Antimonene nanosheets with enhanced electrochemical performance for energy storage applications.

Antimonene is an exfoliated 2D nanomaterial obtained from bulk antimony. It is a novel class of 2D material for energy storage applications. In the present work, antimonene was synthesized using a high-energy ball milling-sonochemical method. The structural, morphological, thermal, and electrochemical properties of antimonene were comparatively analyzed against bulk antimony. X-ray diffractometry (XRD) analysis confirms the crystal structure and 2D structure of antimonene, as a peak shift was observed. The Raman spectra show the peak shift for the Eg and A1g modes of vibration of antimony, which confirms the formation of antimonene. Scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM) images depict the exfoliation of antimonene from bulk antimony. Thermal analysis unveiled the thermal stability of antimonene up to 400 °C with only 3% weight loss. X-ray photoelectron spectroscopy (XPS) analysis reveals the formation of antimonene, which is free from contamination. The electrochemical properties of antimony and antimonene were investigated using cyclic voltammetry (CV) and chronopotentiometric (CP) analysis, using 2 M KOH as an electrolyte. Antimonene exhibited a relatively high specific capacitance of 597 F g-1 compared to ball-milled antimony (101 F g-1) at a scan rate of 10 mV s-1. Moreover, electrochemical impedance spectroscopy (EIS) analysis revealed that antimonene has a relatively low equivalence series resistance (RESR) and low charge transfer resistance (RCT) compared to bulk antimony, which favors high electrochemical performance. The cyclic stability of antimonene was studied for 3000 cycles, and the results show high cyclic stability. The electrochemical results demonstrated that antimonene is a promising material for energy storage applications.

Surfactant-Free Synthesis of Nb2O5 Nanoparticles Anchored Graphene Nanocomposites with Enhanced Electrochemical Performance for Supercapacitor Electrodes.

Nb2O5/graphene nanocomposites without any surfactant are synthesized by an in situ microwave irradiation technique. Structural and morphological studies revealed that the prepared composites were composed of Nb2O5 nanoparticles intercalated into the graphene sheet. The thermal stability of graphene oxide, Nb2O5, and Nb2O5/graphene nanocomposite was studied by the TGA. The electrochemical properties are assessed by cyclic voltammetry, chronopotentiometry and electrochemical impedance spectroscopy analyses. The specific capacitance of Nb2O5/graphene nanocomposites is greater (633 Fg-1) than pure Nb2O5 nanoparticles (221 Fg-1) and graphene (290 Fg-1) at a current density of 1 Ag-1. The long-term cyclic measurement confirms higher cyclic stability of the nanocomposite with capacitance retention of 99.3% after 5000 cycles without performance degradation. The composites exhibit higher electrochemical conductivity and allow effective ions and charge transport over the entire electrode surface with aqueous electrolyte. The electrochemical study suggests that Nb2O5/graphene nanocomposites have the potential to be an effective electrode for superior performance supercapacitor applications.

Bifunctional investigation of ultra-small SnO2 nanoparticle decorated rGO for ozone sensing and supercapacitor applications.

Ultrasmall SnO2 nanoparticles with an average size of 7 nm were synthesized by a hydrothermal method and composited with reduced graphene oxide (rGO) through an ultrasonic assisted solution process. The structural, functional, morphological and compositional properties of synthesised SnO2 and rGO/SnO2 were studied by XRD, FTIR, HRSEM, HRTEM, XPS and Raman analyses. The prepared materials were developed as a film over a PVA/KOH conductive layer coated substrate with varying thickness of 3, 5 and 7 µm to study their ozone sensing characteristics at room temperature. The physico-chemical properties reveal that the fabricated SnO2 and rGO/SnO2 nanocomposite films have a strong interaction with the ozone gas. Among the fabricated composite films rGO/SnO2-S1 film exhibits high ozone sensing response (38%) at room temperature. Additionally, the electrochemical performance of SnO2 and rGO/SnO2 nanocomposites was analysed and the rGO/SnO2 nanocomposite exhibited higher specific capacitance (545 F g-1) than that of pure SnO2 (236 F g-1) at a current density of 1 A g-1 with higher cyclic stability (96%) than that of pure SnO2 (86%) at the current density of 20 A g-1 for a continuous 5000 charge-discharge cycles. Thus, the rGO/SnO2 nanocomposite showed an excellent ozone sensing and energy storage performance.

