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[Display omitted] Marigold analogues micro flowers of tungsten oxide (WO 3) have been grown in thin film form through simple and cost-effective solution chemistry approach on stainless steel substrate. Aqueous precursor involving WO 4 - 2 ions agglomerated as self-sacrificing template growing initially into the nano-petal, followed by self-assembly; leading to marigold analogues micro flower surface architecture. This enthralling morphology motivated us not only to fabricate supercapacitive electrode but also to design complete solid-state supercapacitor devices in dual configurations: flexible pouch cell and coin cell. Interestingly, both devices even in symmetric configuration yields remarkable potential window of 1.82 V when sandwiched by gel inclusive of Li+ ions dispersed in non-conducting polyvinyl alcohol matrix. Solid-state flexible pouch cell and coin cell delivered specific capacitances of 103.98 ± 3.59 and 30.09 ± 1.03 F/g respectively at a scan rate of 5 mV/s. Assembled electrode, coin-cell and flexible pouch-cells have been well assessed in-depth through specific capacitances using cyclic voltammetry and galvanostatic charge discharge, diffusive and capacitive contributions, mechanical bending tests, electrochemical active surface area, and electrochemical impedance analysis. Practical applicability has been demonstrated for designed flexible pouch cell to run small fan and light emitting diode panel whereas coin cell to run light emitting diode panel. [ABSTRACT FROM AUTHOR]

Solid-state batteries offer significant advantages but present several challenges. Given the complexity of these systems, it is good practice to begin the study with simpler models and progressively advance to more complex configurations, all while maintaining an understanding of the physical principles governing solid-state battery operation. The results presented in this work pertain to cells without traditional electrodes, thus providing a foundation for guiding the development of fully functional solid-state cells. The open circuit voltage (OCV) of the Cu/Na2.99Ba0.005ClO composite in a cellulose/Zn pouch cell achieves 1.10 V, reflecting the difference in the chemical potentials of the current collectors (CCs), Zn and Cu, serving as electrodes. After 120 days, while set to discharge, conversely to what was expected, a higher potential difference of 1.13 V was attained (capacity of 5.9 mAh·g−1electrolyte). By incorporating a layer of carbon felt, the OCV became 0.85 V; however, after 95 days, the potential difference increased to 1.20 V. Ab initio simulations were additionally performed on a Cu/Na3ClO/Zn heterojunction showing the formation of dipoles and the Na deposition on Zn which is demonstrated experimentally. The sodium plating on the negative CC (Zn) takes place as the cell is set to discharge at room temperature but is not observed at 40 °C. [ABSTRACT FROM AUTHOR]

The aim of this review is to compile important results of single-crystal X-ray diffraction method, vibrational and NMR studies conducted on alkali metal ion complexes of some small ring benzo-crown ethers namely benzo-15-crown-5, dibenzo-15-crown-5 and benzo-12-crown-4 to determine their structure, stoichiometry and conformation in the solid-state. This review focuses on solid-state architectural diversity of alkali metal ion complexes studied by single-crystal X-ray diffraction method. Investigations of these complexes are significant as the interactions of alkali metal ions with these crown ethers mimic those present in nature between univalent ions and several bioligands. The benzo group in the macrocycle allows to monitor the complexation event by fluorescence studies and extends the applications of these crown ethers to fluorescent ion sensors. The selected small ring benzo oxa-crown ethers have cavities that match the size of the alkali metal ions and give stable complexes with them. The review presents results related to variation in infrared and Raman spectra of the ligands with changes in their crystal structure and conformation on complexation with alkali salts. Single-crystal X-ray diffraction studies of these complexes help to confirm the chemical structure, stoichiometry, stable conformation and presence of associated solvent molecules in the solid state. As noncovalent interactions are involved in the formation of these complexes, they are capable of forming supramolecular assemblies for building smart functional materials. [ABSTRACT FROM AUTHOR]

The human nervous system inspires the next generation of sensory and communication systems for robotics, human‐machine interfaces (HMIs), biomedical applications, and artificial intelligence. Neuromorphic approaches address processing challenges; however, the vast number of sensors and their large‐scale distribution complicate analog data manipulation. Conventional digital multiplexers are limited by complex circuit architecture and high supply voltage. Large sensory arrays further complicate wiring. An ʻin‐electrolyte computingʼ platform is presented by integrating organic electrochemical transistors (OECTs) with a solid‐state polymer electrolyte. These devices use synapse‐like signal transport and spatially dependent bulk ionic doping, achieving over 400 times modulation in channel conductance, allowing discrimination of locally random‐access events without peripheral circuitry or address assignment. It demonstrates information processing from 12 tactile sensors with a single OECT output, showing clear advantages in circuit simplicity over existing all‐electronic, all‐digital implementations. This self‐multiplexer platform offers exciting prospects for circuit‐free integration with sensory arrays for high‐quality, large‐volume analog signal processing. [ABSTRACT FROM AUTHOR]

A new integrated electrode-separator-electrolyte hydrogel is designed and prepared, which is composed of organic liquid crystal, polyvinyl alcohol (PVA), polyaniline (PANI), and reduced graphene oxide (rGO). The organic liquid crystal is introduced into PVA hydrogel, effectively improving compatibility between active materials and hydrogel matrix. The PANI active material is in situ polymerized in hydrogel to prepare PANI-double-network hydrogel. It simultaneously acts as electrode, separator, and electrolyte for assembling flexible solid-state supercapacitor. It obtains an area-specific capacitance of 160.2 mF/cm2 and a power density of 101.5 μW/cm2 with an energy density of 21.0 μWh/cm2. This work provides a new method to reduce interfacial resistance of electrode, separator, and electrolyte of flexible solid-state supercapacitor, further improving its electrochemical performance. [ABSTRACT FROM AUTHOR]

At present, the emerging solid-phase friction-based additive manufacturing technology, including friction rolling additive manufacturing (FRAM), can only manufacture simple single-pass components. In this study, multi-layer multi-pass FRAM-deposited aluminum alloy samples were successfully prepared using a non-shoulder tool head. The material flow behavior and microstructure of the overlapped zone between adjacent layers and passes during multi-layer multi-pass FRAM deposition were studied using the hybrid 6061 and 5052 aluminum alloys. The results showed that a mechanical interlocking structure was formed between the adjacent layers and the adjacent passes in the overlapped center area. Repeated friction and rolling of the tool head led to different degrees of lateral flow and plastic deformation of the materials in the overlapped zone, which made the recrystallization degree in the left and right edge zones of the overlapped zone the highest, followed by the overlapped center zone and the non-overlapped zone. The tensile strength of the overlapped zone exceeded 90% of that of the single-pass deposition sample. It is proved that although there are uneven grooves on the surface of the overlapping area during multi-layer and multi-pass deposition, they can be filled by the flow of materials during the deposition of the next layer, thus ensuring the dense microstructure and excellent mechanical properties of the overlapping area. The multi-layer multi-pass FRAM deposition overcomes the limitation of deposition width and lays the foundation for the future deposition of large-scale high-performance components. [ABSTRACT FROM AUTHOR]

In this paper, we report on the use of a purpose-built hybrid solid-state microwave and radiofrequency generator operating at frequencies of 2.45 GHz and/or 480 kHz for cancer ablation in various tissues. The hybrid generator was tested ex vivo on chicken breast and bovine liver and has demonstrated that the high accuracy of the power delivered to the sample can be achieved by controlling the emitted power versus the temperature profile of the treated sample. In particular, the hybrid generator incorporates control systems based on impedance or reflected power measurements that allow controlled ablation without causing unwanted carbonization and without including areas where tissue damage is not desired. The results of the ex vivo tests showed that radiofrequency ablation (RFA) could be effective for performing controlled ablations with minimally invasive probes, such as cardiac pathologies, small lesions, and tissues with particular composition, while microwave ablation (MWA) could be optimal for performing large ablations in highly vascularized tissues, such as liver cancer, where it is necessary to achieve higher temperatures.

We report on the design and simulation of strip-loaded nanophotonic interfaces aimed at improving resonant coupling and photon routing efficiency. In our design, the guided mode is confined within a plane by a high-index thin film and is loosely confined laterally by a lower index strip. Using a hydrogen silsesquioxane (HSQ) strip, titanium dioxide core, and silicon dioxide substrate, we optimise the waveguide dimensions for maximum lateral confinement of light. Specifically, we propose a polymer-based Bragg grating cavity and ring resonator that achieve near-optimal mode volumes and high Q-factors. These may be further developed to achieve the even higher Q-factors demanded by quantum technologies. Our calculations suggest that a quantum dot embedded in a cavity with a mode volume of Veff ~ 7.0(λ/n)³ and a Q-factor of 7,000 can produce photons with 97% indistinguishability at 4K. Additionally, we investigate directional couplers for efficient photon routing, comparing photonic and plasmonic material structures. While pure photonic structures demonstrate lower loss and improved quality factors, they face practical limitations in terms of bending radius. Conversely, plasmonic structures offer shorter bending radii but higher propagation losses. This research lays the groundwork for future nanophotonic designs, aiming to enhance photon generation and routing capabilities for quantum optical applications. [ABSTRACT FROM AUTHOR]

Acenes, the group of polycyclic aromatic hydrocarbons (PAHs) with linearly fused benzene rings, possess distinctive electronic properties with potential applicability in material science. Hexacene was the largest acene obtained and characterized in the last century, followed by heptacene in 2006. Since then, a race for obtaining the largest acene resulted in the development of several members of this family as well as diverse innovative synthetic strategies, from solid‐state chemistry to the promising on‐surface chemistry. This last technique allows the obtention of large acenes, up to tridecacene, the largest acene so far. This review presents the different methodologies employed for the synthesis of acenes, highlighting the newest studies, to provide a much more thorough understanding of the essence of the electronic structure of this captivating group of organic compounds. [ABSTRACT FROM AUTHOR]

Hard carbon (HC) with low cost and high specific capacity is considered the appropriate anode material for sodium‐ion batteries (SIBs), but the low initial coulombic efficiency (ICE) caused by solid electrolyte interface (SEI) formation and inherent active defects impede its practical battery application. Here, the practicability of solid‐state electrochemical (SSE) pre‐sodiation technique for hard carbon anode is assessed to conquer such challenges. The uniformly pre‐sodiated HC (Pre‐HC) can be fabricated through the SSE reaction between the HC and preloaded sodium metal film without introducing a liquid electrolyte. After being immerged in the electrolyte, a thin artificial SEI with abundant inorganic species is formed on the surface of Pre‐HC due to the spontaneous chemical reaction, and the ICE of HC is improved from 76.0% to 107.9%. Full cell paired with Na3V2(PO4)3 cathode exhibits a high ICE of 94.0% with 70% of energy density augment (from 126.5 to 214.4 Wh kg−1) after anode pre‐sodiation. Pre‐HC anode still retains the pre‐sodiation capacity of 671.1 mAh gNa−1 after being stored in the dry air for 2 h. This work demonstrates the practical applicability of this SSE pre‐sodiation strategy to enhance the energy density of SIBs. [ABSTRACT FROM AUTHOR]

Improving food preservation technologies is a key aspect in the struggle to reduce global food waste, and natural antimicrobial substances, such as essential oil (EO) components represent very promising food preserving agent. However, their intrinsic chemico‐physical properties, such as the low melting point, low water solubility and high volatility, pose some practical difficulties in exploiting them for practical applications. Cocrystallization is used to stabilize liquid or volatile EO components providing them whit a crystalline environment, thus improving their potential application as antibacterial agents. Five EO active ingredients (THY = thymol, CAR = carvacrol, EUG = eugenol, CAD = trans‐cinnamaldehyde, and VAN = o‐vanillin) and two coformers (INA = Isonicotinamide, and HBA = 4‐hydroxybenzoic acid) have been combined and the corresponding cocrystals have been studied for their potential inhibiting effect against four food spoilage bacteria (Bacillus thuringiensis, Enterobacter cloacae, Pseudomonas fluorescens, and Serratia marcescens). The structures of the five cocrystals have been used to derive structure‐activity relationships in terms of release energy of the active ingredients form the crystalline environment, and a correlation has been derived with the Intermolecular Interaction Energies of the EO molecules. [ABSTRACT FROM AUTHOR]

Direct recycling is a key technology for enabling a circular economy of spent lithium ion batteries (LIBs). For cathode active materials (CAMs), it is regarded as the tightest closed‐loop and most efficient approach among current recycling techniques as it simply proceeds via re‐lithiation and reconstruction of aged CAMs instead of separating them into elemental components. In this work, spent, i.e., morphologically and structurally decomposed CAM based on LiNi0.83Co0.12Mn0.05O2 (NCM‐831205) is restored by mimicking conditions of original CAM synthesis. After evaluating and optimizing the high‐temperature duration for CAM restoration and subsequent washing procedure, the recycled CAM is shown to maintain poly‐crystallinity and tap density, successfully recover specific surface area, lithium content, crystal structure in surface and bulk, while, however, only partly the original secondary particle size and shape. Though, comparable in initial 100 charge/discharge cycles with pristine CAM in lithium ion‐cells, the subsequent increase in resistance and capacity fading remains a challenge. High temperature during recycling can be regarded as a key challenge on material level, as it not only promotes detrimental surface carbonate species from residual carbon black but also enhances cation disorder and micro‐/nanoscopic porosity through oxygen release, likely in de‐lithiated, thus less thermally stable regions of cycled NCM. [ABSTRACT FROM AUTHOR]

In this paper, we report on the use of a purpose-built hybrid solid-state microwave and radiofrequency generator operating at frequencies of 2.45 GHz and/or 480 kHz for cancer ablation in various tissues. The hybrid generator was tested ex vivo on chicken breast and bovine liver and has demonstrated that the high accuracy of the power delivered to the sample can be achieved by controlling the emitted power versus the temperature profile of the treated sample. In particular, the hybrid generator incorporates control systems based on impedance or reflected power measurements that allow controlled ablation without causing unwanted carbonization and without including areas where tissue damage is not desired. The results of the ex vivo tests showed that radiofrequency ablation (RFA) could be effective for performing controlled ablations with minimally invasive probes, such as cardiac pathologies, small lesions, and tissues with particular composition, while microwave ablation (MWA) could be optimal for performing large ablations in highly vascularized tissues, such as liver cancer, where it is necessary to achieve higher temperatures. [ABSTRACT FROM AUTHOR]

The combined effect of active shielding packaging and relative phase sweeping on heating performance in a dual-port solid-state microwave heating process was evaluated. Four types of heating strategies that combine two factors (passive and active packaging and fixed and sweeping relative phase) were used in heating a tray of 300 g gellan gel sample for 3 min. The temperature distributions at the top and middle layers of the heated samples were collected and analyzed for heating uniformity index (HUI) and power absorption efficiency (PAE). The results showed that both active shielding package and relative phase sweeping can individually improve the HUI while maintaining high PAE. The packaging factor and relative phase factor showed a significant interaction effect (p = 0.0021) in influencing HUI but not PAE, highlighting the necessity of considering both factors (packaging and relative phase) when optimizing the microwave heating uniformity. The combination of active packaging and sweeping relative phase is a robust heating strategy that delivers the best heating performance that is significantly better than or similar to other combinations of packaging and relative phase strategies. [ABSTRACT FROM AUTHOR]

Hydrogen‐driven energy is fascinating among the everlasting energy sources, particularly for stationary and onboard transportation applications. Efficient hydrogen storage presents a key challenge to accomplishing the sustainability goals of hydrogen economy. In this regard, solid‐state hydrogen storage in nanomaterials, either physically or chemically adsorbed, has been considered a safe path to establishing sustainability goals. Though metal hydrides have been extensively explored, they fail to comply with the set targets for practical utilization. Recently, MXenes, both in bare form and hybrid state with metal hydrides, have proven their flair in ascertaining the hydrides′ theoretical and experimental hydrogen storage capabilities far beyond the fancy materials and current state‐of‐the‐art technologies. This review encompasses the significant accomplishments achieved by MXenes (primarily in 2019–2024) for enhancing the hydrogen storage performance of various metal hydride materials such as MgH2, AlH3, Mg(BH4)2, LiBH4, alanates, and composite hydrides. It also discusses the bottlenecks of metal hydrides for hydrogen storage, the potential use of MXenes hybrids, and their challenges, such as reversibility, H2 losses, slow kinetics, and thermodynamic barriers. Finally, it concludes with a detailed roadmap and recommendations for mechanistic‐driven future studies propelling toward a breakthrough in solid material‐driven hydrogen storage using cost‐effective, efficient, and long‐lasting solutions. [ABSTRACT FROM AUTHOR]

Bovine lactoferrin (bLF) is a multifunctional protein used in the food and pharmaceutical industries. Various commercially available bLF powders (bLFPs) have different ratios of protein monomers to aggregates, which affects the aggregation rate. However, the changes in molecular structure and interactions during aggregation are unclear. This study investigated changes in the structure and interactions of stored bLFPs during aggregation. Five commercially available bLFPs with different molecular weight distributions were analyzed before and after storage using size-exclusion chromatography and X-ray diffraction (XRD) to monitor aggregation and β-strand interaction, respectively. These bLFPs were stored for four weeks under high temperature and humidity conditions as a stress test. The XRD results revealed changes in peak II (around 2θ = 20°), corresponding to β-strand interactions. The peak II change rate suggested that the aggregation occurs due to partial structural fluctuations and interaction changes. Furthermore, time-course analysis of peak II and correlations with the pre-storage monomer ratio and aggregation phase index demonstrated that β-strand interactions decreased during the transformation of monomers to low-molecular-weight (LMW) aggregates, while it increased during the LMW-to-high-molecular-weight aggregate phase. These results provide novel insights into the conformational changes and molecular interactions of bLFPs during aggregation.

Abstract The human nervous system inspires the next generation of sensory and communication systems for robotics, human‐machine interfaces (HMIs), biomedical applications, and artificial intelligence. Neuromorphic approaches address processing challenges; however, the vast number of sensors and their large‐scale distribution complicate analog data manipulation. Conventional digital multiplexers are limited by complex circuit architecture and high supply voltage. Large sensory arrays further complicate wiring. An ʻin‐electrolyte computingʼ platform is presented by integrating organic electrochemical transistors (OECTs) with a solid‐state polymer electrolyte. These devices use synapse‐like signal transport and spatially dependent bulk ionic doping, achieving over 400 times modulation in channel conductance, allowing discrimination of locally random‐access events without peripheral circuitry or address assignment. It demonstrates information processing from 12 tactile sensors with a single OECT output, showing clear advantages in circuit simplicity over existing all‐electronic, all‐digital implementations. This self‐multiplexer platform offers exciting prospects for circuit‐free integration with sensory arrays for high‐quality, large‐volume analog signal processing.

ObjectivesDuring holmium:yttrium-aluminum-garnet (holmium:YAG) laser lithotripsy to break urinary stones, urologists frequently see flashes of light. As infrared laser pulses are invisible, what is the source of light? Here we studied the origin, characteristics, and some effects of flashes of light in laser lithotripsy.MethodsUltrahigh-speed video-microscopy was used to record single laser pulses at 0.2-1.0 J energy lasered with 242 µm glass-core-diameter fibers in contact with whole surgically retrieved urinary stones and hydroxyapatite (HA)-coated glass slides in air and water. Acoustic transients were measured with a hydrophone. Visible-light and infrared photodetectors resolved temporal profiles of visible-light emission and infrared-laser pulses.ResultsTemporal profiles of laser pulses showed intensity spikes of various duration and amplitude. The pulses were seen to produce dim light and bright sparks with submicrosecond risetime. The spark produced by the intensity spike at the beginning of laser pulse generated a shock wave in the surrounding liquid. The subsequent sparks were in a vapor bubble and generated no shock waves. Sparks enhanced absorption of laser radiation, indicative of plasma formation and optical breakdown. The occurrence and number of sparks varied even with the same urinary stone. Sparks were consistently observed at laser energy >0.5 J with HA-coated glass slides. The slides broke or cracked by cavitation with sparks in 63 ± 15% of pulses (1.0 J, N = 60). No glass-slide breakage occurred without sparks (1.0 J, N = 500).ConclusionUnappreciated in previous studies, plasma formation with free-running long-pulse holmium:YAG lasers can be an additional physical mechanism of action in laser procedures.

In order to fulfill the demand for high energy and capacity, an electrode with high-voltage capability, namely LiNi0.5Mn1.5O4 (LNMO) that has an operating potential of up to 4.7 V vs Li/Li+, is currently becoming popular in Li-ion battery chemistries. This research produced LNMO by using a solid-state method with only one-step synthesis route to compare its electrochemical performance with different lithium sources, including hydroxide (LNMO-LiOH), acetate (LNMO-LiAce), and carbonate (LNMO-LiCar) precursors. TGA/DSC was first performed for all three sample precursors to ensure the optimal calcination temperature, while XRD and SEM characterized the physical properties. The electrochemical measurements, including cyclic voltammetry and charge-discharge, were conducted in the half-cell configurations of LNMO//Li-metal using a standard 1 M LiPF6 electrolyte. LNMO-LiOH samples exhibited the highest purity and the smallest particle size, with values of 93.3% and 418 nm, respectively. In contrast, samples with higher impurities, such as LNMO-LiCar, mainly in the form of LixNi1-xO (LiNiO), displayed the largest particle size. The highest working voltage possessed by LNMO-LiOH samples was 4.735 V vs Li/Li+. The results showed that LNMO samples with LiNiO impurities would affect the reaction behavior that occurs at the cathode-electrolyte interface during the release of lithium-ions, resulting in high resistance at the battery operations and decreasing the specific capacity of the LNMO during discharging. The highest value, shown by LNMO-LiOH, was up to 92.75 mAh/g. On the other side, LNMO-LiCar only possessed a specific capacity of 44.57 mAh/g, indicating a significant impact of different lithium sources in the overall performances of LNMO cathode.

