Nanocomposites of polymer and inorganic nanoparticles for optical and magnetic applications

This article provides an up-to-date review on nanocomposites composed of inorganic nanoparticles and the polymer matrix for optical and magnetic applications. Optical or magnetic characteristics can change upon the decrease of particle sizes to very small dimensions, which are, in general, of major interest in the area of nanocomposite materials. The use of inorganic nanoparticles into the polymer matrix can provide high-performance novel materials that find applications in many industrial fields. With this respect, frequently considered features are optical properties such as light absorption (UV and color), and the extent of light scattering or, in the case of metal particles, photoluminescence, dichroism, and so on, and magnetic properties such as superparamagnetism, electromagnetic wave absorption, and electromagnetic interference shielding. A general introduction, definition, and historical development of polymer–inorganic nanocomposites as well as a comprehensive review of synthetic techniques for polymer–inorganic nanocomposites will be given. Future possibilities for the development of nanocomposites for optical and magnetic applications are also introduced. It is expected that the use of new functional inorganic nano-fillers will lead to new polymer–inorganic nanocomposites with unique combinations of material properties. By careful selection of synthetic techniques and understanding/exploiting the unique physics of the polymeric nanocomposites in such materials, novel functional polymer–inorganic nanocomposites can be designed and fabricated for new interesting applications such as optoelectronic and magneto-optic applications

Roadmap on holography

From its inception holography has proven an extremely productive and attractive area of research. While specific technical applications give rise to 'hot topics', and three-dimensional (3D) visualisation comes in and out of fashion, the core principals involved continue to lead to exciting innovations in a wide range of areas. We humbly submit that it is impossible, in any journal document of this type, to fully reflect current and potential activity; however, our valiant contributors have produced a series of documents that go no small way to neatly capture progress across a wide range of core activities. As editors we have attempted to spread our net wide in order to illustrate the breadth of international activity. In relation to this we believe we have been at least partially successful.This work was supported by Ministerio de Economía, Industria y Competitividad (Spain) under projects FIS2017-82919-R (MINECO/AEI/FEDER, UE) and FIS2015-66570-P (MINECO/FEDER), and by Generalitat Valenciana (Spain) under project PROMETEO II/2015/015

Roadmap on holography

From its inception holography has proven an extremely productive and attractive area of research. While specific technical applications give rise to 'hot topics', and three-dimensional (3D) visualisation comes in and out of fashion, the core principals involved continue to lead to exciting innovations in a wide range of areas. We humbly submit that it is impossible, in any journal document of this type, to fully reflect current and potential activity; however, our valiant contributors have produced a series of documents that go no small way to neatly capture progress across a wide range of core activities. As editors we have attempted to spread our net wide in order to illustrate the breadth of international activity. In relation to this we believe we have been at least partially successful

Spontaneous Formation of Fractal Aggregates of Au Nanoparticles in Epoxy-Siloxane Films and Their Application as Substrates for NIR Surface Enhanced Raman Spectroscopy

We present a facile, inexpensive route to free-standing, thermo-mechanically robust and flexible epoxy-siloxane substrates embedded with fractal aggregates of Au nanoparticles, and demonstrate their efficiency as substrates for surface enhanced Raman spectroscopy (SERS) at NIR wavelengths. The metallodielectric films are prepared by generating Au nanoparticles through the in-situ reduction of gold (III) chloride trihydrate in epoxypropoxypropyl terminated polydimethyl siloxane (EDMS). The metal nanoparticles spontaneously aggregate into fractal structures in the colloid, which could then be drop-cast onto a substrate. Subsequent UV-initiated cationic polymerization of epoxide moieties in EDMS transforms the fluid colloid into a thin, free-standing film, which contains a dense distribution of fractal aggregates of Au nanoparticles. We used electron and optical microscopy as well as UV–Vis–NIR spectrometry to monitor the evolution of nanoparticles and to optically and structurally characterize the resulting films. Raman spectroscopy of the chromophore Eosin Y adsorbed onto the metallodielectric films showed that they are excellent SERS substrates at NIR excitation with an enhancement factor of ~9.3 × 103

Spontaneous Emergence of Nonlinear Light Waves and Self-Inscribed Waveguide Microstructure during the Cationic Polymerization of Epoxides

We report spontaneous pattern formation due to modulation instability (MI) of a broad, uniform, incandescent beam as it propagates through a fluid medium undergoing cationic ring-opening polymerization of epoxide moieties and show that the dynamics of the process can be controlled through polymerization kinetics. By strong contrast, MI in the half century-old field of nonlinear light propagation has until now been described predominantly in terms of optical parameters such as coherence, intensity and wavelength. The increase in refractive index (Δ<i>n</i>) originating from the cross-linking polymerization of biscycloaliphatic epoxy monomers pushes the system into a nonlinear regime, where normally negligible spatial noise becomes greatly amplified. The perturbed optical field stabilizes by spontaneously dividing into thousands of self-trapped filaments of light. Because each filament inscribes a permanent microscopic channel along its propagation path, the initially isotropic fluid medium solidifies into a densely packed array of self-induced waveguides. These experiments demonstrated the strong correlation between the kinetics of cationic polymerization and dynamics of MI; the beam becomes unstable only within a narrow parameter range where a critical balance is struck between the photoresponse speed (determined by polymerization rate) and the magnitude of Δ<i>n</i> (determined by extent of cross-linking). The former needs to be sufficiently fast to respond to noise while the latter must be large enough to generate high-refractive index seeds that trigger MI. Outside of this range, MI is entirely suppressed. This study reveals that nonlinear waveforms emerge in a familiar, widely employed epoxide photopolymer system, which for the first time highlights the possibility of tuning MI through the kinetics of a photochemical reaction