Structure Of Soft Materials Research Articles

(Invited) Morphological Diversity and Space-Recognition of Polysaccharide Microfibers on Evaporative Interface

The geometric structures of soft materials can be controlled on the macro-scale by using interfacial or mechanical instability, e.g.fingering patterns of viscous liquids and buckling patterns of gels during swelling/deswelling. These patterns can be used as smart materials for capturing/releasing and mass-transportation applications. Here we introduce the emergence of uniaxially oriented membranes by drying an aqueous liquid-crystalline solution, composed of megamolecular supra-polysaccharides, sacran, in a limited space. In addition, by controlling the geometry of the evaporation front, multiple nuclei emerge that grow into vertical membraneswith uniaxial orientation. Notably, the membrane, composed of microfiber, is rationally formed along the dynamic three-phase contact line. As a result of the self-organization, the membrane macroscopically partitions the three-dimensional cuboid cell. We envision that such uniaxially oriented membranes, obtained through partitioning phenomena, can be used as soft biomaterials, like anisotropic dialysis membranes with directional controllability in the medical and pharmaceutical field.

Structure of surfactant and phospholipid monolayers at the air/water interface modeled from neutron reflectivity data

Specular neutron reflectometry is a powerful technique to resolve interfacial compositions and structures in soft matter. Surprisingly however, even after several decades, a universal modeling approach for the treatment of data of surfactant and phospholipid monolayers at the air/water interface has not yet been established. To address this shortcoming, first a systematic evaluation of the suitability of different models is presented. The result is a comprehensive validation of an optimum model, which is evidently much needed in the field, and which we recommend as a starting point for future data treatment. While its limitations are openly discussed, consequences of failing to take into account various key aspects are critically examined and the systematic errors quantified. On the basis of this physical framework, we go on to show for the first time that neutron reflectometry can be used to quantify directly in situ at the air/water interface the extent of acyl chain compaction of phospholipid monolayers with respect to their phase. The achieved precision of this novel quantification is ∼10%. These advances together enhance significantly the potential for exploitation in future studies data from a broad range of systems including those involving synthetic polymers, proteins, DNA, nanoparticles and drugs.

Unidirectionally-oriented Membrane Formation of Supra-polysaccharides Sacran and Application to Drug Delivery System

The geometric structures of soft materials can be controlled on the macro-scale using interfacial or mechanical instability, e.g., fingering patterns of viscous liquid and buckling patterns of gels during swelling/deswelling. These patterns can be used as smart materials for capturing/releasing and mass-transportation applications. Here we introduce the emergence of a uniaxially oriented membrane by drying an aqueous liquid-crystalline solution, composed of megamolecular supra-polysaccharides "sacran", from a limited space. By controlling the geometries of the evaporation front, multiple nuclei emerge that grow into upright membranes with uniaxial orientation. Notably, the uniaxially orientated membrane composed of rod-like microdomains is rationally formed along the dynamic three-phase contact line. Besides, the membrane macroscopically partitions the three-dimensional cuboid cell for evaporating the aqueous solution. We envision that such a uniaxially oriented membrane can be used as soft biomaterials such as dialysis membranes with directional controllability in medical and pharmaceutical fields.

Silicon Carbide Nanoparticles as an Effective Bioadhesive to Bond Collagen Containing Composite Gel Layers for Tissue Engineering Applications.

Additive manufacturing via layer-by-layer adhesive bonding holds much promise for scalable manufacturing of tissue-like constructs, specifically scaffolds with integrated vascular networks for tissue engineering applications. However, there remains a lack of effective adhesives capable of composite layer fusion without affecting the integrity of patterned features. Here, the use of silicon carbide is introduced as an effective adhesive to achieve strong bonding (0.39 ± 0.03 kPa) between hybrid hydrogel films composed of alginate and collagen. The techniques have allowed us to fabricate multilayered, heterogeneous constructs with embedded high-resolution microchannels (150 µm-1 mm) that are precisely interspaced (500-600 µm). Hydrogel layers are effectively bonded with silicon carbide nanoparticles without blocking the hollow microchannels and high cell viability (90.61 ± 3.28%) is maintained within the scaffold. Nanosilica is also tested and found to cause clogging of smaller microchannels when used for interlayer bonding, but is successfully used to attach synthetic polymers (e.g., Tygon) to the hydrogels (32.5 ± 2.12 mN bond strength). This allows us to form inlet and outlet interconnections to the gel constructs. This ability to integrate hollow channel networks into bulk soft material structures for perfusion can be useful in 3D tissue engineering applications.

