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JOURNALS // Nanosystems: Physics, Chemistry, Mathematics // Archive

Nanosystems: Physics, Chemistry, Mathematics, 2019 Volume 10, Issue 6, Pages 681–685 (Mi nano484)

This article is cited in 7 papers

CHEMISTRY AND MATERIAL SCIENCE

SILD synthesis of the efficient and stable electrocatalyst based on CoO-NiO solid solution toward hydrogen production

I. A. Kodintseva, K. D. Martinsona, A. A. Lobinskyb, V. I. Popkova

a Ioffe Institute, 194021 Saint Petersburg, Russia
b Saint Petersburg State University, Peterhof, 198504 Saint Petersburg, Russia

Abstract: Currently, nanocrystalline NiO is well known as one of the best non-noble metal electrode material with low overpotential (OP) but mediocre stability. On the contrary, CoO has remarkable stability but the high values of OP. In this work, a method is proposed to achieve the stability of nickel oxide-based electrode materials while maintaining a low OP via the synthesis of a nanocrystalline CoO-NiO solid solution. Nanocrystals of CoO-NiO solid solution were synthesized by successive ionic layer deposition (SILD). XRD, SEM, and EDX analysis show that the CoO-NiO sample consists of 3–5 nm isometric crystallites of the solid solution mentioned above and Ni/Co ratio is equal to 45.4 % / 54.6 % at. Electrochemical investigation of the nanocrystalline CoO-NiO solution as electrode material shows OP values of -240 mV at a current density (CD) of 10 mA/cm$^{2}$, Tafel slope values of 78 mV/dec for hydrogen production from water-ethanol solution (10 % vol.) and high cyclic stability - only 3 mV degradation at 10 mA/cm$^{2}$ after 100 cycles of cyclic voltammetry. Thus, it was shown that the synthesis of a solid solution within the proposed approach makes it possible to maintain the high electrocatalytic properties inherent in NiO, but with high stability in a wide range of overpotential and in the high cyclic load inherent in CoO.

Keywords: nickel oxide, cobalt oxide, successive ionic layer deposition, hydrogen evolution, electrocatalytic reforming.

PACS: 73.61.r, 81.15.z, 82.65.+r

Received: 25.07.2019
Revised: 25.11.2019

Language: English

DOI: 10.17586/2220-8054-2019-10-6-681-685



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