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研究论文

Ni-Ru-Ir氧化物阴极涂层的析氢活性

  • 付银辉 ,
  • 黎学明 ,
  • 李武林
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  • 重庆大学化学化工学院;

收稿日期: 2010-05-28

  修回日期: 2010-05-28

  网络出版日期: 2010-05-28

Hydrogen Evolution Reaction Activtity of Ni-Ru-Ir Oxide Cathode Coating

  • FU Yin-hui ,
  • LI Xue-ming ,
  • LI Wu-lin
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  • ( College of Chemistry and Chemical Engineering,Chongqing University,Chongqing 400030,China

Received date: 2010-05-28

  Revised date: 2010-05-28

  Online published: 2010-05-28

摘要

应用热分解氧化法制备Ni-Ru-Ir氧化物活性阴极.循环伏安、Tafel曲线及计时电流测试表明,在90℃、30%(bymass)的NaOH溶液中,电流密度0.3A·cm-2条件下,Ru∶Ir质量比为1∶1的Ni-Ru-Ir氧化物电极的析氢过电位比Ni电极低300mV;表面粗糙度是Ni网电极的32倍;交换电流密度是Ni网电极的4倍;其析氢性能显然远优于Ni网电极,有望应用于氯碱工业以期降低能耗.

本文引用格式

付银辉 , 黎学明 , 李武林 . Ni-Ru-Ir氧化物阴极涂层的析氢活性[J]. 电化学, 2010 , 16(2) : 202 -205 . DOI: 10.61558/2993-074X.3344

Abstract

The Ni-Ru-Ir electrode coating was fabricated by thermal decomposition and oxidation. Electrochemical properties of Ni-Ru-Ir electrode coating and pure nickel cathode in the 30% NaOH solutions at 90 ℃( conditions of the industrial electrolysis) ,have been investigated by cyclic voltammetry,Tafel curves and chronoamperometry. The results show that the Ni-Ru-Ir oxide electrode coating exhibited high catalytic activity. At the current density of 0. 3 A·cm-2,the lowest hydrogen evolution overpotential of Ni-Ru-Ir oxide electrode coating was about 300 mV lower than Ni. The roughness and excharge current density of Ni-Ru-Ir electrode coating were 32 and 4 times,respectively,larger than those of pure nickel cathode. Hence,the Ni-Ru-Ir oxide electrode is expected to be able to reduce energy consumption of chlor-alkali industry.

参考文献

[1]Antonio A L,Bargioni C,Luciano I,et al.EIS study of the service life of activated cathodes for the hydrogen e-volution reaction in the chlor-alkali membrane cell process[J].Electrochimica Acta,2008,53(25):7410-7416. [2]Chiaki Iwakura,Masashi Tanaka,Shuji Nakamatsu,et al.Electrochemical properties of Ni/(Ni+RuO2)ac-tive cathodes for hydrogen evolution in chlor-alkali elec-trolysis[J].Electrochimica Acta,1995,40(8):977-982. [3]Shibli S M A,Dilimon V S.Development of TiO2-sup-ported nano-RuO2-incorporated catalytic nickel coating for hydrogen evolution reaction[J].International Journal of Hydrogen Energy,2008,33(4):1104-1111. [4]Xu Li-kun,Xin Yonglei,Wang Juntao.A comparative study on IrO2-Ta2O5coated titanium electrodes prepared with different methods[J].Electrochimica Acta,2008,54(6):1820-1825. [5]JI Lei(稽雷),WANG Jun-tao(王均涛),LIU Wen-bin(刘文斌),et al.The effect of Ru∶Sn on properties of Ru-Ir-Sn ox ide anode coatings[J].Electrochemistry(电化学),2008,14(3):263-267. [6]Lourdes Vázquez-Gómez,Sandro Cattarin,Paolo Guerri-ero.Preparation and electrochemical characterization of Ni+RuO2composite cathodes of large effective area[J].Electrochimica Acta,2007,52(28):8055-8063. [7]Pani V,Dekanski A,Milonji S,et al.The influence of the aging time of RuO2and TiO2sols on the electro-chemical properties and behavior for the chlorine evolu-tion reaction of activated titanium anodes obtained by the sol-gel procedure[J].Electrochimica Acta,2000,46(2/3):415-421. [8]Zeng Yi,Chen Kangning,Wu Wei,et al.Effect of IrO2loading on RuO2-IrO2-TiO2anodes:A study of micro-structure and working life for the chlorine evolution re-action[J].Ceramics International,2007,33(6):1087-1091.
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