Electric field-directed assembly of fullerene crystal rods into hierarchical films

2018 ◽  
Vol 6 (41) ◽  
pp. 11118-11127 ◽  
Author(s):  
Angela C. Stelson ◽  
Sonny J. Penterman ◽  
Chekesha M. Liddell Watson
Keyword(s):  
Electric Field ◽  
Material Properties ◽  
Self Assembly ◽  
Directed Assembly

Self-assembly of nanomaterials with desired material properties requires assembly control from nanometer to millimeter scales.

scholarly journals Electric-Field-Directed Self-Assembly of Active Enzyme-Nanoparticle Structures

2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
Alexander P. Hsiao ◽  
Michael J. Heller
Keyword(s):  
Electric Field ◽  
Self Assembly ◽  
Microelectrode Array ◽  
Glucose Sensor ◽  
Directed Assembly ◽  
Passive Layer ◽  
Higher Order ◽  
Significant Loss ◽  
Layer By Layer ◽  
Multilayered Structures

A method is presented for the electric-field-directed self-assembly of higher-order structures composed of alternating layers of biotin nanoparticles and streptavidin-/avidin-conjugated enzymes carried out on a microelectrode array device. Enzymes included in the study were glucose oxidase (GOx), horseradish peroxidase (HRP), and alkaline phosphatase (AP); all of which could be used to form a light-emitting microscale glucose sensor. Directed assembly included fabricating multilayer structures with 200 nm or 40 nm GOx-avidin-biotin nanoparticles, with AP-streptavidin-biotin nanoparticles, and with HRP-streptavidin-biotin nanoparticles. Multilayered structures were also fabricated with alternate layering of HRP-streptavidin-biotin nanoparticles and GOx-avidin-biotin nanoparticles. Results showed that enzymatic activity was retained after the assembly process, indicating that substrates could still diffuse into the structures and that the electric-field-based fabrication process itself did not cause any significant loss of enzyme activity. These methods provide a solution to overcome the cumbersome passive layer-by-layer assembly methods to efficiently fabricate higher-order active biological and chemical hybrid structures that can be useful for creating novel biosensors and drug delivery nanostructures, as well as for diagnostic applications.

scholarly journals An In-Situ Reaction Route to Molecular Level Dispersed Bisimide and ZnO Nanorod Hybrids with Efficient Photo-Induced Charge Transfer

2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Chunzheng Lv ◽  
Lirong He ◽  
Jiahong Tang ◽  
Feng Yang ◽  
Chuhong Zhang
Keyword(s):  
Charge Transfer ◽  
Electric Field ◽  
Self Assembly ◽  
Molecular Level ◽  
Surface Photovoltage ◽  
Zno Nanorod ◽  
In Situ Reaction ◽  
Perylene Bisimide ◽  
Induced Charge

AbstractAs an important photoconductive hybrid material, perylene/ZnO has attracted tremendous attention for photovoltaic-related applications, but generally faces a great challenge to design molecular level dispersed perylenes/ZnO nanohybrids due to easy phase separation between perylenes and ZnO nanocrystals. In this work, we reported an in-situ reaction method to prepare molecular level dispersed H-aggregates of perylene bisimide/ZnO nanorod hybrids. Surface photovoltage and electric field-induced surface photovoltage spectrum show that the photovoltage intensities of nanorod hybrids increased dramatically for 100 times compared with that of pristine perylene bisimide. The enhancement of photovoltage intensities resulting from two aspects: (1) the photo-generated electrons transfer from perylene bisimide to ZnO nanorod due to the electric field formed on the interface of perylene bisimide/ZnO; (2) the H-aggregates of perylene bisimide in ZnO nanorod composites, which is beneficial for photo-generated charge separation and transportation. The introduction of ordered self-assembly thiol-functionalized perylene-3,4,9,10-tetracarboxylic diimide (T-PTCDI)/ ZnO nanorod composites induces a significant improvement in incident photo-to-electron conversion efficiency. This work provides a novel mentality to boost photo-induced charge transfer efficiency, which brings new inspiration for the preparation of the highly efficient solar cell.

