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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

QCM-D studies of polypyrrole influence on structure stabilization of beta phase of Ni(OH)(2) nanoparticles during electrochemical cycling

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Author(s):
Miguel, Fernando H. C. [1] ; Benedetti, Tania M. [1] ; Torresi, Roberto M. [1] ; Cordoba de Torresi, Susana I. [1]
Total Authors: 4
Affiliation:
[1] Univ Sao Paulo, Inst Quim, BR-05513970 Sao Paulo - Brazil
Total Affiliations: 1
Document type: Journal article
Source: Electrochemistry Communications; v. 48, p. 164-168, NOV 2014.
Web of Science Citations: 4
Abstract

Pure beta badly crystallized, beta(bc)-Ni(OH)(2), and hybrid beta(bc)-Ni(OH)(2)/polypyrrole nanoparticles (NPs) were synthesized and immobilized by electrophoretic deposition. The influence of polypyrrole (Ppy) on the structural stability with cycling was evaluated by Quartz Crystal Microbalance with Dissipation. The results show that Ppy stabilizes the NP structure avoiding stress features provoked by the formation of gamma-NiOOH. Ppy remains oxidized during the entire process and, as it is doped with a big counter anion such as dodecylbenzenesulfonate (DBS-) which is not removed during cycling, avoids volumetric changes of Ni(OH)(2) leading to higher cyclability. (C) 2014 Elsevier B.V. All rights reserved. (AU)

FAPESP's process: 09/53199-3 - Molecular recognition and energy storage: fundamental studies concerning geometry, size and synthesis effects on the optimization of the chemical properties of electroactive materials
Grantee:Roberto Manuel Torresi
Support Opportunities: Research Projects - Thematic Grants
FAPESP's process: 12/02117-0 - Poly(ionic liquids) in electrochemical devices: polyelectrolytes for energy storage and conversion devices and stabilization of graphene and poly(3,4-etylenedioxidethiophene) (PEDOT) for electroactive films obtention
Grantee:Tania Machado Benedetti
Support Opportunities: Scholarships in Brazil - Post-Doctoral