scholarly journals Role of Entropy in Colloidal Self-Assembly

Entropy ◽  
2020 ◽  
Vol 22 (8) ◽  
pp. 877
Author(s):  
Brunno C. Rocha ◽  
Sanjib Paul ◽  
Harish Vashisth

Entropy plays a key role in the self-assembly of colloidal particles. Specifically, in the case of hard particles, which do not interact or overlap with each other during the process of self-assembly, the free energy is minimized due to an increase in the entropy of the system. Understanding the contribution of entropy and engineering it is increasingly becoming central to modern colloidal self-assembly research, because the entropy serves as a guide to design a wide variety of self-assembled structures for many technological and biomedical applications. In this work, we highlight the importance of entropy in different theoretical and experimental self-assembly studies. We discuss the role of shape entropy and depletion interactions in colloidal self-assembly. We also highlight the effect of entropy in the formation of open and closed crystalline structures, as well as describe recent advances in engineering entropy to achieve targeted self-assembled structures.

Soft Matter ◽  
2021 ◽  
Author(s):  
Jiawei Lu ◽  
Xiangyu Bu ◽  
Xinghua Zhang ◽  
Bing Liu

The shapes of colloidal particles are crucial to the self-assembled superstructures. Understanding the relationship between the shapes of building blocks and the resulting crystal structures is an important fundamental question....


2020 ◽  
Vol 8 (5) ◽  
pp. 838-851 ◽  
Author(s):  
Xiujuan Zhao ◽  
Changren Zhou ◽  
Mingxian Liu

This article reviewed the self-assembly methods of HNTs and biomedical applications of HNT self-assembly patterns.


2015 ◽  
Vol 127 (2) ◽  
pp. 273-280 ◽  
Author(s):  
MILI C NARANTHATTA ◽  
V RAMKUMAR ◽  
DILLIP KUMAR CHAND

2002 ◽  
Vol 739 ◽  
Author(s):  
V. Bouda

ABSTRACTThe growth of the self-assembled structure of carbon colloidal particles has been studied [1]. The system of carbon particles was processed in electrical field in polymer melt with controlled ionic concentration. The interpretation of the complex evolution of the self-assembled structure of carbon particles was given in terms of phase transitions of colloidal systems of carbon particles.Interactions between doublets of carbon black (CB) particles are interpreted in terms of DLVO approximation of interaction energy as multiples of average thermal fluctuation kT. Plots of the sum of energy of electrostatic repulsion and energy of van der Waals attraction versus separation between the doublets show the energy barriers to coagulation of high B and the energy wells with the secondary minima of depth W. The colloidal phase transitions appear at critical conjuncture of the concentration of ions in the medium and surface potential on the colloids. Six transition lines determine five phases of the assembly of carbon colloids in the proposed colloidal phase diagram: lateral vapor + axial vapor (vapor), lateral liquid + axial vapor (columnar liquid crystal), lateral liquid + axial liquid (smectic LC), lateral liquid + axial solid (nematic LC), and lateral solid + axial solid (solid).The diagram provides a tool to control the evolution of carbon self-assembly. The eventual morphology depends on the route of the steps of the processing. During the time elapsed in the LC state, the structure can reorganize and the eventual coagulation produces various crystals. On the contrary, the route outside the LC state can produce glass.


Nanomedicine ◽  
2021 ◽  
Vol 16 (2) ◽  
pp. 139-163
Author(s):  
Sonika Chibh ◽  
Jibanananda Mishra ◽  
Avneet Kour ◽  
Virander S Chauhan ◽  
Jiban J Panda

Molecular self-assembly is a widespread natural phenomenon and has inspired several researchers to synthesize a compendium of nano/microstructures with widespread applications. Biomolecules like proteins, peptides and lipids are used as building blocks to fabricate various nanomaterials. Supramolecular peptide self-assembly continue to play a significant role in forming diverse nanostructures with numerous biomedical applications; however, dipeptides offer distinctive supremacy in their ability to self-assemble and produce a variety of nanostructures. Though several reviews have articulated the progress in the field of longer peptides or polymers and their self-assembling behavior, there is a paucity of reviews or literature covering the emerging field of dipeptide-based nanostructures. In this review, our goal is to present the recent advancements in dipeptide-based nanostructures with their potential applications.


