Potential-sensing electrochemical atomic force microscopy for in operando analysis of water-splitting catalysts and interfaces

Michael R. Nellist, Forrest A. L. Laskowski, Jingjing Qiu, Hamed Hajibabaei, Kevin Sivula, Thomas W. Hamann and Shannon W. Boettcher ()
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Michael R. Nellist: University of Oregon
Forrest A. L. Laskowski: University of Oregon
Jingjing Qiu: University of Oregon
Hamed Hajibabaei: Michigan State University
Kevin Sivula: École Polytechnique Fédérale de Lausanne (EPFL)
Thomas W. Hamann: Michigan State University
Shannon W. Boettcher: University of Oregon

Nature Energy, 2018, vol. 3, issue 1, 46-52

Abstract: Abstract Heterogeneous electrochemical phenomena, such as (photo)electrochemical water splitting to generate hydrogen using semiconductors and/or electrocatalysts, are driven by the accumulated charge carriers and thus the interfacial electrochemical potential gradients that promote charge transfer. However, measurements of the “surface” electrochemical potential during operation are not generally possible using conventional electrochemical techniques, which measure/control the potential of a conducting electrode substrate. Here we show that the nanoscale conducting tip of an atomic force microscope cantilever can sense the surface electrochemical potential of electrocatalysts in operando. To demonstrate utility, we measure the potential-dependent and thickness-dependent electronic properties of cobalt (oxy)hydroxide phosphate (CoPi). We then show that CoPi, when deposited on illuminated haematite (α-Fe2O3) photoelectrodes, acts as both a hole collector and an oxygen evolution catalyst. We demonstrate the versatility of the technique by comparing surface potentials of CoPi-decorated planar and mesoporous haematite and discuss viability for broader application in the study of electrochemical phenomena.

Date: 2018
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DOI: 10.1038/s41560-017-0048-1

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