Soft Chemical Method Research Articles

The role of BaTiO3 nanoparticles as photocatalysts in the synthesis and characterization of novel fruit dyes is investigated.

In the present work, the photocatalytic activity against the natural dye extracted from the novel fruits has been studied by the BaTiO3 nanoparticles (NPs) under a ultra-violet (UV) light source. The large concentrations of an essential phenolic agent present in this phytochemical extract superimposed with cloths fibers make strong stain and degrade into another form of toxic, which is excluded from the many textiles industries as the colorful waste waters without recycling and removal of that dye pigments have been investigated using both photodegradation and photoluminescence techniques. The entitled nanoparticles (NPs) were prepared using the soft chemical root-modified solvothermal synthesis combo method and exposure to heat treatment such that the annealing process has been done for different temperatures ranging from 100°C to 250°C. As for as concern the characterization, as a start, structural and morphology studies have been reported here that highly crystalline oriented peaks data using powder x-ray diffraction techniques (PXRD) as well as the surface morphology including the size, shape, and mass distribution using the field emission scanning electron microscopy (FESEM) techniques, which purely belong to rutile tetragonal structure of the crystal system and circular and noncircular flakes like rough surface morphology materials respectively. The lattice dissociation constant 'ε' value of the BaTiO3 NPs has determined to be ~2.71 × 10-3 using the Williamson-Hall (W-H plot) analysis of crystallographic data. In the UV visible spectroscopy findings, since the extreme quantum confinement of BaTiO3 nanoflakes/nanodisc, the optical energy bandgap has been estimated to be a range of 1.98 to 2.67 eV (~2.48 eV) found from the Tauc plot analysis, which contributes to the significantly owing to the enhanced photocatalytic efficiency with excellent performance along exciton formation, superoxide ions, and hydroxyl free radicals generations under UV-vis light irradiation resulting in efficient degradation of typical novel fruit organic dye. Photoluminescence spectra observed at room temperature and low temperature have been observed for the BaTiO3 nanoflakes, which exhibit the blue emission due to the crystalline defects such as the appearance of Ba vacancies leads to the conceivable beginning of p-type conductivity and the origination of free exciton emission reveals the direct bandgap transition nature of nanoflakes. RESEARCH HIGHLIGHTS: According to our findings, 89.71% of the natural syzygium cumin is degraded by photocatalysis reaction. As a plausible mechanism for the destruction of natural dyes under solar light, photocatalytic destruction has been proposed. The reaction between these reactive free radical species leads to high efficiency photodegradation with a short decay time. In addition to water treatment and environmental cleaning applications, the excellent performance of this photocatalyst makes it a promising candidate for other applications. Hence, the synthesized BaTiO3 nanoflakes showcase a highly significant advancement towards the development of a textiles dye recycling method.

Soft chemistry-derived Al-substituted hydrated nickel hydroxide electrodes for rechargeable aqueous batteries.

Hydrated nickel hydroxides with partial aluminum substitution were synthesized using the conventional coprecipitation and soft chemistry methods. The soft chemistry derived sample showed better reversibility owing to the low activity for oxygen evolution during charging. Operando X-ray diffraction indicated the increased interlayer distance and decreased crystallinity during discharging caused by water accommodation.

Synergy of nitrogen dopants and cobalt single atoms in calcium niobate nanosheets for photocatalytic oxygen evolution

Abstract Successful separation of photoexcited charge carriers and their effective utilization are crucial for overcoming the slow kinetics of the four-electron process for photocatalytic oxygen evolution. Herein, a novel strategy utilizing urea as a source of N-doping on Ca2Nb3O10 nanosheets is adopted followed by the successful deposition of Co single atoms (Co-SAs) to achieve a synergistic effect. The presence of N-dopants and Co-SAs is validated via various experimental techniques. Besides, it is observed that the presence of N-doping contributed towards deposition of higher content of Co-SAs (0.21 wt%) in Ca2Nb3O10-xNx¬-CoSA nanosheets compared to 0.15 wt% for non-doped Ca2Nb3O10-CoSA. The optimized Ca2Nb3O10-xNx-CoSA nanosheets exhibited an impressive photocatalytic O2 evolution of ~727.22 µmol g-1 h-1 via the synergy of N-dopants and Co-SAs. As a result, O2 evolution response of Ca2Nb3O10-xNx-CoSA is 3.6 times higher than pristine Ca2Nb3O10 nanosheets (201.26 µmol g-1 h-1), 2.24 times better than Ca2Nb3O10-xNx nanosheets (323.42 µmol g-1 h-1), and 1.77 times higher compared to Ca2Nb3O10-CoSA, (409.33 µmol g-1 h-1), clearly demonstrated the synergistic effect of N-dopants and Co-SAs in Ca2Nb3O10-xNx-CoSA nanosheets. Base on the finding of various characterization techniques, the co-presence of N-dopants and Co-SAs is observed to contribute towards better charge carriers separation, and utilization to achieve superior photocatalytic response. Thus, this work presents a novel approach for incorporating N-dopants and Co-SAs on Ca2Nb3O10 nanosheets which can be extended to wide range of nanosheets produced by the soft chemical exfoliation method.

