Issue 44, 2023

Two-dimensional nickel cyano-bridged coordination polymer thermally derived potent electrocatalysts for alkaline hydrogen evolution reaction

Abstract

Because of its sustainability and cleanliness, hydrogen has recently been a research focus as a potential fuel. One promising way to produce hydrogen is water electrolysis in an alkaline solution. However, this process requires much energy to split the H–OH bond and transfer multiple electrons/protons. To overcome this challenge, catalytic electrodes have been developed to reduce the energy needed and maintain sustainable water electrolysis. This study explores the potential of utilizing a two-dimensional nickel-based cyanide coordination polymer (2D Ni-CP) precursor to synthesize effective Ni-based inorganic nanostructured electrodes. Various types of electrodes, including Ni-O, Ni-S, Ni-Se, and Ni-P, are synthesized through direct thermal treatment of the coordination polymer. The performance of the as-prepared materials in the hydrogen evolution process (HER) in an alkaline medium is examined. Ni-P demonstrates the most promising HER performance with an overpotential of 266 mV at 10 mA cm−2 and a Tafel slope of 186 mV dec−1. These results are compared to those of the benchmark expensive and scarce Pt/C-40% catalyst (38 mV and 48 mV dec−1) examined under identical conditions. Additionally, Ni-P shows outstanding HER durability over four days, as reflected by chronopotentiometry measurements.

Graphical abstract: Two-dimensional nickel cyano-bridged coordination polymer thermally derived potent electrocatalysts for alkaline hydrogen evolution reaction

Supplementary files

Article information

Article type
Paper
Submitted
29 Jul 2023
Accepted
13 Oct 2023
First published
02 Nov 2023

J. Mater. Chem. A, 2023,11, 24261-24271

Two-dimensional nickel cyano-bridged coordination polymer thermally derived potent electrocatalysts for alkaline hydrogen evolution reaction

M. M. Abdel Naby, M. B. Zakaria, H. M. El-Bery, G. G. Mohamed and M. E. El-Khouly, J. Mater. Chem. A, 2023, 11, 24261 DOI: 10.1039/D3TA04511K

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