Electrolytic Conversion of Sacrificial Metal–Organic Framework Thin Films into an Electrocatalytically Active Monolithic Oxide Coating for the Oxygen-Evolution Reaction

Salma Begum, Tawheed Hashem, Manuel Tsotsalas, Christof Wöll, Mohamed H. Alkordi

Research output: Contribution to journalArticle

Abstract

The electrolytic conversion of SURMOFs, monolithic surface-anchored metal–organic framework (MOF) thin films, to yield Ni(OH)2 coatings for utilization as electrocatalysts in the water oxidation reaction is described. The electrocatalytic properties of the hydroxide coating, namely an oxygen-evolving reaction (OER) onset overpotential of 330 mV and overpotential of only 440 mV at a current density of 10 mA cm−2, are well comparable to some of the most efficient materials used for the OER process. This electrolytic transformation process represents a facile pathway for the fabrication of electrochemically and electrocatalytically active coatings, and is potentially transferrable to several other systems. This approach is an attractive alternative to the commonly utilized, energy intensive pyrolysis, where heating the samples to temperatures above 600 °C is common to induce full transformation into electroactive catalysts.

Original languageEnglish
Article number1900967
JournalEnergy Technology
Volume7
Issue number11
DOIs
Publication statusPublished - 1 Nov 2019
Externally publishedYes

Fingerprint

Thin films
Coatings
Oxides
Oxygen
Electrocatalysts
Pyrolysis
Current density
Heating
Fabrication
Oxidation
Catalysts
Water
Temperature

Keywords

  • electrochemical catalysis
  • metal–organic frameworks
  • Ni catalysis
  • thin films
  • water spitting

ASJC Scopus subject areas

  • Energy(all)

Cite this

Electrolytic Conversion of Sacrificial Metal–Organic Framework Thin Films into an Electrocatalytically Active Monolithic Oxide Coating for the Oxygen-Evolution Reaction. / Begum, Salma; Hashem, Tawheed; Tsotsalas, Manuel; Wöll, Christof; Alkordi, Mohamed H.

In: Energy Technology, Vol. 7, No. 11, 1900967, 01.11.2019.

Research output: Contribution to journalArticle

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