Controlled molecular self-assembly of complex three-dimensional structures in soft materials

Many applications in tissue engineering, flexible electronics, and soft robotics call for approaches that are capable of producing complex 3D architectures in soft materials. Here we present a method using molecular self-assembly to generate hydrogel-based 3D architectures that resembles the appealing features of the bottom-up process in morphogenesis of living tissues. Our strategy effectively utilizes the three essential components dictating living tissue morphogenesis to produce complex 3D architectures: modulation of local chemistry, material transport, and mechanics, which can be engineered by controlling the local distribution of polymerization inhibitor (i.e., oxygen), diffusion of monomers/cross-linkers through the porous structures of cross-linked polymer network, and mechanical constraints, respectively. We show that oxygen plays a role in hydrogel polymerization which is mechanistically similar to the role of growth factors in tissue growth, and the continued growth of hydrogel enabled by diffusion of monomers/cross-linkers into the porous hydrogel similar to the mechanisms of tissue growth enabled by material transport. The capability and versatility of our strategy are demonstrated through biomimetics of tissue morphogenesis for both plants and animals, and its application to generate other complex 3D architectures. Our technique opens avenues to studying many growth phenomena found in nature and generating complex 3D structures to benefit diverse applications.

Laboratory layered latte

Inducing thermal gradients in fluid systems with initial, well-defined density gradients results in the formation of distinct layered patterns, such as those observed in the ocean due to double-diffusive convection. In contrast, layered composite fluids are sometimes observed in confined systems of rather chaotic initial states, for example, lattes formed by pouring espresso into a glass of warm milk. Here, we report controlled experiments injecting a fluid into a miscible phase and show that, above a critical injection velocity, layering emerges over a time scale of minutes. We identify critical conditions to produce the layering, and relate the results quantitatively to double-diffusive convection. Based on this understanding, we show how to employ this single-step process to produce layered structures in soft materials, where the local elastic properties vary step-wise along the length of the material.

Responsive Nanogel Probe for Ratiometric Fluorescent Sensing of pH and Strain in Hydrogels.

In this study a new pH-responsive nanogel probe containing a complementary nonradiative resonance energy transfer (NRET) fluorophore pair is investigated and its ability to act as a versatile probe of network-related changes in three hydrogels demonstrated. Fluorescent sensing using NRET is a powerful method for studying relationships between Angstrom length-scale structure and macroscopic properties of soft matter. Unfortunately, inclusion of NRET fluorophores into such materials requires material-specific chemistry. Here, low concentrations of preformed nanogel probes were included into hydrogel hosts. Ratiometric photoluminescence (PL) data for the gels labeled with the nanogel probes enabled pH-triggered swelling and deswelling to be studied as well as Ca2+-triggered collapse and solute release. PL measurements during compression of a nanogel probe-labeled nanocomposite gel demonstrated mechanochromic behavior and strain sensing. The new nanogel probes have excellent potential for investigating the internal structures of gels and provide a versatile ratiometric fluorescent platform for studying pH and strain.

Rheological Study of Soft Matters: A Review of Microrheology and Microrheometers

AbstractRheological properties of soft matter like polymer solutions/gels, colloidal dispersions, and biological materials have been extensively studied by macroscopic methods. Recently, a set of microrheometers has emerged as powerful tools to investigate the dynamics and structures of homogeneous or heterogeneous soft matter at the micro‐ or nanoscale. In this review, these microrheometers, including some novel hybrid microrheometers are summarized and compared.

Effects of Lateral and Terminal Chains of X-Shaped Bolapolyphiles with Oligo(phenylene ethynylene) Cores on Self-Assembly Behaviour. Part 1: Transition between Amphiphilic and Polyphilic Self-Assembly in the Bulk.

