An all-solid-state-supercapacitor possessing a non-aqueous gel polymer electrolyte prepared using a UV-assisted in situ polymerization strategy

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Ultralight crystalline hybrid composite material for highly efficient sequestration of radioiodine

Abstract Considering the importance of sustainable nuclear energy, effective management of radioactive nuclear waste, such as sequestration of radioiodine has inflicted a significant research attention in recent years. Despite the fact that materials have been reported for the adsorption of iodine, development of effective adsorbent with significantly improved segregation properties for widespread practical applications still remain exceedingly difficult due to lack of proper design strategies. Herein, utilizing unique hybridization synthetic strategy, a composite crystalline aerogel material has been fabricated by covalent stepping of an amino-functionalized stable cationic discrete metal-organic polyhedra with dual-pore containing imine-functionalized covalent organic framework. The ultralight hybrid composite exhibits large surface area with hierarchical macro-micro porosity and multifunctional binding sites, which collectively interact with iodine. The developed nano-adsorbent demonstrate ultrahigh vapor and aqueous-phase iodine adsorption capacities of 9.98 g.g−1 and 4.74 g.g−1, respectively, in static conditions with fast adsorption kinetics, high retention efficiency, reusability and recovery

Pre-Sowing Treatments, Seed Components and Water Imbibition Aids Seed Germination of Gloriosa superba

Gloriosa superba L. is a horticulturally and medicinally important plant. Its seeds have poor, erratic, and deferred germination. The detailed seed structure components and water imbibition mechanism facilitating the process of seed germination in G. superba remain unexplored. Therefore, it is essential to develop methods to ensure consistent and enhanced seed germination in G. superba. Various pre-sowing treatments along with the Brunauer-Emmett-Teller (BET) surface area analysis and 3D X-ray micro-tomography (micro-T) were employed to elucidate seed structure components, porosity network, and the water imbibition mechanism during germination in G. superba. The study revealed that consistent and significantly improved seed germination (>85%) was observed using the pre-sowing treatment mechanical scarification followed by 24 h water soaking in G. superba. BET and micro-T showed that the tegmen of the seed coat exhibited porosity (21%) with a well-connected porosity network (17.50%) that helped in water movement through hilum, which was confirmed by phosphotungstic acid staining. However, the sarcotesta and endosperm were water-impermeable due to their negligible porosity. Multidisciplinary techniques such as BET and micro-T along with conventional methodologies can be employed to address the seed coat structure, porosity, and water imbibition mechanism aiding seed germination. Mechanical scarification enabled the water to penetrate internal seed layers through the permeable tegmen via the reticulate pore network, which significantly improved seed germination. The developed seed germination method can produce a large number of plants in less time and conserve the natural populations of this high-value medicinally important species

Mechanically Tunable Curcumin Incorporated Polyurethane Hydrogels as Potential Biomaterials

We report here on the one-pot synthesis and characterization of curcumin incorporated polyethylene glycol–polyurethane (PU-CUR) hydrogels using PEG-4000, 4, 4′-methylenebis (cyclohexyl isocyanate), curcumin in the presence of a cross-linker, 1,2,6 hexanetriol (HT). Besides the physical entrapment, curcumin also provides a partial cross-linking in the 3-D structure of the hydrogel. The degree of swelling in hydrogels could be controlled by varying the amount of HT as well as curcumin. The structural characterization of hydrogels was performed using Fourier transform infrared spectroscopy, high-resolution mass spectrometry, UV and fluorescence spectroscopy. The wide-angle X-ray scattering studies revealed the existence of crystalline domains of PEG, and the small-angle X-ray scattering studies showed the presence of lamellar microstructures. Porous structure in the hydrogel was created by cryogenic treatment and lyophilization. Scanning electron microscopy and microcomputed tomography imaging of hydrogels showed the presence of interconnected pores. The mechanical strength of the hydrogels was measured using a universal testing machine. The observed tensile and breaking compression strengths for the equilibrium swollen gels were found to be in the range of 0.22–0.73 MPa and 1.65–4.6 MPa, respectively. Detailed in vitro biological experiments showed the biocompatibility of gels, cytostatic dosage of curcumin, selective toxicity toward cancer cell lines, and antibacterial property. These gels show promising applications as scaffolds and implants in tissue engineering