Effect of co-sensitization of InSb quantum dots on enhancing the photoconversion efficiency of CdS based quantum dot sensitized solar cells.

The effect of co-sensitization of CdS and InSb Quantum Dots (QDs) on the enhancement of efficiency of Quantum Dots Sensitized Solar Cells (QDSSCs) has been investigated. InSb is synthesized by a facile solvothermal method using indium metal particles and antimony trichloride as precursors. From TEM images the average particle size of InSb was found to be less than 25 nm. The I-V data showed photoconversion efficiency (PCE) of 0.8% using InSb QDs as a sensitizer layer for QDSSC. However, co-sensitization of InSb QDs and CdS QDs on the TiO2 photoanode in QDSSCs showed an enhanced PCE of 4.94% compared to that of CdS sensitized solar cells (3.52%). The InSb QD layer broadens the light absorption range with reduced spectral overlap causing an improvement in light harvesting along with suppression of surface defects which reduced the recombination losses. As a result, co-sensitized TiO2/CdS/InSb QDSSC exhibits a greatly improved PCE of 4.94%, which is 40% higher than that of TiO2/CdS (3.52%) based QDSSCs due to improved light absorption with low recombination losses.

Enhanced electrochemical performance of α-MoO3/graphene nanocomposites prepared by an in situ microwave irradiation technique for energy storage applications.

Nanoparticles of α-molybdenum oxide (α-MoO3) are directly grown on graphene sheets using a surfactant-free facile one step ultrafast in situ microwave irradiation method. The prepared α-MoO3 and α-MoO3/G nanocomposites are analysed by different characterization techniques to study their structural, morphological and optical properties. Transmission electron microscope images reveal the intercalation of three dimensional (3D) α-MoO3 nanoparticles into 2D graphene sheets without any agglomeration. The electrochemical results exhibit improved performance for the α-MoO3/G composite electrode compared to pristine α-MoO3 owing to its structural superiority. The specific capacitance (C s) values of the α-MoO3/G composite and pristine α-MoO3 are measured to be 483 and 142 F g-1 respectively at a current density of 1 A g-1. The α-MoO3/G composite maintains a very strong cyclic performance after 5000 cycles. The capacitance retention of the composite electrode shows stable behavior without any degradation confirming its suitability as an enduring electrode material for high-performance supercapacitor applications.

Enhancing the thermoelectric power factor of nanostructured ZnCo2O4 by Bi substitution.

Bi x ZnCo2-x O4 (0 ≤ x ≤ 0.2) nanoparticles with different x values have been prepared by the sol-gel method; the structural, morphological, thermal and thermoelectric properties of the prepared nanomaterials are investigated. XRD analysis confirms that Bi is completely dissolved in the ZnCo2O4 lattice till the x values of ≤0.1 and the secondary phase of Bi2O3 is formed at higher x value (x > 0.1). The synthesized nanomaterials are densified and the thermoelectric properties are studied as a function of temperature. The electrical resistivity of the Bi x ZnCo2-x O4 decreased with x value and it fell to 4 × 10-2 Ω m for the sample with x value ≤ 0.1. The Seebeck coefficient value increased with the increase of Bi substitution till the x value of 0.1 and decreased for the sample with higher Bi content (x ≤ 0.2) as the resistivity of the sample increased due to secondary phase formation. With the optimum Seebeck coefficient and electrical resistivity, Bi0.1ZnCo1.9O4 shows the high-power factor (α 2 σ 550 K) of 2.3 µW K-2 m-1 and figure of merit of 9.5 × 10-4 at 668 K respectively, compared with other samples. The experimental results reveal that Bi substitution at the Co site is a promising approach to improve the thermoelectric properties of ZnCo2O4.

Enhancing effects of Te substitution on the thermoelectric power factor of nanostructured SnSe1-xTex.

