Correlated Optical–Electrochemical Measurements Reveal Bidirectional Current Steps for Graphene Nanoplatelet Collisions at Ultramicroelectrodes

Single-entity electrochemistry has emerged as a powerful tool to study the adsorption behavior of single nanoscale entities one-at-a-time on an ultramicroelectrode surface. Classical single-entity collision studies have focused on the behavior of spherical nanoparticles or entities where the orienta...

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Bibliographic Details
Published inAnalytical chemistry (Washington) Vol. 93; no. 5; pp. 2898 - 2906
Main Authors Pendergast, Andrew D, Renault, Christophe, Dick, Jeffrey E
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 09.02.2021
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Summary:Single-entity electrochemistry has emerged as a powerful tool to study the adsorption behavior of single nanoscale entities one-at-a-time on an ultramicroelectrode surface. Classical single-entity collision studies have focused on the behavior of spherical nanoparticles or entities where the orientation of the colliding entity does not impact the electrochemical response. Here, we report a detailed study of the collision of asymmetric single graphene nanoplatelets onto ultramicroelectrodes. The collision of conductive graphene nanoplatelets on biased ultramicroelectrode surfaces can be observed in an amperometric i–t trace, revealing a variety of current transients (both positive and negative steps). To elucidate the dynamics of nanoplatelet adsorption processes and probe response heterogeneity, we correlated the collision events with optical microscopy. We show that positive steps are due to nanoplatelets coming into contact with the ultramicroelectrode, making an electrical connection, and adsorbing partly on the glass surrounding the ultramicroelectrode. Negative steps occur when nanoplatelets adsorb onto the glass without an electrical connection, effectively blocking flux of ferrocenemethanol to the ultramicroelectrode surface. These measurements allow rigorous quantification of current transients and detailed insights into the adsorption dynamics of asymmetric objects at the nanoscale.
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ISSN:0003-2700
1520-6882
DOI:10.1021/acs.analchem.0c04409