Static and dynamic screening effects in the electrostatic self-assembly of nano-particles

2014 ◽  
Vol 16 (46) ◽  
pp. 25449-25460 ◽  
Author(s):  
V. N. Kuzovkov ◽  
E. A. Kotomin
Keyword(s):  
Self Assembly ◽  
3D Structure ◽  
Nano Particles ◽  
Dynamic Screening ◽  
Charged Nanoparticles ◽  
Self Assembled ◽  
Oppositely Charged

3D structure of self-assembled and oppositely charged nanoparticles.

Theory of non-equilibrium critical phenomena in three-dimensional condensed systems of charged mobile nanoparticles

2014 ◽  
Vol 16 (27) ◽  
pp. 13974-13983 ◽  
Author(s):  
V. N. Kuzovkov ◽  
G. Zvejnieks ◽  
E. A. Kotomin
Keyword(s):  
Critical Phenomena ◽  
3D Structure ◽  
Three Dimensional ◽  
Charged Nanoparticles ◽  
Self Assembled ◽  
Oppositely Charged ◽  
Condensed Systems ◽  
Non Equilibrium

The 3d structure of self-assembled and oppositely charged nanoparticles.

Computer simulation of self-assembly (crystallization) of oppositely charged nanoparticles with various size distributions

2009 ◽  
Vol 355 (24-27) ◽  
pp. 1360-1369 ◽  
Author(s):  
R. Orlik ◽  
A.C. Mitus ◽  
B. Kowalczyk ◽  
A.Z. Patashinski ◽  
B.A. Grzybowski
Keyword(s):  
Computer Simulation ◽  
Self Assembly ◽  
Size Distributions ◽  
Charged Nanoparticles ◽  
Oppositely Charged

scholarly journals Mono-patchy zwitterionic microcolloids as building blocks for pH-controlled self-assembly

Soft Matter ◽  
2019 ◽  
Vol 15 (11) ◽  
pp. 2430-2438 ◽  
Author(s):  
Fatemeh Naderi Mehr ◽  
Dmitry Grigoriev ◽  
Nikolay Puretskiy ◽  
Alexander Böker
Keyword(s):  
Self Assembly ◽  
Building Blocks ◽  
Free Surfaces ◽  
Patchy Particles ◽  
Self Assembled ◽  
Oppositely Charged ◽  
Ph Controlled

Not only in theory but also experimentally, mono-patchy particles can be self-assembled via pH-controlled electrostatic attractions between their oppositely charged patchy and patch-free surfaces.

scholarly journals X-Ray Reflectometry Study of Self-Assembled Ionic Nanolayers

2012 ◽  
Vol 2012 ◽  
pp. 1-5
Author(s):  
Szymon Jasiecki ◽  
Jarosław Serafińczuk ◽  
Teodor Gotszalk ◽  
Grzegorz Schroeder
Keyword(s):  
Self Assembly ◽  
Ion Pair ◽  
Multilayered Structures ◽  
X Ray ◽  
Sequential Deposition ◽  
Assembly Technique ◽  
Self Assembled ◽  
Oppositely Charged ◽  
Macrocyclic Molecules ◽  
Polymeric Structures

The self-assembly technique has been applied for the fabrication of thin films including macrocyclic molecules. These multilayered structures, grown by sequential deposition of oppositely charged molecules, were characterised with X-ray reflectometry. The data obtained indicate regular thickness of ion pair layers formed regardless of the number of depositions made as well as the number of ion groups occurring in the molecule. Savitzky-Golay algorithm was used for the calculation of the layer thickness. Formation of self-assembled multilayers (SAMs) occurs not only for polymeric structures but also for small ionic compound systems and results from the electrostatic interaction of many strongly dissipated charges on the whole structure of the molecule.

Nanoscale Self-Assembly Using Ion and Electron Beam Techniques: A Rapid Review

MRS Advances ◽  
2020 ◽  
Vol 5 (64) ◽  
pp. 3507-3520
Author(s):  
Chunhui Dai ◽  
Kriti Agarwal ◽  
Jeong-Hyun Cho
Keyword(s):  
Electron Beam ◽  
Self Assembly ◽  
Ion Beam ◽  
Three Dimensional ◽  
The Self ◽  
Stress Generation ◽  
Rapid Review ◽  
High Yield ◽  
3D Nanostructures ◽  
Self Assembled

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.