Interplay of luminescence and magnetic phenomena in Mn-doped ZnS zinc blende nanocrystals: Influence of magnetic doping

This research comprehensively investigates the interplay between luminescence and magnetic phenomena in the zinc blende phase of manganese-doped and undoped zinc sulfide. The study involves the synthesis of zinc sulfide nanocrystals through a soft chemical method, followed by an in-depth experimental characterization. Theoretical studies were conducted using a 2 × 2 × 2 supercell model with 64 atoms to explore the impact of native defects and manganese doping on zinc sulfide's the electronic, magnetic, and optical properties. The research findings offer a detailed physical description of magnetic and optic phenomena observed, underpinned by a strong correlation between theoretical predictions and experimental results. An essential contribution of this work is developing a depiction that elucidates the relationship between optical transitions and spin-exchange in the context of these phenomena.

Friends not Foes: Exfoliation of Non-van der Waals Materials.

ConspectusTwo-dimensional materials have been a focus of study for decades, resulting in the development of a library of nanosheets made by a variety of methods. However, many of these atomically thin materials are exfoliated from van der Waals (vdW) compounds, which inherently have weaker bonding between layers in the bulk crystal. Even though there are diverse properties and structures within this class of compounds, it would behoove the community to look beyond these compounds toward the exfoliation of non-vdW compounds as well. A particular class of non-vdW compounds that may be amenable to exfoliation are the ionically bonded layered materials, which are structurally similar to vdW compounds but have alkali ions intercalated between the layers. Although initially they may have been more difficult to exfoliate due to a lack of methodology beyond mechanical exfoliation, many synthesis techniques have been developed that have been used successfully in exfoliating non-vdW materials. In fact, as we will show, in some cases it has even proven to be advantageous to start the exfoliation from a non-vdW compound.The method we will highlight here is chemical exfoliation, which has developed significantly and is better understood mechanistically compared to when it was first conceived. Encompassing many methods, such as acid/base reactions, solvent reactions, and oxidative extractions, chemical exfoliation can be tailored to the delamination of non-vdW materials, which opens up many more possibilities of compounds to study. In addition, beginning with intercalated analogues of vdW materials can even lead to more consistent and higher quality results, overcoming some challenges associated with chemical exfoliation in general. To exemplify this, we will discuss our group's work on the synthesis of a 1T'-WS2 monolayer ink. By starting with K0.5WS2, the exfoliated 1T'-WS2 nanosheets obtained were larger and more uniform in thickness than those from previous syntheses beginning with vdW materials. The crystallinity of the nanosheets was high enough that films made from this ink were superconducting. We will also show how soft chemical methods can be used to make new phases from existing compounds, such as HxCrS2 from NaCrS2. This material was found to have alternating amorphous and crystalline layers. Its biphasic structure improved the material's performance as a battery electrode, enabling reversible Cr redox and faster Na-ion diffusion. From these and other examples, we will see how chemical exfoliation of non-vdW materials compares to other methods, as well as how this technique can be further extended to known compounds that can be deintercalated electrochemically and to quasi-one-dimensional crystals.