High-Performance Flexible Solid-State Supercapacitor with an Extended Nanoregime Interface through in Situ Polymer Electrolyte Generation

Here, we report an efficient strategy by which a significantly enhanced electrode–electrolyte interface in an electrode for supercapacitor application could be accomplished by allowing in situ polymer gel electrolyte generation inside the nanopores of the electrodes. This unique and highly efficient strategy could be conceived by judiciously maintaining ultraviolet-triggered polymerization of a monomer mixture in the presence of a high-surface-area porous carbon. The method is very simple and scalable, and a prototype, flexible solid-state supercapacitor could even be demonstrated in an encapsulation-free condition by using the commercial-grade electrodes (thickness = 150 μm, area = 12 cm², and mass loading = 7.3 mg/cm²). This prototype device shows a capacitance of 130 F/g at a substantially reduced internal resistance of 0.5 Ω and a high capacitance retention of 84% after 32000 cycles. The present system is found to be clearly outperforming a similar system derived by using the conventional polymer electrolyte (PVA–H₃PO₄ as the electrolyte), which could display a capacitance of only 95 F/g, and this value falls to nearly 50% in just 5000 cycles. The superior performance in the present case is credited primarily to the excellent interface formation of the in situ generated polymer electrolyte inside the nanopores of the electrode. Further, the interpenetrated nature of the polymer also helps the device to show a low electron spin resonance and power rate and, most importantly, excellent shelf-life in the unsealed flexible conditions. Because the nature of the electrode–electrolyte interface is the major performance-determining factor in the case of many electrochemical energy storage/conversion systems, along with the supercapacitors, the developed process can also find applications in preparing electrodes for the devices such as lithium-ion batteries, metal–air batteries, polymer electrolyte membrane fuel cells, etc

Design of a High Performance Thin All-Solid-State Supercapacitor Mimicking the Active Interface of Its Liquid-State Counterpart

Here we report an all-solid-state supercapacitor (ASSP) which closely mimics the electrode–electrolyte interface of its liquid-state counterpart by impregnating polyaniline (PANI)-coated carbon paper with polyvinyl alcohol-H₂SO₄ (PVA-H₂SO₄) gel/plasticized polymer electrolyte. The well penetrated PVA-H₂SO₄ network along the porous carbon matrix essentially enhanced the electrode–electrolyte interface of the resulting device with a very low equivalent series resistance (ESR) of 1 Ω/cm² and established an interfacial structure very similar to a liquid electrolyte. The designed interface of the device was confirmed by cross-sectional elemental mapping and scanning electron microscopy (SEM) images. The PANI in the device displayed a specific capacitance of 647 F/g with an areal capacitance of 1 F/cm² at 0.5 A/g and a capacitance retention of 62% at 20 A/g. The above values are the highest among those reported for any solid-state-supercapacitor. The whole device, including the electrolyte, shows a capacitance of 12 F/g with a significantly low leakage current of 16 μA². Apart from this, the device showed excellent stability for 10000 cycles with a coulombic efficiency of 100%. Energy density of the PANI in the device is 14.3 Wh/kg

COF-supported zirconium oxyhydroxide as a versatile heterogeneous catalyst for Knoevenagel condensation and nerve agent hydrolysis

Summary: A composite of catalytic Lewis acidic zirconium oxyhydroxides (8 wt %) and a covalent organic framework (COF) was synthesized. X-ray diffraction and infrared (IR) spectroscopy reveal that COF’s structure is preserved after loading with zirconium oxyhydroxides. Electron microscopy confirms a homogeneous distribution of nano- to sub-micron-sized zirconium clusters in the COF. 3D X-ray tomography captures the micron-sized channels connecting the well-dispersed zirconium clusters on the COF. The crystalline ZrOx(OH)y@COF’s nanostructure was model-optimized via simulated annealing methods. Using 0.8 mol % of the catalyst yielded a turnover number of 100–120 and a turnover frequency of 160–360 h−1 for Knoevenagel condensation in aqueous medium. Additionally, 2.2 mol % of catalyst catalyzes the hydrolysis of dimethyl nitrophenyl phosphate, a simulant of nerve agent Soman, with a conversion rate of 37% in 180 min. The hydrolytic detoxification of the live agent Soman is also achieved. Our study unveils COF-stabilized ZrOx(OH)y as a new class of zirconium-based Lewis + Bronsted-acid catalysts