首页 | 本学科首页   官方微博 | 高级检索  
     检索      

Ni-S合金析氢阴极的制备研究
引用本文:司敬沛,张建民,黄伟庆.Ni-S合金析氢阴极的制备研究[J].信阳师范学院学报(自然科学版),2006,19(2):210-213.
作者姓名:司敬沛  张建民  黄伟庆
作者单位:郑州大学,化学系,河南,郑州450052
基金项目:教育部留学回国人员科研启动基金资助项目
摘    要:以硫脲作为硫源,在改进的瓦特镀液体系中用电沉积方法获得N i-S合金镀层,系统地研究了硫脲浓度、电流密度、电沉积时间、镀液温度、pH值、有机添加剂等实验条件对N i-S合金电极析氢活性的影响.用重量分析法测定电沉积层中硫的含量,X-射线衍射技术表征镀层的晶形结构,稳态恒流极化法研究N i-S合金层的电催化活性.实验结果表明,电沉积得到的析氢活性较好的镍硫合金为非晶态结构和弱晶结构,硫含量为11.59%(重量比)时,N i-S合金电极具有优良的电催化性能,且在长期电解条件下电极仍有良好的析氢活性.

关 键 词:电沉积  镍-硫电极  析氢反应
文章编号:1003-0972(2006)02-0210-04
收稿时间:2005-09-26
修稿时间:2005年9月26日

Study on Preparation of Ni-S Alloys as Hydrogen Evolution Reaction Cathodes
SI Jing-pei,ZHANG Jian-min,HUANG Wei-qing.Study on Preparation of Ni-S Alloys as Hydrogen Evolution Reaction Cathodes[J].Journal of Xinyang Teachers College(Natural Science Edition),2006,19(2):210-213.
Authors:SI Jing-pei  ZHANG Jian-min  HUANG Wei-qing
Institution:Department of Chemistry, Zhengzhou University, Zhengzhou 450052, China
Abstract:The coating of nickel-sulfur alloys was obtained by electrodeposition method in a modified Watts bath with thiourea as the sulfur source.The effects of experimental conditions,such as concentration of thiourea,current density, electroplating time,temperature,pH,organic additives,on the catalytic activity of Ni-S alloys for hydrogen evolution reaction were systematically studied. The sulfur content in electrodeposition coatings was analyzed by gravimetric method,the structure of Ni-S alloys was characterized by X-ray diffraction technique,and the electrocatalytic activity of nickel-sulfur electrode was measured by constant current steady polarization method.The results show that Ni-S electro deposits which have better HER activity were amorphous,the Ni-S alloy ele ctrode with sulfur content of 11.59 wt% performed excellent electrocatalytic property and lasts good activity for hydrogen evolution reaction during long-term electrolysis.
Keywords:electrodeposition  nickel-sulfur electrode  hydrogen evolution reaction
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号