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.