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Register a new userSingle step synthesis and organization of gold colloids assisted by copolymer templates
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We report here an original single-step process for synthesis and self-organization of gold colloids by simply incorporating gold salts into a solution prepared with Polystyrene (PS) - Polymethylmethacrylate (PMMA) copolymer, thiolated PS and Propylene Glycol Methyl Ether Acetate (PGMEA) as solvent. The spin-coating and annealing of this solution allows then the formation of PS domains. Depending on the polymer concentration of the as-prepared solution, there can be either one or several gold nanoparticles (NPs) per PS domains. For high concentration of gold nanoparticles in PS domains, the coupling between plasmonic nanoparticles leads to the observation of second peak in the optical extinction spectrum. Such collective effect could be relevant for the development of optical strain sensors in the next future.
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Inverse patchy colloids are nano- to micro-scale particles with a surface divided into differently charged regions. This class of colloids combines directional, selective bonding with a relatively simple particle design: owing to the competitive interplay between the orientation-dependent attraction and repulsion -- induced by the interactions between like/oppositely charged areas -- experimentally accessible surface patterns are complex enough to favor the stabilization of specific structures of interest. Most important, the behavior of heterogeneously charged units can be ideally controlled by means of external parameters, such as the pH and the salt concentration. We present a concise review about this class of systems, spanning the range from the synthesis of model inverse patchy particles to their self-assembly, covering their coarse-grained modeling and the related numerical/analytical treatments.
The investigation of the Localized Surface Plasmon Resonance for plasmonic nanoparticles has opened new perspectives for optical nanosensors. Today, an issue in plasmonics is the development of large scale and low cost devices. We focus here on the Langmuir-Blodgett technique to self-organize gold nanoparticles (~ 7 nm) into rings (~ 60 nm) via polystyrene-b-polymethylmethacrylate templates. In particular, we investigated the optical properties of organized gold nanoparticle rings over large areas and report experimental evidence for plasmon resonances of both individual nanoparticles and collective modes. This paves the way for designing devices with multiple resonances in the visible-Infra-red spectrum and developing optical sensors.
We present here an original process combining top-down and bottom-up approaches by annealing a thin gold film evaporated onto a hole template made by etching a PS-PMMA copolymer film. Such process allows a better control of the gold nanoparticle size distribution which provides a sharper localized surface plasmon resonance. This makes such route appealing for sensing applications since the figure of merit of the Au nanoparticles obtained after thermal evaporation is more than doubled. Such process could besides allow tuning the localized surface plasmon resonance by using copolymer with various molecular weights and thus be attractive for surface enhanced raman spectroscopy.
Polymer assisted spherical FeNi nanoparticles were prepared via wet chemical method using hydrazine as a reducing agent and polymers (PVP and PEG) as reducing and stabilizing agent. Structural studies performed using XRD and TEM shows uniform dispersion of fine FeNi nanocrystallites in nanocomposite particles. The size and thermal stability of FeNi nanoparticles prepared under same reaction condition was found to be dependent on the type and the molecular weight of the polymer used. However, the magnetic properties of nanocomposite particles were not influenced by the polymers. The study highlights subtle differences in using polymers during the synthesis of alloyed nanocomposite particles.
Ternary nitride materials hold promise for many optical, electronic, and refractory applications yet their preparation via solid-state synthesis remains challenging. Often, high pressures or reactive gasses are used to manipulate the effective chemical potential of nitrogen, yet these strategies require specialized equipment. Here we report on a simple two-step synthesis using ion-exchange reactions that yield rocksalt-derived MgZrN$_2$ and Mg$_2$NbN$_3$, as well as layered MgMoN$_2$. All three compounds show nearly temperature-independent and weak paramagnetic responses to an applied magnetic field at cryogenic temperatures indicating phase pure products. The key to synthesizing these ternary materials is an initial low-temperature step (300-450 $^{circ}$C) to promote Mg-M-N bond formation. Then the products are annealed (800-900 $^{circ}$C) to increase crystalline domains of the ternary product. Calorimetry experiments reveal that initial reaction temperatures are determined by phase transitions of reaction precursors, whereas heating directly to high temperatures results in decomposition. These two-step reactions provide a rational guide to material discovery of other bulk ternary nitrides.
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