Ni0.3Co2.7O4 spinel particles/polypyrrole composite electrode: Study by X-ray photoelectron spectroscopy
Description
In this work we have studied the multilayered polypyrrole/oxide composite electrode on glassy carbon having the structure GC/PPy/PPy(Ni0.3Co2.7O4)/PPy, in which the spinel oxide Ni0.3Co2.7O4 is known to be an electrocatalyst of the oxygen reduction reaction in alkaline medium. The successive GC/PPy, GC/PPy/PPy(Ni0.3Co2.7O4) and GC/PPy/PPy(Ni0.3Co2.7O4)/PPy parts of the electrode were examined by X-ray photoelectron spectroscopy. The results indicate that the electronic structure of the PPy is independent of the thickness of the PPy used to prepare the electrodes. The XPS data also show that cobalt is present in both divalent and trivalent states. The PPy doping degree by Cl- ions (in terms of the Cl-/N) and the oxide/PPy mass ratio observed by XPS were 19 and 4.5%, respectively
Additional details
Identifiers
- PII
- S0013468602005145;
Publishing Information
- Journal Title
- Electrochimica Acta
- Journal Volume
- 48
- Journal Issue
- 2
- Journal Page Range
- p. 119-125
- ISSN
- 0013-4686
- CODEN
- ELCAAV
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 38008428
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- CHLORINE IONS; COBALT OXIDES; ELECTRODES; ELECTRONIC STRUCTURE; NICKEL OXIDES; ORGANIC POLYMERS; OXYGEN; PYRROLES; REDUCTION; SPINELS; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- AZOLES; CHALCOGENIDES; CHARGED PARTICLES; CHEMICAL REACTIONS; COBALT COMPOUNDS; ELECTRON SPECTROSCOPY; ELEMENTS; HETEROCYCLIC COMPOUNDS; IONS; MINERALS; NICKEL COMPOUNDS; NONMETALS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; OXIDE MINERALS; OXIDES; OXYGEN COMPOUNDS; PHOTOELECTRON SPECTROSCOPY; POLYMERS; SPECTROSCOPY; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2002 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.