Collagen‐based aerogels have great potential for topical biomedical applications. Collagen's natural affinity with skin, biodegradability, and gelling behavior are compelling properties to combine with the structural integrity of highly porous matrices in the dry form (aerogels). This work aimed to produce a novel collagen‐based aerogel and to perform the material's solid‐state and physicochemical characterization. Aerogels were obtained by performing different solvent exchange approaches of a collagen‐gelled extract and drying the obtained alcogels with supercritical CO2. The resulting aerogels showed a sponge‐like structure with a relatively dense mesoporous network with a specific surface area of 201–203 m2/g, a specific pore volume of 1.08–1.15 cm3/g, and a mean pore radius of ca. 14.7 nm. Physicochemical characterization confirmed that the obtained aerogels are composed of pure collagen, and the aerogel production process does not impact protein tertiary structure. Finally, the material swelling behavior was assessed at various pH values (4, 7, and 10). Collagen aerogels presented a high water uptake capacity up to ~2700 wt. %, pH‐dependent stability, and swelling behavior in aqueous media. The results suggest that this collagen aerogel could be a promising scaffold candidate for topical biomedical applications. [ABSTRACT FROM AUTHOR]

This study introduces a novel approach to address the growing demand for flexible energy storage systems in wearable and human-integrated devices. A flexible supercapacitor (SC) system is developed using a plasticized polyvinyl chloride (PVC)-derived ionogel electrolyte. The ionogel consists of PVC, dibutyl adipate (DBA) plasticizer, and 1-ethyl-3-methyl imidazolium bis(trifluoromethyl sulfonyl)imide ([EMIM]+[TFSI]−) ionic liquid (IL), offering impressive properties such as high stretchability (~ 2050%) and non-volatility. SCs assembled with activated carbon electrodes embedded in the ionogel exhibit remarkable electrochemical performance. They attain near-100% Coulombic efficiency (CE) up to 2.0 V and a specific capacitance of up to 64.8 F g−1, finely tuned by modulating the concentration of [EMIM]+[TFSI]− IL. Significantly, the SC employing the optimized PVC-based ionogel demonstrates exceptional stability over 1000 charge–discharge cycles, maintaining both capacitance and CE. The non-volatile nature of the ionogel enhances its robustness under ambient conditions, contributing to long-term stability. Moreover, the potential integration of the PVC-based ionogel with flexible electrodes and a malleable current collector hints at the possibility of creating a highly stretchable SC system. This work advances the field of SC powering flexible electronics and accelerates their seamless integration into everyday life. [ABSTRACT FROM AUTHOR]

This manuscript shows an innovative water-based processing route to fabricate lead-free piezoceramics. It faces the challenge of substituting conventionally used organic solvents by innocuous water. The procedure involves two methods of widespread use in industry: attrition ball-milling and freezing-lyophilization. Powders with nominal composition (Ba 0.92 Ca 0.08)(Ti 0.95 Zr 0.05)O 3 were effectively obtained. A narrow monomodal size distribution (600 nm) proved high reactivity that allowed solid-state synthesis at ultra-low temperature (700 °C-2 h). Optimal two-step sintering method (900 °C-3 h,1280 °C-6 h) allowed well-sintered homogeneous ceramics with pure tetragonal perovskite phase. They showed high piezo-sensitivity (d 33 =320 pC/N, d 31 =−110 pC/N, k p =31.45% and N p =2750 kHz·mm, ε ′ 33 T =3670, tanδ=0.036 at 1 kHz), comparable to that found for routes in organic media. Therefore, attrition ball milling in water and lyophilization work in synergy to successfully activate the precursors, influencing on the structural, microstructural and electrical properties of the final BCZT ceramics. This is an unprecedented development to produce piezoelectric ceramics using a sustainable, environmentally benign water-based process, with a positive impact in noteworthy industrial applications. • Novel mixed oxides route to fabricate (Ba 0.92 Ca 0.08) (Ti 0.95 Zr 0.05) O 3. • Attrition ball-milling in water, freezing and lyophilization activate the precursors. • Fine lyophilized powder (600 nm) allows ultra-low synthesis at 700 °C. • Two-step sintering at 1280 °C results in a pure tetragonal perovskite phase. • High piezo-sensitivity, alike that obtained by milling in organic media. [ABSTRACT FROM AUTHOR]

The development of single‐platform qubits, predominant for most of the last few decades, has driven the progress of quantum information technologies but also highlighted the limitations of various platforms. Some inherent issues, such as charge/spin noise in materials hinder certain platforms, while increased decoherence upon attempts to scale up severely impacts qubit quality and coupling on others. In addition, a universal solution for coherent information transfer between quantum systems remains lacking. By combining one or more qubit platforms, one could potentially create new hybrid platforms that might alleviate significant issues that current single‐platform qubits suffer from, and in some cases, even facilitate the conversion of static to flying qubits on the same hybrid platform. While nascent, this is an area of rising importance that could shed new light on robust and scalable qubit development and provide new impetus for research directions. Here, the requirements for hybrid systems are defined with artificial atoms in the solid state, exemplified with systems that are proposed or attempted, and conclude with the outlook for such hybrid quantum systems. [ABSTRACT FROM AUTHOR]

