English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse
  1. View item / 
  2. Item Summary

Item

ITEM ACTIONSEXPORT
Add to Basket
  Local TagsRelease HistoryDetailsSummary

Released
Journal Article

Structure and activity relations in the hydrogen peroxide reduction at silver electrodes in alkaline NaF/NaOH electrolytes

MPS-Authors
/persons/resource/persons22054

Savinova,  Elena R.
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons22221

Wasle,  Sabine
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons21471

Doblhofer,  Karl
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)
There are no public fulltexts stored in PuRe
Supplementary Material (public)
There is no public supplementary material available
Citation

Savinova, E. R., Wasle, S., & Doblhofer, K. (1998). Structure and activity relations in the hydrogen peroxide reduction at silver electrodes in alkaline NaF/NaOH electrolytes. Electrochimica Acta, 44(8-9), 1341-1348. doi:10.1016/S0013-4686(98)00256-4.


Cite as: https://hdl.handle.net/21.11116/0000-0006-F9D9-D
Abstract
The electrochemical interface between polycrystalline silver and alkaline NaF/NaOH electrolytes at various pH values has been studied by means of cyclic voltammetry and ac-impedance spectroscopy. Hydroxide electrochemisorption has been observed in a wide potential range (between −1.1 and 0 V SCE depending upon pH). Study of the hydrogen peroxide reduction at silver rotating-disc electrodes in alkaline NaF/NaOH electrolytes has proved the existence of a slow chemical step in the reaction mechanism, its rate being strongly affected by the submonolayer surface oxidation. The reaction scheme is proposed for the hydrogen peroxide reduction, which takes into consideration the structure of the adsorbate layer at the electrode/electrolyte interface at the variable potential.