An improvement on redox reversibility of cobalt oxyhydroxide in nickel hydroxide electrodes
Creators
- 1. Henan Provincial Key Laboratory of Surface and Interface, Zhengzhou University of Light Industry, Zhengzhou 450002 (China)
Description
In this paper, two kinds of cobalt oxyhydroxide conductive networks were introduced into nickel hydroxide electrodes by different methods-electrochemically-oxidized (EO) or chemically oxidized (CO) CoOOH on the surface of nickel hydroxide particles. The redox behaviors of them were studied by using cyclic voltammetry (CV) and X-ray diffraction (XRD) measurements. It shows that because CoOOH(CO) has better redox reversibility than CoOOH(EO), the structure of the former can be kept when nickel hydroxide electrodes are subjected to a negative potential. Thus, 98.5% capacity retention is demonstrated on nickel/metal-hydride (Ni-MH) batteries with CoOOH(CO) after being imposed over-discharge state storage; on the contrary, only 81.4% capacity retention is found on the batteries with CoOOH(EO)
Availability note (English)
Available from http://dx.doi.org/10.1016/j.matchemphys.2008.04.020Additional details
Identifiers
- DOI
- 10.1016/j.matchemphys.2008.04.020;
- PII
- S0254-0584(08)00217-4;
Publishing Information
- Journal Title
- Materials Chemistry and Physics
- Journal Volume
- 111
- Journal Issue
- 2-3
- Journal Page Range
- p. 331-334
- ISSN
- 0254-0584
- CODEN
- MCHPDR
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 40019767
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- COBALT COMPOUNDS; ELECTRIC BATTERIES; ELECTROCHEMISTRY; ELECTRODES; NICKEL HYDROXIDES; OXIDATION; VOLTAMETRY; X-RAY DIFFRACTION
- Descriptors DEC
- CHEMICAL REACTIONS; CHEMISTRY; COHERENT SCATTERING; DIFFRACTION; ELECTROCHEMICAL CELLS; ENERGY STORAGE SYSTEMS; ENERGY SYSTEMS; HYDROGEN COMPOUNDS; HYDROXIDES; NICKEL COMPOUNDS; OXYGEN COMPOUNDS; SCATTERING; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.