Nanostructured SnSe1-xTex (0 < x < 0.2) was prepared by the planetary ball milling method. The prepared materials were studied by various analytical techniques. XRD analysis shows the pure phase of SnSe when x ≤ 0.1 and the secondary phase of SnTe was observed when x ≥ 0.1, possibly due to the low solid solubility limit of Te in SnSe. FESEM images revealed that the grain sizes of all the samples were in the range of 100 to 500 nm. TEM images showed the grain structures, sizes and grain boundaries of the samples. XPS analysis confirmed the incorporation of Te in SnSe1-xTex and the binding states of the elements in the samples. The samples were made into pellets and sintered at high temperature. The electrical resistivity of the SnSe1-xTex pellets decreased by up to two orders of magnitude as the x value increased in the samples. Concomitantly, the Seebeck coefficient of the SnSe1-xTex samples decreased drastically as the x value increased in the samples. A power factor (PF) of 102.8 µW K-2 m-1 was obtained for the SnSe0.9Te0.1 sample at 550 K, which is higher than the reported values for SnSe and SnSe1-xTex. When substituting Se with Te, the band structure of SnSe changes, which significantly enhances the thermoelectric PF of SnSe1-xTex for x ∼ 0.1. The PF decreased when the x value was increased further (x ≥ 0.1), possibly due to the precipitation of the SnTe phase. These experimental results demonstrate that the addition of a reasonable amount of Te is a promising approach for improving the thermoelectric properties of SnSe.

Electrochemical Sensor Based on Fe Doped Hydroxyapatite-Carbon Nanotubes Composite for L-Dopa Detection in the Presence of Uric Acid.

A novel amperometric sensor based on iron doped hydroxyapatite (Fe-HA) and multiwalled carbon nanotubes (CNT) composite immobilized on a glassy carbon electrode (GCE) has been fabricated. The hybrid composite made of Fe-HA nanoparticles and CNT promotes electron transfer kinetics between the analyte levodopa (L-dopa) and the modified GC electrode. Under optimum conditions, the fabricated sensor gave a linear response range of 1.0 x 10(-7)-1.1 x 10(-6) M with the detection limit as low as 62 nM. The Fe-HA/CNT modified electrode showed good selectivity towards the determination of L-dopa in the presence of ascorbic acid (AA), uric acid (UA) and other common interferents. The sensor displays a high sensitivity, good reproducibility and long-term stability and it was successfully applied for the detection of L-dopa in pharmaceutical and medicinal plant samples.

Graphene decorated with MoS2 nanosheets: a synergetic energy storage composite electrode for supercapacitor applications.

The two-dimensional (2D) transition metal dichalcogenide nanosheet-carbon composite is an attractive material for energy storage because of its high Faradaic activity, unique nanoconstruction and electronic properties. In this work, a facile one step preparation of a molybdenum disulfide (MoS2) nanosheet-graphene (MoS2/G) composite with the in situ reduction of graphene oxide is reported. The structure, morphology and composition of the pure MoS2 and composites were comparatively analyzed by various characterization techniques. The electrochemical performance of the pure MoS2, graphene oxide and the MoS2/G composite electrode materials was evaluated by cyclic voltammogram, galvanostatic charge-discharge and electrochemical impedance spectroscopy. The MoS2/G composite showed a higher specific capacitance (270 F g(-1) at a current density of 0.1 A g(-1)) compared to the pure MoS2 (162 F g(-1)) in a neutral aqueous electrolyte. Moreover, the energy density of the composite electrode is also higher (12.5 Wh kg(-1)) with a high power density (2500 W kg(-1)) compared to the pure MoS2. In addition, the MoS2/G composite electrode showed excellent cyclic stability even after 1000 cycles. The enhancement in specific capacitance, excellent cyclic stability and high energy density of the composite electrode are mainly due to the interconnected conductive network of the composite as well as the synergetic effect of the pure MoS2 and graphene. The experimental results demonstrated that the MoS2/G composite is a promising electrode material for high-performance supercapacitors.

Facile synthesis of graphene-CeO2 nanocomposites with enhanced electrochemical properties for supercapacitors.

