Self-Assembly Growth and Size Control of Silver Nanocrystals for Nonvolatile Memory Applications

2009 ◽  
Vol 610-613 ◽  
pp. 585-590 ◽  
Author(s):  
Li Wang ◽  
Hong Fang Sun ◽  
Hui Hua Zhou ◽  
Jing Zhu
Keyword(s):  
Self Assembly ◽  
Nonvolatile Memory ◽  
Single Layer ◽  
Size Control ◽  
Transmission Electron ◽  
Sputtering Power ◽  
High Uniformity ◽  
Memory Applications ◽  
Magnetic Sputtering ◽  
The Relationship

A film with a single-layer of size controlled silver nanocrystals embedded in silicon dioxide (SiO2) dielectric film by magnetic sputtering has been fabricated for nonvolatile memory applications. The effects of sputtering power, deposition time and substrate temperature on Ag nanocrystals formation were investigated. Transmission electron microscopy (TEM) images showed the as-prepared Ag nanocrystals had high uniformity in their size and distribution. The relationship between Ag nanocrystal size, density and electron storage capability as well as date retention time has been discussed.

Pd Nanocrystals-Embedded TiO2 Film Sandwiched Between Al2O3 Layers for Nonvolatile Memory Applications

2011 ◽  
Vol 422 ◽  
pp. 139-145
Author(s):  
Wan Yi Huang ◽  
Hong Bing Chen ◽  
Sun Chen ◽  
Shi Jin Ding ◽  
David Wei Zhang
Keyword(s):  
Self Assembly ◽  
Nonvolatile Memory ◽  
Photoelectron Spectra ◽  
Oxide Semiconductor ◽  
Mos Capacitor ◽  
Injection Speed ◽  
Average Size ◽  
A Charge ◽  
Memory Applications ◽  
Memory Characteristics

Pd nanocrystals embedded in TiO2film are formed in a self-assembly manner by rapid thermal annealing (RTA) of reactively co-sputtered TiPdO films. The cross-section transmission-electron microscopy (TEM) image and X-ray photoelectron spectra (XPS) reveal that the RTA at 800°C for 15 s results in the formation of Pd nanocrystals with an average size of around 10 nm. Further, the metal-oxide-semiconductor (MOS) capacitor with Pd-nanocrystals-embedded TiO2film sandwiched between Al2O3layers has been fabricated and characterized electrically in comparison with the counterpart without Pd nanocrystals, indicating that the formed Pd nanocrystals are dominant charge storage nodes. The fabricated MOS capacitor with Pd nanocrystals exhibits obvious memory characteristics, demonstrating a C-V hysteresis window of about 8.2 V at the sweeping voltage rang of +/-9 V, a flatband voltage shift of ~2V under a constant voltage stress of +9V for 10ns corresponding to a charge injection speed of 6×1012cm-2μs-1. The underlying mechanisms of the memory characteristics under different C-V sweeps have also been discussed.

Monolayer FePt nanocrystal self-assembly embedded into atomic-layer-deposited Al2O3 films for nonvolatile memory applications

2014 ◽  
Vol 588 ◽  
pp. 103-107 ◽  
Author(s):  
Xiao-Jie Liu ◽  
Mo-Yun Gao ◽  
Ai-Dong Li ◽  
Yan-Qiang Cao ◽  
Xue-Fei Li ◽  
...  
Keyword(s):  
Self Assembly ◽  
Nonvolatile Memory ◽  
Atomic Layer ◽  
Memory Applications ◽  
Al2o3 Films

Wüstite nanocrystals: Synthesis, structure and superlattice formation

2007 ◽  
Vol 22 (7) ◽  
pp. 1987-1995 ◽  
Author(s):  
Ming Yin ◽  
Zhuoying Chen ◽  
Brian Deegan ◽  
Stephen O’Brien
Keyword(s):  
Self Assembly ◽  
Three Dimensional ◽  
Size Control ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
Salt Crystal ◽  
Uniform Size ◽  
Nonpolar Solvents ◽  
Transmission Electron ◽  
State Kinetic

Monodisperse ligand-capped cubic wüstite FexO nanocrystals were prepared by a novel thermal decomposition method of iron (II) acetate in the presence of oleic acid as the surfactant. Controlled size distributions of cubic nanoparticles possessing the rock salt crystal structure were isolated in the range 10–18 nm. The influence of molar ratio of surfactant to precursor was investigated to understand size control and monodispersity. Using inexpensive, nontoxic metal salts as reactants, we were able to synthesize gram-scale quantities of relatively monodisperse nanocrystals in a single reaction, without further size selection, characterized by x-ray diffraction and transmission electron microscopy. The procedure enables the collection of samples of uniform size as a function of time, thus permitting a preliminary solid-state kinetic analysis of the reaction as a function of increasing particle size. Following controlled evaporation from nonpolar solvents, self-assembly into two-dimensional arrays, three-dimensional single-component superlattices, and binary superlattices with gold nanoparticles were observed and characterized.

