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Understanding the surface state and proton adsorption phenomena on ni-based alloys at the hydrogen evolution zone in alkaline medium by EIS-XPS

机译:通过EIS-XPS了解在碱性介质中氢释放区的镍基合金的表面状态和质子吸附现象

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摘要

In this work, well-defined Ni-based alloys, labeled M1 (Ni_(0.8)CoO_(0.1)Zn_(0.05)MnO_(0.02)Ti_(0.01)Y_(0.01)Al_(0.01)) and M2 (NiO_(0.8)CoO_(0.1)Zn_(0.05)MnO_(0.02)Ti_(0.01)Y_(0.01)Al_(0.01)), were prepared by ball-milling technique and used as electrodes for the generation of hydrogen. Electrochemical Impedance Spectroscopy (EIS) and X-ray photoelectron spectroscopy (XPS) were employed in order to understand the surface state and proton adsorption phenomena during cathodic polarization. It was found that high concentration species such as NiO and/or Ni(OH)_2 induces passivation effect, suppressing the HER by increasing the electrode resistance. The charge transfer, double layer capacitance and adsorption of protons toward the electrode interface ware found to be highly controlled by the intrinsic nature of the alloy in turn.
机译:在这项工作中,定义明确的Ni基合金被标记为M1(Ni_(0.8)CoO_(0.1)Zn_(0.05)MnO_(0.02)Ti_(0.01)Y_(0.01)Al_(0.01))和M2(NiO_(0.8通过球磨技术制备了CoO_(0.1)Zn_(0.05)MnO_(0.02)Ti_(0.01)Y_(0.01)Al_(0.01)),并用作产生氢的电极。为了了解阴极极化过程中的表面状态和质子吸附现象,采用了电化学阻抗谱(EIS)和X射线光电子能谱(XPS)。发现高浓度物质如NiO和/或Ni(OH)_2诱导钝化作用,通过增加电极电阻来抑制HER。电荷转移,双层电容和质子向电极界面的吸附依次受合金的内在特性控制。

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