Co-Electrodeposition and Characterization of Ni+RuO2 Nano-Electrocatalyst for Hydrogen Evolution in Chlor-Alkali Process

F. Mohammadi, R. Zandi-zand, M. Yousefi
{"title":"Co-Electrodeposition and Characterization of Ni+RuO2 Nano-Electrocatalyst for Hydrogen Evolution in Chlor-Alkali Process","authors":"F. Mohammadi, R. Zandi-zand, M. Yousefi","doi":"10.1109/NEMS.2006.334711","DOIUrl":null,"url":null,"abstract":"(Ni+RuO2)/Ni active cathodes were prepared by electrochemical co-deposition of suspended RuO2 particles along with Ni2+ ions onto Ni substrates from an electrolyte solution (Watt bath). Morphology and composition of the cathodes were investigated by SEM and EDX analysis. The observations revealed the RuO 2-Ni layers covered by cauliflower-like particles which distributed homogeneously on the Ni substrate. Particle size and distribution of RuO2 particles in suspension and on the cathode surface were studied by light scattering (LS) and X-ray map techniques, respectively. The LS results revealed a Gaussian distribution with an average RuO2 particle size of 527nm in suspension while X-ray map showed a non-uniform nano particle size distribution below 100 nm. Electrochemical activity of the cathodes were evaluated by linear sweep voltametry (LSV) and the results showed that the enhanced activity of the cathodes were mainly ascribable to the RuO 2 content or the increase in the active sites. The effect of Ni substrates pre-treatment on activity and morphology of prepared cathodes showed morphology changes and enhanced effect on electrochemical activity of the cathodes","PeriodicalId":6362,"journal":{"name":"2006 1st IEEE International Conference on Nano/Micro Engineered and Molecular Systems","volume":"43 1","pages":"1258-1262"},"PeriodicalIF":0.0000,"publicationDate":"2006-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"2006 1st IEEE International Conference on Nano/Micro Engineered and Molecular Systems","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/NEMS.2006.334711","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

(Ni+RuO2)/Ni active cathodes were prepared by electrochemical co-deposition of suspended RuO2 particles along with Ni2+ ions onto Ni substrates from an electrolyte solution (Watt bath). Morphology and composition of the cathodes were investigated by SEM and EDX analysis. The observations revealed the RuO 2-Ni layers covered by cauliflower-like particles which distributed homogeneously on the Ni substrate. Particle size and distribution of RuO2 particles in suspension and on the cathode surface were studied by light scattering (LS) and X-ray map techniques, respectively. The LS results revealed a Gaussian distribution with an average RuO2 particle size of 527nm in suspension while X-ray map showed a non-uniform nano particle size distribution below 100 nm. Electrochemical activity of the cathodes were evaluated by linear sweep voltametry (LSV) and the results showed that the enhanced activity of the cathodes were mainly ascribable to the RuO 2 content or the increase in the active sites. The effect of Ni substrates pre-treatment on activity and morphology of prepared cathodes showed morphology changes and enhanced effect on electrochemical activity of the cathodes
氯碱析氢Ni+RuO2纳米电催化剂的共电沉积及表征
在电解液(瓦特浴)中,将悬浮的RuO2颗粒与Ni2+离子电化学共沉积在Ni衬底上,制备了(Ni+RuO2)/Ni活性阴极。通过扫描电镜和EDX分析研究了阴极的形貌和组成。观察发现,在Ni衬底上均匀分布着由菜花状颗粒覆盖的tio2 -Ni层。利用光散射(LS)和x射线图技术分别研究了悬浮体和阴极表面RuO2颗粒的粒径和分布。LS结果显示,悬浮颗粒的平均粒径为527nm,呈高斯分布;x射线图显示,悬浮颗粒的粒径分布在100 nm以下,呈非均匀分布。用线性扫描伏安法(LSV)评价了阴极的电化学活性,结果表明阴极活性的增强主要是由于氧化锆含量的增加或活性位点的增加。Ni衬底预处理对阴极活性和形貌的影响表明,制备的阴极形貌发生了变化,对阴极电化学活性的影响增强
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:481959085
Book学术官方微信