Polyphilic self-assembly leads to compartmentalization of space and development of complex structures in soft matter on different length scales, reaching from the morphologies of block copolymers to the liquid crystalline (LC) phases of small molecules. Whereas block copolymers are known to form membranes and interact with phospholipid bilayers, liquid crystals have been less investigated in this respect. Here, series of bolapolyphilic X-shaped molecules were synthesized and investigated with respect to the effect of molecular structural parameters on the formation of LC phases (part 1), and on domain formation in phospholipid bilayer membranes (part 2). The investigated bolapolyphiles are based on a rod-like π-conjugated oligo(phenylene ethynylene) (OPE) core with two glycerol groups being either directly attached or separated by additional ethylene oxide (EO) units to both ends. The X-shape is provided by two lateral alkyl chains attached at opposite sides of the OPE core, being either linear, branched, or semiperfluorinated. In this report, the focus is on the transition from polyphilic (triphilic or tetraphilic) to binary amphiphilic self-assembly. Polyphilic self-assembly, i.e., segregation of all three or four incorporated units into separate nano-compartments, leads to the formation of hexagonal columnar LC phases, representing triangular honeycombs. A continuous transition from the well-defined triangular honeycomb structures to simple hexagonal columnar phases, dominated by the arrangement of polar columns on a hexagonal lattice in a mixed continuum formed by the lipophilic chains and the OPE rods, i.e., to amphiphilic self-assembly, was observed by reducing the length and volume of the lateral alkyl chains. A similar transition was found upon increasing the length of the EO units involved in the polar groups. If the lateral alkyl chains are enlarged or replaced by semiperfluorinated chains, then the segregation of lateral chains and rod-like cores is retained, even for enlarged polar groups, i.e., the transition from polyphilic to amphiphilic self-assembly is suppressed.

Synthesis of Lipophilic Guanine N-9 Derivatives: Membrane Anchoring of Nucleobases Tailored to Fatty Acid Vesicles.

Covalent or noncovalent surface functionalization of soft-matter structures is an important tool for tailoring their function and stability. Functionalized surfaces and nanoparticles have found numerous applications in drug delivery and diagnostics, and new functionalization chemistry is continuously being developed in the discipline of bottom-up systems chemistry. The association of polar functional molecules, e.g., molecular recognition agents, with soft-matter structures can be achieved by derivatization with alkyl chains, allowing noncovalent anchoring into amphiphilic membranes. We report the synthesis of five new guanine-N9 derivatives bearing alkyl chains with different attachment chemistries, exploiting a synthesis pathway that allows a flexible choice of hydrophobic anchor moiety. In this study, these guanine derivatives were functionalized with C10 chains for insertion into decanoic acid bilayer structures, in which both alkyl chain length and attachment chemistry determined their interaction with the membrane. Incubation of these guanine conjugates, as solids, with a decanoic acid vesicle suspension, showed that ether- and triazole-linked C10 anchors yielded an increased partitioning of the guanine derivative into the membranous phase compared to directly N-9-linked saturated alkyl anchors. Decanoic acid vesicle membranes could be loaded with up to 5.5 mol % guanine derivative, a 6-fold increase over previous limits. Thus, anchor chemistries exhibiting favorable interactions with a bilayer's hydrophilic surface can significantly increase the degree of structure functionalization.

Heuristics for precise supramolecular control of soft matter structure and properties - 2,3,4-tris(dodecyloxy)benzenesulfonates with alkaline and organic cations.

Comprehensive analysis of the structure and phase behavior for a number of 2,3,4-tris(dodecyloxy)benzenesulfonates with alkali metal and organic focal groups revealed that the shape of the mesogenic group plays a decisive role in phase behavior of the material. Cubic and layered types of packing prevail when the size of the cation is small and, thus, the shape of the mesogenic molecule is close to conic one. With increasing cation size, the shape becomes more tapered, and columnar mesophases appear to be more stable. Interactions of the focal groups however determine the stability of mesophases. Comparatively strong interactions may, morever, provide substantial deviations from a phase diagram plotting the transition temperatures versus the radius of focal group, as in the case of pyridinium 2,3,4-tris(dodecyloxy)benzenesulfonate.

A stress-controlled shear cell for small-angle light scattering and microscopy.

We develop and test a stress-controlled, parallel plates shear cell that can be coupled to an optical microscope or a small angle light scattering setup, for simultaneous investigation of the rheological response and the microscopic structure of soft materials under an imposed shear stress. In order to minimize friction, the cell is based on an air bearing linear stage, the stress is applied through a contactless magnetic actuator, and the strain is measured through optical sensors. We discuss the contributions of inertia and of the small residual friction to the measured signal and demonstrate the performance of our device in both oscillating and step stress experiments on a variety of viscoelastic materials.

