Integral Role of the NiS Electrode/Electrolyte Interface in the Redox Reaction with Lithium

R. D. Apostolova, E. M. Shembel’, B. Markovsky, D. Aurbach

Research output: Contribution to journalArticlepeer-review

1 Scopus citations


Abstract: Electrochemically synthesized thin-layer NiS electrodes were studied in lithium perchlorate dissolved in 1.3-dioxolane or in a mixture of 1.3-dioxolane and tetrahydrofuran. In the 1.3-dioxolane 1 M LiClO4 electrolyte, the irreversible capacity was reduced by 20% сompared to the initial capacity. However, the stability of the electrochemical characteristics of NiS electrodes in redox reactions with lithium is unsatisfactory. Much better results of charge–discharge cycling of NiS electrodes were obtained in the electrolyte solutions of 1.3-dioxolane, tetrahydrofuran, and 1 M LiClO4 demonstrating a stable reversible capacity of 400–450 mAh/g during 50–75 cycles. Using the methods of electron microscopy and IR spectroscopy with Fourier transform, it was established that the reason for the discharge capacity fading of NiS electrodes was associated with the formation of a surface film, which reduces the adhesion and cohesion of NiS particles. This, in turn, leads to a loss in the mechanical strength of NiS electrodes.

Original languageEnglish
Pages (from-to)665-674
Number of pages10
JournalSurface Engineering and Applied Electrochemistry
Issue number6
StatePublished - Nov 2020

Bibliographical note

Publisher Copyright:
© 2020, Allerton Press, Inc.


  • NiS electrode
  • dioxolane
  • dioxolane/LiClO
  • electrochemical characteristics
  • lithium battery
  • surface film
  • tetrahydrofuran/LiClO


Dive into the research topics of 'Integral Role of the NiS Electrode/Electrolyte Interface in the Redox Reaction with Lithium'. Together they form a unique fingerprint.

Cite this