Investigation of ferroelectrics using conventional and in situ electron microscopy

1994 ◽  
Vol 52 ◽  
pp. 586-587
Author(s):  
V. Saikumar ◽  
H. M. Chan ◽  
M. P. Harmer
Keyword(s):  
Nonvolatile Memory ◽  
Ferroelectric Materials ◽  
Gate Insulator ◽  
Sensors And Actuators ◽  
In Situ Electron Microscopy ◽  
Ferroelectric Domains ◽  
Domain Boundaries ◽  
Domain Interactions ◽  
Memory Applications

In recent years, there has been a growing interest in the application of ferroelectric thin films for nonvolatile memory applications and as a gate insulator in DRAM structures. In addition, bulk ferroelectric materials are also widely used as components in electronic circuits and find numerous applications in sensors and actuators. To a large extent, the performance of ferroelectric materials are governed by the ferroelectric domains (with dimensions in the micron to sub-micron range) and the switching of domains in the presence of an applied field. Conventional TEM studies of ferroelectric domains structures, in conjunction with in-situ studies of the domain interactions can aid in explaining the behavior of ferroelectric materials, while providing some answers to the mechanisms and processes that influence the performance of ferroelectric materials. A few examples from bulk and thin film ferroelectric materials studied using the TEM are discussed below.Figure 1 shows micrographs of ferroelectric domains obtained from undoped and Fe-doped BaTiO3 single crystals. The domain boundaries have been identified as 90° domains with the boundaries parallel to <011>.

Bottom-up Evolution from Disks to High-Genus Polymersomes

2018 ◽  
Author(s):  
Claudia Contini ◽  
Russell Pearson ◽  
Linge Wang ◽  
Lea Messager ◽  
Jens Gaitzsch ◽  
...  
Keyword(s):  
Self Assembly ◽  
The Self ◽  
Amphiphilic Copolymers ◽  
Chain Entanglement ◽  
Bottom Up ◽  
New Approach ◽  
High Genus ◽  
Transmission Electron ◽  
Minimal Radius ◽  
Stop Flow

<div><div><div><p>We report the design of polymersomes using a bottom-up approach where the self-assembly of amphiphilic copolymers poly(2-(methacryloyloxy) ethyl phosphorylcholine)–poly(2-(diisopropylamino) ethyl methacrylate) (PMPC-PDPA) into membranes is tuned using pH and temperature. We study this process in detail using transmission electron microscopy (TEM), nuclear magnetic resonance (NMR) spectroscopy, dynamic light scattering (DLS), and stop-flow ab- sorbance disclosing the molecular and supramolecular anatomy of each structure observed. We report a clear evolution from disk micelles to vesicle to high-genus vesicles where each passage is controlled by pH switch or temperature. We show that the process can be rationalised adapting membrane physics theories disclosing important scaling principles that allow the estimation of the vesiculation minimal radius as well as chain entanglement and coupling. This allows us to propose a new approach to generate nanoscale vesicles with genus from 0 to 70 which have been very elusive and difficult to control so far.</p></div></div></div>

Bottom-up Evolution from Disks to High-Genus Polymersomes

2018 ◽  
Author(s):  
Claudia Contini ◽  
Russell Pearson ◽  
Linge Wang ◽  
Lea Messager ◽  
Jens Gaitzsch ◽  
...  
Keyword(s):  
Self Assembly ◽  
The Self ◽  
Amphiphilic Copolymers ◽  
Chain Entanglement ◽  
Bottom Up ◽  
New Approach ◽  
High Genus ◽  
Transmission Electron ◽  
Minimal Radius ◽  
Stop Flow

