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Thin films of amorphous silicon (a-Si) coated on metals such as nickel (Ni) are one of the most promising anode architectures for high-energy-density lithium-ion (Li-ion) batteries. The performance and longevity of batteries with this type of electrode depend on the integrity of the Ni/a–Si interface. The integrity of the a-Si /Ni bonded interface during cycling is critical, but the experimental characterization of interfacial failure of this material system is highly challenging and there is a sparsity of interface strength data in the literature. Here, we describe a laser spallation (LS) technique to characterize the interfacial adhesion strength of Ni/a–Si multilayer films created by chemical vapor deposition (CVD). The LS technique enables the non-contact measurement of the tensile interfacial strength with high precision when compared to conventional methods for characterizing adhesion. Interferometric measurement combined with finite element analysis shows that the Ni/a–Si interface, created via the CVD of a-Si on Ni surfaces can withstand ≈46–72 MPa in tension before failure initiation. To ensure successful and precise characterization of interfacial adhesion strength using LS, we further develop a design criterion for multi-layer samples by analyzing the thin-film mechanics. Our study provides insights into the strength of the Ni/a–Si interface that governs the performance and durability of high-energy-density anodes and offers design guidelines for improving thin-film electrode integrity. [ABSTRACT FROM AUTHOR]

A nanostructured copper oxide (nCO) coating which can be electrochemically reduced to copper metal is demonstrated as an anti‐reflection coating, enabling interference lithography of three‐dimensionally structured templates on a surface compatible with subsequent electrodeposition steps. The nCO presents a black needle‐like structure which effectively absorbs the incident radiation during interference lithography. Specular and diffused reflectivity measurements confirm nCO has near‐zero reflectivity from at least UV (350 nm) to near IR (700 nm) wavelengths. A particularly important aspect of the nCO is its ability to be reduced to copper metal, enabling electrodeposition inside porous templates fabricated on the nCO. It is demonstrated electrodeposition of copper within 3D templates defined by interference lithography and proximity field nano‐patterning processes, forming mesostructured metals which enhance two‐phase cooling. The resultant 5 µm thick structures exhibited up to 3 times the critical heat flux and 2 times heat transfer coefficient of bare silicon. The structures are optimized via computational tools including Finite Difference Time Domain (FDTD) and COMSOL Multiphysics. The use of the approach demonstrated here can potentially find application in many areas given the broad importance of mesostructured metals for energy, biomedical, and mechanical applications. [ABSTRACT FROM AUTHOR]

The coupled transport of charge and heat provide fundamental insights into the microscopic thermodynamics and kinetics of materials. We describe a sensitive ac differential resistance bridge that enables measurements of the temperature difference on two sides of a coin cell with a resolution of better than 10 μK. We use this temperature difference metrology to determine the ionic Peltier coefficients of symmetric Li-ion electrochemical cells as a function of Li salt concentration, solvent composition, electrode material, and temperature. The Peltier coefficients Π are negative, i.e., heat flows in the direction opposite to the drift of Li ions in the applied electric field, large, −Π > 30 kJ mol−1, and increase with increasing temperature at T > 300 K. The Peltier coefficient is approximately constant on time scales that span the characteristic time for mass diffusion across the thickness of the electrolyte, suggesting that heat of transport plays a minor role in comparison to the changes in partial molar entropy of Li at the interface between the electrode and electrolyte. Our work demonstrates a new platform for studying the non-equilibrium thermodynamics of electrochemical cells and provides a window into the transport properties of electrochemical materials through measurements of temperature differences and heat currents that complement traditional measurements of voltages and charge currents. [ABSTRACT FROM AUTHOR]

A key display characteristic is its efficiency (emitted light power divided by input power). Although display efficiencies are being improved through emissive (for example, quantum dot and organic light-emitting) display designs, which remove the highly inefficient colour filters found in traditional liquid crystal displays, polarization filters, which block about 50% light, remain necessary to inhibit ambient light reflection. We introduce a luminescent concentrator design to replace both colour and polarization filters. Narrow-band, large-Stokes-shift, CdSe/CdS quantum dot emitters are embedded in a luminescent concentrator pixel element with a small top aperture. The remainder of the top surface is coated black, reducing ambient light reflection. A single pixel demonstrates an extraction efficiency of 40.9% from a pixel with an aperture opening of 11.0%. A simple proof-of-concept multipixel array is demonstrated. Inefficient filters and overall efficiency are issues for display technology. Luminescent concentrator pixels have been used with CdSe/CdS quantum dot emitters, which enable both colour and polarization filtering, as well as nearly 41% extraction efficiency. [ABSTRACT FROM AUTHOR]

