Atomic force microscopy of confined liquids using the thermal bending fluctuations of the cantilever

Liu, Fei; van den Ende, Dirk; de Beer, Sissi; Mugele, Frieder

doi:10.1103/PhysRevE.87.062406

Journal Article

FZJ-2013-04327

Atomic force microscopy of confined liquids using the thermal bending fluctuations of the cantilever

Liu, F. ; de Beer, S.FZJ* ; van den Ende, D. ; Mugele, F.

2013
APS College Park, Md.

Physical review / E 87(6), 062406 (2013) [10.1103/PhysRevE.87.062406]

This record in other databases:

Please use a persistent id in citations: http://hdl.handle.net/2128/5406 doi:10.1103/PhysRevE.87.062406

Abstract: We use atomic force microscopy to measure the distance-dependent solvation forces and the dissipation across liquid films of octamethylcyclotetrasiloxane (OMCTS) confined between a silicon tip and a highly oriented pyrolytic graphite substrate without active excitation of the cantilever. By analyzing the thermal bending fluctuations, we minimize possible nonlinearities of the tip-substrate interaction due to finite excitation amplitudes because these fluctuations are smaller than the typical 1 Å, which is much smaller than the characteristic interaction length. Moreover, we avoid the need to determine the phase lag between cantilever excitation and response, which suffers from complications due to hydrodynamic coupling between cantilever and fluid. Consistent results, and especially high-quality dissipation data, are obtained by analyzing the power spectrum and the time autocorrelation of the force fluctuations. We validate our approach by determining the bulk viscosity of OMCTS using tips with a radius of approximately 1 μm at tip-substrate separations >5 nm. For sharp tips we consistently find an exponentially decaying oscillatory tip-substrate interaction stiffness as well as a clearly nonmonotonic variation of the dissipation for tip-substrate distances up to 8 and 6 nm, respectively. Both observations are in line with the results of recent simulations which relate them to distance-dependent transitions of the molecular structure in the liquid.

Classification: