Fabrication of graphene: CdSe quantum dots/CdS nanorod heterojunction photodetector and role of graphene to enhance the photoresponsive characteristics.

Integration of graphene with semiconducting quantum dots (QDs) provides an elegant way to access the intrinsic properties of graphene and optical properties of QDs concurrently to realize the high-performance optoelectronic devices. In the current article, we have demonstrated the high-performance photodetector based on graphene: CdSe QDs/CdS nanorod heterostructures. The resulting heterojunction photodetector with device configuration ITO/graphene: CdSe/CdS nanorods/Ag show excellent operating characteristics including a maximum photoresponsivity of 15.95 AW-1and specific detectivity of 6.85 × 1012Jones under 530 nm light illumination. The device exhibits a photoresponse rise time of 545 ms and a decay time of 539 ms. Furthermore, the study of the effect of graphene nanosheets on the performance enhancement of heterojunction photodetector is carried out. The results indicate that, due to the enhanced energy transfer from photoexcited QDs to graphene layer, light absorption is increased and excitons are generated led to the enhancement of photocurrent density. In addition to that, the graphene: CdSe QDs/CdS nanorod interface can facilitate charge carrier transport effectively. This work provides a promising approach to develop high-performance visible-light photodetectors and utilizing advantageous features of graphene in optoelectronic devices.

Green synthesis, characterization and antimicrobial activity of silver nanoparticles using methanolic root extracts of Diospyros sylvatica.

The current research study focuses to formulate the biosynthesized silver nanoparticles for the first time from silver acetate using methanolic root extracts of Diospyros sylvatica, a member of family Ebenaceae. TEM analysis revealed the average diameter of Ag NPs around 8nm which is in good agreement with the average crystallite size (10nm) calculated from X-ray Diffraction (XRD) analysis. Further the study has been extended to the antimicrobial activity against test pathogenic Gram (+) ve, Gram (-) ve bacterial and fungal strains. The bioinspired Ag-NP showed promising activity against all the tested bacterial strains and the activity was enhanced with increased dosage levels.

Single-phase BiFeO3 and BiFeO3-Fe2O3 nanocomposite photocatalysts for photodegradation of organic dye pollutants.

The application of a novel BiFeO3 (BFO)-Fe2O3 composite (called BFOF) as a photocatalyst for the degradation of methylene blue is reported. To improve the photocatalytic effectiveness of BiFeO3, we synthesized the first BFOF photocatalyst by adjusting the molar ratio of Fe2O3 in BiFeO3 using microwave-assisted co-precipitation. The UV-visible properties of the nanocomposites showed excellent absorption of visible light and reduced electron-hole recombination properties compared to the pure phase BFO. Photocatalytic studies on BFOF10 (90% BFO, 10% Fe2O3), BFOF20 (80% BFO, 20% Fe2O3), and BFOF30 (70% BFO, 30% Fe2O3) have shown that they decompose Methylene Blue (MB) in sunlight better than the pure BFO phase in 70 minutes. The BFOF30 photocatalyst was the most effective at reducing MB when exposed to visible light (94%). Magnetic studies confirm that the most effective catalyst BFOF30 has excellent stability and magnetic recovery properties due to the presence of magnetic phase Fe2O3 in the BFO.

BiFeO3-Black TiO2 Composite as a Visible Light Active Photocatalyst for the Degradation of Methylene Blue.

The application of a novel BiFeO3 (BFO)-black TiO2 (BTO) composite (called BFOT) as a photocatalyst for the degradation of methylene blue is reported. The p-n heterojunction photocatalyst was synthesized for the first time through microwave-assisted co-precipitation synthesis to change the molar ratio of BTO in BiFeO3 to increase the photocatalytic efficiency of the BiFeO3 photocatalyst. The UV-visible properties of p-n heterostructures showed excellent absorption of visible light and reduced electron-hole recombination properties compared to the pure-phase BFO. Photocatalytic studies on BFOT10, BFOT20, and BFOT30 have shown that they decompose methylene blue (MB) in sunlight better than pure-phase BFO in 70 min. The BFOT30 photocatalyst was the most effective at reducing MB when exposed to visible light (97%). Magnetic studies have shown that BTO is diamagnetic, and the BFOT10 photocatalyst exhibits a very weak antiferromagnetic behavior, whereas BFOT20 and BFO30 show diamagnetic behavior. This study confirms that the catalyst has poor stability and weak magnetic recovery properties due to the non-magnetic phase BTO in the BFO.

