应用射频反应磁控溅射法制备阳极催化氧化铁镍薄膜,由循环伏安、线性扫描伏安、极化曲线和电化学交流阻抗谱等研究发生在该电极上的氧化反应.结果表明,作为活化中心的铁能使过电势降低,并且随着溅射过程氧流量的增加催化性能增强,铁的掺入使得速率限定步骤由OH-的释放变为氧原子的结合.与镍相比,氧化铁镍是更理想的催化阳极材料,当电流密度为50 mA/cm2时,其氧的过电势比镍的下降了500 mV.
In this paper,the iron-doped nickel oxide thin film as anode catalyst was prepared by RF reactivesputtering method.The oxygen evolution reaction(OER) on the iron-doped nickel oxide was investigated withcyclic voltammetry,liner sweep voltammetry,polarization curves and electrochemical impedance spectroscopy.Results showthat the iron acts as active site in the film which makes the overpotential lower,and changes therate-limiting from primary discharge of OH-ions to the recombination of oxygen atom.With the increasing of ox-ygen content in flu ratio during sputtering,the electrocatalytic activities of the film increase.Iron-doped nickeloxide thin film is promising material as OER electrocatalyst for hydrogen production than the nickel electrode.The oxygen overpotential on the film was over 500 mV lower than the overpotential with nickel at50mA/cm2.
[1]Barreto L,Makihira A,Riahi K.The hydrogen econo-my in the 21stcentury:a sustainable development scena-rioc[J].Int.J.Hydrogen Energy,2003,28:267.
[2]Midilli A,Dincer I,Rosen M A.On hydrogen and hy-drogen energy strategies II:future projections affectingglobal stability and unrest[J].Renew.Sust.EnergyRev.,2005,9:273.
[3]Massimo S,Mickele C,Sara M.Design and analysis ofstand-alone hydrogen energy systems with different re-newable sources[J].Int.J.Hydrogen Energy,2004,29:1571.
[4]Tsuneo H.Research and development of internationalclean energy network using hydrogen energy(WE-NET)[J].Int.J.Hydrogen Energy,2002,27:115.
[5]Seth D.Hydrogen futures:toward a sustainable energysystem[J].Int.J.Hydrogen Energy,2002,27:235.
[6]Bak T,Nowotny J,Rekas M,et al.Photo-electrochem-ical hydrogen generation from water using solar energy[J].Int.J.Hydrogen Energy,2002,27:991.
[7]Trasatti S.Electrocatalysis in the anodic evolution of ox-ygen and chlorine[J].Electrochimica Acta,1983,29:1503.
[8]Suredini HB,Cerne J L,Crnkovic F C,et al.Recentdevelopments in electrode materials for water electrolysis[J].Int.J.Hydrogen Energy,2000,25:415.
[9]Tiwari S K,Chartier P,Singh R N.Preparation of per-ovskite-type oxides of cobalt by the malic acid aidedprocess and their electrocatalytic surface properties inrelation to oxygen evolution[J].J.Electrochem.Soc.,1995,142:148.
[10]Kibria M F,Mridha M SH.Electrochemical studies ofthe nickel electrode for the oxygen evolution reaction[J].Int.J.Hydrogen Energy,1996,21:179.
[11]Choquette Y,Brossard L,Lasia A,et al.Investigationof hydrogen evolution on raney-nickel composite-coatedelectrodes[J].Electrochimica Acta.,1990,35:1251.
[12]Choquette Y,Menard H,Brossard L,Electrocatalyticperformance of composite-coated electrodes for alkalinewater electrolysis[J].Int.J.Hydrogen Energy,1990,15:21.
[13]Kamnev AA,Ezhov B B.Electron spectroscopy of solu-ble anodic oxidation products of iron in alkaline solu-tions[J].Soviet Electrochemistry,1989,24:1027.
[14]Corrigan D.The catalysis of the oxygen evolution reac-tion by iron impurities in thin film nickel oxide elec-trodes[J].J.Electrochem.Soc.,1987,134(2):377.