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Further exploration of this topic would not only broaden the knowledge of Soft Mattonics, but also encourage multidisciplinary research from specialists across different disciplines and promote diverse soft and smart photonic applications. [44] This research is therefore an important step towards the understanding and efficient use of colloidal mixtures and block copolymers which helps the design of soft matter systems with desired properties. [43] NUS physicists have discovered a theoretical behavior known as the "critical skin effect" influencing how changes between different phases of matter occur.
Rivista del Nuovo Cimento, 2012
We present a review of a series of nano/micro, soft-matter-based, periodic, composite structures, along with a theoretical model, which explains their main physical and optical features as determined by a suitable choice of the values of given physical and geometrical parameters. The historical development is illustrated by starting from the fabrication technique, which enables obtaining a structure made of films of well-aligned Liquid Crystal alternated to polymer slices. Realised samples, which exhibit a spatial periodicity in the range 0.2-15 μm, are given the generic name POLICRYPS (as an acronym of POlymer LIquid CRYstal Polymer Slices) and are obtained by curing a homogeneous mixture of mesogenic material, monomer and curing agent under suitable conditions and by means of a UV radiation. A number of interesting applications are determined by the possibility of tuning, or even switching on/off, the spatial modulation (from polymer to LC) of the refractive index of these structures; this effect of tuneability can be obtained by applying an electric field of few V/μm or, in some cases, by irradiating the sample with a light beam of suitable wavelength. We show that, depending on the used geometry, these particular structures can be exploited as switchable diffraction gratings, tuneable beam splitters, switchable optical phase modulators, tuneable Bragg filters, soft matter templates for aligning different kinds of LCs, arrays of tuneable microlaser, or can enable realising "active plasmonics" devices.
Chimia, 2008
We demonstrate how we can tune the size, shape, surface functionality and properties of nanoparticles and use them as ideal model systems for fundamental investigations as well as for materials applications. We in particular describe ways to create functionalized core-shell particles with various degree of anisotropy and interesting magnetic properties. We show how we can use these particles in order to study the equilibrium and non-equilibrium phase behavior of colloidal suspensions with different interaction potentials and summarize our current understanding of the phenomenon of dynamical arrest, i.e., gel and glass formation. While different nanoparticles are vital for fundamental studies of various aspects of soft condensed matter, they also offer fascinating possibilities in materials science. We will demonstrate this with the example of nanocomposites made through an in-situ polymerization reaction.
Materials
Soft matters include polymers, liquid crystals, colloids, biological tissues, and many smart materials [...]
2017
interactions can facilitate double-stranded DNA adsorption onto conducting carbon nanotubes.
2008
Colloids are present in a large variety of biological, chemical and physical systems. In the last few years, they have been used as model systems which allow understanding fundamental processes in atomic systems or elucidating problems in soft condensed matter. The success of colloids to be used as well-controlled model systems resides in the fact that the relevant interactions between colloids are easily and independently tuneable and the colloid position is accessible by means of optical techniques, thus allowing a direct comparison with simulations and theoretical calculations. In this contribution, we briefly show the versatility of colloids as model systems to, on one hand, understand the effective interactions that emerge in soft matter physics when unobservable components of the system are integrated out or contracted of the description and, on the other hand, to quantify the effects of soft and periodic external fields on the structural and dynamics properties of many-body systems.
Soft Matter, 2008
Chaos: An Interdisciplinary Journal of Nonlinear Science
Nonlinear optics and polymer systems are distinct fields that have been studied for decades. These two fields intersect with the observation of nonlinear wave propagation in photoreactive polymer systems. This has led to studies on the nonlinear dynamics of transmitted light in polymer media, particularly for optical self-trapping and optical modulation instability. The irreversibility of polymerization leads to permanent capture of nonlinear optical patterns in the polymer structure, which is a new synthetic route to complex structured soft materials. Over time more intricate polymer systems are employed, whereby nonlinear optical dynamics can couple to nonlinear chemical dynamics, opening opportunities for self-organization. This paper discusses the work to date on nonlinear optical pattern formation processes in polymers. A brief overview of nonlinear optical phenomenon is provided to set the stage for understanding their effects. We review the accomplishments of the field on studying nonlinear waveform propagation in photopolymerizable systems, then discuss our most recent progress in coupling nonlinear optical pattern formation to polymer blends and phase separation. To this end, perspectives on future directions and areas of sustained inquiry are provided. This review highlights the significant opportunity in exploiting nonlinear optical pattern formation in soft matter for the discovery of new light-directed and light-stimulated materials phenomenon, and in turn, soft matter provides a platform by which new nonlinear optical phenomenon may be discovered.
2005
We predict that spatial self-trapping of light can occur in soft matter encompassing a wide class of new materials such as colloids, foams, gels, fractal aggregates etc. We develop a general nonlocal theory that allows to relate the properties of the trapped state of Maxwell equations to the measurable static structure factor of the specific material. We give numerical evidence for stable trapping in fractal aggregates and suggest also the possibility of soliton spectroscopy of soft-matter.
Condensed Matter Physics, 2010
Shape variation under the action of small external fields is a peculiar feature of soft matter. In the present paper we demonstrate a possibility of the analogous shape variation in the solids that combine the properties of antiferro-and ferromagnetic materials and show strong magnetoelastic coupling. The antiferromagnetic subsystem provides a macroscopic deformation of a sample in the external magnetic field while the ferromagnetic component ensures high susceptibility of the domain structure.
