Title of article :
Formation of novel assembled silver nanostructures from polyglycol solution
Author/Authors :
Jie Zhang، نويسنده , , Ke Liu، نويسنده , , Zhihui Dai، نويسنده , , Yuying Feng، نويسنده , , Jianchun Bao، نويسنده , , Xiangyin Mo، نويسنده ,
Issue Information :
دوهفته نامه با شماره پیاپی سال 2006
Pages :
6
From page :
313
To page :
318
Abstract :
This paper described a simple and mild chemical reduction approach to prepare novel silver nanostructures with different morphologies. Dendritic silver nanostructure was obtained by a fast reduction reaction using hydrazine as a reducing agent in aqueous solution of polyglycol, while both the zigzag and linear Ag nanostructures were slowly assembled using polyglycol as a reducing agent. Powder X-ray diffraction (XRD), transmission electron microscopy (TEM), high-resolution TEM (HRTEM) and field emission scanning electron microscopy (FE-SEM) were used to characterize the obtained silver nanostructures. Fourier transform infrared absorption (FT-IR) spectra were recorded to show that there exists a certain coordination of the oxygen atoms in the polyglycol with Ag+ ions in aqueous solution of the AgNO3/polyglycol. Furthermore, the examination of the morphologies of the products obtained at different stages of the reaction of Ag+ ions with polyglycol revealed that such a coordination is of utmost importance for the formation of the silver nanostructures, namely polyglycol provided lots of active sites for the coordination, nucleation, growth and serves as backbones for directing the assembly of the metal particles formed. The formation mechanism of the dendritic silver nanostructure was called a coordination–reduction–nucleation–growth–fractal growth process. The strong surface plasmon absorption bands at 470 nm for the zigzag silver and at 405 nm for the dendritic silver were found.
Keywords :
electron microscopy , Nanostructures , metals
Journal title :
Materials Chemistry and Physics
Serial Year :
2006
Journal title :
Materials Chemistry and Physics
Record number :
1064897
Link To Document :
بازگشت