We report on the design and simulation of strip-loaded nanophotonic interfaces aimed at improving resonant coupling and photon routing efficiency. In our design, the guided mode is confined within a plane by a high-index thin film and is loosely confined laterally by a lower index strip. Using a hydrogen silsesquioxane (HSQ) strip, titanium dioxide core, and silicon dioxide substrate, we optimise the waveguide dimensions for maximum lateral confinement of light. Specifically, we propose a polymer-based Bragg grating cavity and ring resonator that achieve near-optimal mode volumes and high Q-factors. These may be further developed to achieve the even higher Q-factors demanded by quantum technologies. Our calculations suggest that a quantum dot embedded in a cavity with a mode volume of Veff∼7.0λ/n3 and a Q-factor of 7,000 can produce photons with 97% indistinguishability at 4K. Additionally, we investigate directional couplers for efficient photon routing, comparing photonic and plasmonic material structures. While pure photonic structures demonstrate lower loss and improved quality factors, they face practical limitations in terms of bending radius. Conversely, plasmonic structures offer shorter bending radii but higher propagation losses. This research lays the groundwork for future nanophotonic designs, aiming to enhance photon generation and routing capabilities for quantum optical applications.

PurposeTo investigate the preparation of inclusion complexes of diphenylcyclopropenone (DPCP)/β-cyclodextrin (β-CD) derivatives using a three-dimensional (3D) ball mill, and verify the inclusion behavior of the solid dispersion. Additionally, we aimed to investigate the effect of DPCP/β-CDs complex formation on the spleens of male C57BL/6 mice in terms of anti-inflammatory effects.MethodsThe inclusion complexes of DPCP with β-CD and hydroxypropyl-β-cyclodextrin (HPβCD) were prepared using a 3D ball mill. Powder X-ray diffraction (PXRD) and Fourier-transform infrared spectroscopy (FT-IR) were used to evaluate the solid-state properties. The solubility of the prepared DPCP/β-CD and HPβCD complexes and the intermolecular interaction between DPCP and β-CD derivatives in solution were assessed using 1H nuclear magnetic resonance (NMR). Furthermore, the anti-inflammatory effects of DPCPs in the prepared DPCP/CD complexes were investigated using spleens from male C57BL/6 mice, with measurement of interferon gamma (IFN-γ) secretion as an endpoint. Additionally, the protective effects of each drug on NIH-3T3 cells exposed to ultraviolet (UV) irradiation were examined.ResultsSolid-state characterization confirmed the formation of inclusion complexes in the 3D ground mixture (3DGM) (DPCP/β-CD = 1/1) and 3DGM (DPCP/HPβCD = 1/1) complexes through PXRD and IR analysis. The solubility of 3DGM (DPCP/β-CD = 1/1) and 3DGM (DPCP/HPβCD = 1/1) was 17.5 μg/mL and 58.4 μg/mL, respectively, indicating higher solubility than that of DPCP alone. NMR analysis of 3DGM samples suggested that DPCP/β-CD and DPCP/HPβCD form inclusion complexes at a molar ratio of 1/1 but with different inclusion modes. Regarding the anti-inflammatory activity of DPCP, 3DGM (DPCP/HPβ-CD) showed anti-inflammatory effects at lower doses compared to 3DGM (DPCP/β-CD) in terms of IFN-γ and NIH-3T3 cells injured by UV irradiation.ConclusionWe successfully formed inclusion complexes of DPCP/β-CD and DPCP/HPβCD using the 3D ground mixture method. NMR analysis suggested that DPCP/β-CD and DPCP/HPβCD form inclusion complexes at a molar ratio of 1/1 but with different inclusion modes. The anti-inflammatory activity of DPCP was more pronounced in 3DGM (DPCP/HPβCD) at lower doses compared to that in 3DGM (DPCP/β-CD), indicating that the HPβCD derivatives were more effective in enhancing the anti-inflammatory properties of DPCP.