Compact visible wavelength achromats are essential for miniaturized and lightweight optics. However, fabrication of such achromats has proved to be exceptionally challenging. Here, using subsurface 3D printing inside mesoporous hosts we densely integrate aligned refractive and diffractive elements, forming thin high performance hybrid achromatic imaging micro-optics. Focusing efficiencies of 51–70% are achieved for 15μm thick, 90μm diameter, 0.3 numerical aperture microlenses. Chromatic focal length errors of less than 3% allow these microlenses to form high-quality images under broadband illumination (400–700 nm). Numerical apertures upwards of 0.47 are also achieved at the cost of some focusing efficiency, demonstrating the flexibility of this approach. Furthermore, larger area images are reconstructed from an array of hybrid achromatic microlenses, laying the groundwork for achromatic light-field imagers and displays. The presented approach precisely combines optical components within 3D space to achieve thin lens systems with high focusing efficiencies, high numerical apertures, and low chromatic focusing errors, providing a pathway towards achromatic micro-optical systems. Creating compact, lightweight and powerful optics that work well under visible light has been challenging. Here, the authors 3D print optically transparent polymers inside nanoporous glass in order to densely integrate refractive and diffractive elements, forming thin, high-performance hybrid achromatic imaging micro-optics. [ABSTRACT FROM AUTHOR]

We present an electrically switchable, compact metasurface device based on the metallic polymer PEDOT:PSS in combination with a gel polymer electrolyte. Applying square-wave voltages, we can reversibly switch the PEDOT:PSS from dielectric to metallic. Using this concept, we demonstrate a compact, standalone, and CMOS compatible metadevice. It allows for electrically controlled ON and OFF switching of plasmonic resonances in the 2–3 µm wavelength range, as well as electrically controlled beam switching at angles up to 10°. Furthermore, switching frequencies of up to 10 Hz, with oxidation times as fast as 42 ms and reduction times of 57 ms, are demonstrated. Our work provides the basis towards solid state switchable metasurfaces, ultimately leading to submicrometer-pixel spatial light modulators and hence switchable holographic devices. [ABSTRACT FROM AUTHOR]

Materials which selectively transport molecules offer powerful opportunities for concentrating and separating chemical agents. Here, utilizing static and dynamic chemical gradients, transport of molecules within swollen crosslinked polymers is demonstrated. Using an ≈200 μm static hydroxyl to hexyl gradient, the neutral ambipolar nerve agent surrogate diethyl (cyanomethyl)phosphonate (DECP) is directionally transported and concentrated 60‐fold within 4 hours. To accelerate transport kinetics, a dynamic gradient (a "travelling wave") is utilized. Here, the non‐polar dye pyrene was transported. The dynamic gradient is generated by an ion exchange process triggered by the localized introduction of an aqueous NaCl solution, which converts the gel from hydrophobic to hydrophilic. As the hydrophilic region expands, associated water enters the gel, and pyrene is pushed ahead of the expansion front. The dynamic gradient provides about 10‐fold faster transport kinetics than the static gradient. [ABSTRACT FROM AUTHOR]

Materials which selectively transport molecules offer powerful opportunities for concentrating and separating chemical agents. Here, utilizing static and dynamic chemical gradients, transport of molecules within swollen crosslinked polymers is demonstrated. Using an ≈200 μm static hydroxyl to hexyl gradient, the neutral ambipolar nerve agent surrogate diethyl (cyanomethyl)phosphonate (DECP) is directionally transported and concentrated 60‐fold within 4 hours. To accelerate transport kinetics, a dynamic gradient (a "travelling wave") is utilized. Here, the non‐polar dye pyrene was transported. The dynamic gradient is generated by an ion exchange process triggered by the localized introduction of an aqueous NaCl solution, which converts the gel from hydrophobic to hydrophilic. As the hydrophilic region expands, associated water enters the gel, and pyrene is pushed ahead of the expansion front. The dynamic gradient provides about 10‐fold faster transport kinetics than the static gradient. [ABSTRACT FROM AUTHOR]