Nanoscopic imaging of thick heterogeneous soft-matter structures in aqueous solution.

Precise nanometre-scale imaging of soft structures at room temperature poses a major challenge to any type of microscopy because fast thermal fluctuations lead to significant motion blur if the position of the structure is measured with insufficient bandwidth. Moreover, precise localization is also affected by optical heterogeneities, which lead to deformations in the imaged local geometry, the severity depending on the sample and its thickness. Here we introduce quantitative thermal noise imaging, a three-dimensional scanning probe technique, as a method for imaging soft, optically heterogeneous and porous matter with submicroscopic spatial resolution in aqueous solution. By imaging both individual microtubules and collagen fibrils in a network, we demonstrate that structures can be localized with a precision of ∼10 nm and that their local dynamics can be quantified with 50 kHz bandwidth and subnanometre amplitudes. Furthermore, we show how image distortions caused by optically dense structures can be corrected for.

Hydrostatic 3D-printing for soft material structures using low one-photon polymerization

This paper studies the feasibility of a 3D printing method that enables a hydrostatic condition for support-free fabrication, named hydrostatic 3D printing (H3P). Soft structures are difficult to build in additive manufacturing due to the low stiffness. H3P utilizes low one-photon polymerization (LOPP) to achieve “in-liquid” curing surrounded by the hydrostatic pressure. Single-spot curing and continuous printing were investigated for a UV-curable silicone material under different light intensities and exposure times. Initial results have demonstrated LOPP effects for H3P. The equivalent exposure time in continuous printing was found shorter than a stationary single-spot curing due to a non-linear intensity distribution.

Visualizing the Dynamics of Nanoparticles in Liquids by Scanning Electron Microscopy.

Taking advantage of ionic liquid nonvolatility, the Brownian motions of nanospheres and nanorods in free-standing liquid films were visualized in situ by scanning electron microscopy. Despite the imaging environment's high vacuum, a liquid cell was not needed. For suspensions that are dilute and films that are thick compared to the particle diameter, the translational and rotational diffusion coefficients determined by single-particle tracking agree with theoretical predictions. In thinner films, a striking dynamical pairing of nanospheres was observed, manifesting a balance of capillary and hydrodynamic interactions, the latter strongly accentuated by the two-dimensional film geometry. Nanospheres at high concentration displayed subdiffusive caged motion. Concentrated nanorods in the thinner films transiently assembled into finite stacks but did not achieve high tetratic order. The illustrated imaging protocol will broadly apply to the study of soft matter structure and dynamics with great potential impact.

Directed peptide amphiphile assembly using aqueous liquid crystal templates in magnetic fields.

An alignment technique based on the combination of magnetic fields and a liquid crystal (LC) template uses the advantages of both approaches: the magnetic fields offer non-contact methods that apply to all sample sizes and shapes, whilst the LC templates offer high susceptibilities. The combination introduces a route to control the spatial organization of materials with low intrinsic susceptibilities. We demonstrate that we can unidirectionally align one such material, peptide amphiphiles in water, on a centimeter scale at a tenfold lower magnetic field by using a lyotropic chromonic liquid crystal as a template. We can transform the aligned supramolecular assemblies into optically active π-conjugated polymers after photopolymerization. Lastly, by reducing the magnetic field strength needed for addressing these assemblies, we are able to create more complex structures by initiating self-assembly of our supramolecular materials under competing alignment forces between the magnetically induced alignment of the assemblies (with a positive diamagnetic anisotropy) and the elastic force dominated alignment of the template (with a negative diamagnetic anisotropy), which is directed orthogonally. Although the approach is still in its infancy and many critical parameters need optimization, we believe that it is a very promising technique to create tailor-made complex structures of (aqueous) functional soft matter.