Objectives: Porcelain chipping and delamination are among the shortcomings of all-ceramic restorations. This study aimed to assess the effect of laser irradiation and sandblasting on shear bond strength (SBS) of zirconia to veneering porcelain. Materials and Methods: In this in vitro, experimental study, 60 zirconia blocks were randomly divided into three groups (n=20) for surface treatment with Er:YAG laser, sandblasting, and no surface treatment (control). Each group was randomly divided into two subgroups (n=10) for porcelain application by the layering or the pressing technique. The surface roughness, SBS, and failure mode were determined and analyzed using two-way ANOVA, Tukey’s HSD test, Chi-square test, and Pearson’s correlation test (alpha=0.05). Results: The mean SBS was 8.16±3.66 MPa, 9.32±2.7 MPa, and 11.85±3.06 MPa in the control, laser, and sandblasting groups, respectively. The SBS was significantly different among the three groups (P=0.002). The failure mode of the three groups was not significantly different (P>0.05). The sandblasted group showed significantly higher surface roughness than the control and laser groups (P

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SignificanceTraditional pathology workflow suffers from limitations including biopsy invasiveness, small fraction of large tissue samples being analyzed, and complex and time-consuming processing.AimWe address limitations of conventional pathology workflow through development of a laser microbiopsy device for minimally invasive harvest of sub-microliter tissue volumes. Laser microbiopsy combined with rapid diagnostic methods, such as virtual hematoxylin and eosin (H&E) imaging has potential to provide rapid minimally invasive tissue diagnosis.ApproachLaser microbiopsies were harvested using an annular shaped Ho:YAG laser beam focused onto the tissue surface. As the annulus was ablated, the tissue section in the center of the annulus was ejected and collected directly onto a glass slide for analysis. Cryogen spray cooling was used before and after laser harvest to limit thermal damage. Microbiopsies were collected from porcine skin and kidney. Harvested microbiopsies were imaged with confocal microscopy and digitally false colored to provide virtual H&E images.ResultsMicrobiopsies were successfully harvested from porcine skin and kidney. Computational and experimental results show the benefit of cryogen pre- and post-cooling to limit thermal damage. Virtual H&E images of microbiopsies retained observable cellular features including cell nuclei.ConclusionsLaser microbiopsy with virtual H&E imaging shows promise as a potential rapid and minimally invasive tool for biopsy and diagnosis.

A pyridine-fused triazapentalene shows weak fluorescence in solution and is readily accessible via nitrene-mediated cyclization. In this study, a modified Cadogan reaction was used to synthesize HetATAP 1. Palladium-catalyzed reactions have been used as post-functionalization methods. Interestingly, modified Suzuki cross-couplings with various boronic acids resulted in poor to moderate yields of HetATAPs 2–5 which were arylated at the azole moiety. Direct CH arylation of HetATAP 1 gave the products with the same regiochemistry in satisfactory yields. The structures of HetATAPs 2–5 were confirmed using NMR analysis. In addition, the photophysical properties of HetATAPs 1–5 were studied under various conditions. Particularly, the emission of HetATAPs 2–5 is enhanced in the solid and aggregate state.

Herein, we report the first solid-state protocol for nickel(0)-mediated Yamamoto-coupling reactions using ball milling. A variety of aryl halides reacted efficiently in the presence of bis(cyclooctadiene)nickel(0) [Ni(cod)2] and 4,4'-di-tert-butyl-2,2'-bipyridyl under solid-state mechanochemical conditions, affording the corresponding biaryls in high yields. Considering that potentially harmful and high-boiling organic solvents are not required, the present study provides a more convenient, environmentally friendly, and sustainable alternative to conventional solution-based Yamamoto coupling. Solid-state Yamamoto-coupling polymerization and the development of a catalytic variant are also described. [ABSTRACT FROM AUTHOR]

Despite being discovered over five decades ago, little is still known about ivermectin. Ivermectin has several physico-chemical properties that can result in it having poor bioavailability. In this study, polymorphic and co-crystal screening was used to see if such solid-state modifications can improve the oil solubility of ivermectin. Span® 60, a lipophilic non-ionic surfactant, was chosen as co-former. The rationale behind attempting to improve oil solubility was to use ivermectin in future topical and transdermal preparations to treat a range of skin conditions like scabies and head lice. Physical mixtures were also prepared in the same molar ratios as the co-crystal candidates, to serve as controls. Solid-state characterization was performed using X-ray powder diffraction (XRPD), Fourier-transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The FTIR spectra of the co-crystal candidates showed the presence of Span® 60's alkyl chain peaks, which were absent in the spectra of the physical mixtures. Due to the absence of single-crystal X-ray data, co-crystal formation could not be confirmed, and therefore these co-crystal candidates were referred to as co-processed crystalline solids. Following characterization, the solid-state forms, physical mixtures and ivermectin raw material were dissolved in natural penetration enhancers, i.e., avocado oil (AVO) and evening primrose oil (EPO). The co-processed solids showed increased oil solubility by up to 169% compared to ivermectin raw material. The results suggest that co-processing of ivermectin with Span® 60 can be used to increase its oil solubility and can be useful in the development of oil-based drug formulations. [ABSTRACT FROM AUTHOR]