<div><div><div><p>We report the design of polymersomes using a bottom-up approach where the self-assembly of amphiphilic copolymers poly(2-(methacryloyloxy) ethyl phosphorylcholine)–poly(2-(diisopropylamino) ethyl methacrylate) (PMPC-PDPA) into membranes is tuned using pH and temperature. We study this process in detail using transmission electron microscopy (TEM), nuclear magnetic resonance (NMR) spectroscopy, dynamic light scattering (DLS), and stop-flow ab- sorbance disclosing the molecular and supramolecular anatomy of each structure observed. We report a clear evolution from disk micelles to vesicle to high-genus vesicles where each passage is controlled by pH switch or temperature. We show that the process can be rationalised adapting membrane physics theories disclosing important scaling principles that allow the estimation of the vesiculation minimal radius as well as chain entanglement and coupling. This allows us to propose a new approach to generate nanoscale vesicles with genus from 0 to 70 which have been very elusive and difficult to control so far.</p></div></div></div>

Preparation of BSA Nanoparticles by Desolvation Technique Using Acetone as Desolvating Agent

2012 ◽  
Vol 5 (1) ◽  
pp. 1643-1647
Author(s):  
Krishna Sailaja A ◽  
Amareshwar P
Keyword(s):  
Aqueous Solution ◽  
Standard Deviation ◽  
Process Parameters ◽  
Self Assembly ◽  
Size Control ◽  
Polymeric Materials ◽  
Preparation Condition ◽  
Assembly Process ◽  
Average Size

In order to see the functionality and toxicity of nanoparticles in various food and drug applications, it is important to establish procedures to prepare nanoparticles of a controlled size. Desolvation is a thermodynamically driven self-assembly process for polymeric materials. In this study, we prepared BSA nanoparticles using the desolvation technique using acetone as desolvating agent. Acetone was added intermittently into 1% BSA solution at different pH under stirring at 700 rpm. Amount of acetone added, intermittent timeline of acetone addition, and pH of solution were considered as process parameters to be optimized. The effect of the process parameters on size of the nanoparticles was studied. The results indicated that the size control of BSA nanoparticles was achieved by adding acetone intermittently. The standard deviation of average size of BSA nanoparticles at each preparation condition was minimized by adding acetone intermittently. The intermittent addition in polymeric aqueous solution can be useful for size control for food or drug applications.  

scholarly journals Understanding the role of conjugation length on the self-assembly behaviour of oligophenyleneethynylenes

2021 ◽  
Author(s):  
Beatriz Matarranz ◽  
Goutam Ghosh ◽  
Ramesh Kandanelli ◽  
Angel Sampedro ◽  
Kalathil K. Kartha ◽  
...  
Keyword(s):  
Self Assembly ◽  
The Self ◽  
Conjugation Length ◽  
The Relationship

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

Synthesis and size control of Si nanocrystals by SiO/SiO2 superlattices and Er doping

2002 ◽  
Vol 737 ◽  
Author(s):  
J. Heitmann ◽  
D. Kovalev ◽  
M. Schmidt ◽  
L.X. Yi ◽  
R. Scholz ◽  
...  
Keyword(s):  
Phase Separation ◽  
Crystal Size ◽  
Radiative Lifetime ◽  
Size Control ◽  
Luminescence Signal ◽  
Er Doping ◽  
Size Dependent ◽  
Transmission Electron ◽  
Si Nanocrystals ◽  
Ultrathin Layers

ABSTRACTThe synthesis of nc-Si by reactive evaporation of SiO and subsequent thermal induced phase separation is reported. The size control of nc-Si is realized by evaporation of SiO/SiO2 superlattices. By this method an independent control of crystal size and density is possible. The phase separation of SiO into SiO2 and nc-Si in the limit of ultrathin layers is investigated. Different steps of this phase separation are characterized by photoluminescence, infrared absorption and transmission electron microscopy measurements. The strong room temperature luminescence of nc-Si shows a strong blueshift of the photoluminescence signal from 850 to 750 nm with decreasing crystal size. Several size dependent properties of this luminescence signal, like decreasing radiative lifetime and increasing no-phonon transition properties with decreasing crystal size are in good agreement with the quantum confinement model. Er doping of the nc-Si shows an enhancement of the Er luminescence at 1.54 μm by a factor of 5000 compared to doped SiO2 layers. The decreasing transfer time for the nc-Si to Er transition with decreasing crystal size can be understood as additional proof of increasing recombination probability within the nc-Si for decreasing crystal size.

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