NH2-MIL-125(Ti) doped CdS/Graphene composite as electro and photo catalyst in basic medium under light irradiation.

The development of active electrocatalysts and photocatalysts for hydrogen evolution reaction (HER) and for environmental remediation is a huge challenge. Research is still underway on the development of low-cost catalytic materials with appreciable efficiency for HER. In the present study, a composite of metal organic framework (MOF) with CdS and graphene (NH2-MIL-125(Ti)/CdS-graphene) composites were developed with different loadings of graphene material via solvothermal technique. Further the electrocatalytic activity of the synthesized catalysts were investigated for HER and photocatalytic degradation of dye. Results show that the synthesized catalyst with a less amount of graphene was more active. HER results showed a less Tafel slope of 70.8 and 61.9 mVdec-1 with 15.6 mA/cm2 and 15.46 mA/cm2 current densities under light on and off conditions. Further the dye degradation activity of the synthesized catalysts was tested with Rhodamine B dye and results showed that the catalyst showed excellent activity for low weight loading of graphene with a degradation efficiency of 95 % and followed pseudo first order kinetic model. Overall results showed that the synthesized composites are promising for HER and photocatalytic applications.

Development of Cu3N electrocatalyst for hydrogen evolution reaction in alkaline medium.

A wide variety of electrocatalysts has been evolved for hydrogen evolution reaction (HER) and it is reasonable to carry out HER with low cost electrocatalyst and a good efficiency. In this study, Cu3N was synthesized by nitridation of Cu2O and further utilized as an electrocatalyst towards HER. The developed Cu3N electrocatalyst was tested and results showed a low overpotential and moderate Tafel slope value (overpotential: 149.18 mV and Tafel slope 63.28 mV/dec at 10 mA/cm2) in alkaline medium with a charge transfer resistance value as calculated from electrochemical impendence spectroscopy being 1.44 Ω. Further from the experimental results, it was observed that the reaction kinetics was governed by Volmer-Heyrovsky mechanism. Moreover, Cu3N has shown an improved rate of electron transfer and enhanced accessible active sites, due to its structural properties and electrical conductivity. Thus the overall results show an excellent electrochemical performance, leading to a new pathway for the synthesis of low cost electrocatalyst for energy conversion and storage.

Facile synthesis of gold and platinum doped titanium oxide nanoparticles for antibacterial and photocatalytic activity: A photodynamic approach.

A simple method has been needed to synthesize nanoparticles (NPs) to avoid environmental pollution, an alternative chemical and physical method. This current study deals with phytosynthesis of gold (Au) and platinum (Pt) metal doped with titanium oxide (TiO2) NPs using Enterolobium saman bark extract. This extract plays a vital role in reducing and stabilizing Au and Pt doped into the TiO2 NPs lattices. Phytosynthesized samples were characterized by XRD, SEM, ED-XRF, TEM, FTIR, Raman, and UV-vis-DRS analyses. The metal doping effect has decreased bandgap energy and particle size, whereas increased conductivity for TiO2/M-Au and TiO2/M-Pt NPs compared to pristine TiO2 NPs. Phytosynthesized NPs were fabricated for dye-sensitized solar cell (DSSC) and photocatalytic behaviour against methylene blue (MB) dye was studied. An obtained result demonstrates that TiO2/M-Au NPs have excellent feasibility for applying DSSC and photocatalytic application due to particle size, crystallite size, absorption ability, and bandgap energy. Besides, synthesized samples were measured with cyclic voltammetry and impedance spectroscopy found that the metal doping is drifted the dielectric and increases that the metal doping is drifted the dielectric increases electro-catalytic of the TiO2. Different concentrations of all NPs were tested against Escherichia coli MTCC 40 and S. aureus ATCC 6633 bacteria by a well-diffusion method. The 10 mg concentration of all NPs showed better antibacterial activity. However, we believe that the proposed simple phytosynthesized method provides an efficient way to overcome the chemical and physical methods.

Highly Porous MIL-100(Fe) for the Hydrogen Evolution Reaction (HER) in Acidic and Basic Media.

The present study reports the synthesis of a porous Fe-based MOF named MIL-100(Fe) by a modified hydrothermal method without the HF process. The synthesis gave a high surface area with the specific surface area calculated to be 2551 m2 g-1 and a pore volume of 1.407 cm3 g-1 with an average pore size of 1.103 nm. The synthesized electrocatalyst having a high surface area is demonstrated as an excellent electrocatalyst for the hydrogen evolution reaction investigated in both acidic and alkaline media. As desired, the electrochemical results showed low Tafel slopes (53.59 and 56.65 mV dec-1), high exchange current densities (76.44 and 72.75 mA cm-2), low overpotentials (148.29 and 150.57 mV), and long-term stability in both media, respectively. The high activity is ascribed to the large surface area of the synthesized Fe-based metal-organic framework with porous nature.

Role of MIL-53(Fe)/hydrated-dehydrated MOF catalyst for electrochemical hydrogen evolution reaction (HER) in alkaline medium and photocatalysis.

The role of breathing behavior in hydrated and dehydrated forms of MIL-53(Fe) is investigated here. The material can be used as an efficient electrocatalyst and photocatalyst for a hydrogen evolution reaction (HER) in an alkaline medium and the same was further tested for the degradation of organic pollutants. The as-synthesized MIL-53(Fe)/hydrated and dehydrated forms were characterized by different analytical techniques to study their structure, morphology, surface analysis, thermal, physical and chemical properties. The breathing behavior of the hydrated and dehydrated forms of MIL-53(Fe) was studied through BET surface analysis. Our results show a low onset potential (-0.155 V and -0.175 V), Tafel slope (71.6 mV per decade, 88.7 mV per decade) and a large exchange current density (1.6 × 10-4 mA cm-2 and 2.5 × 10-4 mA cm-2). Hydrated and dehydrated MIL-53(Fe) degraded an RhB dye solution within 30 minutes thus proving their efficiency as efficient photocatalysts.

Removal of cationic and anionic heavy metals from water by 1D and 2D-carbon structures decorated with magnetic nanoparticles.

In this study, cobalt ferrites (C) decorated onto 2D material (porous graphene (PG)) and 1D material (carbon nanofibers (CNF)), denoted as PG-C and CNF-C nanocomposites, respectively, were synthesized using solvothermal process. The prepared nanocomposites were studied as magnetic adsorbents for the removal of lead (cationic) and chromium(VI) (anionic) metal ions. The structural and chemical analysis of synthesized nanocomposites was conducted using different characterization techniques including Brunauer-Emmett-Teller (BET) analysis, field emission-scanning electron microscopy (FE-SEM), Fourier-transform infrared spectroscopy (FTIR), high resolution-transmission electron microscopy (HR-TEM), vibrating sample magnetometer (VSM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). Batch mode adsorption studies were conducted with the prepared nanocomposites to examine their maximum adsorption potential for lead and chromate ions. Performance parameters (time, pH, adsorbent dosage and initial ion concentrations) effecting the adsorption capacity of the nanocomposites were optimized. Different kinetic and isotherm models were examined to elucidate the adsorption process. Synthesized nanocomposites exhibited significant potential for the studied metal ions that can be further examined at pilot scale for the removal of metal ions from contaminated water.