4.8 Article

Optimization of synthesis of the nickel-cobalt oxide based anode electrocatalyst and of the related membrane-electrode assembly for alkaline water electrolysis

Journal

JOURNAL OF POWER SOURCES
Volume 347, Issue -, Pages 247-258

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jpowsour.2017.02.057

Keywords

Alkaline water electrolysis; Oxygen evolution; Spinel oxides; Synthesis route; Catalyst binder

Funding

  1. Grant Agency of the Czech Republic [1620728S]
  2. Operational Programme Prague - Competitiveness [CZ.2.16/3.1.00/24501]
  3. National Program of Sustainability [NPU I L01613, MSMT-43760/2015]

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In this work, the Ni-Co spinel oxides are synthesized via different methods and using different calcination temperatures. Properties of the prepared materials are compared. The best route is selected and used to prepare a Ni1+xCo2-xO4 (-1 <= x <= 1) series of materials in order to investigate their catalytic activity towards the oxygen evolution reaction (OER). The results show that hydroxide preparation yields NiCo2O4 oxide with the highest activity. 325 degrees C is identified as the optimum calcination temperature. Subsequently, the catalysts are tested in an electrolysis cell. To prepare an anode catalyst layer based on NiCo2O4 catalyst on top of a nickel foam substrate for membrane electrode assembly (MEA) construction, following polymer binders are used: anion-selective quaternized polyphenylene oxide (qPPO), inert polytetrafluoroethylene (PTFE (R)), and cation-selective Nafion (R). qPPO ionomer containing MEA exhibited highest OER activity. The current density obtained using a MEA containing qPPO binder attains a value of 135 mA cm(-2) at a cell voltage of 1.85 V. After 7 h chronopotentiometric experiment at a constant current density of 225 mA cm 2, the MEA employing PTFE (R) binder shows higher stability than the other binders in alkaline water electrolysis at 50 degrees C. Under similar conditions, stability of the PTFE (R)-binding MEA is examined for 135 h. Crown Copyright (C) 2017 Published by Elsevier B.V. All rights reserved.

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