Silver Nanoparticles In Polymer Research Articles

Mesalmine Targeted Water-Compatible Molecularly Imprinted Polymer-Silver Nanoparticles with Surface-Enhanced Raman Spectroscopic (SERS) and Voltammetric Detection

Mesalmine Targeted Water-Compatible Molecularly Imprinted Polymer-Silver Nanoparticles with Surface-Enhanced Raman Spectroscopic (SERS) and Voltammetric Detection

Novel hybrid polymer photovoltaics made by generating silver nanoparticles in polymer:fullerene bulk-heterojunction structures

Here, we developed the high efficient poly(3-hexylthiophene) (P3HT):[6,6]-phenyl C 61-butyric acid butyl ester (PCBB):Ag nanoparticle hybrid photovoltaic cells by generating the silver nanoparticles in the bulk-heterojunction structures of P3HT:PCBB prior to the spin-coating process. Hybrid bulk-heterojunction solar cells with an ITO/(G)-PEDOT/P3HT:PCBB:Ag/Al was fabricated, which shows open-circuit voltage, short-circuit current density, and power conversion efficiency of 0.639 V, 12.29 mA/cm 2, and 4.30% under AM1.5 irradiation (100 mW/cm 2), respectively.

Plasmonic properties of silver in polymer

In the present research silver nanoparticles were produced by e-beam evaporation of metal on polymer-modified silica substrate at room temperature (20 °C) and elevated temperature (80 °C). Modification of the silica substrate was done by different weight concentration polymer (PMMA/PS) blends formed from the polymer solutions by spin coating. The silver layer thickness varied from 1 nm to 10 nm. Silver nanoparticles in polymer matrix were characterized by XRD, AFM and UV–vis spectrometry. The crystalline silver nanoparticles showed surface plasmon resonance (SPR) with absorption maximum at 420–550 nm that was dependent on the silver layer thickness, PMMA and PS weight concentration in polymer blends and substrate temperature during vacuum deposition. The silver nanoparticles in polymer with selective light properties resulting from the controlled SPR shifting to the UV–vis wavelength region were produced.

Effect of the polymer matrix on the formation of silver nanoparticles in polymer–silver salt complex membranes

AbstractWhen polymer–silver salt complex membranes were exposed to UV irradiation, the separation performances of both the permeance and selectivity for propylene–propane decreased, which was primarily attributed to the reduction of the silver ions in the membranes to silver nanoparticles. Here, the effect of the polymer matrix on the formation of silver nanoparticles in the polymer–silver salt complex membranes was investigated. This effect was assessed for the complexes of two kinds of silver salts (AgBF4 and AgCF3SO3) with several polymeric ligands containing three different carbonyl groups, including poly(vinyl pyrrolidone) (PVP) with an amide group, poly(vinyl methyl ketone) (PVMK) with a ketone group, and poly(methyl methacrylate) (PMMA) with an ester group. UV–vis spectra and transmission electron microscopy (TEM) images clearly indicated that the reduction rate of the silver ions has the following order in the various polymer matrices: PVP > PVMK > PMMA, whereas the size and the distribution of the nanoparticles exhibited the reverse order. The tendency to form silver nanoparticles was explained in terms of the differences between the comparative strengths of the interactions of the silver ions with the different carbonyl oxygens in the matrices, as well as that of the silver ions with counteranions, which was characterized by X‐ray photoelectron spectroscopy (XPS) and FT‐Raman spectroscopy. It was concluded that when the concentration of free silver ions was low due to weak polymer–silver ion and strong silver ion–anion interactions, as found with PMMA, the reduction rate of silver ions to silver nanoparticles was slow. Therefore, the PMMA–silver complex membranes were less sensitive to decreases in separation performance upon UV irradiation than compared to the PVP membranes. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 1168–1178, 2006