Silver Nanoparticles Ag Research Articles

Plant-based synthesis of silver nanoparticles and their characteristic properties

Biosynthesised metallic nanoparticles (NPs) have a wide range of applications in the fields of medicine and engineering. Among various metallic NPs, silver (Ag) NPs have gained extraordinary fame due to their unique properties. Conventional methods for the synthesis of silver NPs are pernicious due to chemical toxicity and various serious biological concerns. Plant extract-mediated synthesis can rapidly and simply produce eco-friendly, well-dispersed and stable silver NPs from silver nitrate in aqueous conditions without employing any reducing and stabilising agent. This paper intends to present an overview of the potential use of various plants for silver NP synthesis with particular emphasis on the extraordinary anticancer and antimicrobial properties of these NPs against a wide range of cancerous cell lines and bacterial strains. Several plant extracts have naturally biodegradable antioxidants which simultaneously act as reducing and stabilising agents for silver NP. Furthermore, this paper highlights optimum situations for the green synthesis of silver NPs by controlling critical parameters, such as pH, temperature, duration of incubation and concentrations of both silver salt and plant extract. Hence, green synthesis of silver NPs is a promising method which allows for synthesis with low cost and low energy requirement.

N-Vinylcarbazole: As an Additive for Thermal Polymerization at Room Temperature with in situ Formation of Ag(0) Nanoparticules

N-vinylcarbazole (NVK) is proposed as an additive for acrylates thermal free radical polymerization (FRP) and epoxy thermal ring opening polymerization (ROP) at room temperature. The new initiating systems are based on a silane/silver salt/N-vinylcarbazole interaction, which ensures good to excellent polymerization. Moreover, the polymerization is much more efficient under air than under argon. The effects of the N-vinylcarbazole, silane, silver salt and monomer structures are investigated. Interestingly, silver nanoparticles Ag(0) are formed in situ. The as-synthesized nanocomposite materials contained spherical nanoparticles homogeneously dispersed in the polymer matrices. Polymers and nanoparticles were characterized by Differential Scanning Calorimetry (DSC), Transmission Electron Microscopy (TEM), Energy-Dispersive X-ray Spectrometry (EDS), Fourier Transform Infrared Spectroscopy (FTIR), and UV-vis spectroscopy. A coherent picture of the involved chemical mechanisms is presented.

Regeneration of aged-AgNPs via density gradient ultracentrifugal nanoseparation

To reuse aged-silver nanoparticles (AgNPs) and recover the mono-dispersed AgNPs separately, we attempted to recycle the aged-AgNPs with high polydispersity in particle size distribution using the density gradient ultracentrifugation rate (DGUR) separation with five media. Results for the microscopic and spectroscopic showed that Tween series media, which have low density compared to other media, are suitable for the application of DGUR separation for recycling aged-AgNPs. This method might be helpful to regenerate and recycle the precious metal nanoparticles with polydispersity due to long-term storage.

Multimetallic Complexes and Functionalized Nanoparticles Based on Oxygen- and Nitrogen-Donor Combinations

The versatile precursors [Ru(CH═CHC6H4Me-4)Cl(CO)(BTD)(PPh3)2] (BTD = 2,1,3-benzothiadiazole) and [Ru(C(C≡CPh)═CHPh)Cl(CO)(PPh3)2] were treated with isonicotinic acid, 4-cyanobenzoic acid, and 4-(4-pyridyl)benzoic acid under basic conditions to yield [Ru(vinyl)(O2CC5H4N)(CO)(PPh3)2], [Ru(vinyl)(O2CC6H4CN-4)(CO)(PPh3)2], and [Ru(vinyl){O2CC6H4(C5H4N)-4}(CO)(PPh3)2], respectively. The osmium analogue [Os(CH═CHC6H4Me-4)(O2CC5H4N)(CO)(PPh3)2] was also prepared. cis-[RuCl2(dppm)2] was used to prepare the cationic compounds [Ru(O2CC5H4N)(dppm)2](+) and [Ru{O2CC6H4(C5H4N)-4}(dppm)2](+). The treatment of 2 equiv of [Ru(C(C≡CPh)═CHPh)(O2CC5H4N)(CO)(PPh3)2] and [Ru(O2CC5H4N)(dppm)2](+) with AgOTf led to the trimetallic compounds [{Ru(C(C≡CPh)═CHPh)(CO)(PPh3)2(O2CC5H4N)}2Ag](+) and [{Ru(dppm)2(O2CC5H4N)}2Ag](3+). In a similar manner, the reaction of [Ru(O2CC5H4N)(dppm)2](+) with PdCl2 or K2PtCl4 yielded [{Ru(dppm)2(O2CC5H4N)}2MCl2](2+) (M = Pd, Pt). The reaction of [RuHCl(CO)(BTD)(PPh3)2] with HC≡CC6H4F-4 provided [Ru(CH═CHC6H4F-4)Cl(CO)(BTD)(PPh3)2], which was treated with isonicotinic acid and base to yield [Ru(CH═CHC6H4F-4)(O2CC5H4N)(CO)(PPh3)2]. The addition of [Au(C6F5)(tht)] (tht = tetrahydrothiophene) resulted in the formation of [Ru(CH═CHC6H4F-4){O2CC5H4N(AuC6F5)}(CO)(PPh3)2]. Similarly, [Ru(vinyl)(O2CC6H4CN-4)(CO)(PPh3)2] reacted with [Au(C6F5)(tht)] to provide [Ru(vinyl){O2CC6H4(CNAuC6F5)-4}(CO)(PPh3)2]. The reaction of 4-cyanobenzoic acid with [Au(C6F5)(tht)] yielded [Au(C6F5)(NCC6H4CO2H-4)]. This compound was used to prepare [Ru(CH═CHC6H4F-4){O2CC6H4(CNAuC6F5)-4}(CO)(PPh3)2], which was also formed on treatment of [Ru(CH═CHC6H4F-4)(O2CC6H4CN-4)(CO)(PPh3)2] with [Au(C6F5)(tht)]. The known compound [RhCl2(NC5H4CO2)(NC5H4CO2Na)3] and the new complex [RhCl2{NC5H4(C6H4CO2)-4}{NC5H4(C6H4CO2Na)-4}3] were prepared from RhCl3·3H2O and isonicotinic acid or 4-(4-pyridyl)benzoic acid, respectively. The former was treated with [Ru(CH═CHC6H4Me-4)Cl(CO)(BTD)(PPh3)2] to yield [RhCl2{NC5H4CO2(Ru(CH═CHC6H4Me-4)(CO)(PPh3)2}4]Cl. As an alternative route to pentametallic compounds, the Pd-coordinated porphyrin [(Pd-TPP)(p-CO2H)4] was treated with 4 equiv of [Ru(CH═CHR)Cl(CO)(BTD)(PPh3)2] in the presence of a base to yield [(Pd-TPP){p-CO2Ru(CH═CHR)(CO)(PPh3)2}4] (R = C6H4Me-4, CPh2OH). Where R = CPh2OH, treatment with HBF4 led to the formation of [(Pd-TPP){p-CO2Ru(═CHCH═CPh2)(CO)(PPh3)2}4](BF4)4. [(Pd-TPP){p-CO2Ru(dppm)2}4](PF6)4 was prepared from [(Pd-TPP)(p-CO2H)4] and cis-[RuCl2(dppm)2]. The reaction of AgNO3 with sodium borohydride in the presence of [Ru(O2CC5H4N)(dppm)2](+) or [RuR{O2CC6H4(C5H4N)-4}(dppm)2](+) provided silver nanoparticles Ag@[NC5H4CO2Ru(dppm)2](+) and Ag@[NC5H4{C6H4CO2Ru(dppm)2}-4](+).

