In-situ localized pH, pNa and dissolved O2 measurements during charge-discharge of mixed Ni–Co hydroxide electrodes
ADÁN-MÁS, Alberto
Centro de Quimica Estrutural [CQE]
Institut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
Voir plus >
Centro de Quimica Estrutural [CQE]
Institut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
ADÁN-MÁS, Alberto
Centro de Quimica Estrutural [CQE]
Institut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
Centro de Quimica Estrutural [CQE]
Institut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
GUERLOU-DEMOURGUES, Liliane
Réseau sur le stockage électrochimique de l'énergie [RS2E]
Institut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
< Réduire
Réseau sur le stockage électrochimique de l'énergie [RS2E]
Institut de Chimie de la Matière Condensée de Bordeaux [ICMCB]
Langue
en
Article de revue
Ce document a été publié dans
Journal of The Electrochemical Society. 2020, vol. 167, n° 8, p. 080511
Electrochemical Society
Résumé en anglais
This work reports, for the first time, the use of ion-selective localized electrochemical techniques to elucidate the charge-discharge mechanism of nickel-cobalt hydroxide electrodes for electrochemical energy storage. The ...Lire la suite >
This work reports, for the first time, the use of ion-selective localized electrochemical techniques to elucidate the charge-discharge mechanism of nickel-cobalt hydroxide electrodes for electrochemical energy storage. The charge-discharge mechanism of electrodeposited nickel-cobalt hydroxide electrodes was studied in Na2SO4 0.05 M by localized in situ measurements of pH, pNa and dissolved O2 during cyclic voltammetry. Local pH and pNa distributions were recorded using micro-potentiometric sensors with liquid membrane, while dissolved O2 was monitored using a fiber-optic microsensor. These original results highlight how localized potentiometry can provide new insights to better understand the charge mechanism of metal (hydr)oxide electrodes by directly measuring the concentrations/activities of relevant species at the electrode-electrolyte interface during charge-discharge.< Réduire
Origine
Importé de halUnités de recherche