Microwave-Assisted Solvothermal Route for One-Step Synthesis of Pure Phase Bismuth Ferrite Microflowers with Improved Magnetic and Dielectric Properties.

The prototypical plum-free, one-phase multiferric ferrite BiFeO3 (BFO) is solid, parallel, with a high ferroelectric Curie temperature and Neel temperature and antiferromagnetic and ferroelectric propagation. This work aims to synthesize pure-phase BFO in the quickest possible way. We followed the microwave-assisted solvothermal (MWAST) method to achieve pure-phase BFO in the shortest duration of 3 min. The experiment involves simple optimizations with KOH concentration and microwave power levels. The surface morphology along with magnetic properties of BFO synthesized via the MWAST method are altered with varying KOH concentrations and microwave (MW) power levels. Our X-ray diffraction findings reveal that the pure-phase BFO is formed at 800 W MW power, and the structural characterizations like transmission electron microscopy, field emission scanning electron microscopy with energy-dispersive X-ray analysis have displayed the formation of uniformly distributed spherical microflowers of pure-phase BFO exhibiting a single-crystalline nature. Besides, the magnetic measurements affirmed a reliable weak ferromagnetic behavior (magnetization ∼1.25 emu/g) in BFO synthesized at 800 W MW power. In addition, good dielectric behavior with low dielectric loss was accompanied by frequency-dependent dielectric studies indicating an excellent frequency response of the material, and also the room-temperature ferroelectric properties were studied using a ferroelectric analyzer. The polarization of pure-phase BFO increases with the applied electric field and exhibits unsaturated polarization-electric field loops due to leakage current. Moreover, the Fourier transform infrared spectrum of the synthesized material has indicated the pure-phase BFO, and the Raman data have elucidated the vibrational modes of BFO. Further, the analysis of X-ray photoelectron spectroscopy data has confirmed the presence of fewer Fe2+ ions and oxygen vacancies in the pure-phase BFO. Therefore, the collective characterizations and detailed analysis of BFO material have revealed the uniqueness of the MWAST method in producing the pure-phase BFO in 3 min with improved magnetic and dielectric properties, and hence the BFO synthesized via the MWAST method can be a potential candidate for multiferroic applications.

Green Biosynthesis of Tin Oxide Nanomaterials Mediated by Agro-Waste Cotton Boll Peel Extracts for the Remediation of Environmental Pollutant Dyes.

The sustainable synthesis of metal oxide materials provides an ecofriendly and more exciting approach in the domain of a clean environment. Besides, plant extracts to synthesize nanoparticles have been considered one of the more superior ecofriendly methods. This paper describes the biosynthetic preparation route of three different sizes of tetragonal structure SnO2 nanoparticles (SNPs) from the agro-waste cotton boll peel aqueous extract at 200, 500, and 800 °C for 3 h and represents a low-cost and alternative preparation method. The samples were characterized by X-ray diffraction, Fourier transform infrared spectrophotometry, ultraviolet-visible absorption spectroscopy, high-resolution transmission electron microscopy (HR-TEM), and energy-dispersive X-ray spectroscopy. Surface area and porosity size distribution were identified by nitrogen adsorption-desorption isotherms and Brunauer-Emmett-Teller analysis. The photocatalytic properties of the SNP samples were studied against methylene blue (MB) and methyl orange (MO), and the degradation was evaluated with three different size nanomaterials of 3.97, 8.48, and 13.43 nm. Photocatalytic activities were carried out under a multilamp (125 W Hg lamps) photoreactor. The smallest size sample exhibited the highest MB degradation efficiency within 30 min than the most significant size sample, which lasted 80 min. Similarly, in the case of MO, the smallest sample showed a more superior degradation efficiency with a shorter period (40 min) than the large-size samples (100 min). Therefore, our studies suggested that the developed SNP nanomaterials could be potential, promising photocatalysts against the degradation of industrial effluents.

Biogenic Photo-Catalyst TiO2 Nanoparticles for Remediation of Environment Pollutants.

