Electric-field-assisted growth of highly uniform and oriented gold nanotriangles on conducting glass substrates

A method for the growth of highly aligned gold nanotriangles (NTs) on conducting glass surfaces is described. This may be described as 'potential-assisted seed mediated growth'. Atomic force microscopy confirms that all the triangles observed are equilateral and are uniformly stacked. The NT-coated glass exhibits intense near-infrared absorption and strong surface-enhanced Raman activity

Molecular precursor-mediated tuning of gold mesostructures: synthesis and SERRS studies

This article describes the high yield synthesis of a range of anisotropic gold mesostructures such as flowers, cubes, plates, and quasispherical mesostructures using a seed-mediated approach. These structures were formed from precursor seed nanoparticles of gold stabilized by the template, 1,2-phenylenediamine (1,2-PDA). We demonstrated that control of the morphologies from mesoflowers to quasispherical structures is possible with the molecular precursors used in the synthesis of seeds. It was found that concentration of the template, 1,2-PDA added during seed preparation played an important role in the conversion of mesoflowers to quasispherical and cube-like structures. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV-vis spectroscopy and energy dispersive analysis of X-rays (EDAX) were used for the determination of physical and chemical composition of the nano/mesostructures formed. The seed nanoparticles responsible for the formation of these various anisotropic structures were further characterized and analyzed using laser desorption ionization mass spectrometry (LDI MS) and TEM. We demonstrated high surface-enhanced resonance Raman scattering (SERRS) activity of the mesoflowers using crystal violet (CV) as the analyte molecule. The shape-dependent SERRS activity of various meso/nanostructures was also studied. A ~0.8×102 decrease in the SERRS intensity was observed in quasispherical structures compared to mesoflowers. The increased SERRS activity is attributed to the unique shape and nanofeatures present on the mesoflowers, which were absent in the quasispherical mesostructures. We believe that the high SERRS activity exhibited by the mesoflowers may be utilized for developing novel sensors

A fifteen atom silver cluster confined in bovine serum albumin

Luminescent Ag15 clusters confined in bovine serum albumin (BSA) have been prepared by a simple wet chemical route. The luminescence, exhibiting a maximum at 685 nm, is observable to the naked eye. The chemical composition of these clusters was analyzed using matrix assisted laser desorption ionization mass spectrometry (MALDI MS), X-ray photoelectron spectroscopy (XPS), and energy dispersive analysis of X-rays (EDAX). Intact Ag15@BSA is observed by MALDI MS. Multiple charge states of the cluster are observed confirming the mass assignment. The clusters showed a quantum yield of 10.71% in water and the luminescence was stable in a pH range of 1-12. Stability of the clusters was enhanced by the addition of polyvinylpyrrolidone (PVP). The clusters showed luminescence in the solid state as well. Evolution of clusters with variation in the amount of reducing agent added shows that the cluster formation goes through an intermediate state of bound silver, formed instantaneously after the addition of Ag+, which transforms to the cluster. High yield synthesis and exciting photophysical properties make our new material interesting for various applications such as biolabeling and imaging

Electric field enhancement and concomitant Raman spectral effects at the edges of a nanometre-thin gold mesotriangle

The local electric field enhancement at various regions of an individual nanometre-thin gold mesotriangle has been demonstrated both numerically and experimentally. This work provides, for the first time, direct experimental evidence of localized enhancement of Raman signals at three edges of nanometre-thin gold mesotriangles at single particle level, using Raman microscopy. Raman images were collected from mesotriangles of ~11 mm edge length and ~30 nm thickness, using adsorbed crystal violet as the probe molecule. Spatial distribution and the extent of electric field enhancement around a single mesotriangle are investigated theoretically by finite-difference time-domain (FDTD) simulations. Confocal Raman studies provided direct proof for the substantial electrical field enhancement at the edges and corners compared to the face of the mesotriangle. The simulated electric field enhancement was in the order, corner > edge > surface, which is in complete agreement with the experimental results