In the article "Interference Lithography-Based Fabrication of 3D Metallic Mesostructures on Reflective Substrates using Electrodeposition-Compatible Anti-Reflection Coatings for Power Electronics Cooling," published in Advanced Electronic Materials, the authors explore the use of nanostructured copper oxide (nCO) coatings to improve cooling efficiency. These coatings allow for intricate interference lithography processes on reflective semiconductor substrates, enabling the electrodeposition of mesostructured metals. The mesostructured coatings demonstrate significant improvements in heat flux and heat transfer coefficient compared to conventional systems, particularly in the context of power electronics cooling. The findings of this study have the potential to impact the field of power electronics cooling. [Extracted from the article]

The shuttling behavior and slow conversion kinetics of the intermediate lithium polysulfides are the severe obstacles for the application of lithium‐sulfur (Li‐S) batteries over a wide temperature range. Here, an engineered lamellar yolk–shell structure of In2O3@void@carbon for the Li‐S battery cathode is developed for the first time to construct a powerful barrier that effectively inhibits the shuttling of polysulfides. On the basis of the unique nanochannel‐containing morphology, the continuous kinetic transformation of sulfur and polysulfides is confined in a stable framework, which is demonstrated by using X‐ray nanotomography. The constructed Li‐S battery exhibits a high cycling capability over 1000 cycles at 1.0 C with a capacity decay rate as low as 0.038% per cycle, good rate performance, and temperature tolerance at −10, 25, and 50 °C. A nondestructive in situ monitoring method of the interfacial reaction resistance in different cycling stages is proposed, which provides a new analysis perspective for the development of emerging electrochemical energy‐storage systems. [ABSTRACT FROM AUTHOR]

Templating with self‐assembled colloidal crystals has enabled fabrication of porous materials with potential for sensing, heat transfer, and energy storage applications. Herein, electrical, thermal, and mechanical properties of templated electroplated metallic copper inverse opals (CIO) containing close‐packed 500 nm pores are evaluated via a four‐point probe, eddy current, lap shear measurements, thermal cycling, and finite‐element analysis (FEA). CIOs are found to have an electrical conductivity of ≈4 × 106 S m−1, about 15% of pure copper, about the expected value based on the measured electroplated copper conductivity and the CIO pore structure. The good electrical and thermal properties of this structure, coupled with its connected porosity, make it attractive for two‐phase cooling applications. However, the thermal reliability of this structure raises questions about its integrity. It is found that this structure fails around 150 cycles when cycled between −40 and 200 °C at 10 °C min−1. Scanning electron micrograph (SEM) images of failed samples show that the failure plane lies within the CIO and generally at the thinnest interconnects in the structure, which agrees with FEA of the CIO structure, which shows stress concentrations at thin regions of the interconnects in the structure. [ABSTRACT FROM AUTHOR]

Three-dimensional (3D) photonic crystals are one class of materials where epitaxy, and the resultant attractive electronic properties, would enable new functionalities for optoelectronic devices. Here we utilize self-assembled colloidal templates to fabricate epitaxially grown single crystal 3D mesostructured GaxIn1–xP (GaInP) semiconductor photonic crystals using hydride vapor phase epitaxy (HVPE). The epitaxial relationship between the 3D GaInP and the substrate is preserved during the growth through the complex geometry of the template as confirmed by X-ray diffraction (XRD) and high resolution transmission electron microscopy. XRD reciprocal space mapping of the 3D epitaxial layer further demonstrates the film to be nearly fully relaxed with a negligible strain gradient. Fourier transform infrared spectroscopy reflection measurement indicates the optical properties of the photonic crystal which agree with finite difference time domain simulations. This work extends the scope of the very few known methods for the fabrication of epitaxial III-V 3D mesostructured materials to the well-developed HVPE technique. [ABSTRACT FROM AUTHOR]

