When self-assembly meets topology: an enhanced micelle stability

2017 ◽  
Vol 53 (27) ◽  
pp. 3822-3825 ◽  
Author(s):  
Xiaopeng Dong ◽  
Xuliang Guo ◽  
Guangqin Liu ◽  
Aiping Fan ◽  
Zheng Wang ◽  
...  

Curvature-induced dipole moment and unique geometry can enhance micelle stability.

Author(s):  
E. Amah ◽  
N. Musunuri ◽  
Ian S. Fischer ◽  
Pushpendra Singh

We numerically study the process of self-assembly of particle mixtures on fluid-liquid interfaces when an electric field is applied in the direction normal to the interface. The force law for the dependence of the electric field induced dipole-dipole and capillary forces on the distance between the particles and their physical properties obtained in an earlier study by performing direct numerical simulations is used for conducting simulations. The inter-particle forces cause mixtures of nanoparticles to self-assemble into molecular-like hierarchical arrangements consisting of composite particles which are organized in a pattern. However, there is a critical electric intensity value below which particles move under the influence of Brownian forces and do not self-assemble. Above the critical value, when the particles sizes differed by a factor of two or more, the composite particle has a larger particle at its core and several smaller particles forming a ring around it. Approximately same sized particles, when their concentrations are approximately equal, form binary particles or chains (analogous to polymeric molecules) in which positively and negatively polarized particles alternate, but when their concentrations differ the particles whose concentration is larger form rings around the particles with smaller concentration.


1985 ◽  
Vol 63 (1) ◽  
pp. 99-103
Author(s):  
John Courtenay Lewis

The intercollisional interference dip in the Q-branch of the fundamental band of collision-induced spectra of H2–He mixtures partially fills in at low temperatures. In contradiction to claims that this ia a quantum effect, we show 1. that if the induced dipole moment is exactly proportional to the intermolecular force then the interference dip goes to zero at all temperatures; 2. that the filling-in of the dip is essentially a classical phenomenon and is due mainly to the discontinuity in the distance of closest approach during binary collisions as a function of impact parameter.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Oleksandr Shyshov ◽  
Shyamkumar Vadakket Haridas ◽  
Luca Pesce ◽  
Haoyuan Qi ◽  
Andrea Gardin ◽  
...  

AbstractThe development of powerful methods for living covalent polymerization has been a key driver of progress in organic materials science. While there have been remarkable reports on living supramolecular polymerization recently, the scope of monomers is still narrow and a simple solution to the problem is elusive. Here we report a minimalistic molecular platform for living supramolecular polymerization that is based on the unique structure of all-cis 1,2,3,4,5,6-hexafluorocyclohexane, the most polar aliphatic compound reported to date. We use this large dipole moment (6.2 Debye) not only to thermodynamically drive the self-assembly of supramolecular polymers, but also to generate kinetically trapped monomeric states. Upon addition of well-defined seeds, we observed that the dormant monomers engage in a kinetically controlled supramolecular polymerization. The obtained nanofibers have an unusual double helical structure and their length can be controlled by the ratio between seeds and monomers. The successful preparation of supramolecular block copolymers demonstrates the versatility of the approach.


2006 ◽  
Vol 05 (06) ◽  
pp. 895-900 ◽  
Author(s):  
NOBUYUKI ISHIDA ◽  
AGUS SUBAGYO ◽  
KAZUHISA SUEOKA

We performed STM measurements on the K/GaAs (110) surface with high K coverage. The K atoms gradually disappeared while scanning the tip over the surface at negative sample bias voltage. The phenomenon strongly occurred over the scanning area and can be explained by the field-induced surface diffusion from the scanning area to radial direction. Considering the interaction between the dipole moment of the adsorbed K atoms and the electric field, we discuss the relationship between the static and induced dipole moment of K atoms on a GaAs (110) surface.


2002 ◽  
Vol 32 (5) ◽  
pp. 301-312 ◽  
Author(s):  
Wynand S. Verwoerd

To describe mutual polarisation in bulk materials containing high polarisability molecules, local fields beyond the linear approximation need to be included. A second order tensor equation is formulated, and it describes this in the case of crystalline or at least locally ordered materials such as an idealised polymer. It is shown that this equation is solved by a set of recursion equations that relate the induced dipole moment, linear polarisability, and first hyperpolarisability in the material to the intrinsic values of the same properties of isolated molecules. From these, macroscopic susceptibility tensors up to second order can be calculated for the material.


2013 ◽  
Vol 113 (6) ◽  
pp. 064314 ◽  
Author(s):  
F. Dujardin ◽  
E. Feddi ◽  
A. Oukerroum ◽  
J. Bosch Bailach ◽  
J. Martínez-Pastor ◽  
...  

MRS Bulletin ◽  
1989 ◽  
Vol 14 (2) ◽  
pp. 22-31 ◽  
Author(s):  
P.E. Dunn ◽  
S.H. Carr

This article provides an overview of the piezoelectric effect in all the classes of materials in which it is found to occur. This includes select materials from the categories of naturally occurring single crystals, polycrystalline ceramics, and semicrystalline polymers. Throughout this development, an attempt is made to point out the common factor for the piezoelectric effect in all these materials, namely, the presence of dipolar moieties, whose orientation brings about a net polarization in the material as a whole.The applications of each of these classes of materials are covered briefly. Each such application has a specific value based on the aggregate properties of the material as a whole, making each material complementary rather than competitive in device applications.Brief mention is made of the mathematics and geometry of the piezoelectric effect in order to define the piezoelectric constants by which the properties of these materials are described. The article then focuses on the basis of the piezoelectric response in synthetic polymers.Piezoelectricity or “pressure electricity” was coined from the Greek verb “piezen,” to press, by Pierre and Jacques Curie in the 1880s during an investigation of the symmetry in crystals. In this work it was found that certain crystals, lacking a center of symmetry, produced an electrical charge when mechanically deformed. The converse effect was also found to occur, whereby applying an electric field caused the crystal to change its shape. This phenomenon was attributed to a deformation of the net internal polarization in the crystal. When no external forces are present, the centers of positive and negative charges will coincide, and there is no net polarization. The application of a stress, be it mechanical (pressure) or electrical (applied field), causes a displacement of the centers of gravity of the positive and negative charges. In the absence of a center of symmetry, the charge displacement will be nonsymmetrical and thereby produce an induced dipole moment. This dipole moment, if produced by a mechanical stress, will cause the surfaces to develop an effective charge. If an external field displaces the charges, by electrostatic attraction or repulsion, it produces a mechanical strain which causes the material to deform. The mathematical relations describing this effect were developed in the few years following their discovery, making use of tensor notation to describe the directionality of the applied stress and the resultant strain.


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