Issue 24, 2020

Highly porous Ni–P electrode synthesized by an ultrafast electrodeposition process for efficient overall water electrolysis

Abstract

The development of high-efficiency catalysts for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is essential to lower the energy losses during water electrolysis. Herein, a highly porous Ni–P (HP Ni–P) electrode, prepared by an ultrafast electrodeposition within only ten seconds, is presented with superior electrocatalytic activity towards both HER and OER in alkaline media: overpotentials of 96 and 323 mV are required to reach a current density level of 100 mA cm−2 for HER and OER, respectively, with corresponding Tafel slopes of 32.9 and 44.0 mV dec−1. Experimental analyses and theoretical calculations show that charge transfer occurs from Ni to P and the HER kinetics is accelerated by the increased hydrogen coverage, enhanced water dissociation ability, and optimized hydrogen adsorption energy on the HP Ni–P. Under OER conditions, surface P is oxidized into PO43−, promoting oxidation of Ni to OER-active NiOOH and exposing abundant OER-active sites on the HP Ni–P surface. An alkaline electrolysis cell was constructed with HP Ni–P as the cathode and anode (Ni–P‖Ni–P) and outperformed the Pt/C‖IrO2 cell at cell voltages exceeding 1.68 V. This work provides a practically applicable method to prepare HER and OER electrodes for use in industrial water electrolyzers, with insight into the activities of the catalysts.

Graphical abstract: Highly porous Ni–P electrode synthesized by an ultrafast electrodeposition process for efficient overall water electrolysis

Supplementary files

Article information

Article type
Paper
Submitted
05 Apr 2020
Accepted
08 Jun 2020
First published
08 Jun 2020

J. Mater. Chem. A, 2020,8, 12069-12079

Highly porous Ni–P electrode synthesized by an ultrafast electrodeposition process for efficient overall water electrolysis

D. Song, D. Hong, Y. Kwon, H. Kim, J. Shin, H. M. Lee and E. Cho, J. Mater. Chem. A, 2020, 8, 12069 DOI: 10.1039/D0TA03739G

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