This article reports a benign environmentally friendly fabrication method of titanium dioxide (TDO) nanoparticles (named TDO NPs3, TDO NPs5, and TDO NPs8) using aqueous extract of durva herb waste. This synthesis process avoids use of harmful substances and persistent chemicals throughout the order and enables us to control the size of the nanomaterials. Characterization of TDO nanoparticles was analyzed by ultraviolet-visible spectroscopy, X-ray diffraction, and Fourier transform infrared spectroscopy. The morphological nature of the TDO samples was inspected by transmission electron microscopy, which indicated that the TDO NPs3, TDO NPs5, and TDO NPs8 were spherical in shape, with average sizes of 5.14, 12.54, and 29.61 nm, respectively. The stability of TDO nanoparticles was assessed using thermogravimetric analysis and dynamic light scattering analysis. These samples could be used for degradation of polluting industrial textile dyes, such as methylene blue (MB) and rhodamine B (Rh-B). Remarkably, the TDO NPs3 sample (5.14 nm size) exhibits a noticeable degradation of the MB dye in a shorter time period (50 min) than the TDO NPs8 sample with a size of 29.61 nm (120 min). The TDO NPs3 sample was also tested for degradation of Rh-B dye, showing high degradation efficiency over a short period of time (60 min). In contrast, the TDO NPs8 sample showed degradation of the Rh-B dye in 120 min. The effect of the dye concentration and the catalyst dose to remove dye pollutants has also been investigated. The synthesized TDO NPs act as exceptional catalysts for the degradation of dyes, and they are promising materials for the degradation of industrial polluting dyes.

Effect of the Graphene- Ni/NiFe2O4 Composite on Bacterial Inhibition Mediated by Protein Degradation.

Recent investigations have demonstrated that nickel ferrite nanoparticles and their derivatives have toxicity effects on bacterial cells. In this study, we have prepared nickel ferrite nanoparticles (Ni/NiFe2O4) and nickel/nickel ferrite graphene oxide (Ni/NiFe2O4-GO) nanocomposite and evaluated their toxic effects on E. coli cells ATCC 25922. The prepared nanomaterials were characterized using X-ray diffraction, Raman spectroscopy, scanning electron microscopy, transmission electron microscopy, and vibrating sample magnetometry techniques. The toxicity was evaluated using variations in cell viability, cell morphology, protein degradation, and oxidative stress. Ni/NiFe2O4-GO nanocomposites likewise prompt oxidative stress proved by the age of reactive oxygen species (ROS) and exhaustion of antioxidant glutathione. This is the first report indicating that Ni/NiFe2O4-GO nanocomposite-initiated cell death in E. coli through ROS age and oxidative stress.

Pyroelectric Properties of BaxSr(1-x)TiO3/PVDF-TrFE Coating on Silicon.

Bilayer coatings of barium strontium titanate (BaxSr(1-x)TiO3)/poly [(vinylidenefluoride-co-trifluoroethylene] (PVDF-TrFE) were integrated on silicon Si (100) for pyroelectric devices. Pyroelectric properties of the composite were determined for different electrode materials (silver and aluminum) and different electrodes configurations creating an electric field in parallel and in-plane direction in the ferroelectric coating. For this purpose, parallel-plate and planar interdigital capacitors were fabricated. Anisotropy in the pyroelectric response was noted for the different directions of the measured electrical potential. The dynamic method was used to evaluate the pyroelectric properties in the temperature range of 22 to 48 °C. Pyroelectric response with a higher value was observed at the one plate's configuration of interdigital electrodes. The voltage response was the strongest when silver contacts were used. At temperatures near room temperature, the voltage increased by 182 µV at resolution of 7 µV/°C for the in-plain device configuration, vs. 290 µV at a resolution of 11 µV/°C for the out-of-plain configuration. A relationship between the surface morphology of the ferroelectric oxide and oxide/polymer coating and the pyroelectric voltage was also found, proving the smoothening effect of the introduction of polymer PVDF-TrFE over the BaSrTiO3 grains.

New Method for the Synthesis of 2D Vanadium Nitride (MXene) and Its Application as a Supercapacitor Electrode.