Biofabrication of Anisotropic Gold Nanotriangles Using Extract of Endophytic Aspergillus clavatus as a Dual Functional Reductant and Stabilizer

Biosynthesis of metal and semiconductor nanoparticles using microorganisms has emerged as a more eco-friendly, simpler and reproducible alternative to the chemical synthesis, allowing the generation of rare forms such as nanotriangles and prisms. Here, we report the endophytic fungus Aspergillus clavatus, isolated from surface sterilized stem tissues of Azadirachta indica A. Juss., when incubated with an aqueous solution of chloroaurate ions produces a diverse mixture of intracellular gold nanoparticles (AuNPs), especially nanotriangles (GNT) in the size range from 20 to 35 nm. These structures (GNT) are of special interest since they possess distinct plasmonic features in the visible and IR regions, which equipped them with unique physical and optical properties exploitable in vital applications such as optics, electronics, catalysis and biomedicine. The reaction process was simple and convenient to handle and was monitored using ultraviolet–visible spectroscopy (UV–vis). The morphology and crystalline nature of the GNTs were determined from transmission electron microscopy (TEM), atomic force spectroscopy (AFM) and X-ray diffraction (XRD) spectroscopy. This proposed mechanistic principal might serve as a set of design rule for the synthesis of anisotropic nanostructures with desired architecture and can be amenable for the large scale commercial production and technical applications

Anisotropic nanomaterials: structure, growth, assembly, and functions

Comprehensive knowledge over the shape of nanomaterials is a critical factor in designing devices with desired functions. Due to this reason, systematic efforts have been made to synthesize materials of diverse shape in the nanoscale regime. Anisotropic nanomaterials are a class of materials in which their properties are direction-dependent and more than one structural parameter is needed to describe them. Their unique and fine-tuned physical and chemical properties make them ideal candidates for devising new applications. In addition, the assembly of ordered one-dimensional (1D), two-dimensional (2D), and three-dimensional (3D) arrays of anisotropic nanoparticles brings novel properties into the resulting system, which would be entirely different from the properties of individual nanoparticles. This review presents an overview of current research in the area of anisotropic nanomaterials in general and noble metal nanoparticles in particular. We begin with an introduction to the advancements in this area followed by general aspects of the growth of anisotropic nanoparticles. Then we describe several important synthetic protocols for making anisotropic nanomaterials, followed by a summary of their assemblies, and conclude with major applications

Adhesion and proliferation of living cell on surface functionalized with glycine nanostructures

This research presents the application of glycine amino acid for establishing firm cell-substrate interaction instead of expensive adhesion proteins, peptides and peptide derivatives. The glycine amino acid is chemically functionalized on the coverslip to achieve self-assembled nanostructure. Glycine self-assembly on NaCl treated coverslips is initiated with SiONa+:COO− linkage while their nanostructure is achieved with formation of glycine chain through NH3+:COO− covalent linkage between the adjacent molecules. The functionalization steps are confirmed by Fourier-transform infrared spectroscopy (FTIR) investigation. The atomic force microscopy (AFM) and scanning electron microscopy (SEM) investigations reveal that glycine growth initiates at 4 Hours (H) post-treatment while maximum growth appears after 8H-10H. Both the vertical and horizontal growth of nanostructures show dependence on functionalization periods. Various levels of glycine functionalized surface show different levels of baby hamster kidney (BHK-21) cell adhesion and proliferation efficiency with maximum performance for 10H functionalized surface. The adhesion and proliferation performance of 10H glycine functionalized surface shows negligible difference when compared with glycine-aspartic acid (RGD) functionalized surface. Finally, growth curves obtained from both glycine and RGD functionalized surface reveal exponential growth phage up to 48H followed by stationary phage between 48H and 72H while death of many cells appears from 72H to 96H. Thus, this research concluded that glycine functionalized surface is equally effective for cell adhesion and proliferation