DNA-based self-assembly of nanostructures

2017 ◽  
Author(s):  
Joshua D. Carter ◽  
Chenxiang Lin ◽  
Yan Liu ◽  
Hao Yan ◽  
Thomas H. LaBean
Keyword(s):  
Self Assembly ◽  
Materials Science ◽  
Directed Assembly ◽  
Building Blocks ◽  
Hierarchical Assembly ◽  
Synthetic Dna ◽  
Nanoscale Manufacturing ◽  
Covalently Linked ◽  
Design Construction ◽  
Proteins And Peptides

This article examines the DNA-based self-assembly of nanostructures. It first reviews the development of DNA self-assembly and DNA-directed assembly, focusing on the main strategies and building blocks available in the modern molecular construction toolbox, including the design, construction, and analysis of nanostructures composed entirely of synthetic DNA, as well as origami nanostructures formed from a mixture of synthetic and biological DNA. In particular, it considers the stepwise covalent synthesis of DNA nanomaterials, unmediated assembly of DNA nanomaterials, hierarchical assembly, nucleated assembly, and algorithmic assembly. It then discusses DNA-directed assembly of heteromaterials such as proteins and peptides, gold nanoparticles, and multicomponent nanostructures. It also describes the use of complementary DNA cohesion as 'smart glue' for bringing together covalently linked functional groups, biomolecules, and nanomaterials. Finally, it evaluates the potential future of DNA-based self-assembly for nanoscale manufacturing for applications in medicine, electronics, photonics, and materials science.

Self-Assembly of Monolayers of Submicron Sized Particles on Thin Liquid Films

2013 ◽  
Author(s):  
Shriram Pillapakkam ◽  
N. A. Musunuri ◽  
P. Singh
Keyword(s):  
Electric Field ◽  
Self Assembly ◽  
Uv Light ◽  
Capillary Forces ◽  
Liquid Films ◽  
Thin Liquid Films ◽  
Liquid Interfaces ◽  
Uv Curable ◽  
Particle Monolayer ◽  
Uv Curable Resin

In this paper, we present a technique for freezing monolayers of micron and sub-micron sized particles onto the surface of a flexible thin film after the self-assembly of a particle monolayer on fluid-liquid interfaces has been improved by the process we have developed where an electric field is applied in the direction normal to the interface. Particles smaller than about 10 microns do not self-assemble under the action of lateral capillary forces alone since capillary forces amongst them are small compared to Brownian forces. We have overcome this problem by applying an electric field in the direction normal to the interface which gives rise to dipoledipole and capillary forces which cause the particles to arrange in a triangular pattern. The technique involves assembling the monolayer on the interface between a UV-curable resin and another liquid by applying an electric field, and then curing the resin by applying UV light. The monolayer becomes embedded on the surface of the solidified resin film.

Numerical Simulations of Electric Field Driven Self-Assembly of Monolayers of Mixtures of Nanoparticles

2017 ◽  
Author(s):  
E. Amah ◽  
N. Musunuri ◽  
Ian S. Fischer ◽  
Pushpendra Singh
Keyword(s):  
Electric Field ◽  
Physical Properties ◽  
Numerical Simulations ◽  
Self Assembly ◽  
Composite Particle ◽  
Critical Value ◽  
Direct Numerical Simulations ◽  
Composite Particles ◽  
Liquid Interfaces ◽  
Induced Dipole

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.

PIEZOELECTRIC MATERIAL AND ONE-DIMENSIONAL PHONONIC CRYSTAL

2019 ◽  
Vol 26 (02) ◽  
pp. 1850144 ◽  
Author(s):  
ARAFA H. ALY ◽  
AHMED NAGATY ◽  
Z. KHALIFA
Keyword(s):  
Electric Field ◽  
Piezoelectric Material ◽  
Material Properties ◽  
Phononic Crystal ◽  
Defect Layer ◽  
Phononic Crystals ◽  
Localized Modes ◽  
One Dimensional ◽  
Energy Applications ◽  
Relative Change

We have theoretically obtained the transmittance properties of one-dimensional phononic crystals incorporating a piezoelectric material as a defect layer. We have used the transfer matrix method in our analysis with/without defect materials. By increasing the thickness of the defect layer, we obtained a sharp peak created within the bandgap, that indicates to the significance of defect layer thickness on the band structure. The localized modes and a particular intensity estimated within the bandgap depend on the piezoelectric material properties. By applying different quantities of an external electric field, the position of the peak shifts to different frequencies. The electric field induces a relative change in the piezoelectric thickness. Our structure may be very useful in some applications such as sensors, acoustic switches, and energy applications.

Molecular Self-Assembly under Nanoconfinement: Indigo Carmine Scroll Structures Entrapped Within Polymeric Capsules

Nanoscale ◽  
2021 ◽  
Author(s):  
Inbal Maor ◽  
Naama Koifman ◽  
Ellina Kesselman ◽  
Pnina Matsanov ◽  
Ilan Shumilin ◽  
...  
Keyword(s):  
Material Properties ◽  
Self Assembly ◽  
Indigo Carmine ◽  
The Self

Molecular self-assembly forms structures of well-defined organization that allow control over material properties, affording many advanced technological applications. Although the self-assembly of molecules is seemingly spontaneous, the structure into which...

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