The hydrogen evolution reaction of HCOOH, CH 3 COOH, and C 2 H 5 COOH solutions consists of two different reduction processes depending on the evaluated potential region; (1) independent reduction of RCOOH and (2) simultaneous reduction of RCOOH and H 2 O. The reduction of each carboxylic acid generates an apparent convective diffusion-controlled limiting current. The first achievement of the present study is that by using a rotating disk electrode (RDE) and a sinusoidal hydrodynamic modulated-rotating disk electrode (SHM), it was elucidated that the additive property of the reduction currents of RCOOH and H 2 O was not effective, and the convective-diffusion current was successfully distinguished from the total current. The second achievement is the successful analysis of the rotation-speed dependency of the limiting current in RDE and SHM using a modified theory of the Koutecky-Levich equation. The slopes of the plots for each carboxylic acid increased in the following sequence: RDE, SHM ( p = 0.05), and SHM ( p = 0.24), which is consistent with the theory. The dissociation rates of the carboxylic acids and the reverse recombination rate were calculated.
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Kanzaki et al. (2014) studied this question.
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