Metallic Glass Nanofoam Anode Catalysts for Anion-Exchange Membrane Water Electrolyzers

Qiurong Shi, Michael J. Zachman, Deborah J. Myers, Hui Xu, Gang Wu
{"title":"Metallic Glass Nanofoam Anode Catalysts for Anion-Exchange Membrane Water Electrolyzers","authors":"Qiurong Shi, Michael J. Zachman, Deborah J. Myers, Hui Xu, Gang Wu","doi":"10.1149/ma2023-01362068mtgabs","DOIUrl":null,"url":null,"abstract":"Alkaline anion-exchange membrane water electrolyzers (AEMWEs) for hydrogen production are now receiving intensive attention due to their feasibility to use sustainable, low-cost platinum group metal (PGM-free) catalysts. Although a variety of highly efficient PGM-free catalysts for the oxygen evolution reaction (OER) have been explored, few of them demonstrated satisfied performance in real AEMWEs due to the insufficient electrical conductivity and unfavorable interfaces with ionomers in 3D porous electrodes. Herein, we report a series of highly porous ternary NiFeM (M: Cu, Co, and Mn) metallic glassy catalysts featured with nanofoam network morphologies, which are composed of amorphous OER active metal oxide shells and highly electrically conductive metallic glass alloy cores. Due to these unique properties, these NiFeM nanofoam catalysts demonstrated promising OER activities and stabilities in the half-cell with aqueous alkaline electrolytes, especially at high potentials. We also examined their magnetic properties and found no direct correlation with measured OER activity. These ternary NiFeM catalysts are further integrated with unique ionomers and AEMs to fabricate AEMWEs, showing superior performance to binary NiFe and commercial IrO 2 catalysts when utilizing diluted KOH electrolytes. A different trend was identified when directly using desirable but challenging pure water, and the NiFeCu catalyst performed the best comparable to IrO 2 especially at high current densities. Although deep understanding on limiting factor of pure water AEMWEs is still required, these NiFeM catalysts with favorable catalytic and morphological properties representing a new class of highly efficient PGM-free anode catalysts for viable AEMWEs toward clean hydrogen generation.","PeriodicalId":11461,"journal":{"name":"ECS Meeting Abstracts","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ECS Meeting Abstracts","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1149/ma2023-01362068mtgabs","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

Alkaline anion-exchange membrane water electrolyzers (AEMWEs) for hydrogen production are now receiving intensive attention due to their feasibility to use sustainable, low-cost platinum group metal (PGM-free) catalysts. Although a variety of highly efficient PGM-free catalysts for the oxygen evolution reaction (OER) have been explored, few of them demonstrated satisfied performance in real AEMWEs due to the insufficient electrical conductivity and unfavorable interfaces with ionomers in 3D porous electrodes. Herein, we report a series of highly porous ternary NiFeM (M: Cu, Co, and Mn) metallic glassy catalysts featured with nanofoam network morphologies, which are composed of amorphous OER active metal oxide shells and highly electrically conductive metallic glass alloy cores. Due to these unique properties, these NiFeM nanofoam catalysts demonstrated promising OER activities and stabilities in the half-cell with aqueous alkaline electrolytes, especially at high potentials. We also examined their magnetic properties and found no direct correlation with measured OER activity. These ternary NiFeM catalysts are further integrated with unique ionomers and AEMs to fabricate AEMWEs, showing superior performance to binary NiFe and commercial IrO 2 catalysts when utilizing diluted KOH electrolytes. A different trend was identified when directly using desirable but challenging pure water, and the NiFeCu catalyst performed the best comparable to IrO 2 especially at high current densities. Although deep understanding on limiting factor of pure water AEMWEs is still required, these NiFeM catalysts with favorable catalytic and morphological properties representing a new class of highly efficient PGM-free anode catalysts for viable AEMWEs toward clean hydrogen generation.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
阴离子交换膜水电解槽用金属玻璃纳米泡沫阳极催化剂
碱性阴离子交换膜水电解槽(AEMWEs)因其使用可持续、低成本的铂族金属(PGM-free)催化剂的可行性而受到广泛关注。尽管人们已经探索了各种用于析氧反应(OER)的高效无pgm催化剂,但由于其导电性不足以及在三维多孔电极中与离聚体的界面不利,很少有催化剂在实际的AEMWEs中表现出令人满意的性能。在此,我们报道了一系列具有纳米泡沫网络形态的高多孔三元NiFeM (M: Cu, Co和Mn)金属玻璃催化剂,它们由非晶OER活性金属氧化物壳和高导电性金属玻璃合金芯组成。由于这些独特的性质,这些NiFeM纳米泡沫催化剂在含碱性电解质的半电池中表现出了良好的OER活性和稳定性,特别是在高电位下。我们还检查了它们的磁性,发现与测量的OER活动没有直接关联。这些三元NiFeM催化剂进一步与独特的离聚体和AEMs相结合,制备了AEMWEs,在使用稀释的KOH电解质时,表现出比二元NiFe和商用io2催化剂更优越的性能。当直接使用理想但具有挑战性的纯水时,发现了不同的趋势,NiFeCu催化剂的表现与io2相比最好,特别是在高电流密度下。虽然对纯水AEMWEs的限制因素仍需深入了解,但这些具有良好催化性能和形态性能的NiFeM催化剂代表了一类高效的无pgm阳极催化剂,可用于清洁制氢的AEMWEs。
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Redox Tolerant Solid Oxide Electrolysis Cathode for CO2 and Steam (Keynote) Releasing the Bubbles: Efficient Phase Separation in (Photo-)Electrochemical Devices in Microgravity Environment Phase Stability of SrTi1-XFexO3- δ Under Solid Oxide Cell Fuel-Electrode Conditions: Implications for Related Exsolution Electrode Materials Long-Term Stability of Perovskite-Based Fuel Electrode Material Sr2Fe2-XMoxO6-δ – GDC for Enhanced High-Temperature Steam and CO2 Electrolysis GC:BiFE As an Useful Tool for the Quantification of Health Harmful Organic Compounds in Artisanal Spiritus Beverages Via ADSV
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1