TIME-RESOLVED INVESTIGATION OF THE HYDROGEN EVOLUTION REACTION ON AG(111), AG(100), SMOOTH POLYCRYSTALLINE, AND ACTIVATED POLYCRYSTALLINE SILVER SURFACES
D. Diesing et al., TIME-RESOLVED INVESTIGATION OF THE HYDROGEN EVOLUTION REACTION ON AG(111), AG(100), SMOOTH POLYCRYSTALLINE, AND ACTIVATED POLYCRYSTALLINE SILVER SURFACES, Physica status solidi. a, Applied research, 159(1), 1997, pp. 243-254
Experiments on the hydrogen evolution by hot electrons at activated si
lver top electrodes of metal/insulator/metal (MIM) junctions demonstra
ted the existence of a transient adsorbed hydrogen species at the silv
er electrolyte interface. In the present work we investigated the hydr
ogen evolution on Ag(lll): Ag(100), smooth polycrystalline, and activa
ted silver surfaces in neutral and acid elec trolytes with the help of
cyclovoltammograms and potentiostatic current transients after cathod
ic potential pulses. In neutral electrolytes the hydrogen overpotentia
l of kg(100) was found to be 90 mV more negative compared to Ag(lll).
No difference was found under acid conditions (pH = 1). After cathodic
pulses a transient hydrogen oxidation reaction was observed for the f
irst time on activated silver surfaces in neutral electrolytes. The de
resistance of Ag(100) thin film electrodes is very little influenced
by the hydrogen evolution reaction, compared to the increase induced b
y the adsorption of perchlorate.