MXenes are the class of two-dimensional transition metal carbides and nitrides that exhibit unique properties and are used in a multitude of applications such as biosensors, water purification, electromagnetic interference shielding, electrocatalysis, supercapacitors, and so forth. Carbide-based MXenes are being widely explored, whereas investigations on nitride-based ones are seldom. Among the nitride-based MXenes obtained from their MAX phases, only Ti4N3 and Ti2N are reported so far. Herein, we report a novel synthesis of V2NT x (T x is the surface termination) obtained by the selective removal of "Al" from V2AlN by immersing powders of V2AlN in the LiF-HCl mixture (salt-acid etching) followed by sonication to obtain V2NT x (T x = -F, -O) MXene which is then delaminated using the dimethyl sulfoxide solvent. The V2NT x MXene is characterized by X-ray diffraction studies, field emission scanning electron microscope imaging, energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, and high-resolution transmission electron microscope imaging. Supercapacitor electrodes are prepared using V2NT x MXenes and their electrochemical performances are examined by cyclic voltammetry, galvanostatic charge/discharge measurement, and electrochemical impedance spectroscopy. The V2NT x MXene electrode exhibits a specific capacitance of 112.8 F/g at a current density of 1.85 mA/cm2 with an energy and power density of 15.66 W h/kg and 3748.4 W/kg, respectively, in 3.5 M KOH aqueous electrolyte. The electrode exhibits an excellent capacitance retention of 96% even after 10,000 charge/discharge cycles. An asymmetric supercapacitor fabricated with V2NT x as a negative electrode and Mn3O4 nanowalls as a positive electrode helps obtain a cell voltage of 1.8 V in aqueous KOH electrolyte.

Pt-free, low-cost and efficient counter electrode with carbon wrapped VO2(M) nanofiber for dye-sensitized solar cells.

The present study reports the use of one-dimensional carbon wrapped VO2(M) nanofiber (VO2(M)/C) as a cost-effective counter electrode for dye-sensitized solar cells (DSSCs); where M denotes monoclinic crystal system. Uniform short length nanofiber was synthesised by a sol-gel based simple and versatile electrospinning and post carbonization technique. The investigation of nanostructure and morphological analysis were performed by X-ray diffraction (XRD), field emission scanning electron microscope (FE-SEM), and transmission electron microscope (TEM) with EDAX. The electrochemical response was comprehensively characterized by cyclic voltammetry, electrochemical impedance spectroscopy and Tafel polarization. The electrochemical analysis of the VO2(M)/C nanofiber counter electrode exhibits significant electrocatalytic activity towards the reduction of triiodide and low charge transfer resistance at the electrode-electrolyte interface. The DSSCs fabricated with carbon-wrapped VO2(M) nanofiber CE showed high power conversion efficiency of 6.53% under standard test condition of simulated 1SUN illumination at AM1.5 G, which was comparable to the 7.39% observed for conventional thermally decomposed Pt CE based DSSC under same test conditions. This result encourages the next step of modification and use of low-cost VO2(M) as an alternate counter electrode for DSSCs to achieve a substantial efficiency for future energy demand.

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.

Natural biomass derived hard carbon and activated carbons as electrochemical supercapacitor electrodes.

With every moving day, the aspect that is going to be the most important for modern science and technology is the means to supply sufficient energy for all the scientific applications. As the resource of fossil fuel is draining out fast, an alternative is always required to satisfy the needs of the future world. Limited resources also force to innovate something that can utilise the resource more efficiently. This work is based on a simple synthesis route of biomass derived hard carbon and to exploring the possibility of using it as electrochemical supercapacitors. A cheap, eco-friendly and easily synthesized carbon material is utilized as electrode for electrochemical energy-storage. Four different hard carbons were synthesized from KOH activated banana stem (KHC), phosphoric acid treated banana stem derived carbons (PHC), corn-cob derived hard carbon (CHC) and potato starch derived hard carbons (SHC) and tested as supercapacitor electrodes. KOH-activated hard carbon has provided 479.23 F/g specific capacitance as calculated from its cycle voltammograms. A detailed analysis is done to correlate the results obtained with the material property. Overall, this work provides an in depth analysis of the science behind the components of an electrochemical energy-storage system as well as why the different characterization techniques are required to assess the quality and reliability of the material for electrochemical supercapacitor applications.

Photocatalytic degradation of toxic aquatic pollutants by novel magnetic 3D-TiO2@HPGA nanocomposite.