Physical Review E
We explore the glassy dynamics of soft colloids using microgels and charged particles interacting by steric and screened Coulomb interactions, respectively. In the supercooled regime, the structural relaxation time τα of both systems grows steeply with volume fraction, reminiscent of the behavior of colloidal hard spheres. Computer simulations confirm that the growth of τα on approaching the glass transition is independent of particle softness. By contrast, softness becomes relevant at very large packing fractions when the system falls out of equilibrium. In this non-equilibrium regime, τα depends surprisingly weakly on packing fraction and time correlation functions exhibit a compressed exponential decay consistent with stress-driven relaxation. The transition to this novel regime coincides with the onset of an anomalous decrease of local order with increasing density typical of ultrasoft systems. We propose that these peculiar dynamics results from the combination of the non-equilibrium aging dynamics expected in the glassy state and the tendency of colloids interacting through soft potentials to refluidize at high packing fractions.
An alternating electric fi eld is employed to induce a tunable dipolar contribution in soft-ionic microgel colloids, where eff ective volume fractions far above close packing can be reached. Novel fi eld-induced structural transitions are discovered, both at intermediate as well as at very high eff ective volume fractions.
arXiv (Cornell University), 2018
Development of artificial materials exhibiting unusual optical properties is one of the major strands of current photonics research [1]. Of particular interest are soft-matter systems reconfigurable by external stimuli that play an important role in research fields ranging from physics to chemistry and life sciences [2-7]. Here, we prepare and study unconventional self-assembled colloidal optical waveguides (CWs) created from wavelength-size dielectric particles held together by long-range optical forces [8]. We demonstrate robust non-linear optical properties of these CWs that lead to optical transformation characteristics remarkably similar to those of gradient refractive index materials and enable reversible all-optical tuning of light propagation through the CW. Moreover, we characterize strong optomechanical interactions responsible for the CW self-assembly; in particular, we report self-sustained oscillations of the whole CW structure tuned so that the wavelength of the laser beams forming the CW is not allowed to propagate through. The observed significant coupling between the mechanical motion of the CW and the intensity of light transmitted through the CW can form a base for designing novel mesoscopic-scale photonic devices that are reconfigurable by light.
We use monodisperse poly(N-isopropylacrylamide) (PNIPAM) microgels as a model system for soft repulsive colloids and study their density dependent structural ordering and phase behaviour using confocal laser scanning microscopy (CLSM). The experiments are carried out at low temperatures, where the particles are in the swollen state and interact via a Hertzian potential, evidenced through a quantitative comparison of the pair correlation functions g(r) obtained with CLSM and computer simulations. We worked over a broad range of effective volume fractions f eff below and above close packing (f cp ). CLSM allows us to identify a fluid-glass and a fluid-crystal transition by looking at the structure and dynamics of the suspensions. The density dependent g(r) values exhibit clearly visible anomalies at high f eff > f cp which we interpret as a structural signature of the glass transition related to the particle softness. These results are discussed in light of the previously studied phase behaviour of colloidal systems interacting with hard and soft repulsive interaction potentials.
Nature communications, 2014
Refraction at a dielectric interface can take an anomalous character in anisotropic crystals, when light is negatively refracted with incident and refracted beams emerging on the same side of the interface normal. In soft matter subject to reorientation, such as nematic liquid crystals, the nonlinear interaction with light allows tuning of the optical properties. We demonstrate that in such material a beam of light can experience either positive or negative refraction depending on input power, as it can alter the spatial distribution of the optic axis and, in turn, the direction of the energy flow when traveling across an interface. Moreover, the nonlinear optical response yields beam self-focusing and spatial localization into a self-confined solitary wave through the formation of a graded-index waveguide, linking the refractive transition to power-driven readdressing of copolarized guided-wave signals, with a number of output ports not limited by diffraction.
2007
Preface. List of Contributors. Part I: Experimental Advances. Microemulsion Templating W.F.C. Sager. Nanofabrication of Block Copolymer Bulk and Thin Films: Microdomain Structures as Templates Takeji Hashimoto and Kenji Fukunaga. Characterization of Surfactant Water Systems by X-Ray Scattering and 2H NMR Michael C. Holmes. Polyelectrolyte Diblock Copolymer Micelles: Small Angle Scattering Estimates of the Charge Ordering in the Coronal Layer Johan R.C. van der Maarel. Structure and Shear-Induced Order in Blends of a Diblock Copolymer with the Corresponding Homopolymers I.W. Hamley, V. Castelletto and Z. Yang. Electric Field Alignment of Diblock Copolymer Thin Films T. Xu, J. Wang and T.P. Russell. Control of Block Copolymer Microdomain Orientation from Solution Using Electric Fields: Governing Parameters and Mechanisms Alexander Boker. Structure and Dynamics of Cylinder Forming Block Copolymers in Thin Films Larissa Tsarkova. Part II: Mathematical and Theoretical Approaches. Mathema...
2015
Please note that technical editing may introduce minor changes to the text and/or graphics, which may alter content. The journal’s standard Terms & Conditions and the Ethical guidelines still apply. In no event shall the Royal Society of Chemistry be held responsible for any errors or omissions in this Accepted Manuscript or any consequences arising from the use of any information it contains. Accepted Manuscript
Journal of Nanoscience and Nanotechnology, 2006
We review the forces that rule interactions between phospholipid membranes and other soft nanomaterials such as polymers and colloids. Contrary to traditional nanostructures, soft materials display a high susceptibility to the fluctuations of the thermal environment, leading to new forces of an essentially entropic nature.
Testing showed the device capable of measuring nanoparticles in the range of 200 to 900 nm. [45] Further exploration of this topic would not only broaden the knowledge of Soft Mattonics, but also encourage multidisciplinary research from specialists across different disciplines and promote diverse soft and smart photonic applications. [44] This research is therefore an important step towards the understanding and efficient use of colloidal mixtures and block copolymers which helps the design of soft matter systems with desired properties. [43] NUS physicists have discovered a theoretical behavior known as the "critical skin effect" influencing how changes between different phases of matter occur.
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