Abstract

Kinetics of the oxygen evolution reaction on rhodium electrodes with different electrocatalytic activity

Highlights

  • Instituto de Investigaciones Fisicoquimicas TeOricas y Aplicadas. (INIFTA), DivisiOn Electroquimica, Sucursal 4 --Casilla de Correo 16 (1900), La Plata (Argentina)

  • It has recently been demonstrated [1] that the potentiodynamic behaviour of Rh/H2SO4(aq) interphases in the potential range of the thermodynamic stability of bulk water is associated with at least two-well defined and different electrochemical characteristics of rhodium, which were referred to as Aand B-type Rh electrodes [ 1 ]

  • The aim of the present report is to show the electrocatalytic difference of A- and B-type electrodes for the 02 evolution reaction, on the basis that the corresponding structures of the electrodes remain stable during the time the electrochemical measurements last

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Summary

Short communication

Instituto de Investigaciones Fisicoquimicas TeOricas y Aplicadas. (INIFTA), DivisiOn Electroquimica, Sucursal 4 --Casilla de Correo 16 (1900), La Plata (Argentina). The A-type Rh electrodes are characterized by an Eli potentiodynamic profile in the 0--1.60 V range (vs RHE), which involves the already known contributions of the H-electrosorption/H-electrodesorption (0.0--0.24 V)and the O-electrosorption/O-electrodesorption (0.6--1.6 V) (Fig. 1) These electrodes were first subjected to repetitive triangular potential sweeps (RTPS) in the 0---1.60 V range at one preset potential sweep rate (v) in the 0.03 V s -1 ~< v ~< 0.3 V s-' range in order to attain a stabilized E / / display. These electrodes are characterized by a stabilized potentiodynamic Eli profile, including a fast response conjugated redox system in the 1.54--1.66 V range Once this situation has been attained v is changed from 80 to 0.03 V s -1 ~< v ~< 0.3 V s -I and the anodic potential limit is extended to 1.9 V (Fig. 1) to cover a part of the 02 evolution potential range.

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