Green synthesis of mixed metallic nanoparticles using room temperature self-assembly

2017 ◽  
Vol 13 (2) ◽  
pp. 4671-4677 ◽  
Author(s):  
A. M. Abdelghany ◽  
A.H. Oraby ◽  
Awatif A Hindi ◽  
Doaa M El-Nagar ◽  
Fathia S Alhakami
Keyword(s):  
Self Assembly ◽  
Metallic Nanoparticles ◽  
Room Temperature ◽  
Bimetallic Nanoparticles ◽  
Reduction Process ◽  
Nano Particles ◽  
Nano Structure ◽  
Small Shift ◽  
Molar Ratios ◽  
Vis Spectroscopy

Bimetallic nanoparticles of silver (Ag) and gold (Au) were synthesized at room temperature using Curcumin. Reduction process of silver and gold ions with different molar ratios leads to production of different nanostructures including alloys and core-shells. Produced nanoparticles were characterized simultaneously with FTIR, UV/vis. spectroscopy, transmission electron microscopy (TEM), and Energy-dispersive X-ray (EDAX). UV/vis. optical absorption spectra of as synthesized nanoparticles reveals presence of surface palsmon resonance (SPR) of both silver at (425 nm) and gold at (540 nm) with small shift and broadness of gold band after mixing with resucing and capping agent in natural extract which suggest presence of bimetallic nano structure (Au/Ag). FTIR and EDAX data approve the presence of bimetallic nano structure combined with curcumin extract. TEM micrographs shows that silver and gold can be synthesized separately in the form of nano particles using curcumin extract. Synthesis of gold nano particles in presence of silver effectively enhance and control formation of bi-metallic structure.

Self-Assembly of a Chiral Cubic Three-Connected Net from the High Symmetry Molecules C60 and SnI4

2020 ◽  
Author(s):  
Daniel B. Straus ◽  
Robert J. Cava
Keyword(s):  
Organic Synthesis ◽  
Self Assembly ◽  
Van Der Waals ◽  
Van Der Waals Forces ◽  
High Symmetry ◽  
Molecular Chirality ◽  
Chiral Materials ◽  
Self Assembled ◽  
Chiral Centers

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.

scholarly journals Nano- and Micropatterning on Optical Fibers by Bottom-Up Approach: The Importance of Being Ordered

2021 ◽  
Vol 11 (7) ◽  
pp. 3254
Author(s):  
Marco Pisco ◽  
Francesco Galeotti
Keyword(s):  
Optical Fiber ◽  
Optical Fibers ◽  
Self Assembly ◽  
Ordered Structures ◽  
Bottom Up ◽  
Photonic Structures ◽  
Fiber Technology ◽  
Optical Fiber Probes ◽  
Fiber Probes ◽  
Self Assembled

The realization of advanced optical fiber probes demands the integration of materials and structures on optical fibers with micro- and nanoscale definition. Although researchers often choose complex nanofabrication tools to implement their designs, the migration from proof-of-principle devices to mass production lab-on-fiber devices requires the development of sustainable and reliable technology for cost-effective production. To make it possible, continuous efforts are devoted to applying bottom-up nanofabrication based on self-assembly to decorate the optical fiber with highly ordered photonic structures. The main challenges still pertain to “order” attainment and the limited number of implementable geometries. In this review, we try to shed light on the importance of self-assembled ordered patterns for lab-on-fiber technology. After a brief presentation of the light manipulation possibilities concerned with ordered structures, and of the new prospects offered by aperiodically ordered structures, we briefly recall how the bottom-up approach can be applied to create ordered patterns on the optical fiber. Then, we present un-attempted methodologies, which can enlarge the set of achievable structures, and can potentially improve the yielding rate in finely ordered self-assembled optical fiber probes by eliminating undesired defects and increasing the order by post-processing treatments. Finally, we discuss the available tools to quantify the degree of order in the obtained photonic structures, by suggesting the use of key performance figures of merit in order to systematically evaluate to what extent the pattern is really “ordered”. We hope such a collection of articles and discussion herein could inspire new directions and hint at best practices to fully exploit the benefits inherent to self-organization phenomena leading to ordered systems.

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