Effect of Ga doping on the structural, optical, and electrical properties of ZnO nanopowders elaborated by sol-gel method

Nanostructured ZnO has received a considerable amount of interest, owing to its unique physical and chemical characteristics, as well as its remarkable performance in the fields of electronics, optics, and photonics. This work aims to study the influence of Ga dopant on the structural, optical, and electrical properties of ZnO nanopowders. Undoped and Ga-doped ZnO (GZO) nanopowders were successfully synthesised with the soft chemical sol-gel method. The solution was prepared using zinc acetate dihydrate and gallium (III) nitrate hydrate as precursors. The ethylene glycol is used as solvent. The X-ray diffractometer, scanning electronic microscope (SEM), UV–Vis, FTIR, and four-point probe method are used to analyse the properties of the synthesised powders. XRD and FTIR measurements show the growth of pure and Ga-doped ZnO crystals, which have a hexagonal wurtzite structure, and the average crystallite size varies from 9.09 nm to 24.8 nm. The nanospherical morphology of the nanopowders synthesised can be seen in the SEM images. The UV–visible spectroscopy shows that the optical gap energy increases with Ga concentration, from 3.59 eV to 3.67 eV. The I-V electrical measurements indicate that the breakdown voltage and the non-linear coefficient increase with Ga doping. This study will open the way for the investigation of a relationship between the electrical and nanostructural features of ZnO-based varistors for future device applications.

Room-Temperature Synthesis and Low Thermal Conductivity in Nanocrystalline Ag3CuS2.

Noble-metal-based chalcogenide materials recently gained massive attention in the field of thermoelectrics. In most cases, materials are synthesized using (i) high-temperature solid-state reactions or (ii) soft chemical methods where temperature requirements are lower than those of solid-state reactions (generally below 400 °C). Herein, we present a simple, surfactant-free, room-temperature, and energy-efficient synthesis of Ag3CuS2 nanocrystals. The present synthesis technique is scalable and capable of gram-scale production. A spark plasma sintering (SPS) pressed sample exhibits ultralow thermal conductivity (∼0.31 W/mK at room temperature). We found that Ag3CuS2 exhibits low sound velocity, as well as a non-Debye-like behavior based on a low-temperature heat capacity measurement. A high degree of anharmonicity of bonding, soft vibrations modes, and nanoscale grain boundary scattering in Ag3CuS2 lead to ultralow thermal conductivity, which can be important for thermoelectrics, optoelectronics, and thermal barrier coating applications.

Magnetic and optical properties of ZnO nanoparticles and nanorods synthesized by green chemistry

ZnO nanostructures have attracted considerable attention because of their physicochemical properties and applications as antibacterial agents, photocatalytic reactions for pollutant removal, and electronics. Hence, efficient production and knowledge of their properties under different synthesis conditions are essential. Biosynthesis has emerged as an excellent growth-directing method for synthesizing nanomaterials, representing a soft and cleaner alternative for their production. In this study, we synthesized different ZnO nanostructures using a soft chemistry method at different growth temperatures, from 200 to 800 °C every 200 °C. The crystalline structure was estudied by x-ray Diffraction (XRD) and High-Resolution Transmission Electron Microscopy (HRTEM). The shape and size were studied by Field Emission Scanning Electron Microscopy (FESEM) and Transmission Electron Microscopy (TEM), which revealed a ZnO hexagonal phase with two shapes: nanoparticles (NPs) with irregular shapes and nanorods of different sizes. The optical properties were studied by Raman and UV-visible spectroscopy, and optical absorption measurements showed bandgap tuning of the produced nanostructures. Finally, the magnetic characteristics of the samples demonstrated magnetic anisotropy due to the preference for crystalline formation and the size of the nanoparticles. The magnetic interaction between the two types of NPs increased the diamagnetism associated with the nanorods.

Mild chemistry synthesis of ultrathin Bi2O2S nanosheets exhibiting 2D-ferroelectricity at room temperature.

Modern technology demands miniaturization of electronic components to build small, light, and portable devices. Hence, discovery and synthesis of new non-toxic, low cost, ultra-thin ferroelectric materials having potential applications in various electronic and optoelectronic devices are of paramount importance. However, achieving room-temperature ferroelectricity in two dimensional (2D) ultra-thin systems remains a major challenge as conventional three-dimensional ferroelectric materials lose their ferroelectricity when the thickness is brought down below a critical value owing to the depolarization field. Herein, we report room-temperature ferroelectricity in ultra-thin single-crystalline 2D nanosheets of Bi2O2S synthesized by a simple, rapid, and scalable solution-based soft chemistry method. The ferroelectric ground state of Bi2O2S nanosheets is confirmed by temperature-dependent dielectric measurements as well as piezoelectric force microscopy and spectroscopy. High resolution transmission electron microscopy analysis and density functional theory-based calculations suggest that the ferroelectricity in Bi2O2S nanosheets arises due to the local distortion of Bi2O2 layers, which destroys the local inversion symmetry of Bi2O2S.

