Published May 25, 2006 | Version v1
Journal article

Inherent emf relaxation of electrochemical cells with nanocrystalline Ag electrodes

  • 1. Max-Planck-Institute for Solid State Research, Heisenbergstrasse 1, D-70569 Stuttgart (Germany)
  • 2. University of Leoben, Department of General, Analytical and Physical Chemistry, Franz-Josef-Strasse 18, A-8700 Leoben (Austria)

Description

The open circuit voltage of the electrochemical cell Ag (nano)|solid silver electrolyte|Ag (macro) is found to be inherently unstable. Even under conditions which support the morphological stability of the arrangement of nanocrystalline silver, the particles grow significantly as soon as they function as electrodes; i.e. when they are in contact with a silver electrolyte and connected electronically at the same time. The process is shown to be due to electrochemical Ostwald ripening with the interfacial transfer of Ag+ through the Ag/electrolyte interface being the rate limiting step. Its activation energy is 0.01 eV. The decay is in good agreement with modelling results

Additional details

Identifiers

DOI
10.1016/j.electacta.2005.11.048;
PII
S0013-4686(05)01341-1;

Publishing Information

Journal Title
Electrochimica Acta
Journal Volume
51
Journal Issue
20
Journal Page Range
p. 4176-4181
ISSN
0013-4686
CODEN
ELCAAV

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
38016354
Subject category
S36: MATERIALS SCIENCE;
Descriptors DEI
ACTIVATION ENERGY; CRYSTALS; ELECTROCHEMICAL CELLS; ELECTRODES; GRAIN GROWTH; MILLI EV RANGE; NANOSTRUCTURES; RELAXATION; SILVER; SILVER IONS; SOLID ELECTROLYTES
Descriptors DEC
CHARGED PARTICLES; ELECTROLYTES; ELEMENTS; ENERGY; ENERGY RANGE; IONS; METALS; TRANSITION ELEMENTS

Optional Information

Copyright
Copyright (c) 2005 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.