Pulse Electrodeposition of a Superhydrophilic and Binder-Free Ni-Fe-P Nanostructure as Highly Active and Durable Electrocatalyst for Both Hydrogen and Oxygen Evolution Reactions

Ghasem Barati Darband, Mahmood Aliofkhazraei, Suyeon Hyun, Sangaraju Shanmugam

Research output: Contribution to journalArticlepeer-review

87 Scopus citations

Abstract

Development and fabrication of electrodes with favorable electrocatalytic activity, low-cost, and excellent electrocatalytic durability are one of the most important issues in the hydrogen production area using the electrochemical water splitting process. We use the pulse electrodeposition method as a versatile and cost-effective approach to synthesize three-dimensional Ni-Fe-P electrocatalysts on nickel nanostructures under various applied frequencies and duration times, in which nanostructures exhibit excellent intrinsic electrocatalytic activity. Benefiting from the three-dimensional structure, as well as the simultaneous presence of the three elements nickel, iron, and phosphorus, the electrode fabricated at the optimal conditions has indicated outstanding electrocatalytic activity with a η10 of 66 and 198 mV for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), respectively, in a 1.0 M KOH solution. Also, the water electrolysis cell constructed with this electrode and tested as a bifunctional electrode exhibited 1.508 V for 10 mA cm-2 in overall water splitting. In addition, the lowest amount of potential change in 100 mA cm-2 was observed for HER and OER, indicating excellent electrocatalytic stability. This study proposes a binder-free and economical technique for the synthesis of three-dimensional electrocatalysts.

Original languageEnglish
Pages (from-to)53719-53730
Number of pages12
JournalACS Applied Materials and Interfaces
Volume12
Issue number48
DOIs
StatePublished - 2 Dec 2020

Bibliographical note

Publisher Copyright:
© 2020 American Chemical Society. All rights reserved.

Keywords

  • Ni-Fe-P nanostructure
  • hydrogen evolution reaction
  • oxygen evolution reaction
  • pulse electrodeposition

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