Interfacial stiffness of nematic–smectic B interface in Gay–Berne liquid crystals using capillary wave theory

2021 ◽  
Vol 155 (4) ◽  
pp. 044901
Author(s):  
Jagroop Kaur ◽  
Debabrata Deb
1982 ◽  
Vol 60 (2) ◽  
pp. 137-153 ◽  
Author(s):  
Luis de Sobrino ◽  
Jože Peternelj

We use van Kampen's expression for the partition function of a van der Waals gas to investigate the effect of noncritical fluctuations on the interface of an inhomogeneous fluid. Such a procedure combines in a consistent manner the results of mean field theory and of capillary wave theory and, in addition, uncovers contributions due to fluctuations of the interface profile. Although the latter add negligibly to the interfacial width, they result in corrections to the mean field surface tension comparable to those resulting from capillary fluctuations. The effect of the walls in limiting the fluctuations is explicitly taken into account.


1989 ◽  
Vol 177 ◽  
Author(s):  
M. L. Schlossman ◽  
D. K. Schwartz ◽  
E. H. Kawamoto ◽  
G. J. Kellogg ◽  
P. S. Pershan ◽  
...  

ABSTRACTX-ray specular reflectivity is used to study the liquid-vapor interface of pure water and of fatty acid and polymer monolayers at that interface. For the pure water surface the reflectivity was measured for three different spectrometer resolutions and simultaneous fits with only one free parameter to all of the data are in excellent agreement with the prediction of capillary wave theory for the RMS surface roughness. Diffuse scattering away from the specular condition, at wavevectors corresponding to those of the capillary waves, yields intensities and line shapes in agreement with theory with no significant adjustable parameters. Reflectivity from separate monolayers of co-poly 1,2-butadiene/butyl alcohol (50% random substitution) and lignoceric acid (CH3(CH2)22COOH) at the water/vapor interface are interpreted to obtain profiles of the average electron density ρ(z) as a function of distance z along the surface normal. For the polymer monolayer we find the following: 1) a local maximum in the electron density approximately 10% larger than that of the bulk polymer and 2) the RMS roughness of the vapor/polymer interface agrees with capillary wave theory predictions for the lower surface pressures. For the highest surface pressure the RMS roughness exceeds the value predicted by the capillary wave model. Measurements of reflectivity from a lignoceric acid monolayer, as a function of surface pressure throughout an isotherm (near room temperature), reveal the following behavior: 1) the overall thickness of the monolayer increases with increasing pressure and 2) the head groups occupy a progressively larger region along the surface normal as the pressure increases, indicating that they rearrange normal to the interface.


1986 ◽  
Vol 33 (1) ◽  
pp. 614-616 ◽  
Author(s):  
J. R. Henderson

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Zihao Ou ◽  
Lehan Yao ◽  
Hyosung An ◽  
Bonan Shen ◽  
Qian Chen

Abstract Development of the surface morphology and shape of crystalline nanostructures governs the functionality of various materials, ranging from phonon transport to biocompatibility. However, the kinetic pathways, following which such development occurs, have been largely unexplored due to the lack of real-space imaging at single particle resolution. Here, we use colloidal nanoparticles assembling into supracrystals as a model system, and pinpoint the key role of surface fluctuation in shaping supracrystals. Utilizing liquid-phase transmission electron microscopy, we map the spatiotemporal surface profiles of supracrystals, which follow a capillary wave theory. Based on this theory, we measure otherwise elusive interfacial properties such as interfacial stiffness and mobility, the former of which demonstrates a remarkable dependence on the exposed facet of the supracrystal. The facet of lower surface energy is favored, consistent with the Wulff construction rule. Our imaging–analysis framework can be applicable to other phenomena, such as electrodeposition, nucleation, and membrane deformation.


Sign in / Sign up

Export Citation Format

Share Document