Long-Term Stability of Ni-Sn-Fe-Based Coatings Prepared by Electrodeposition for the Oxygen Evolution Reaction

IF 1.9
Nobuhiro Nakamura, Wataru Fujita, Takehiko Muranaka, Masaharu Nakayama
{"title":"Long-Term Stability of Ni-Sn-Fe-Based Coatings Prepared by Electrodeposition for the Oxygen Evolution Reaction","authors":"Nobuhiro Nakamura, Wataru Fujita, Takehiko Muranaka, Masaharu Nakayama","doi":"10.1149/2754-2734/acfe8d","DOIUrl":null,"url":null,"abstract":"A coating comprising Ni, Sn, and Fe was deposited on a Ni mesh by cathodic polarization from a bath containing Ni 2+ , Sn 2+ , and Fe 3+ salts in solution, and the oxygen evolution reaction properties of the thus obtained electrode were investigated. The lattice volume of the Ni–Sn–Fe-based coating was estimated to be 77.1 Å 3 , a much larger value than that (44.0 Å 3 ) of the Ni–Fe-based coating obtained in the absence of Sn 2+ . The Ni–Sn–Fe-coated electrode manufactured by cathodic polarization at a current density of −120 mA cm −2 afforded a current density of 10 mA cm −2 at an overpotential of 276 mV in 1 M KOH. The said electrode’s Tafel slope was estimated to be 37 mV dec −1 . When electrolyzed at constant current density (+50 mA cm −2 to +800 mA cm −2 ), it exhibited a stable potential for at least 162 h. The Ni–Sn–Fe-coated electrode was also used as the anode in a two-electrode cell (80 °C; 30 wt% KOH) and electrolyzed for 3 d. Evidence indicated a low cell voltage of 1.81 V at a current density of +600 mA cm −2 , which is at an industrial level.","PeriodicalId":338397,"journal":{"name":"ECS Advances","volume":"60 1","pages":"0"},"PeriodicalIF":1.9000,"publicationDate":"2023-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ECS Advances","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1149/2754-2734/acfe8d","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

A coating comprising Ni, Sn, and Fe was deposited on a Ni mesh by cathodic polarization from a bath containing Ni 2+ , Sn 2+ , and Fe 3+ salts in solution, and the oxygen evolution reaction properties of the thus obtained electrode were investigated. The lattice volume of the Ni–Sn–Fe-based coating was estimated to be 77.1 Å 3 , a much larger value than that (44.0 Å 3 ) of the Ni–Fe-based coating obtained in the absence of Sn 2+ . The Ni–Sn–Fe-coated electrode manufactured by cathodic polarization at a current density of −120 mA cm −2 afforded a current density of 10 mA cm −2 at an overpotential of 276 mV in 1 M KOH. The said electrode’s Tafel slope was estimated to be 37 mV dec −1 . When electrolyzed at constant current density (+50 mA cm −2 to +800 mA cm −2 ), it exhibited a stable potential for at least 162 h. The Ni–Sn–Fe-coated electrode was also used as the anode in a two-electrode cell (80 °C; 30 wt% KOH) and electrolyzed for 3 d. Evidence indicated a low cell voltage of 1.81 V at a current density of +600 mA cm −2 , which is at an industrial level.
析氧反应制备ni - sn - fe基镀层的长期稳定性
在含有Ni 2+、Sn 2+和fe3 +盐的溶液中,通过阴极极化在Ni网上沉积了Ni、Sn和Fe镀层,并研究了该镀层的析氧反应性能。ni - Sn - fe基镀层的晶格体积为77.1 Å 3,远高于无Sn 2+时ni - fe基镀层的晶格体积(44.0 Å 3)。阴极极化制备的ni - sn - fe包覆电极在- 120 mA cm - 2的电流密度下,在1 M KOH的过电位为276 mV时,电流密度为10 mA cm - 2。所述电极的塔菲尔斜率估计为37 mV dec−1。在恒电流密度(+50 mA cm - 2至+800 mA cm - 2)下电解时,其电位稳定时间至少为162小时。ni - sn - fe涂层电极也用作双电极电池的阳极(80°C;30 wt% KOH),电解3天。有证据表明,在+600 mA cm - 2的电流密度下,电池电压低至1.81 V,处于工业水平。
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
自引率
0.00%
发文量
0
×
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
小红书