Localized surface plasmon enhanced microcrystalline–silicon solar cells

A novel type of substrate named “Ag–SP substrate”, in which silver nanoparticles are incorporated, is introduced and utilized as a back reflector for hydrogenated microcrystalline-silicon solar cell in a substrate-type (n-i-p) configuration. Optical and morphological analyses of Ag–SP substrates fabricated with various sizes of silver nanoparticles are systematically performed. It is shown that silver nanoparticles in Ag–SP substrate structure can lead to significant scattering of light when their diameter increases up to 300nm. Furthermore, the photocurrent of the solar cell fabricated on an Ag–SP substrate with RMS roughness as small as 16.5nm and a proper lateral diameter (approximately 300nm) of silver nanoparticles is improved as compared to that of the solar cell prepared on reference textured substrate with RMS roughness of 25.3nm, owing to strong scattering of light by silver nanoparticles in the red-infrared region.

A Complete Green Protocol: Wrapping of Multiwall Carbon Nanotubes with Silver Nanoparticles

Silver nanoparticles have been wrapped on multiwall carbon nanotubes though a green synthesis approach that has advantages over other conventional methods that involve chemical agents associated with environmental toxicity and damage of carbon nanotubes. Acacia was used as a green stabilizer for multiwall carbon nanotubes as well as a stabilizer and reducing agent for silver nanoparticles. Generation of silver-decorated multiwall carbon nanotubes was confirmed by UV-Vis spectrophotometry and X-ray diffraction. Generation of silver nanoparticles (5-10 nm) wrapped on MWCNTs was confirmed by field emission scanning electron microscopy and transmission electron microscopy.

New Initiating Systems for Thermal Cationic Polymerization at Ambient Temperature with in situ Formation of Ag(0) Nanoparticles: A Silane/Silver Salt Combination

AbstractNew initiating systems for the thermal cationic polymerization of epoxides and vinyl ether derivatives are proposed. They are based on a silane/silver salt interaction, which ensures a good to excellent polymerization at room temperature. Moreover, the polymerization is much more efficient under air. The effects of the silane, silver salt, and monomer structures are investigated. Interestingly, silver nanoparticles Ag(0) are formed in situ. A coherent picture of the involved chemical mechanisms is presented.magnified image

Formation of nanoparticles and nanorods via UV irradiation of AgNO 3 solutions

The synthesis of silver nanoparticles via UV irradiation of AgNO 3 solutions was controlled by using UV–vis absorption spectra and TEM (transmission electron microscope) images. The UV–vis absorption method is good enough for the general control of synthesis process, and TEM images give us information about size of formed species. For investigated solutions of silver nitrate in ethanol and water, we observed formation of large nanoparticles (size about 100 nm) and nanorods (100 nm in length). Moreover, there was effort to confirm evidence of formation of these particles by using TOF mass spectrometer. Due to laser desorption/ionization process there is only evidence of small silver nanoparticles Ag x , x ≤ 4 (clusters), and variety of silver compounds Ag x N y O z ( x ≤ 5, y ≤ 2, z ≤ 3).