Biowastes-derived enzyme-powered zinc oxide and titanium oxide nanomaterials synthesis for anticancer and eco-friendly photocatalytic activity

Biowastes derived enzyme powered zinc oxide (ZnO) and titanium oxide (TiO2) nanomaterials were prepared using a soft-chemical method and their photocatalytic dye degradation efficiencies against toxic Methylene Blue (MB - cationic) and Methyl Orange (MO-anionic) dyes were studied. The enzymes prevalent in certain biowastes (vegetable wastes and fruit peels) are derived through eco-friendly fermentation process and used for nanomaterial synthesis. The enzyme quantitative assay confirmed the presence of the enzymes viz., protease, peroxidase, cellulase, amylase and lipase in the synthesized nanopowders. The photocatalytic results showed the enhanced combined effect of the semiconductor photocatalyst (ZnO and TiO2) and the bio-catalyst (enzymes). The efficiency of the resultant photocatalysts: ZnO - 95% (60 min) and TiO2 99% (60 min). The XRD results confirm the crystallized form of enzymes in the nanomaterial. The desirable morphological changes caused by the enzyme coupling with semiconductor was evidenced from SEM images. The study showed that the synthesized material (enzyme powered ZnO and TiO2) are desirable candidates for environmentally friendly, biocompatible photocatalysis for toxic dyes degradation. The cytotoxicity studies revealed that the material may effectively destroy the lung cancer A-549 cells. The half maximal inhibitory concentration (IC50) values of enzyme powered ZnO and TiO2 are 51.75 ± 0.05 μg/mL and 52.25 ± 0.05 μg/mL, respectively. Thus, the biowastes derived enzyme powered ZnO and TiO2 can be considered as promising materials for cost-effective dye degradation and anticancer activities.

Structural and Electrochemical Investigation of 3D Tunnel Type Li0.44MnO2 Cathode Material for Secondary Li-Ion Batteries

The design of new cathode materials remains a key goal in the development of (post) Li-ion batteries. In that regard, densely packed structures like Li0.44MnO2 are judicious for study. The presence of Mn as a transition metal makes it more attractive due to its sustainable nature, low cost, elemental abundance, structural diversity/polymorphism, and rich oxidation states (2+ to 7+) offering tunable redox potential [1]. Here, we have investigated Mn-based tunnel-type Li0.44MnO2 oxide for secondary LIBs. i) Li44MnO2 (LMO) was prepared by a soft chemical method using the corresponding sodium manganese oxide (Na0.44MnO2) as a parent compound [2]. The crystal structure of Li0.44MnO2 maintains the parent Na0.44MnO2-type tunnel structure which is analogous to Na4Mn4Ti5O18 having an orthorhombic (s.g. Pbam) crystal system [3]. To understand redox chemistry, this material was studied for both cationic (Mn) and anionic (O) redox reactions using ex-situ X-ray photoelectron spectroscopy. The lithium (de)insertion mechanism of Li0.44MnO2 was explored involving ab initio calculations and in-situ X-ray diffraction experiments. Combined with electrochemical measurements, structural characterizations, and first principles DFT calculations revealed the capacity correlated strongly with both cationic and anionic redox reactions. ii) We have studied the phase transition of Li44MnO2 from a 3D tunnel-type structure to a cubic spinel structure by in-situ X-ray diffraction and Raman spectroscopy. The mechanism of transformation was elucidated by employing transmission electron microscopy. In this case, diffusion-less transformation occurs involving the rearrangement of atoms during heating [4]. An increase in the average redox potential from the pristine orthorhombic phase to the final spinel phase was observed by electrochemical studies. iii) Further to improve the electrochemical performance of Li0.44MnO2, Ti was used as a dopant. The Li0.44[Mn1-xTix]O2 (x=0, 0.11, 0.22, 0.33, 0.44, 0.56) series were obtained with chemical ion exchange from Na precursors. The Na precursors (Na0.44[Mn1-xTix]O2) were prepared via a simple solid-state route. Ti-substituted compositions exhibited similar crystal structures to their parent LMO i.e. orthorhombic framework with Pbam symmetry. A tunnel-type morphology was observed in all cases. The electrochemical performance of Ti-substituted LMO as cathode material for LIBs was studied in a half-cell configuration. The structure and electrochemical properties of Ti-doped LMO, reaching the highest capacity of 128 mAh/g, will be described. Keywords: batteries; cathode; tunnel type manganese oxides; phase transformation; doping

