CuO cathode in lithium cells—III. Its discharge kinetics
✍ Scribed by Petr Novák
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- English
- Weight
- 496 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0013-4686
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✦ Synopsis
The kinetics of discharge of CuO cathode was followed in 1 M LiCIO, in propylene carbonate. The cathode intercalation reaction is probably accompanied by several parallel and follow-up reactions. The reduction of CuO is irreversible and is controlled by transport in solid phase at current densities j up to 0.04 mA cm '; a contribution of activation control sets in at higher current densities. The dependence of the closed circuit potential on j can formally be expressed by the Tafel equation E = A -B In 1 j I. NOMENCLATURE Tafel constant, V Tafel constant, V theoretical capacity of CuO, 0.674 Ah g I thickness of the CuO layer, pm closed circuit potential, V open circuit potential, V peak potential, V ohmic potential drop, V current density, mA cmez peak current density, mAcm_' charge delivered from unit geometric surface area of electrode, cm-* scan rate, mV mint number of atoms or electrons activation overpotential, V concentration overpotential at the time T after current interruption, V time, s rotation speed, min-1
📜 SIMILAR VOLUMES
Time resolved synchrotron X-ray powder diffraction methods have been used to study the kinetics of oxidation of lanthanum strontium manganates(III, IV) in a flow of oxygen. The process studied is La 1؊x Sr x MnO 3.00 ; /2O 2 La 1؊x Sr x MnO 3.00؉ (for x,00.0؍ 0.10, 0.15). A contraction of the unit