Tracking Catalyst Redox States and Reaction Dynamics in Ni–Fe Oxyhydroxide Oxygen Evolution Reaction Electrocatalysts: The Role of Catalyst Support and Electrolyte pH

• Published in: Journal of the American Chemical Society Vol. 139; no. 5; pp. 2070 - 2082
• Main Authors: Görlin, Mikaela, Ferreira de Araújo, Jorge, Schmies, Henrike, Bernsmeier, Denis, Dresp, Sören, Gliech, Manuel, Jusys, Zenonas, Chernev, Petko, Kraehnert, Ralph, Dau, Holger, Strasser, Peter
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 08.02.2017
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/jacs.6b12250

Ni–Fe oxyhydroxides are the most active known electrocatalysts for the oxygen evolution reaction (OER) in alkaline electrolytes and are therefore of great scientific and technological importance in the context of electrochemical energy conversion. Here we uncover, investigate, and discuss previously unaddressed effects of conductive supports and the electrolyte pH on the Ni–Fe­(OOH) catalyst redox behavior and catalytic OER activity, combining in situ UV–vis spectro-electrochemistry, operando electrochemical mass spectrometry (DEMS), and in situ cryo X-ray absorption spectroscopy (XAS). Supports and pH > 13 strongly enhanced the precatalytic voltammetric charge of the Ni–Fe oxyhydroxide redox peak couple, shifted them more cathodically, and caused a 2–3-fold increase in the catalytic OER activity. Analysis of DEMS-based faradaic oxygen efficiency and electrochemical UV–vis traces consistently confirmed our voltammetric observations, evidencing both a more cathodic O2 release and a more cathodic onset of Ni oxidation at higher pH. Using UV–vis, which can monitor the amount of oxidized Ni+3/+4 in situ, confirmed an earlier onset of the redox process at high electrolyte pH and further provided evidence of a smaller fraction of Ni+3/+4 in mixed Ni–Fe centers, confirming the unresolved paradox of a reduced metal redox activity with increasing Fe content. A nonmonotonic super-Nernstian pH dependence of the redox peaks with increasing Fe contentdisplaying Pourbaix slopes as steep as −120 mV/pHsuggested a two proton–one electron transfer. We explain and discuss the experimental pH effects using refined coupled (PCET) and decoupled proton transfer–electron transfer (PT/ET) schemes involving negatively charged oxygenate ligands generated at Fe centers. Together, we offer new insight into the catalytic reaction dynamics and associated catalyst redox chemistry of the most important class of alkaline OER catalysts.