Chimie Douce Derived K-Based P2-Type Transition Metal(s) Layered Oxides for Secondary K-Ion Batteries

Owing to great societal and technological benefits, there has been a remarkable growth in the industrial demand for enhanced energy storage for many target applications including electric vehicles, aerospace applications, and portable electronics. Secondary K-ion batteries (KIBs) are among the potentially inexpensive candidates for energy storage systems beyond state-of-the-art Li-ion batteries (LIBs). Electrochemical cells based on mobile carrier K+ can provide efficient energy storage because of comparative ionic diffusion in bulk and swift charge transfer at the interface due to weak Lewis’s acidity.1,2 Despite various advantages over LIBs and NIBs, the roadblock of practical KIB implementation lies in identifying suitable cathodes that reversibly (de)intercalate K+ at optimum voltage, swift rate, and with prolonged cycle life.Despite constant efforts to develop new cathodes for K+ -ion batteries, several challenges such as low concentrations of K-ions due to strong electrostatic repulsions between the K+ - K+ ions and difficulty in preparation from direct synthesis routes3 limit its practical application. In this scenario, we have adopted the chimie douce (soft chemistry) method to design the novel layered transition metal oxide cathode from the parent P2 type Na-based system. In addition, we have probed the ion exchange mechanism using X-ray diffraction and transmission electron microscopy (TEM) techniques. Rietveld analysis confirmed the structure having a P2-type stacking sequence with hexagonal symmetry and P6/3mmc space group. Further, we have successfully examined the chemical ion-exchanged novel layered P2- K2/3Co1/3Mn2/3O2 as a cathode for KIB at ambient and high temperatures. It delivered a good capacity (~70 mAh/g) with an average redox potential of 3.0 V along with good cycling stability and coulombic efficiency (CE) in temperature ranging from 25-50 ºC. Ex-situ X-ray diffraction analysis and potentio/galvanostatic titration techniques were used to analyse the K+ insertion mechanism. This study can assist in developing new insertion K+ host materials for viable and reliable practical applications.

BaRuO3 coated Ti plate as an efficient and stable electro-catalyst for water splitting reaction in alkaline medium

Water splitting using an electrochemical device to produce hydrogen fuel is a green and economic approach to solve the energy and environmental crisis. The realistic design of durable electro-catalysts and their synthesis using a simplistic technique is a great challenge to produce hydrogen by water electrolysis. Herein, we report a stable highly active barium ruthenium oxide (BRO) electro-catalysts over Ti plate using a soft chemical method at low temperature. The synthesized material shows facile hydrogen evolution reaction (HER) as well as oxygen evolution reaction (OER) in alkaline medium with over-potentials of 195 mV and 300 mV, respectively at a current density of 10 mA cm−2. The excellent stability lasts for at least 24 h without any degradation for both the HER and OER at the current density of 10 mA cm−2, inferring the practical applications of the material toward production of green hydrogen energy. Certainly, the synthesized catalyst is capable adequately for the overall water splitting at a cell voltage of 1.60 V at a current density of 10 mA cm−2 with an impressive stability for at least 24 h, showing a minimum loss of potential. Thus the present work contributes to the rational design of stable and efficient electro-catalysts for overall water splitting reaction in alkaline media.

