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January 1, 1966Journal of The Electrochemical Society236 citations

Periodic Variation of Exchange Current Density of Hydrogen Electrode Reaction with Atomic Number and Reaction Mechanism

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HKHideaki Kita

Key Points

  • To investigate the periodic dependence of hydrogen electrode reaction rates on atomic number and assess the underlying reaction mechanisms across different metal classes.
  • Surveyed reported activity data (exchange current density, log i0) for the hydrogen electrode reaction across elements in each long period.
  • Analyzed correlations between exchange current density, heat of adsorption, and work function for transition and post-transition metals.
  • Hydrogen electrode activity (log i0) exhibits periodic variation with atomic number across each long period, demonstrating that bulk electrode properties govern activity.
  • For transition metals, log i0 decreases linearly with heat of adsorption and increases linearly with work function, consistent with a catalytic mechanism.
  • For post-transition ascending metals, log i0 remains unchanged with variation in heat of adsorption and work function, interpreted via an electrochemical mechanism.

Abstract

A survey of recent results shows that the activity log io is a periodic function of the atomic number for each long period. It is concluded that the bulk properties of electrode dominate its activity. Also, log io decreases l inearly with heat o ~ adsorption or increases l inearly with work function for the transition metals, but remains unchanged for the metals following them (the ascending metals). These relations are qualitatively interpreted by the catalytic and the electrochemical mechanism for the transition and the ascend-ing metals, respectively. The hydrogen electrode reaction 2H + 4- 2e- = He 1 is one of the simplest and the most fundamental ly important reactions among various kinds of hetero-geneous catalyses, and its solid understanding would be a milestone in the approach toward complicated

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Cite This Study

Hideaki Kita (1966) studied this question.

synapsesocial.com/papers/6a128852c031bb6829a6d1fdhttps://doi.org/10.1149/1.2423772
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