Metal organic frameworks as electrocatalysts: Hydrogen evolution reactions and overall water splitting

The development of clean energy technologies to protect the environment is an important demand of the times. Electrocatalysis is emerging as a promising method for evolution of hydrogen and overall water splitting. Nowadays, metal organic frameworks (MOFs) have emerged as electrocatalysts having uniformly distributed active sites and high electrical conductivity. This review summarizes the latest advances in heterogeneous catalysis by MOFs and their composite/derivatives for efficient hydrogen evolution reaction (HER) and water splitting. Pristine MOFs with their recent development are summarized first followed by composites of MOFs with their enhanced electrocatalytic performances. Overall water splitting by using bifunctional electrocatalysts derived from MOFs with different synthetic approaches is provided and this review gives the metal-based categorisation of precursor MOFs. Different strategies to improve chemical stability, conductivity, and overall electrocatalytic properties have been discussed. In the last, perspectives on the synthesis of efficient MOF-based electrocatalyst materials are provided.     

Periodic nano/micro-hole array silicon solar cell

In this study, we applied a metal catalyst etching method to fabricate a nano/microhole array on a Si substrate for application in solar cells. In addition, the surface of an undesigned area was etched because of the attachment of metal nanoparticles that is dissociated in a solution. The nano/microhole array exhibited low specular reflectance (<1%) without antireflection coating because of its rough surface. The solar spectrum related total reflection was approximately 9%. A fabricated solar cell with a 40-μm hole spacing exhibited an efficiency of 9.02%. Comparing to the solar cell made by polished Si, the external quantum efficiency for solar cell with 30 s etching time was increased by 16.7%.     

Structural and Luminescence Studies on Barium Sodium Borosilicate Glasses Containing Uranium Oxides

Barium sodium borosilicate glasses containing different amounts of uranium oxides were prepared by conventional melt quench method and investigated for their structural aspects by ²⁹Si and ¹¹B MAS NMR technique combined with steady‐state luminescence and lifetime measurements. Based on MAS NMR studies, it is confirmed that uranium ions act as network modifier up to 15 wt% and beyond which a separate uranium containing phase is formed. From the luminescence studies, it is inferred that uranyl species is in a highly distorted environment. For more than 15 wt% uranium oxide incorporation, weaker U–O–U linkages are formed at the expense stronger U–O–Si/B linkages, as suggested by the excited state lifetime value of the uranyl species as well as red shift in emission peak maximum. For glass samples containing more than 25 wt% uranium oxides, crystalline barium uranium silicate gets phase separated from glass matrix as confirmed by XRD studies.     

CNSL: an environment friendly alternative for the modern coating industry

Considering ecological and economical issues in the new generation coating industries, the maximum utilization of naturally occurring materials for polymer synthesis can be an obvious option. In the same line, one of the promising candidates for substituting partially, and to some extent totally, petroleum-based raw materials with an equivalent or even enhanced performance properties, is the Cashew Nut Shell Liquid (CNSL). This dark brown-colored viscous liquid obtained from shells of the cashew nut can be utilized for a number of polymerization reactions due to its reactive phenolic structure and a meta-substituted unsaturated aliphatic chain. Therefore, a wide variety of resins can be synthesized from CNSL, such as polyesters, phenolic resins, epoxy resins, polyurethanes, acrylics, vinyl, alkyds, etc. The present article discusses the potential of CNSL and its derivatives as an environment friendly alternative for petroleum-based raw materials as far as polymer and coating industries are concerned.     

The outlook of zeolite-Y hampered metal–ligand framework as heterogeneous catalysts: synthesis,spectral account and catalytic features

Zeolite-Y enslaved complexes were prepared by the Flexible ligand method. Synthesized materials were characterized by various spectral tools like powder X-ray diffraction, spectral studies (UV–Vis and FT-IR), chemical analysis (ICP-OES and elemental), scanning electron microscopy, AAS and ¹H-NMR techniques. Further, BET and thermogravimetric (TG) analysis were also done for characterization of surface area, pore volume, thermal behavior, and related parameters. Baeyer–Villiger oxidation of cyclohexanone was carried out over Zeolite-Y enslaved complexes using hydrogen peroxide (H₂O₂) as an oxidant. The performance of the heterogeneous system with the homogeneous system was compared to determine the protection effect of the zeolitic matrix over the active center on the catalytic properties. In addition, the effect of experimental variables (various solvents, amount of catalyst, the mole ratio of substrate and oxidant, temperature, and reaction time) was examined in order to get absolute reaction conditions. Under the optimized reaction conditions, [Fe(nbab)₂]-Y was found to be a potential candidate, achieving 70 % ?-caprolactone selectivity.     

Iodine speciation studies on Bunsen reaction of S–I cycle using spectroscopic techniques

Bunsen reaction is an important step of sulfur–iodine cycle for hydrogen production from thermochemical splitting of water. Polyiodide species generated during the separation process need to be identified for complete understanding of the mechanism involved. Speciation of these polyiodide species formed during Bunsen reaction can lead to better understanding of kinetics of the process. HIx species formed have been analyzed using UV–visible and Raman spectroscopic techniques. Peak corresponding to HI₃ species have been ascertained and their conversion to higher HI₅, HI₇ …… species has been observed.     

A sub-space method to detect multiple wireless microphone signals in TV band white space

The main hurdle in the realization of dynamic spectrum access systems from the physical layer perspective is the reliable sensing of low power licensed users. One such scenario shows up in the unlicensed use of the TV bands where the TV band devices are required to sense extremely low power wireless microphones (WMs). The lack of technical standards among various wireless manufacturers and the resemblance of certain WM signals to narrow-band interference signals, such as spurious emissions, further aggravate the problem. Due to these uncertainties, it is extremely difficult to abstract the features of WM signals and hence develop robust sensing algorithms. To partly counter these challenges, we develop a two-stage sub-space algorithm that detects multiple narrow-band analog frequency-modulated signals generated by WMs. The performance of the algorithm is verified by using the real WM signals experimentally captured under low SNR conditions. The problem of differentiating between the WM and other narrow-band signals is left as future work.     

On the Effect of Birefringence on Light Transmission in Polycrystalline Magnesium Fluoride

Light transmission in polycrystalline magnesium fluoride was studied as a function of the mean grain size at different wavelengths. The mean grain size was varied by annealing hot‐pressed billets in argon atmosphere at temperatures ranging from 600°C to 800°C for 1 h. The grain‐size and grain‐orientation distributions were characterized by electron back scatter diffraction. The scattering coefficients were calculated from the in‐line transmittance measured at various wavelengths. The scattering coefficient of polycrystalline magnesium fluoride increased linearly with the mean grain size and inversely with the square of the wavelength of light. It is shown that these trends are consistent with theoretical models based on both a limiting form of the Raleigh–Gans–Debye (RGD) theory of particle scattering and light retardation theories that take refractive index variations along the light path. Quantitative predictions of the theories are, however, subject to uncertainly due to the restrictive assumptions made in the theories and difficulties in representing the microstructure in the theoretical models. In particular, grain‐size distribution has a significant influence on the scattering coefficient calculated using particle scattering models.