Production of Two‐Dimensional Nanomaterials via Liquid‐Based Direct Exfoliation

Tremendous efforts have been devoted to the synthesis and application of two‐dimensional (2D) nanomaterials due to their extraordinary and unique properties in electronics, photonics, catalysis, etc., upon exfoliation from their bulk counterparts. One of the greatest challenges that scientists are confronted with is how to produce large quantities of 2D nanomaterials of high quality in a commercially viable way. This review summarizes the state‐of‐the‐art of the production of 2D nanomaterials using liquid‐based direct exfoliation (LBE), a very promising and highly scalable wet approach for synthesizing high quality 2D nanomaterials in mild conditions. LBE is a collection of methods that directly exfoliates bulk layered materials into thin flakes of 2D nanomaterials in liquid media without any, or with a minimum degree of, chemical reactions, so as to maintain the high crystallinity of 2D nanomaterials. Different synthetic methods are categorized in the following, in which material characteristics including dispersion concentration, flake thickness, flake size and some applications are discussed in detail. At the end, we provide an overview of the advantages and disadvantages of such synthetic methods of LBE and propose future perspectives.     

Multiwall carbon-nanotube-doped ion conducting polymer electrolyte for electrochemical application

Electrical, structural and optical properties of a composite containing a polymer electrolyte (namely polyethylene oxide complexed with sodium iodide) and multiwall carbon nanotube (MWCNT) are reported. The films of these composites were ‘solution casted’ using the viscous solution of polyethylene oxide (PEO) complexed with sodium iodide (NaI) in desired ratios and characterised using various techniques. The conductivity versus composition plot in PEO:NaI shows conductivity maxima at 12?wt% NaI concentration while in MWCNTs doped polymer electrolyte it occurs at 40?wt% MWCNTs concentration. The surface morphology by scanning electron microscopy (SEM) shows the enhancement in amorphous reason by MWCNTs doping which is a well-known favourable condition for conductivity enhancement. The differential scanning calorimetry shows that dispersal of MWCNTs reduces the crystallinity of polymer electrolyte that is well-supported by our polarised optical micrographs and SEM measurements.     

A framework for understanding institutional factors affecting the success and failure of offshoring models in India

The objective of this paper is to identify and analyse the factors that influence offshore location decisions from an institutional theory perspective. In the years, emerging economies have shown great growth potential and have attracted significant foreign direct investment, especially from companies willing to set up operations. Despite such a seemingly favourable trade environment, not all companies that entered an emerging economy have been successful. Thus, there is a need to understand the factors that influence the success of any offshore location decision. It is also important to understand the relative importance of these factors, in order to develop novel insights useful to practitioners. There is a lack of literature addressing this issue, which this study aims to fill. We conducted a multi-case analysis with examples of European companies entering India. The findings indicate that successful companies employed locally focused business strategies that enabled them to acquire important relationships and knowledge, and also to adapt to formal institutions, including governmental and regulatory procedures. It was found that, irrespective of size, disregarding collaborative strategies was the main reason for exiting India. These findings are highly relevant for managers and policy makers.     

Physicochemical investigations of Pd2+ substituted ZnO nanoflowers for liquefied petroleum gas sensing

Journal of Materials Science: Materials in Electronics - Present study portrays, physicochemical investigations of pristine and Pd2+ modified ZnO nanoflowers (NFs) compositional series...     

Conduction mechanism and dielectric properties of BiFeO3–BaTiO3 solid solutions

The first measurements are reported for the frequency-dependent conductivity of (1?x)BiFeO₃–xBaTiO₃ (x = 0.10, 0.15 and 0.30) solid solutions in the frequency range of 10⁰–10⁶ Hz and in the temperature range of 50–300 °C. Powder X-ray diffraction confirms the formation of solid solutions. The dielectric properties were seen to improve with increasing BaTiO₃ (BT) content. The conductivity (AC and DC) measurements reveal an inverse variation of the frequency exponent ‘s’ with temperature, high density of states and thermally activated process. The calculated density of states was found to be N(E_f) = 80.2 × 10³² eV^?1 cm^?1 at 1 kHz and 50 °C for BiFeO₃–10 % BaTiO₃ (BFO–10 % BT) solid solution. The impedance spectroscopy analysis confirms the presence of grain and grain boundary affecting the conductivity. Our results provide the first unambiguous evidence of conduction in crystallite BFO–BT solid solutions through correlated-barrier-hopping model.     

