Abstract

Scanning specimens in liquids using commercial atomic force microscopy (AFM) is very time-consuming due to the necessary try-and-error iteration for determining appropriate triggering frequencies and probes. In addition, the iteration easily contaminates the AFM tip and damages the samples, which consumes probes. One reason for this could be inaccuracy in the resonant frequency in the feedback system setup. This paper proposes a frequency function which varies with the tip-sample separation, and it helps to improve the frequency shift in the current feedback system of commercial AFMs. The frequency function is a closed-form equation, which allows for easy calculation, as confirmed by experimental data. It comprises three physical effects: the quasi-static equilibrium condition, the atomic forces gradient effect, and hydrodynamic load effect. While each of these has previously been developed in separate studies, this is the first time their combination has been used to represent the complete frequency phenomenon. To avoid “jump to contact” issues, experiments often use probes with relatively stiffer cantilevers, which inevitably reduce the force sensitivity in sensing low atomic forces. The proposed frequency function can also predict jump to contact behavior and, thus, the probe sensitivity could be increased and soft probes could be widely used. Additionally, various tip height behaviors coupling with the atomic forces gradient and hydrodynamic effects are discussed in the context of carbon nanotube probes.

Highlights

  • In the last ten years, the atomic-scale resolution of frequency-modulation atomic force microscopy (FM AFM) has been taken advantage of to image and conduct force spectroscopy measurements of biological samples in liquids

  • Soft probes are highly susceptible to the problem of “jump to contact,” which is minor reason why the soft probe has not been adopted in FM AFM

  • Various tip height behaviors coupling with the atomic forces gradient and hydrodynamic effects are discussed in the context of carbon nanotube probes

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Summary

Introduction

In the last ten years, the atomic-scale resolution of frequency-modulation atomic force microscopy (FM AFM) has been taken advantage of to image and conduct force spectroscopy measurements of biological samples in liquids. Scanning specimens in liquids using commercial atomic force microscopy (AFM) is time-consuming due the need for a try-and-error iteration to determine appropriate triggering frequencies This iteration contaminates the AFM tip and damages samples, which consumes probes. This approximation is suitable for the probe in far field, but it does not adequately represent the resonance frequency when the probe approaches close to the specimen This equation is used in commercial AFM devices, and the differences could be on the order of a few hundred hertz. The aforementioned frequency function contains an opened-integration ( z ), which is problematic for AFM engineers To improve it and allow for the use of soft probes, this paper provides an equation for the frequency shift as a function of tip-sample separation. Various tip height behaviors coupling with the atomic forces gradient and hydrodynamic effects are discussed in the context of carbon nanotube probes

Quasi-Static Equilibrium Condition
Atomic Force Gradient Effect
A ts k0 A0
Hydrodynamic Effect
Hydrodynamic Function
Tip Heights and Frequency Shifts
Conclusions
Conflicts of Interest
Full Text
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