Graphene-ceria (CeO2G) nanocomposites were prepared by using a low-temperature solution process with different weight percentages of graphene, and their electrochemical properties were investigated. Structural properties of the nanocomposites were studied by X-ray diffraction, Raman spectroscopy, and FTIR spectral analyses. FE-SEM and HRTEM images revealed a "wrinkled paper"-like morphology of the prepared composites. Elemental mapping images were recorded by using the FE-EPMA technique. XPS analyses revealed the binding states of different elements present in the composites. The composite with 5% graphene displayed a specific capacitance of 110 F g(-1), according to cyclic voltammetric studies, which is higher than that observed for pure CeO2 (75 F g(-1)). The significant increase in the specific capacitance suggests that the CeO2G is a promising material for supercapacitor applications.

Effect of solvents on the bulk growth of 4-aminobenzophenone single crystals: a potential material for blue and green lasers.

Although 4-aminobenzophenone (4-ABP) is the best derivative of benzophenone with 260 times higher second harmonic generation (SHG) efficiency than potassium dihydrogen phosphate (KDP), growth of high quality bulk crystal still remains a difficult task. In the present work, the effect of solvents on solubility and growth aspects of 4-ABP was investigated to grow inclusion free 4-ABP crystals. The growth processes were discussed based on solute-solvent interaction in two different growth media of ethyl acetate and ethanol. The growth rate and thereby solvent inclusions are relatively higher in ethyl acetate grown crystal than the crystal grown from ethanol. The structural, thermal and optical properties of 4-ABP crystals were studied. The enthalpy of 4-ABP melting process was estimated from differential thermal analysis. The optical transmission study shows that 4-ABP crystals grown from ethanol has high transparency compared to ethyl acetate grown sample due to solvent inclusion in the later crystal.

Growth of In x Ga1-x Sb alloy semiconductor at the International Space Station (ISS) and comparison with terrestrial experiments.

BACKGROUND: In x Ga1-x Sb is an important material that has tunable properties in the infrared (IR) region and is suitable for IR-device applications. Since the quality of crystals relies on growth conditions, the growth process of alloy semiconductors can be examined better under microgravity (µG) conditions where convection is suppressed. AIMS: To investigate the dissolution and growth process of In x Ga1-x Sb alloy semiconductors via a sandwiched structure of GaSb(seed)/InSb/GaSb(feed) under normal and µG conditions. METHODS: In x Ga1-x Sb crystals were grown at the International Space Station (ISS) under µG conditions, and a similar experiment was conducted under terrestrial conditions (1G) using the vertical gradient freezing (VGF) method. The grown crystals were cut along the growth direction and its growth properties were studied. The indium composition and growth rate of grown crystals were calculated. RESULTS: The shape of the growth interface was nearly flat under µG, whereas under 1G, it was highly concave with the initial seed interface being nearly flat and having facets at the peripheries. The quality of the µG crystals was better than that of the 1G samples, as the etch pit density was low in the µG sample. The growth rate was higher under µG compared with 1G. Moreover, the growth started at the peripheries under 1G, whereas it started throughout the seed interface under µG. CONCLUSIONS: Kinetics played a dominant role under 1G. The suppressed convection under µG affected the dissolution and growth process of the In x Ga1-x Sb alloy semiconductor.

Shape controlled synthesis of hierarchical nickel sulfide by the hydrothermal method.

Hierarchical structures of nickel sulfide have been grown by the hydrothermal method. Nickel nitrate hexahydrate and thiourea were used as precursor materials to synthesize nickel sulfide. Ethylenediaminetetraacetic acid was used as a capping agent to achieve monodispersity. The different phases of nickel sulfide and its dependency on the precursor concentration were analyzed by X-ray diffractometry. Transmission electron microscopy analysis was used to confirm the phase changes and morphological behavior of the synthesized material. The morphological evolution of the hierarchical structure formation was studied systematically by scanning electron microscopy. In this study, we explore a novel method to control the synthesis of nickel sulfide hierarchical structures by varying the precursor concentration. The two mixed phases enhanced the catalytic activity in the 4-nitro phenol reduction reaction.

Crystal growth, structural, thermal and mechanical behavior of l-arginine 4-nitrophenolate 4-nitrophenol dihydrate (LAPP) single crystals.