Enhanced acetone detection using Au doped ZnO thin film sensor

Zinc oxide (ZnO) thin films are prepared using sol–gel method for acetone vapor sensing. Zinc acetate dihydrate (Zn(CH₃COO)₂·2H₂O) was taken as starting material and a stable and homogeneous solution was prepared in ethanol by deliquescing the zinc acetate and distinct amount of monoethanolamine as a stabilizing agent. The prepared solution was then coated on silicon substrates by spin coating method and then annealed at 650 °C for preparing ZnO thin films. The thickness of the film was maintained at 410 nm. The structural, morphological and optical studies were done for the synthesized ZnO thin films. The operating temperature and sensor response is considered to be an important parameter for the gas sensing behavior of any material. Therefore, the present study examined the effect of sensing behavior of 3% v/v gold (Au) doped ZnO thin films as a sensor. The response characteristics of 410 nm ZnO thin film for temperature ranging from 180 to 360 °C were determined for the acetone vapors. The reported study provides a significant development towards acetone sensors, where a very high sensitivity with rapid response and recovery times are reported with lowered optimal operating temperature as compared to bare ZnO nano-chains like structured thin films. In comparison to the bare ZnO thin films giving a response of 63 at an operating temperature of 320 °C, a much better response of 132.3 was observed for the Au doped ZnO thin films at an optimised operating temperature of 280 °C for a concentration of 500 ppm of acetone vapors.     

Transition from ferro- to ferrimagnetic ordering via Mn-disorder in (Ni,Co)MnGa quaternary Heusler alloy

An inclusive investigation of electronic and magnetic properties of ordered and disordered (Ni,Co)MnGa quaternary Heusler alloy has been undertaken using the density functional theory-based full potential linearized augmented plane wave method within generalized gradient approximation as exchange–correlation potentials. We observe that the increasing Mn concentration in Ni_1?x CoMn_1+x Ga (x = 0, 0.25, 0.50 and 0.75) lowers the ferromagnetic (FM) character of the parent (Ni,Co)MnGa alloy. This change creates two inequivalent Mn sites aligning antiparallel to each other and generates the ferrimagnetic (FiM) ordering in all resultant disordered alloys. Further, this replacement sets off a structural change from Y- to X_a-structure. The highest magnetic moment has been found to be 4.95 μ_B for ordered (Ni,Co)MnGa alloy, whereas it decreases with increase in Mn-concentration for disordered systems. The variation of half-metallicity with increasing Mn concentration is analysed. The stability of FM and FiM state for the present ordered and disordered alloys, respectively, is also examined.     

Temperature stability and bioadhesive properties of delta9-tetrahydrocannabinol incorporated hydroxypropylcellulose polymer matrix systems

The purpose of this study was to determine and compare the bioadhesive profiles of hydroxypropylcellulose (HPC) polymer matrices as a function of Δ⁹-tetrahydrocannabinol (THC) content. In addition, the effect of processing temperature on the stability of THC and its extent of degradation to cannabinol (CBN) was investigated. A hot-melt cast molding method was used to prepare HPC polymer matrix systems incorporated with THC at 0, 4, 8, and 16 percent. Bioadhesive measurements including peak adhesive force, area under the curve, and elongation at adhesive failure were recorded utilizing the TA.XT2i Texture Analyzer^™. Data obtained from these tests at various contact time intervals suggested that the incorporation of THC led to an increase in the bioadhesive strength of the HPC polymer matrices. To determine the stability of THC and the resulting CBN content in the matrices, three different processing temperatures were utilized (120, 160, and 200°C). Post-production High Performance Liquid Chromotography (HPLC) analysis revealed that the processed systems contained at least 94% of THC and the relative percent formation of CBN was 0.5% at 120°C and 0.4% at 160°C compared to 1.6% at 200°C. These findings indicate that the cannabinoid may be a plausible candidate for incorporation into systems utilizing hot-melt extrusion techniques for the development of an effective mucoadhesive transmucosal matrix system for delivery of THC.     

Rapid, online quantification of H2S in JP-8 fuel reformate using near-infrared cavity-enhanced laser absorption spectroscopy

One of the key challenges in reforming military fuels for use with fuel cells is their high sulfur content, which can poison the fuel cell anodes. Sulfur-tolerant fuel reformers can convert this sulfur into H(2)S and then use a desulfurizing bed to remove it prior to the fuel cell. In order to optimize and verify this desulfurization process, a gas-phase sulfur analyzer is required to measure H(2)S at low concentrations (<1 ppm(v)) in the presence of other reforming gases (e.g., 25-30% H(2), 10-15% H(2)O, 15% CO, 5% CO(2), 35-40% N(2), and trace amounts of light hydrocarbons). In this work, we utilize near-infrared cavity-enhanced optical absorption spectroscopy (off-axis ICOS) to quantify H(2)S in a JP-8 fuel reformer product stream. The sensor provides rapid (2 s), highly precise (±0.1 ppm(v)) measurements of H(2)S in reformate gases over a wide dynamic range (0-1000 ppm(v)) with a low detection limit (3σ = ±0.09 ppm(v) in 1 s) and minimal cross-interferences from other present species. It simultaneously quantifies CO(2) (±0.2%), CH(4) (±150 ppm(v)), C(2)H(4) (±30 ppm(v)), and H(2)O (±300 ppm(v)) in the reformed gas for a better characterization of the fuel reforming process. Other potential applications of this technology include measurement of coal syngas and H(2)S in natural gas. By including additional near-infrared, distributive feedback diode lasers, the instrument can also be extended to other reformate species, including CO and H(2).