УПАКОВКА И РАЗВЕРТЫВАНИЕ ВНУТРЕННИМ ДАВЛЕНИЕМ КРУПНОГАБАРИТНЫХ ОБОЛОЧЕЧНЫХ КОНСТРУКЦИЙ

The packaging of large composite shell structures (corrugation, a cylinder and a truncated cone) and their deployment by internal pressure loading are explored. It is believed that the medial surfaces of the constituent elements have involutes which coincide with them in a packed state. The corrugation consists of the ring components, the cylinder and cone consist of trapezoidal plane components. These components are made of carbon fiber with orthotropic or transversely isotropic elastic properties and stapled by joints. The joints do not perceive resistance to rotation about the tangent to the weld line. The contemplated structures perceive bending loads (unlike pneumatic ones) made of soft materials (fabrics, films). Geometrically nonlinear solid mechanics problems with the internal pressure loading are solved by using the engineering computing system ANSYS. The deployment pressure dependence on the shell material structure, shell thickness and amount of constituent elements are investigated. It is shown that the deployment pressure of the large shell is commensurate with the pressure of pneumatic structures of soft materials. It was found that the stresses in the corrugation shells can reach critical values but in the cylinder and the truncated cone the stresses are insignificant. The task formulation and its solution on the thermodynamic state of the injected gas under quasi-static internal pressure loading of the shell are suggested. It is shown that in the beginning of deployment the gas temperature will drop by about 50-80 degrees Celsius according to gas composition, and then its temperature is tending to increase to the injected gas temperature. These results enable to expand the choice of materials for the pneumatic products manufacturing including space applications design.

Compartmentalization Approaches in Soft Matter Science: From Nanoreactor Development to Organelle Mimics

Compartmentalization is an essential feature found in living cells to ensure that biological processes occur without being affected by undesired external influences. Over the years many scientists have designed self-assembled soft matter structures that mimic these natural catalytic compartments. The rationale behind this research is threefold. First of all, compartmentalization leads to the creation of a secluded environment for the catalytic species, which solves compatibility issues and which can improve catalyst efficiency and selectivity. Secondly, nano- and micro-compartments are constructed with the aim to obtain microenvironments that more closely mimic the cellular architecture. These biomimetic platforms are used to attain a better understanding of how cellular processes are executed. Thirdly, natural design rules are applied to create biomolecular assemblies with unusual functionality, which for example are used as artificial organelles. Here, recent developments will be discussed regarding these compartmentalized catalytic systems, with a selected number of illustrative examples to demonstrate which strategies have been followed, and to show to what extent the ambitious goals of this field of science have been reached. The focus here is on the field of soft matter science, covering the wide spectrum from polymeric assemblies to protein nanocages.

Nanostructural analysis of water distribution in hydrated multicomponent gels using thermal analysis and NMR relaxometry.

Highly complex, multicomponent gels and water-containing soft materials have varied applications in biomedical, pharmaceutical, and food sciences, but the characterization of these nanostructured materials is extremely challenging. The aim of this study was to use stearoyl macrogol-32 glycerides (Gelucire 50/13) gels containing seven different species of glycerides, PEG, and PEG-esters, as model, complex, multicomponent gels, to investigate the effect of water content on the micro- and nanoarchitecture of the gel interior. Thermal analysis and NMR relaxometry were used to probe the thermal and diffusional behavior of water molecules within the gel network. For the highly concentrated gels (low water content), the water activity was significantly lowered due to entrapment in the dense gel network. For the gels with intermediate water content, multiple populations of water molecules with different thermal responses and diffusion behavior were detected, indicating the presence of water in different microenvironments. This correlated with the network architecture of the freeze-dried gels observed using SEM. For the gels with high water content, increased quantities of water with similar diffusion characteristics as free water could be detected, indicating the presence of large water pockets in these gels. The results of this study provide new insights into structure of Gelucire gels, which have not been reported before because of the complexity of the material. They also demonstrate that the combination of thermal analysis and NMR relaxometry offers insights into the structure of soft materials not available by the use of each technique alone. However, we also note that in some instances the results of these measurements are overinterpreted and we suggest limitations of the methods that must be considered when using them.

Nucleation and growth of a helical nanofilament (B4) liquid-crystal phase confined in nanobowls.

The B4 helical nanofilament (HNF) liquid crystal (LC) phase is a three-dimensional (3D) helical structure composed of 2D smectic layers. Because of the complex shape of the HNF phase, it is difficult to understand the generation mechanism of HNFs in the bulk as well as in the thin-film condition. Here, we directly investigated the nucleation and growth of HNFs in nanobowls. A combination of electron microscopy and X-ray diffraction was used to reveal the transitional surface structures, in which barrel-like structures as well as short HNFs with random handedness were observed, depending on the LC film thickness. These results will be useful in achieving a better understanding of thin film structures of complex chiral structures in soft matter.