Issue 21, 2022

Phase-controlled solvothermal syntheses and oxygen evolution reaction (OER) activity of nickel sulfide nanoparticles obtained from 1,2-bis(diphenylphosphino)ethane nickel(ii) acetylacetonatedithiolate

Abstract

A new heteroleptic nickel(II) complex, [Ni(dppe)(acac)]·CHCl3 (1) (where acac = acetylacetonatedithiolate, dppe = 1,2-bis(diphenylphosphino)ethane), has been synthesized and characterized using different spectroscopic techniques and single-crystal X-ray diffraction. The solvothermal decomposition of the complex in two different solvents, viz. 1-dodecanethiol (DT) and octadecyl amine (ODA), yielded two different nickel sulfides, viz.Ni-DT and Ni-ODA, respectively. These sulfides have been characterized by PXRD and SEM. Rietveld refinement analyses of Ni-DT revealed that it comprises two phases of nickel sulfide, viz. NiS and Ni3S3, while Ni-ODA possesses only a single phase of Ni2S3. The newly synthesized materials have been used as electrocatalysts for the oxygen evolution half-cell reaction of water splitting. The electrochemical studies suggest that Ni-DT/Ni-ODA has a good electrocatalytic activity towards the OER at a low overpotential of ∼200 mV with η1 being 342 mV and 243 mV for Ni-DT and Ni-ODA, respectively, at a scan rate of 1 mV s−1.

Graphical abstract: Phase-controlled solvothermal syntheses and oxygen evolution reaction (OER) activity of nickel sulfide nanoparticles obtained from 1,2-bis(diphenylphosphino)ethane nickel(ii) acetylacetonatedithiolate

Supplementary files

Article information

Article type
Paper
Submitted
09 Mar 2022
Accepted
26 Apr 2022
First published
26 Apr 2022

New J. Chem., 2022,46, 10246-10255

Phase-controlled solvothermal syntheses and oxygen evolution reaction (OER) activity of nickel sulfide nanoparticles obtained from 1,2-bis(diphenylphosphino)ethane nickel(II) acetylacetonatedithiolate

A. Singh, A. Singh, G. Kociok-Köhn, R. Chauhan, S. W. Gosavi, A. Singh, A. K. Singh, A. Kumar and Mohd. Muddassir, New J. Chem., 2022, 46, 10246 DOI: 10.1039/D2NJ01177H

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