for the generation of hydrogen as a sustainable alternative to fossil fuels. For alkaline water splitting, perovskite phases (ABO<jats:sub>3</jats:sub>) with earth‐abundant first‐row transition‐metals have emerged as a promising material class for OER electrocatalysts. Among these, LaNiO<jats:sub>3</jats:sub> has been found to exhibit high intrinsic OER activity. To increase catalyst utilization, a high surface area of the catalyst is desirable and can be achieved by impregnation of porous templates. In this work, La–Ni‐based oxides were prepared via impregnation of activated carbon and subsequent heating, combining precursor calcination and template removal into one step. The phase structure of the samples is analyzed via powder X‐ray diffractometry, and the morphology is determined by scanning electron microscopy. The synergistic effect of B‐site mixing iron as well as A‐site mixing strontium into LaNiO<jats:sub>3</jats:sub> is studied and found to increase its OER activity, confirming the activity‐enhancing effect of Fe in Ni‐based OER electrocatalysts. To allow for facile technical application of the catalysts, the electrodes are prepared by coating a perovskite ink onto Ni‐metal as industrially relevant substrates, followed by calcination.","PeriodicalId":12566,"journal":{"name":"Fuel Cells","volume":null,"pages":null},"PeriodicalIF":2.6000,"publicationDate":"2024-07-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fuel Cells","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1002/fuce.202300239","RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0

Abstract

The anodic oxygen evolution reaction (OER) remains a bottleneck for electrocatalytic water splitting due to its sluggish kinetics and, thus, high overpotentials. This limits water electrolysis as a key technology for the generation of hydrogen as a sustainable alternative to fossil fuels. For alkaline water splitting, perovskite phases (ABO3) with earth‐abundant first‐row transition‐metals have emerged as a promising material class for OER electrocatalysts. Among these, LaNiO3 has been found to exhibit high intrinsic OER activity. To increase catalyst utilization, a high surface area of the catalyst is desirable and can be achieved by impregnation of porous templates. In this work, La–Ni‐based oxides were prepared via impregnation of activated carbon and subsequent heating, combining precursor calcination and template removal into one step. The phase structure of the samples is analyzed via powder X‐ray diffractometry, and the morphology is determined by scanning electron microscopy. The synergistic effect of B‐site mixing iron as well as A‐site mixing strontium into LaNiO3 is studied and found to increase its OER activity, confirming the activity‐enhancing effect of Fe in Ni‐based OER electrocatalysts. To allow for facile technical application of the catalysts, the electrodes are prepared by coating a perovskite ink onto Ni‐metal as industrially relevant substrates, followed by calcination.
用于 OER 电催化的镧镍基混合氧化物涂层镍电极
由于阳极氧进化反应(OER)的动力学缓慢,因此过电位较高,它仍然是电催化水分离的瓶颈。这限制了水电解作为一种可持续替代化石燃料的制氢关键技术。在碱性水分离方面,富含第一排过渡金属的过氧化物相(ABO3)已成为一种很有前途的 OER 电催化剂材料。其中,LaNiO3 已被发现具有很高的固有 OER 活性。为了提高催化剂的利用率,需要催化剂具有较高的比表面积,这可以通过浸渍多孔模板来实现。在这项工作中,通过浸渍活性炭并随后加热制备了 La-Ni 基氧化物,将前驱体煅烧和模板去除合二为一。样品的相结构通过粉末 X 射线衍射仪进行分析,形貌则通过扫描电子显微镜进行测定。研究发现,在 LaNiO3 中加入 B 位混合铁和 A 位混合锶可提高其 OER 活性,从而证实了镍基 OER 电催化剂中铁的活性增强效应。为了便于催化剂的技术应用,电极的制备方法是在工业相关基底镍金属上涂覆包晶油墨,然后进行煅烧。
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
Fuel Cells
Fuel Cells 工程技术-电化学
CiteScore
5.80
自引率
3.60%
发文量
31
审稿时长
3.7 months
期刊介绍: This journal is only available online from 2011 onwards. Fuel Cells — From Fundamentals to Systems publishes on all aspects of fuel cells, ranging from their molecular basis to their applications in systems such as power plants, road vehicles and power sources in portables. Fuel Cells is a platform for scientific exchange in a diverse interdisciplinary field. All related work in -chemistry- materials science- physics- chemical engineering- electrical engineering- mechanical engineering- is included. Fuel Cells—From Fundamentals to Systems has an International Editorial Board and Editorial Advisory Board, with each Editor being a renowned expert representing a key discipline in the field from either a distinguished academic institution or one of the globally leading companies. Fuel Cells—From Fundamentals to Systems is designed to meet the needs of scientists and engineers who are actively working in the field. Until now, information on materials, stack technology and system approaches has been dispersed over a number of traditional scientific journals dedicated to classical disciplines such as electrochemistry, materials science or power technology. Fuel Cells—From Fundamentals to Systems concentrates on the publication of peer-reviewed original research papers and reviews.
文献相关原料
公司名称 产品信息 采购帮参考价格
×
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:481959085
Book学术官方微信