Magnetic and photoluminescence behavior of transitional metal ions-doped ZnO nanoparticles

Soft-chemical methods were used to create ZnO nanoparticles that were doped with transition metal (Ni and Co) ions. By using a variety of characterization approaches, the crystal phases, microstructural, magnetic, and optical characteristics of doped ZnO NPs were fully examined. Electron mapping and chemical analysis were performed with SEM-EDS and ICP-AES, respectively, showing that the doping of metal ions was successful. TEM and XRD)analyses of doped ZnO NPs showed the confirmation of the wurtzite structure of ZnO. X-ray photoelectron spectroscopy (XPS) further confirmed the doping of metal ions into the ZnO matrix. When compared to pristine ZnO, the PL spectra of the doped ZnO NPs indicated a greater defect concentration. Moreover, the magnetic measurement results of doped ZnO NPs showed defect-mediated room temperature ferromagnetic behavior without any coercivity and remanence magnetization. It has been found that the ferromagnetic behavior of doped ZnO NPs is mainly reliant on the defect concentrations in the sample.

Novel experimental methodology and optical analysis of (Ni, Co, Fe, and Cr) iodate nanocrystals

We reported a new experimental approach for a cost-effective production route towards the nanoparticles of 3d transition metal iodates of cobalt Np-CoI, Nickel Np-NiI, Iron Np-FeI and Chrome Np-CrI, exhibit nonlinear optical behavior. This soft chemistry method, we named the Hebboul's saturated solution method, creates the necessary nanoparticles in a couple of minutes demonstrate its usefulness in this family of metal iodate. By using X-ray diffraction, scanning electron microscopy, EDX, and FTIR spectroscopy, the produced samples have been evaluated. Identification of nanocrystal agglomerations was made easier by SEM analysis, XRD and EDX. Furthermore, XRD allowed researchers to determine that the average nanocrystal size of Np-CoI, Np-FeI, and Np-NiI are 13 nm, 17 nm, and 53 nm, respectively. From UV-V analysis, it was determined that the optical bandgap of the pure nanoparticles Np-CoI, Np-FeI, Np-NiI and Np-CrI was, respectively, 3.6 eV, 3.04 eV, 2.61 eV and 3.23 eV.

Facile and Sustainable Synthesis of ZnO Nanoparticles: Effect of Gelling Agents on ZnO Shapes and Their Photocatalytic Performance.

The present work involves investigating an unexplored soft-chemical method for synthesizing nanostructured ZnO through biopolymer gelation. Our objective was to exploit (i) the difference in the gelation mechanism of four tested biopolymers, namely, alginate, chitosan, carboxymethylcellulose (CMC), and pectin and (ii) numerous experimental parameters that govern this process in order to allow the control of the growth of nanostructured ZnO, with a view to using the prepared oxides as photocatalysts for the oxidation of the Orange G dye. So, the effect of biopolymer's nature on the microstructural, morphological, and textural properties was examined by thermogravimetric analysis (TGA), X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, field-emission gun-scanning electron microscopy-high resolution (FEG-SEM) with energy-dispersive spectrometry (SEM-EDS), ultraviolet-visible (UV-vis) spectroscopy, and N2 adsorption/desorption. As-prepared oxides were crystallized in a hexagonal wurtzite structure, with a clear difference in their morphologies. The sample prepared by using chitosan has a specific surface area of around 36.8 m2/g in the form of aggregated and agglomerated nanostructured minirods and thus shows the best photocatalytic performance with 99.3% degradation of the Orange G dye in 180 min.

Tysonite Type Nanocrystalline Solid Solutions R1 – xScxF3 (R = La, Pr): Synthesis and Electrical Conductivity

The single-phase nanocrystalline R0.9Sc0.1F3 solutions (R = La, Pr) were synthesized by soft chemistry methods as transparent xerogels with the tysonite structure (space group). The ionic conductivity of ceramic samples prepared from these materials was 4.5 × 10–4 and 2.1 × 10–3 S/cm at 773 K for R = La and Pr, respectively. The activation energy of the ion transfer in ceramic samples was 0.43 (R = Pr) and 0.48 eV (R = La) in the high-temperature segment and 0.56 eV (R = Pr) in the low-temperature segment. It was shown that the isovalent replacement of La3+ (Pr3+) cations in the R0.9Sc0.1F3 tysonite solid solutions with Sc3+ leads to 3–4-fold decrease in the conductivity of the ceramic electrolytes.

