Achieving Stable Patterns in Multicomponent Polymer Thin Films Using Marangoni and van der Waals Forces

Langmuir ◽  
2021 ◽  
Author(s):  
Saurabh Shenvi Usgaonkar ◽  
Christopher J. Ellison ◽  
Satish Kumar
2015 ◽  
Vol 117 (1) ◽  
pp. 015103 ◽  
Author(s):  
Kyeong Hyun Park ◽  
Mohamed Mohamed ◽  
Zlatan Aksamija ◽  
Umberto Ravaioli

2018 ◽  
Vol 20 (34) ◽  
pp. 21949-21959 ◽  
Author(s):  
Fernando G. Echeverrigaray ◽  
Saron R. S. de Mello ◽  
Leonardo M. Leidens ◽  
Marcelo E. H. Maia da Costa ◽  
Fernando Alvarez ◽  
...  

Energy dissipation associated with frictional damping mechanisms owing to van der Waals (vdW) forces by induced polarizability at the sliding interface of a-C:H thin films.


Nonlinearity ◽  
2007 ◽  
Vol 20 (2) ◽  
pp. 299-317 ◽  
Author(s):  
Kai-Seng Chou ◽  
Ying-Chuen Kwong

2020 ◽  
Author(s):  
Daniel B. Straus ◽  
Robert J. Cava

The design of new chiral materials usually requires stereoselective organic synthesis to create molecules with chiral centers. Less commonly, achiral molecules can self-assemble into chiral materials, despite the absence of intrinsic molecular chirality. Here, we demonstrate the assembly of high-symmetry molecules into a chiral van der Waals structure by synthesizing crystals of C<sub>60</sub>(SnI<sub>4</sub>)<sub>2</sub> from icosahedral buckminsterfullerene (C<sub>60</sub>) and tetrahedral SnI4 molecules through spontaneous self-assembly. The SnI<sub>4</sub> tetrahedra template the Sn atoms into a chiral cubic three-connected net of the SrSi<sub>2</sub> type that is held together by van der Waals forces. Our results represent the remarkable emergence of a self-assembled chiral material from two of the most highly symmetric molecules, demonstrating that almost any molecular, nanocrystalline, or engineered precursor can be considered when designing chiral assemblies.


2019 ◽  
Author(s):  
Henrik Pedersen ◽  
Björn Alling ◽  
Hans Högberg ◽  
Annop Ektarawong

Thin films of boron nitride (BN), particularly the sp<sup>2</sup>-hybridized polytypes hexagonal BN (h-BN) and rhombohedral BN (r-BN) are interesting for several electronic applications given band gaps in the UV. They are typically deposited close to thermal equilibrium by chemical vapor deposition (CVD) at temperatures and pressures in the regions 1400-1800 K and 1000-10000 Pa, respectively. In this letter, we use van der Waals corrected density functional theory and thermodynamic stability calculations to determine the stability of r-BN and compare it to that of h-BN as well as to cubic BN and wurtzitic BN. We find that r-BN is the stable sp<sup>2</sup>-hybridized phase at CVD conditions, while h-BN is metastable. Thus, our calculations suggest that thin films of h-BN must be deposited far from thermal equilibrium.


2008 ◽  
Vol 64 (a1) ◽  
pp. C560-C560
Author(s):  
K. Honda ◽  
M. Morita ◽  
S. Sasaki ◽  
O. Sakata ◽  
A. Takahara

Sign in / Sign up

Export Citation Format

Share Document