In this study, a series of photocatalysts were prepared, namely bare 3D-TiO2 (b-3D-T), magnetic 3D-TiO2: (m3D-T) and magnetic 3D-TiO2@Hierarchical Porous Graphene Aerogels (HPGA) nanocomposite: (m3D-T-HPGA NC) by solvothermal process. The prepared photocatalysts were analyzed by using X-ray diffraction (XRD), Field emission scanning electron microscope (FE-SEM), transmission electron microscope (TEM), Vibrating sample magnetometer (VSM), Brunauer-Emmett-Teller (BET) and Diffuse Reflectance Measurement - Ultraviolet (DRS-UV) to know their physical and chemical properties. The photocatalytic degradations of two toxic aquatic pollutants viz., Cr(VI) and bisphenol A (BPA) were tested by using the prepared photocatalysts. Parameters such as initial pollutant concentration, solution pH, photocatalyst dosage, wavelength and light intensity were investigated to optimize the process. The photocatalytic properties of prepared catalyst were analyzed based on the degradation of Cr(VI) and BPA under UV irradiation. The modified photocatalysts showed better performance as compared to b-3D-T photocatalyst. This better performance is ascribed to efficient charge transfer between b-3D-T nanoparticles to the porous graphene sheets. The maximum photocatalytic degradation of Cr(VI) was found to be 100% with m3D-T-HPGA NC within 140 min, whereas a removal efficacy of 100% and 57% was noticed in case of m3D-T and b-3D-T within 200 and 240 min, respectively. In the case of BPA, the maximum degradation efficiency was found to be 90% with m3D-T-HPGA NC within 240 min.

Enhanced wound healing activity of Ag-ZnO composite NPs in Wistar Albino rats.

In the present study, silver (Ag) and Ag-zinc oxide (ZnO) composite nanoparticles (NPs) were synthesised and studied their wound-healing efficacy on rat model. Ultraviolet-visible spectroscopy of AgNPs displayed an intense surface plasmon (SP) resonance absorption at 450 nm. After the addition of aqueous Zn acetate solution, SP resonance band has shown at 413.2 nm indicating a distinct blue shift of about 37 nm. X-ray diffraction analysis Ag-ZnO composite NPs displayed existence of two mixed sets of diffraction peaks, i.e. both Ag and ZnO, whereas AgNPs exhibited face-centred cubic structures of metallic Ag. Scanning electron microscope (EM) and transmission EM analyses of Ag-ZnO composite NPs revealed the morphology to be monodispersed hexagonal and quasi-hexagonal NPs with distribution of particle size of 20-40 nm. Furthermore, the authors investigated the wound-healing properties of Ag-ZnO composite NPs in an animal model and found that rapid healing within 10 days when compared with pure AgNPs and standard drug dermazin.

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.

Green synthesis of silver nanoparticles using methanolic root extracts of Diospyros paniculata and their antimicrobial activities.

Since the discovery and subsequent widespread use of antibiotics, a variety of bacterial species of human and animal origin have developed numerous mechanisms that render bacteria resistant to some, and in certain cases to nearly all antibiotics, thereby limiting the treatment options and compromising effective therapy. In the present study, the green synthesis of nanoparticles is carried out by the reduction of silver acetate in the presence of crude methanolic root extracts of Diospyros paniculata, a member of family Ebenaceae. The UV-Vis absorption spectrum of the biologically reduced reaction mixture showed the surface plasmon peak at 428 nm, a characteristic peak of silver nanoparticles. X-ray diffraction (XRD) analysis confirmed the face-centered cubic crystalline structure of metallic silver. The average diameter of Ag NPs is about 17 nm from Transmission Electron Microscopy (TEM) which is in good agreement with the average crystallite size (19 nm) calculated from XRD analysis. Further the study has been extended to the antimicrobial activity against test pathogenic Gram (+), Gram (-) bacterial and fungal strains. The biologically synthesized silver nanoparticles showed promising activity against all the tested pathogenic strains and the activity has been enhanced with the increased dose levels.

The Scanning TMR Microscope for Biosensor Applications.

We present a novel tunnel magnetoresistance (TMR) scanning microscope set-up capable of quantitatively imaging the magnetic stray field patterns of micron-sized elements in 3D. By incorporating an Anderson loop measurement circuit for impedance matching, we are able to detect magnetoresistance changes of as little as 0.006%/Oe. By 3D rastering a mounted TMR sensor over our magnetic barcodes, we are able to characterize the complex domain structures by displaying the real component, the amplitude and the phase of the sensor's impedance. The modular design, incorporating a TMR sensor with an optical microscope, renders this set-up a versatile platform for studying and imaging immobilised magnetic carriers and barcodes currently employed in biosensor platforms, magnetotactic bacteria and other complex magnetic domain structures of micron-sized entities. The quantitative nature of the instrument and its ability to produce vector maps of magnetic stray fields has the potential to provide significant advantages over other commonly used scanning magnetometry techniques.