Hematite Nano Cubes and the Prototypes of Their Self Assembly Investigated Using Tem

1996 ◽  
Vol 432 ◽  
Author(s):  
San Yu ◽  
Shihai Kan ◽  
Guangtian Zou ◽  
Xiaogang Peng ◽  
Dongmei Li ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Self Assembly ◽  
Short Range ◽  
The Self ◽  
Magnetic Feature ◽  
Preferential Growth ◽  
Single Crystalline ◽  
Transmission Electron ◽  
Assembly Feature ◽  
Equilibrium Shapes

AbstractMonodisperse hematite cubes about 30nm in size have been prepared by aging a refluxing acidified aqueous solution of FeCl3 in an open vessel. The as grown nano cubes were determined to be single crystalline hematite in perfect cubic shapes using transmission electron microscope and electron diffraction. The nano cube is one of the equilibrium shapes of hematite, which is resumed to be formed by preferential growth in certain crystallographic directions through the species diffusion in the aqueous solutions.Some self-assembly prototypes have been observed, such as the short range ordered buildup consisting of several brick-like hematite nano cubes and the nano box consisted of square plates of hematite nanocrystals. The drive force for the formation of the above assemblies is assumed to be the unique magnetic feature of the single crystalline hematite nano cubes.The perfect shape and the self-assembly feature give a possibility to fabricate bulk ceramics orderly assembled using hematite nano cubes.

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>

scholarly journals Self-Assembled Nanomaterials Based on Complementary Sn(IV) and Zn(II)-Porphyrins, and Their Photocatalytic Degradation for Rhodamine B Dye

Molecules ◽  
2021 ◽  
Vol 26 (12) ◽  
pp. 3598
Author(s):  
Nirmal K. Shee ◽  
Hee-Joon Kim
Keyword(s):  
Aqueous Solution ◽  
Visible Light Irradiation ◽  
Rhodamine B ◽  
Self Assembly ◽  
The Self ◽  
Assembly Process ◽  
Absorption Bands ◽  
Ligand Coordination ◽  
Rhodamine B Dye ◽  
Metal Ligand

A series of porphyrin triads (1–6), based on the reaction of trans-dihydroxo-[5,15-bis(3-pyridyl)-10,20-bis(phenyl)porphyrinato]tin(IV) (SnP) with six different phenoxy Zn(II)-porphyrins (ZnLn), was synthesized. The cooperative metal–ligand coordination of 3-pyridyl nitrogens in the SnP with the phenoxy Zn(II)-porphyrins, followed by the self-assembly process, leads to the formation of nanostructures. The red-shifts and remarkable broadening of the absorption bands in the UV–vis spectra for the triads in CHCl3 indicate that nanoaggregates may be produced in the self-assembly process of these triads. The emission intensities of the triads were also significantly reduced due to the aggregation. Microscopic analyses of the nanostructures of the triads reveal differences due to the different substituents on the axial Zn(II)-porphyrin moieties. All these nanomaterials exhibited efficient photocatalytic performances in the degradation of rhodamine B (RhB) dye under visible light irradiation, and the degradation efficiencies of RhB in aqueous solution were observed to be 72~95% within 4 h. In addition, the efficiency of the catalyst was not impaired, showing excellent recyclability even after being applied for the degradation of RhB in up to five cycles.

Facile synthesis of ultrathin single-crystalline palladium nanowires with enhanced electrocatalytic activities

2016 ◽  
Vol 52 (88) ◽  
pp. 12996-12999 ◽  
Author(s):  
Dongdong Xu ◽  
Xiaoli Liu ◽  
Min Han ◽  
Jianchun Bao
Keyword(s):  
Self Assembly ◽  
The Self ◽  
Facile Synthesis ◽  
Single Crystalline ◽  
Palladium Nanowires

Ultrathin single-crystalline palladium nanowires could be rapidly synthesized by the self-assembly of a specific surfactant dioctadecyldimethylammonium chloride.

scholarly journals Self-assembled chromogen-loaded polymeric cocoon for respiratory virus detection

Nanoscale ◽  
2021 ◽  
Vol 13 (1) ◽  
pp. 388-396
Author(s):  
Indra Memdi Khoris ◽  
Akhilesh Babu Ganganboina ◽  
Tetsuro Suzuki ◽  
Enoch Y. Park
Keyword(s):  
Aqueous Solution ◽  
Self Assembly ◽  
Respiratory Virus ◽  
Virus Detection ◽  
The Self ◽  
Signal Molecules ◽  
Self Assembled

Inspired by the self-assembly approach, in this work, the chromogen, 3,3′,5,5′-tetramethylbenzidine (TMB), was successfully co-precipitated in aqueous solution to form collective nanoparticles (NPs) of signal molecules (TMB-NPs).

Preparation and Characterization of Carbon Nanotubes/Al2O3 Inorganic Hybrid Material - A Bio-Inspired Poly(Dopamine) Approach

2018 ◽  
Vol 54 ◽  
pp. 127-135
Author(s):  
Wen Zhao ◽  
Wen Cai Wang ◽  
Yong Lai Lu ◽  
Li Qun Zhang
Keyword(s):  
Carbon Nanotubes ◽  
Aqueous Solution ◽  
Photoelectron Spectroscopy ◽  
Oxidative Polymerization ◽  
The Self ◽  
Liquid Phase Deposition ◽  
X Ray ◽  
Transmission Electron ◽  
Cnts Surface

Carbon nanotubes/alumina (CNTs/Al2O3) nanocomposites were prepared by the poly (dopamine) assisted chemical liquid phase deposition (CLPD). The poly (dopamine) layers were firstly coated on the CNTs surface uniformly by the self-oxidative polymerization of dopamine in mild aqueous solution and then the Al2O3 nanoparticles formed on the poly (dopamine) coated CNTs surface by the CLPD. The hydrophilic poly (dopamine) layers on the CNTs surface can improve the dispersion of CNTs in aqueous solution. Moreover, it can be used as a key linker between the CNTs and Al2O3 because of the nitrogen-containing group in poly (dopamine) could coordinate with Al3+ ions. The as-prepared poly (dopamine) coated CNTs and CNTs/Al2O3 nanohybrids were characterized by X-ray photoelectron spectroscopy (XPS), X-radial diffractometer (XRD) and high resolution transmission electron microscopy (HRTEM). These results showed that the poly (dopamine) layers were coated on the surface of CNTs uniformly, and the Al2O3 nanoparticles embellished with the poly (dopamine) coated CNTs surface. Compared with pristine NR composites, the thermal conductivity of the as-prepared NR/CNTs@Al2O3 composites increased 17%.

scholarly journals Relationship between Side-Chain Polarity and the Self-Assembly Characteristics of Perylene Diimide Derivatives in Aqueous Solution

ChemistryOpen ◽  
2017 ◽  
Vol 6 (2) ◽  
pp. 266-272 ◽  
Author(s):  
Jurgen Schill ◽  
Lech-Gustav Milroy ◽  
Jody A. M. Lugger ◽  
Albertus P. H. J. Schenning ◽  
Luc Brunsveld
Keyword(s):  
Aqueous Solution ◽  
Self Assembly ◽  
The Self ◽  
Perylene Diimide ◽  
Side Chain ◽  
Perylene Diimide Derivatives
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