Next generation mobile devices and computing architectures would benefit from ultra-high bandwidth technologies that efficiently transport and process optical signals. Subsurface fabrication can address this challenge by forming volumetric photonic integrated circuits with a more compact aerial footprint than planar on-chip circuits. These 3D optical systems may utilize densely packed low-loss, freeform optical interconnects for high volume data transfer. In this Perspective, we provide a comparative overview of the two main methods for subsurface fabrication, including our recently developed SCRIBE process, and assess the advantages and future directions of each approach. After analyzing the underlying technologies, we provide a roadmap of important steps to transition from laboratory demonstrations of individual elements to industrial-scale production of subsurface volumetric photonic integrated circuits. [ABSTRACT FROM AUTHOR]

3D‐structured Se‐loaded bicontinuous porous carbon (BPC) electrodes are fabricated through colloidal templating of BPC followed by pulsed‐voltage Se electrodeposition. The resultant electrodes are found to deliver a specific capacity of 665 mAh g−1 at a rate of 0.1 C, near the theoretical value for Se. When a vinylene carbonate (VC) containing electrolyte is utilized, the capacity fade over 500 cycles at 1 C rate is as small as a few percent. Impedance measurements and physical characterization of cycled electrodes indicate the exceptionally stable cycling performance is possibly due to VC resulting in the formation of a stable solid electrolyte interface (SEI) during cycling. Along with the cycling stability, the rate performance of the 3D Se/BPC electrodes is also good. Due to the bicontinuous structure of carbonaceous current collector at rates as high as 5 C, the deliverable capacity is about 300 mAh g−1. [ABSTRACT FROM AUTHOR]

We introduce an intermediate-temperature (350 °C) dry molten sodium hydroxide-mediated binder-free electrodeposition process to grow the previously electrochemically inaccessible air- and moisture-sensitive layered sodium transition metal oxides, NaxMO2 (M = Co, Mn, Ni, Fe), in both thin and thick film form, compounds which are conventionally synthesized in powder form by solid-state reactions at temperatures =700 °C. As a key motivation for this work, several of these oxides are of interest as cathode materials for emerging sodium-ion-based electrochemical energy storage systems. Despite the low synthesis temperature and short reaction times, our electrodeposited oxides retain the key structural and electrochemical performance observed in high-temperature bulk synthesized materials. We demonstrate that tens of micrometers thick >75%dense NaxCoO2 and NaxMnO2 can be deposited in under 1 h. When used as cathodes for sodium-ion batteries, these materials exhibit near theoretical gravimetric capacities, chemical diffusion coefficients of Na+ ions (~10-12 cm²·s-1), and high reversible areal capacities in the range ~0.25 to 0.76 mA·h·cm-2, values significantly higher than those reported for binder-free sodium cathodes deposited by other techniques. The method described here resolves longstanding intrinsic challenges associated with traditional aqueous solution-based electrodeposition of ceramic oxides and opens a general solution chemistry approach for electrochemical processing of hitherto unexplored air- and moisture-sensitive high valent multinary structures with extended frameworks. [ABSTRACT FROM AUTHOR]

Microencapsulated materials are receiving broad attention for applications as diverse as energy storage and conversion, biomedicine, self‐healing materials, and electronics. Here, a general microfluidic approach is presented to prepare phase‐change material‐infilled microcapsules with unique thermal and mechanical properties. Aqueous sodium acetate solutions are encapsulated by an acrylate‐based shell via a microfluidic method. To understand and optimize microcapsule formation, flow behavior during the encapsulation is numerically simulated. When the microcapsules are embedded in an acrylate matrix (same composition as the shell wall material), the microcapsules exhibit a significant 46.6 ºC difference between the crystallization and melting temperatures as determined by differential scanning calorimetry at a rate of 10 ºC per min. Variable temperature dynamic mechanical analysis over the range of 50 to ‐90 ºC reveals up to a 50% change in the composite's elastic modulus at a given temperature, depending on if the sample is being cooled or heated, due to significant undercooling of the core material crystallization as shown by X‐ray diffraction. [ABSTRACT FROM AUTHOR]