2016 ◽  
Vol 18 (39) ◽  
pp. 27165-27169 ◽  
Author(s):  
B. Reiser ◽  
D. Gerstner ◽  
L. Gonzalez-Garcia ◽  
J. H. M. Maurer ◽  
I. Kanelidis ◽  
...  

We describe solvent effects in the self-assembly of ultrathin gold nanowires and highlight the role of intermolecular ligand–solvent interactions.


MRS Advances ◽  
2020 ◽  
Vol 5 (64) ◽  
pp. 3507-3520
Author(s):  
Chunhui Dai ◽  
Kriti Agarwal ◽  
Jeong-Hyun Cho

AbstractNanoscale self-assembly, as a technique to transform two-dimensional (2D) planar patterns into three-dimensional (3D) nanoscale architectures, has achieved tremendous success in the past decade. However, an assembly process at nanoscale is easily affected by small unavoidable variations in sample conditions and reaction environment, resulting in a low yield. Recently, in-situ monitored self-assembly based on ion and electron irradiation has stood out as a promising candidate to overcome this limitation. The usage of ion and electron beam allows stress generation and real-time observation simultaneously, which significantly enhances the controllability of self-assembly. This enables the realization of various complex 3D nanostructures with a high yield. The additional dimension of the self-assembled 3D nanostructures opens the possibility to explore novel properties that cannot be demonstrated in 2D planar patterns. Here, we present a rapid review on the recent achievements and challenges in nanoscale self-assembly using electron and ion beam techniques, followed by a discussion of the novel optical properties achieved in the self-assembled 3D nanostructures.


2020 ◽  
Vol 27 (9) ◽  
pp. 923-929
Author(s):  
Gaurav Pandey ◽  
Prem Prakash Das ◽  
Vibin Ramakrishnan

Background: RADA-4 (Ac-RADARADARADARADA-NH2) is the most extensively studied and marketed self-assembling peptide, forming hydrogel, used to create defined threedimensional microenvironments for cell culture applications. Objectives: In this work, we use various biophysical techniques to investigate the length dependency of RADA aggregation and assembly. Methods: We synthesized a series of RADA-N peptides, N ranging from 1 to 4, resulting in four peptides having 4, 8, 12, and 16 amino acids in their sequence. Through a combination of various biophysical methods including thioflavin T fluorescence assay, static right angle light scattering assay, Dynamic Light Scattering (DLS), electron microscopy, CD, and IR spectroscopy, we have examined the role of chain-length on the self-assembly of RADA peptide. Results: Our observations show that the aggregation of ionic, charge-complementary RADA motifcontaining peptides is length-dependent, with N less than 3 are not forming spontaneous selfassemblies. Conclusion: The six biophysical experiments discussed in this paper validate the significance of chain-length on the epitaxial growth of RADA peptide self-assembly.


2021 ◽  
Author(s):  
Beatriz Matarranz ◽  
Goutam Ghosh ◽  
Ramesh Kandanelli ◽  
Angel Sampedro ◽  
Kalathil K. Kartha ◽  
...  

We unravel the relationship between conjugation length and self-assembly behaviour of oligophenyleneethynylenes (OPEs).


Soft Matter ◽  
2021 ◽  
Author(s):  
Meng Sun ◽  
Qintang Li ◽  
Xiao Chen

Luminescent gels have been successfully fabricated through the self-assembly of sodium cholate and a europium ion in choline chloride-based deep eutectic solvents.


Sign in / Sign up

Export Citation Format

Share Document