4.8 Article

High-Frequency Electromechanical Imaging of Ferroelectrics in a Liquid Environment

Journal

ACS NANO
Volume 6, Issue 6, Pages 5559-5565

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/nn301489g

Keywords

scanning probe microscopy; liquid; ferroelectrics

Funding

  1. U.S. Department of Energy, Basic Energy Sciences, Materials Sciences and Engineering Division through the Office of Science Early Career Research Program
  2. Scientific User Facilities Division, Office of Basic Energy Sciences, U.S. Department of Energy
  3. National Science Council [NSC-100-2119-M-009-003]

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The coupling between electrical and mechanical phenomena is a ubiquitous feature of many information and energy storage materials and devices. In addition to involvement in performance and degradation mechanisms, electromechanical effects underpin a broad spectrum of nanoscale imaging and spectroscopies including piezoresponse force and electrochemical strain microscopies. Traditionally, these studies are conducted under ambient conditions. However, applications related to imaging energy storage and electrophysiological phenomena require operation in a liquid phase and therefore the development of electromechanical probing techniques suitable to liquid environments. Due to the relative high conductivity of most liquids and liquid decomposition at low voltages, the transfer of characterization techniques from ambient to liquid is not straightforward. Here we present a detailed study of ferroelectric domain imaging and manipulation in thin film BiFeO3 using piezoresponse force microscopy in liquid environments as model systems for electromechanical phenomena in general. We explore the use of contact resonance enhancement and the application of multifrequency excitation and detection principles to overcome the experimental problems introduced by a liquid environment. Understanding electromechanical sample characterization in liquid is a key aspect not only for ferroelectric oxides but also for biological and electrochemical sample systems.

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