For 20 years, nanoscale 3D printing has been based on two-photon absorption, requiring expensive pulsed lasers. Now, via a two-step absorption process, such printing has been demonstrated using a low-cost, low-power continuous-wave laser diode, showing the potential for dramatic cost reductions in 3D nanoprinting. [ABSTRACT FROM AUTHOR]

Self‐assembly of 3D structures presents an attractive and scalable route to realize reconfigurable and functionally capable mesoscale devices without human intervention. A common approach for achieving this is to utilize stimuli‐responsive folding of hinged structures, which requires the integration of different materials and/or geometric arrangements along the hinges. It is demonstrated that the inclusion of Kirigami cuts in planar, hingeless bilayer thin sheets can be used to produce complex 3D shapes in an on‐demand manner. Nonlinear finite element models are developed to elucidate the mechanics of shape morphing in bilayer thin sheets and verify the predictions through swelling experiments of planar, millimeter‐scaled PDMS (polydimethylsiloxane) bilayers in organic solvents. Building upon the mechanistic understandings, The transformation of Kirigami‐cut simple bilayers into 3D shapes such as letters from the Roman alphabet (to make "ADVANCED FUNCTIONAL MATERIALS") and open/closed polyhedral architectures is experimentally demonstrated. A possible application of the bilayers as tether‐less optical metamaterials with dynamically tunable light transmission and reflection behaviors is also shown. As the proposed mechanistic design principles could be applied to a variety of materials, this research broadly contributes toward the development of smart, tetherless, and reconfigurable multifunctional systems. [ABSTRACT FROM AUTHOR]

Composite phase change materials consisting of a high-latent-heat phase change material (PCM) embedded in a high-thermal-conductivity matrix are desirable for thermally buffering pulsed heat loads via rapid absorption and release of thermal energy at a constant temperature. This paper reports a composite PCM thermal buffer consisting of a Field's metal PCM having high volumetric latent heat (315 MJ/m3) embedded in a copper (Cu) matrix having high intrinsic thermal conductivity [384 W/(m·K)]. We demonstrate thermal buffer samples fabricated with Cu volume fractions from 0.05 to 0.2 and sample thicknesses ranging between 1 mm and 4 mm. Experiments coupled with finite element method simulations were used to determine the figures of merit (FOMs), cooling capacity ηeff, energy density Eeff, effective thermal conductivity keff, and the buffering time constant τ. The cooling capacity was measured to be as high as ηeff = 72 ± 4 kJ/(m2·K1/2·s1/2) for the 1.45 mm thick thermal buffer sample having a Cu volume fraction of 0.13, significantly higher than theoretical values for aluminum–paraffin composites [45 kJ/(m2·K1/2·s1/2)] or pure paraffin wax [8 kJ/(m2·K1/2·s1/2)]. Our work develops design guidelines for high-FOM thermal buffer devices for pulsed heat load thermal management. [ABSTRACT FROM AUTHOR]

Template-directed assembly has been shown to yield a broad diversity of highly ordered mesostructures1,2, which in a few cases exhibit symmetries not present in the native material3–5. However, this technique has not yet been applied to eutectic materials, which underpin many modern technologies ranging from high-performance turbine blades to solder alloys. Here we use directional solidification of a simple AgCl-KCl lamellar eutectic material within a pillar template to show that interactions of the material with the template lead to the emergence of a set of microstructures that are distinct from the eutectic’s native lamellar structure and the template’s hexagonal lattice structure. By modifying the solidification rate of this material–template system, trefoil, quatrefoil, cinquefoil and hexafoil mesostructures with submicrometre-size features are realized. Phase-field simulations suggest that these mesostructures appear owing to constraints imposed on diffusion by the hexagonally arrayed pillar template. We note that the trefoil and hexafoil patterns resemble Archimedean honeycomb and square–hexagonal–dodecagonal lattices6, respectively. We also find that by using monolayer colloidal crystals as templates, a variety of eutectic mesostructures including trefoil and hexafoil are observed, the former resembling the Archimedean kagome lattice. Potential emerging applications for the structures provided by templated eutectics include non-reciprocal metasurfaces7, magnetic spin-ice systems8,9, and micro- and nano-lattices with enhanced mechanical properties10,11.Directional solidification of a simple AgCl-KCl lamellar eutectic material is modified by the presence of a pillar template, leading to disordered, trefoil, quatrefoil, cinquefoil and hexafoil mesostructures. [ABSTRACT FROM AUTHOR]

