Size and Morphology Adjustment of PVP-Stabilized Silver and Gold Nanocrystals Synthesized by Hydrodynamic Assisted Self-Assembly

2009 ◽  
Vol 113 (20) ◽  
pp. 8595-8600 ◽  
Author(s):  
Licheng Liu ◽  
Ting Wei ◽  
Xiao Guan ◽  
Xuehong Zi ◽  
Hong He ◽  
...  
RSC Advances ◽  
2016 ◽  
Vol 6 (62) ◽  
pp. 57320-57326 ◽  
Author(s):  
Yanting Liu ◽  
Jun Zhou ◽  
Lu Zhou ◽  
Edwin Yue-Bun Pun ◽  
Tao Jiang ◽  
...  

Self-assembly structures of different types of polyhedral nanocrystals through drop casting method and their plasmonic enhancement characteristics and SERS performances due to the nano-antenna effect.


2011 ◽  
Vol 133 (28) ◽  
pp. 10760-10763 ◽  
Author(s):  
Jibin Song ◽  
Lin Cheng ◽  
Aiping Liu ◽  
Jun Yin ◽  
Min Kuang ◽  
...  

Polymers ◽  
2020 ◽  
Vol 12 (11) ◽  
pp. 2572
Author(s):  
Jaleesa Bresseleers ◽  
Mahsa Bagheri ◽  
Coralie Lebleu ◽  
Sébastien Lecommandoux ◽  
Olivier Sandre ◽  
...  

The careful design of nanoparticles, in terms of size and morphology, is of great importance to developing effective drug delivery systems. The ability to precisely tailor nanoparticles in size and morphology during polymer self-assembly was therefore investigated. Four poly(ethylene glycol)-b-poly(N-2-benzoyloxypropyl methacrylamide) mPEG-b-p(HPMA-Bz) block copolymers with a fixed hydrophilic block of mPEG 5 kDa and a varying molecular weight of the hydrophobic p(HPMA-Bz) block (A: 17.1, B: 10.0, C: 5.2 and D: 2.7 kDa) were self-assembled into nanoparticles by nanoprecipitation under well-defined flow conditions, using microfluidics, at different concentrations. The nanoparticles from polymer A, increased in size from 55 to 90 nm using lower polymer concentrations and slower flow rates and even polymer vesicles were formed along with micelles. Similarly, nanoparticles from polymer D increased in size from 35 to 70 nm at slower flow rates and also formed vesicles along with micelles, regardless of the used concentration. Differently, polymers B and C mainly self-assembled into micelles at the different applied flow rates with negligible size difference. In conclusion, this study demonstrates that the self-assembly of mPEG-b-p(HPMA-Bz) block copolymers can be easily tailored in size and morphology using microfluidics and is therefore an attractive option for further scaled-up production activities.


2013 ◽  
Vol 24 (5) ◽  
pp. 055601 ◽  
Author(s):  
Shu Jun Zhen ◽  
Zhong Yue Zhang ◽  
Na Li ◽  
Zhi Dong Zhang ◽  
Jian Wang ◽  
...  

2017 ◽  
Vol 8 (23) ◽  
pp. 3647-3656 ◽  
Author(s):  
Ryoto Tanaka ◽  
Kodai Watanabe ◽  
Takuya Yamamoto ◽  
Kenji Tajima ◽  
Takuya Isono ◽  
...  

The effect of intramolecular cross-linking on aqueous self-assembly behavior was systematically investigated based on an amphiphilic block copolymer system.


Nanoscale ◽  
2017 ◽  
Vol 9 (43) ◽  
pp. 16922-16936 ◽  
Author(s):  
Ke-Yi Jiang ◽  
Ya-Li Weng ◽  
Si-Yi Guo ◽  
Yan Yu ◽  
Fang-Xing Xiao

A cooperative synergy arising from the SPR and electron-withdrawal effects of gold nanocrystals was simultaneously and unambiguously unraveled for plasmonic photoredox catalysis.


2012 ◽  
Vol 48 (11) ◽  
pp. 1677-1679 ◽  
Author(s):  
Abdennour Abbas ◽  
Limei Tian ◽  
Ramesh Kattumenu ◽  
Abigail Halim ◽  
Srikanth Singamaneni

2019 ◽  
Vol 123 (40) ◽  
pp. 24714-24722 ◽  
Author(s):  
Shuang Lin ◽  
Xiang Lin ◽  
Yuxin Shang ◽  
Siqingaowa Han ◽  
Wuliji Hasi ◽  
...  

2014 ◽  
Vol 1706 ◽  
Author(s):  
Hiroaki Wakayama ◽  
Hirotaka Yonekura ◽  
Yasuaki Kawai

ABSTRACTPeriodically ordered nanohetero inorganic structures offer great promise due to their unique electric, ionic, magnetic, and photonic properties. Many studies have focused on the formation of periodically ordered nano-hetero inorganic structures through layer-by-layer adsorption, sputtering, and self-assembly methods. However, the construction of three-dimensional periodically ordered nanohetero inorganic structures with desired sizes and morphologies remains a great challenge. We present a simple method for producing three-dimensional periodically ordered inorganic nanoheterostructures with controlled shape and size by replicating self-assembled block copolymers (BCPs) containing precursors of metals and metal oxides. Precursors were dissolved with BCPs in a solvent. Upon evaporation of the solvent, each precursor was selectively introduced into a separate polymer block. Application of an external magnetic field (10 T) to the BCP-precursor composites resulted in a phase transition of from spheres to hexagonal cylinders. Subsequent pyrolytic removal of the BCPs produced periodically ordered nanoheterostructures that were structural replicates of the precursor–BCP composites. Self-assembled nano-hetero inorganic structures of nanoparticles, nanorods and layers in a matrix were produced. The morphology and domain size can be tailored by controlling the molecular weight and relative block length of block copolymers. The controlled size and morphology of the inorganic nanoheterostructures demonstrate the method’s utility for producing highly functional materials.


Molecules ◽  
2021 ◽  
Vol 26 (22) ◽  
pp. 6943
Author(s):  
Jesus G. Ovejero ◽  
Miguel A. Garcia ◽  
Pilar Herrasti

The Pechini method has been used as a synthetic route for obtaining self-assembling magnetic and plasmonic nanoparticles in hybrid silica nanostructures. This manuscript evaluates the influence of shaking conditions, reaction time, and pH on the size and morphology of the nanostructures produced. The characterization of the nanomaterials was carried out by transmission electron microscopy (TEM) to evaluate the coating and size of the nanomaterials, Fourier-transform infrared spectroscopy (FT-IR) transmission spectra to evaluate the presence of the different coatings, and thermogravimetric analysis (TGA) curves to determine the amount of coating. The results obtained show that the best conditions to obtain core–satellite nanostructures with homogeneous silica shells and controlled sizes (<200 nm) include the use of slightly alkaline media, the ultrasound activation of silica condensation, and reaction times of around 2 hours. These findings represent an important framework to establish a new general approach for the click chemistry assembling of inorganic nanostructures.


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