Complex impedance analysis of soft chemical synthesized NZCF systems


 
 
 
 The soft chemical method was adopted to prepare of cobalt-substituted nickel-zinc ferrites (Ni0.95-x Zn0.05COx Fe2O4 for x = 0.01, 0.02 and 0.03). We have recently studied their structural, morphological, and magnetic properties, initial permeability, and dielectric constant. They were found to be with cubic ferromagnetic spinel structure, the morphology of which is suitable for high-density recording media. The impedance has a major role in characterizing the electrical and magnetic properties of the sample, which are dependent on their permeability and dielectric constant. So, this study will verify the values obtained before. Next, the energy stored in a capacitor is directly proportional, and its size is inversely proportional to the dielectric constant. Similarly, the resistance offered by a material to the magnetic field to pass through it is related to permeability. This study will focus on the variation of impedance with Co2+ concentration. The results were derived with the equivalent circuit model. The impedance analysis is also important in the biological field having a name of Bio-Impedance Analysis (BIA), for determining nutritional status, and many more.
 
 
 

Synthesis of SnO2 nanoparticles coated ZnO–g–C3N4 composite nanostructures with novel antibacterial activity

Abstract In this work, composite nanostructures (CNs) of SnO2–ZnO–g–C3N4 have been prepared by a soft chemical method and investigated for their potential application in photocatalytic remediation of organics in water and antibacterial agents. Structural study revealed the presence of three phases related to hexagonal wurtzite phase of ZnO, tetragonal phase of SnO2 and monoclinic phase of g–C3N4 having nanocrystalline nature which confirms the formation of CNs. Formation of nanoscale morphology along with elemental composition of the CNs have been validated through scanning electron microscopy (SEM) coupled with energy dispersive X-ray (EDX) spectroscopy. The presence of only A 1g mode of SnO2 in Raman spectrum of ternary CNs suggested that SnO2 nanoparticles have been coated on the surfaces of ZnO and g–C3N4 which is also evident from SEM results. SnO2–ZnO–g–C3N4 CNs have shown much higher photocatalytic degradation efficiency and produced 7 mm greater zone of inhibition (ZOI) against Gram-positive S. Aureus bacteria as compared to pure ZnO which is quite significant result when compared to previously reported results for SnO2–ZnO CNs. These synthesized CNs may have potential uses in healthcare technology and treatment of organics in water.

From Layered Antiferromagnet to 3D Ferromagnet: LiMnBi-to-MnBi Magneto-Structural Transformation

The intermetallic compound LiMnBi was synthesized by the two-step solid-state reaction from the elements. A synthesis temperature of 850 K was selected based on in situ high-temperature powder X-ray diffraction data. LiMnBi crystalizes in the layered-like PbClF structure type (a = 4.3131(7) Å, c = 7.096(1) Å at 100 K, P4/nmm space group, Z = 2). The LiMnBi structure is built of alternating [MnBi] and Li layers, as determined from single-crystal X-ray diffraction data. Magnetic property measurements and solid-state 7Li nuclear magnetic resonance data collected for polycrystalline LiMnBi samples indicate the long-range antiferromagnetic ordering of the Mn sublattice at ∼340 K, with no superconductivity detected down to 5 K. LiMnBi is air- and water-sensitive. Under aerobic conditions, Li can be extracted from the LiMnBi structure to form Li2O/LiOH and MnBi (NiAs structure type, P63/mmc). The obtained MnBi polymorph was previously reported to be one of the strongest rare-earth-free ferromagnets, yet its bulk synthesis in powder form is cumbersome. The proposed magneto-structural transformation from ternary LiMnBi to ferromagnetic MnBi involves condensation of the MnBi4 tetrahedra upon Li deintercalation and is exclusive to LiMnBi. In contrast, ferromagnetic MnBi cannot be obtained from either isostructural NaMnBi and KMnBi or from the structurally related CaMn2Bi2. Such a distinctive transformation in the case of LiMnBi is presumed to be due to its fitting reactivity to yield MnBi and a favorable interlayer distance between [MnBi] layers, while the interlayer distance in NaMnBi and KMnBi structural analogues is unfavorably long. The studies of delithiation from layered-like LiMnBi under different chemical environments indicate that the yield of MnBi depends on the type of solvent used and the kinetics of the reaction. A slow rate and mild reaction media lead to a high fraction of the MnBi product. The saturation magnetization of the “as-prepared” MnBi is ∼50% of the expected value of 81.3 emu/g. Overall, this study adds a missing member to the family of ternary pnictides and illustrates how soft-chemistry methods can be used to obtain “difficult-to-synthesize” compounds.