Eccrine sweat is a rich and largely unexplored biofluid that contains a range of important biomarkers, from electrolytes, metabolites, micronutrients and hormones to exogenous agents, each of which can change in concentration with diet, stress level, hydration status and physiologic or metabolic state. Traditionally, clinicians and researchers have used absorbent pads and benchtop analyzers to collect and analyze the biochemical constituents of sweat in controlled, laboratory settings. Recently reported wearable microfluidic and electrochemical sensing devices represent significant advances in this context, with capabilities for rapid, in situ evaluations, in many cases with improved repeatability and accuracy. A limitation is that assays performed in these platforms offer limited control of reaction kinetics and mixing of different reagents and samples. Here, we present a multi-layered microfluidic device platform with designs that eliminate these constraints, to enable integrated enzymatic assays with demonstrations of in situ analysis of the concentrations of ammonia and ethanol in microliter volumes of sweat. Careful characterization of the reaction kinetics and their optimization using statistical techniques yield robust analysis protocols. Human subject studies with sweat initiated by warm-water bathing highlight the operational features of these systems. [ABSTRACT FROM AUTHOR]

Selective transport and concentration of molecules to specified regions on a substrate both enhances the potential to detect such molecules and provides a path to spatially localize such molecules prior to initiation of subsequent chemical reactions. Here, we first embed radially symmetric α‐, β‐, and γ‐cyclodextrin gradients in a hydrogel matrix. Driven by host‐guest interactions between the cyclodextrins and the target molecule, we observe these gradients can serve to direct 2D molecular transport. Using xanthene dyes and organophosphates as target molecules, we found the transport metrics, e.g. selectivity, rate, and concentration limits, are strongly dependent on the specific cyclodextrin forming the gradient. In all cases, as the concentrating power of the gradient increased, the rate of target concentration slowed, which we hypothesize is because stronger interactions between the target and the cyclodextrin decrease the rate of target diffusion. The concentration enhancement for the nerve agent simulant 4‐methylumbelliferyl phosphate (15.8) is the greatest when the gradient is formed using β‐cyclodextrin while directed concentration of cyanomethyl phosphonate, a smaller non‐aromatic organophosphate, is observed only for the smaller α‐CD. To provide a near real‐time read‐out of the concentration of the analyte, we used an array of IR resonant metallic nanoantennas tuned to a specific IR absorption band of the analyte to enhance the IR signal generated by the analyte. [ABSTRACT FROM AUTHOR]

Selective transport and concentration of molecules to specified regions on a substrate both enhances the potential to detect such molecules and provides a path to spatially localize such molecules prior to initiation of subsequent chemical reactions. Here, we first embed radially symmetric α‐, β‐, and γ‐cyclodextrin gradients in a hydrogel matrix. Driven by host‐guest interactions between the cyclodextrins and the target molecule, we observe these gradients can serve to direct 2D molecular transport. Using xanthene dyes and organophosphates as target molecules, we found the transport metrics, e.g. selectivity, rate, and concentration limits, are strongly dependent on the specific cyclodextrin forming the gradient. In all cases, as the concentrating power of the gradient increased, the rate of target concentration slowed, which we hypothesize is because stronger interactions between the target and the cyclodextrin decrease the rate of target diffusion. The concentration enhancement for the nerve agent simulant 4‐methylumbelliferyl phosphate (15.8) is the greatest when the gradient is formed using β‐cyclodextrin while directed concentration of cyanomethyl phosphonate, a smaller non‐aromatic organophosphate, is observed only for the smaller α‐CD. To provide a near real‐time read‐out of the concentration of the analyte, we used an array of IR resonant metallic nanoantennas tuned to a specific IR absorption band of the analyte to enhance the IR signal generated by the analyte. [ABSTRACT FROM AUTHOR]

