Quantification of in-contact probe-sample electrostatic forces with dynamic atomic force microscopy

abstract

Atomic force microscopy (AFM) methods utilizing resonant mechanical vibrations of cantilevers in contact with a sample surface have shown sensitivities as high as few picometers for detecting surface displacements. Such a high sensitivity is harnessed in several AFM imaging modes. Here, we demonstrate a cantilever-resonance-based method to quantify electrostatic forces on a probe in the probe-sample junction in the presence of a surface potential or when a bias voltage is applied to the AFM probe. We find that the electrostatic forces acting on the probe tip apex can produce signals equivalent to a few pm of surface displacement. In combination with modeling, the measurements of the force were used to access the strength of the electrical field at the probe tip apex in contact with a sample. We find an evidence that the electric field strength in the junction can reach ca. 1 V nm(-1) at a bias voltage of a few volts and is limited by non-ideality of the tip-sample contact. This field is sufficiently strong to significantly influence material states and kinetic processes through charge injection, Maxwell stress, shifts of phase equilibria, and reduction of energy barriers for activated processes. Besides, the results provide a baseline for accounting for the effects of local electrostatic forces in electromechanical AFM measurements as well as offer additional means to probe ionic mobility and field-induced phenomena in solids.

keywords

FERROELECTRIC THIN-FILMS; STRONG ELECTRIC-FIELD; DOMAIN-STRUCTURE; PIEZORESPONSE; SURFACE; SPECTROSCOPY; NANOSCALE; CANTILEVER; RESOLUTION; NANOLITHOGRAPHY

subject category

Science & Technology - Other Topics; Materials Science; Physics

authors

Balke, N; Jesse, S; Carmichael, B; Okatan, MB; Kravchenko, II; Kalinin, SV; Tselev, A

our authors

acknowledgements

Experiments were planned and conducted through personal support provided by the US Department of Energy, Basic Energy Sciences, Materials Sciences and Engineering Division through the Office of Science Early Career Research Program (NB). The facilities to perform the experiments were provided at the Center for Nanophase Materials Sciences, which is sponsored at Oak Ridge National Laboratory by the Scientific User Facilities Division, Office of Basic Energy Sciences, US Department of Energy, which also provided additional personal support (SJ, BC, MBO, IK, SVK, AT). AT also acknowledges CICECO-Aveiro Institute of Materials (Ref. FCT UID/CTM/50011/2013) financed by national funds through the FCT/MEC and, when applicable, co-financed by FEDER under the PT2020 Partnership Agreement. IK provided the HfO2 sample.

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