Single crystals of l-arginine 4-nitrophenolate 4-nitrophenol dihydrate (LAPP) have been grown successfully from the solution of l-arginine and 4-nitrophenol. Slow evaporation of solvent technique was adopted to grow the bulk single crystals. Single crystal X-ray diffraction analysis confirms the grown crystal has monoclinic crystal system with space group of P21. Powder X-ray diffraction analysis shows the good crystalline nature. The crystalline perfection of the grown single crystals was analyzed by HRXRD by employing a multicrystal X-ray diffractometer. The functional groups were identified from proton NMR spectroscopic analysis. Linear and nonlinear optical properties were determined by UV-Vis spectrophotometer and Kurtz powder technique respectively. It is found that the grown crystal has no absorption in the green wavelength region and the SHG efficiency was found to be 2.66 times that of the standard KDP. The Thermal stability of the crystal was found by obtaining TG/DTA curve. The mechanical behavior of the grown crystal has been studied by Vicker's microhardness method.

Synthesis, growth, crystal structure and characterization of a new organic NLO crystal: L-lysine 4-nitrophenolate monohydrate (LLPNP).

L-lysine 4-nitrophenolate monohydrate (LLPNP) has been synthesized and grown by solution growth method at room temperature using deionised water as a solvent. The crystal structure of the materials was solved by single crystal X-ray diffraction analysis and it was found that the material has orthorhombic system. The crystallinity of the grown crystals was studied by the powder X-ray diffraction analysis. Molecular structure of the grown crystal was investigated by 1H NMR spectroscopy. The various functional groups of the sample were identified by Fourier transform infrared and Fourier transform-Raman spectroscopic analyses. Thermal stability of the grown crystal has been studied by Thermogravimetric and Differential thermal (TG&DTA) analysis. The optical absorption of the grown crystals has been ascertained by UV-Vis-NIR absorption studies. Second harmonic generation (SHG) efficiency of the material has been determined by Kurtz and Perry technique and the efficiency was found to be 4.45 and 1.4 times greater than that of standard KDP and urea samples, respectively.

Investigations on the growth aspects and characterization of semiorganic nonlinear optical single crystals of L-histidine and its hydrochloride derivative.

Semiorganic single crystals of l-histidine and l-histidine hydrochloride monohydrate have been obtained in a single solution prepared from the mixture of l-histidine and hydrochloric acid in 1:2M ratio. Growth aspects of the single crystals have been discussed along with characterization studies. Crystal system and lattice parameters have been identified by X-ray diffraction analyses. It has been observed that the grown crystals possess orthorhombic system but with different set of lattice parameters. Presence of various functional groups has been identified and formation of two different crystals has been confirmed by Fourier transform infrared spectral analyses and FT-Raman studies. Linear and nonlinear optical properties have been studied by UV-Vis spectral analyses and Kurtz-Perry powder technique respectively. The thermal stability of the grown crystals was determined by thermal analyses. From the characterization studies it is found that both the crystals are useful for second harmonic generation applications.

Growth and characterization of a novel nonlinear optical borate crystal--yttrium calcium borate (YCB).

A new nonlinear optical single crystal yttrium calcium borate Y2CaB10O19 (YCB) was grown for the first time from its melt. The starting materials were prepared by the solid-state reaction method. The melting point of the synthesized material was identified to be 967 °C. YCB crystal exhibits monoclinic crystal structure with the space group C2. The crystalline perfection of the grown YCB crystal was found to be good. From the UV-VIS-NIR studies, the lower cutoff wavelength of the crystal occurs below 200 nm. The functional groups of the grown crystal were assigned using the FTIR data. The second harmonic generation (SHG) of the YCB crystal was observed using a Nd:YAG laser with a fundamental wavelength of 1064 nm. The laser damage threshold value of the YCB crystal was found to be very high - 10.5 GW/cm(2).

Ethyl 4-(dimethyl-amino)benzoate.

Mol-ecules of the title compound, C(11)H(15)NO(2), are essentially planar (r.m.s. deviation = 0.035 Å) and are linked into a chain along the a axis by weak C-H⋯O hydrogen bonds.