Inexorable demand for increasing bandwidth is driving future wireless communications systems into the 100 GHz–1 THz region, thereby fueling demand for new sources and modulators but also complementary devices such as resonators, phase shifters, and filters. Few such devices exist at present, and the electromagnetic properties of those available at millimeter-wavelengths are generally fixed and characterized by broad (i.e., low Q) resonances. We introduce a class of 3D plasma/metal/dielectric photonic crystals (PPCs), operating in the 120–170 GHz spectral range, that are dynamic (tunable and reconfigurable at electronic speeds) and possess attenuation and transmission resonances with bandwidths below 50 MHz. Interference between sublattices of the crystal, which controls the resonance line shapes, is manipulated through the crystal structure. Incorporating Bragg arrays of low-temperature plasma microcolumns into a dielectric/metal scaffold that is itself a static crystal forms two interwoven and electromagnetically coupled crystals. Plasma-scaffold lattices produce multiple, narrowband attenuation resonances that shift monotonically to higher frequencies by as much as 1.6 GHz with increasing plasma electron density. Controlling the longitudinal geometry of the PPC through electronic activation of successive Bragg planes of plasma columns reveals an unexpected double-crystal symmetry interaction at 138.4 GHz and resonance Q values above 5100. The introduction of point or line defects into plasma column/polymer/metal crystals increases transparency at resonances of the scaffold (Borrmann effect) and yields Fano line shapes characteristic of coupled resonators. The experimental results suggest the suitability of PPC-based metamaterials for applications including multichannel communications, millimeter-wave spectroscopy, and fundamental studies of multiple, coupled resonators. [ABSTRACT FROM AUTHOR]

We describe an optical beam deflection technique for measurements of the thermal diffusivity of fluid mixtures and suspensions of nanoparticles with a precision of better than 1%. Our approach is tested using the thermal conductivity of ethanol-water mixtures; in nearly pure ethanol, the increase in thermal conductivity with water concentration is a factor of 2 larger than predicted by effective medium theory. Solutions of C60–C70 fullerenes in toluene and suspensions of alkanethiolate-protected Au nanoparticles were measured to maximum volume fractions of 0.6% and 0.35 vol %, respectively. We do not observe anomalous enhancements of the thermal conductivity that have been reported in previous studies of nanofluids; the largest increase in thermal conductivity we have observed is 1.3%±0.8% for 4 nm diam Au particles suspended in ethanol. [ABSTRACT FROM AUTHOR]

Emerging power batteries with both high volumetric energy density and fast charge/discharge kinetics are required for electric vehicles. The rapid ion/electron transport of mesostructured electrodes enables a high electrochemical activity in secondary batteries. However, the typical low fraction of active materials leads to a low volumetric energy density. Herein, we report a novel biomimetic “bee pupa infilled honeycomb”-structured 3D mesoporous cathode. We found previously the maximum active material filing fraction of an opal template before pinch-off was about 25%, whereas it could be increased to ∼90% with the bee pupa-infilled honeycomb-like architecture. Importantly, even with a high infilling fraction, fast Li+/e− transport kinetics and robust mechanical property were achievable. As the demonstration, a bee pupa infilled honeycomb-shaped Li2MnSiO4/C cathode was constructed, which delivered a high volumetric energy density of 2443 W h L−1. The presented biomimetic bee pupa infilled honeycomb configuration is applicable for a broad set of both cathodes and anodes in high energy density batteries. [ABSTRACT FROM AUTHOR]

Materials that can be switched between low and high thermal conductivity states would advance the control and conversion of thermal energy. Employing in situ time-domain thermoreflectance (TDTR) and in situ synchrotron X-ray scattering, we report a reversible, light-responsive azobenzene polymer that switches between high (0.35 W m-1 K-1) and low thermal conductivity (0.10 W m-1 K-1) states. This threefold change in the thermal conductivity is achieved by modulation of chain alignment resulted from the conformational transition between planar (trans) and nonplanar (cis) azobenzene groups under UV and green light illumination. This conformational transition leads to changes in the π-π stacking geometry and drives the crystal-to-liquid transition, which is fully reversible and occurs on a time scale of tens of seconds at room temperature. This result demonstrates an effective control of the thermophysical properties of polymers by modulating interchain π-π networks by light. [ABSTRACT FROM AUTHOR]