Hsiang Chih Chiu

The interplay between apparent viscosity and wettability in nanoconfined water

Understanding and manipulating fluids at the nanoscale is a matter of growing scientific and technological interest. Here we show that the viscous shear forces in nanoconfined water can be orders of magnitudes larger than in bulk water if the confining surfaces are hydrophilic, whereas they greatly decrease when the surfaces are increasingly hydrophobic. This decrease of viscous forces is quantitatively explained with a simple model that includes the slip velocity at the water surface interface. The same effect is observed in the energy dissipated by a tip vibrating in water perpendicularly to a surface. Comparison of the experimental data with the model shows that interfacial viscous forces and compressive dissipation in nanoconfined water can decrease up to two orders of magnitude due to slippage. These results offer a new understanding of interfacial fluids, which can be used to control flow at the nanoscale.

Demonstration of the asymmetric lateral Casimir force between corrugated surfaces in the nonadditive regime

The measurement of the lateral Casimir force between two aligned sinusoidally corrugated Au-coated surfaces has been performed in the nonadditive regime. The use of deeper corrugations also allowed to demonstrate an asymmetry in the phase dependences of the lateral Casimir force, as predicted earlier. The measurement data are found to be in excellent agreement with the exact theoretical results computed at T=300 K including effect of real material properties. The deviations between the exact theory and the proximity force approximation are quantified. The obtained results are topical for applications in nanomachines.

Structure and charge transport properties in MEH-PPV

The charge carrier transport in MEH-PPV is investigated with respect to different molecular weight distributions and with different tetrahedral defect densities. The defect density influences the charge transport behaviors significantly. With smaller defect density, MEH-PPV exhibits better charge transport which further depends upon the morphology. Position disorder parameter which is due to the morphology difference dominates the charge transport properties of low defect samples.

Experimental procedures for precision measurements of the Casimir force with an atomic force microscope

Experimental methods and procedures required for precision measurements of the Casimir force are presented. In particular, the best practices for obtaining stable cantilevers, calibration of the cantilever, correction of thermal and mechanical drift, measuring the contact separation, sphere radius and the roughness are discussed.

Morphology dependence of radial elasticity in multiwalled boron nitride nanotubes

We report on the measurement of the radial modulus of boron nitride nanotubes (BN-NTs) with various sizes and thicknesses. These BN-NTs are radially much stiffer than previously reported thinner and smaller BN-NTs. Here, we show the key role of the morphology of the nanotubes in determining their radial rigidity; in particular, we find that the external and internal radii, Rext and Rint, have a stronger influence on the radial modulus than the nanotube’s thickness. The radial modulus decreases nonlinearly with 1/Rext until reaching, for a large number of layers and a large radius, the transverse elastic modulus of bulk h-BN.

Hydrogen-mediated long-range magnetic ordering in Pd-rich alloy film

The effect of hydrogenation on a 14 nm Co14Pd86/Al2O3(0001) thin film was investigated on the basis of the magnetooptical Kerr effect. After exposure to H2 gas, the squareness of the hysteresis loop showed a large transition from approximately 10% to 100% and the saturation Kerr signal was reduced to nearly 30% of the pristine value. The reversibility of the transition was verified and the response time was within 2–3 s. These observations indicate that the hydride formation transformed the short-range coupled and disordered magnetic state of the Co14Pd86 film to a long-range-ordered ferromagnetic state and induced appreciable decrease in the magnetic moment. The enhanced long-range-ordering and the reduction of the magnetic moment were attributed to the change of electronic structure in Co14Pd86 with hydrogen uptake.

Nanorheology by atomic force microscopy

We present an Atomic Force Microscopy (AFM) based method to investigate the rheological properties of liquids confined within a nanosize gap formed by an AFM tip apex and a solid substrate. In this method, a conventional AFM cantilever is sheared parallel to a substrate surface by means of a lock-in amplifier while it is approaching and retracting from the substrate in liquid. The normal solvation forces and lateral viscoelastic shear forces experienced by the AFM tip in liquid can be simultaneously measured as a function of the tip-substrate distance with sub-nanometer vertical resolution. A new calibration method is applied to compensate for the linear drift of the piezo transducer and substrate system, leading to a more precise determination of the tip-substrate distance. By monitoring the phase lag between the driving signal and the cantilever response in liquid, the frequency dependent viscoelastic properties of the confined liquid can also be derived. Finally, we discuss the results obtained with this technique from different liquid-solid interfaces. Namely, octamethylcyclotetrasiloxane and water on mica and highly oriented pyrolytic graphite.

Adhesion and size dependent friction anisotropy in boron nitride nanotubes

The frictional properties of individual multiwalled boron nitride nanotubes (BN-NTs) synthesized by chemical vapour deposition (CVD) and deposited on a silicon substrate are investigated using an atomic force microscope tip sliding along (longitudinal sliding) and across (transverse sliding) the tubes principal axis. Because of the tubes transverse deformations during the tip sliding, a larger friction coefficient is found for the transverse sliding as compared to the longitudinal sliding. Here, we show that the friction anisotropy in BN-NTs, defined as the ratio between transverse and longitudinal friction forces per unit area, increases with the nanotube-substrate contact area, estimated to be proportional to (L(NT)R(NT))(1/2), where L(NT) and R(NT) are the length and the radius of the nanotube, respectively. Larger contact area denotes stronger surface adhesion, resulting in a longitudinal friction coefficient closer to the value expected in the absence of transverse deformations. Compared to carbon nanotubes (C-NTs), BN-NTs display a friction coefficient in each sliding direction with intermediate values between CVD and arc discharge C-NTs. CVD BN-NTs with improved tribological properties and higher oxidation temperature might be a better candidate than CVD C-NTs for applications in extreme environments.

Sliding on a Nanotube: Interplay of Friction, Deformations and Structure

The frictional properties of individual carbon nanotubes (CNTs) are studied by sliding an atomic force microscopy tip across and along its principle axis. This direction-dependent frictional behavior is found to correlate strongly with the presence of structural defects, surface chemistry, and CNT chirality. This study shows that it is experimentally possible to tune the frictional/adhesion properties of a CNT by controlling the CNT structure and surface chemistry, as well as use friction force to predict its structural and chemical properties.

Influence of Oxygen Vacancies on the Frictional Properties of Nanocrystalline Zinc Oxide Thin Films in Ambient Conditions

Oxygen vacancy is the most studied point defect and has been found to significantly influence the physical properties of zinc oxide (ZnO). By using atomic force microscopy (AFM), we show that the frictional properties on the ZnO surface at the nanoscale greatly depend on the amount of oxygen vacancies present in the surface layer and the ambient humidity. The photocatalytic effect (PCE) is used to qualitatively control the amount of oxygen vacancies in the surface layer of ZnO and reversibly switch the surface wettability between hydrophobic and superhydrophilic states. Because oxygen vacancies in the ZnO surface can attract ambient water molecules, during the AFM friction measurement, water meniscus can form between the asperities at the AFM tip-ZnO contact due to the capillary condensation, leading to negative dependence of friction on the logarithm of tip sliding velocity. Such dependence is found to be a strong function of relative humidity and can be reversibly manipulated by the PCE. Our results indicate that it is possible to control the frictional properties of ZnO surface at the nanoscale using optical approaches.