Ibrahim Khan

Sonochemical assisted hydrothermal synthesis of pseudo-flower shaped Bismuth vanadate (BiVO4) and their solar-driven water splitting application

Bismuth vanadate (BiVO4) is a well-known photocatalyst due to its lower bandgap (Eg) and visible electromagnetic light absorption capacity. Herein, we reported the pulse ultra-sonochemical assisted hydrothermal approach to synthesize S-BiVO4. For the comparison purpose, H-BiVO4 is also synthesized via conventional hydrothermal approach. The surface morphology of S-BiVO4 through scanning electron microscope (SEM) indicates condensed microarrays (MAs) having pseudo-flower shapes. The energy dispersive X-rays (EDX) spectrum also confirmed the elemental percent composition of Bi, V and O in BiVO4. X-rays diffraction (XRD) pattern further confirmed the monoclinic scheelite phase of S-BiVO4. Fourier transformed infrared (FTIR) spectrum showed Bi-O and Bi-V-O vibrational bands at 1382 and 1630cm-1, respectively. The diffuse reflectance spectroscopy (DRS) indicated absorption edge at ∼515nm, corresponds to bandgap value (Eg) of 2.41eV, which is suitable range for water splitting applications. The photocurrent density from water splitting under artificial 1 SUN visible light source found at 60 and 50μA/cm2 for S-BiVO4 and H-BiVO4, respectively. The stability test through chronoamperometry showed that S-BiVO4 was more stable than H-BiVO4. It can be depicted from the growth mechanism that ultrasonication played a definite role in the overall synthesis of pseudo-flower shaped S-BiVO4 MAs.

Sonochemical-driven ultrafast facile synthesis of SnO2 nanoparticles: Growth mechanism structural electrical and hydrogen gas sensing properties

Synthesis of SnO2 nanoparticles have been successfully accomplished moderately at lower temperature by facile, rapid, efficient and mild ultrasonic irradiation method. The as-grown SnO2 nanoparticles are investigated by various characterization techniques in terms of structural, optical, electrical and gas sensing properties. XRD investigation has shown that the SnO2 nanoparticles materials exhibit single rutile crystal phase with high crystallinity. FESEM studies showed uniform and monodisperse morphology of SnO2 nanoparticles. The chemical composition of SnO2 was systematically studied by EDX measurements. Additional confirmation of three Raman shifts (432, 630, 772cm-1) indicated the characteristic properties of the rutile phase of the as-grown SnO2 nanoparticles. The optical properties of SnO2 nanoparticles were examined by DRS, and the electronic band gap of SnO2 nanoparticles were around 3.6eV. Electrical properties of the SnO2 nanoparticles measured at various temperatures have shown the semiconducting properties. Surface area and pore size of synthesized nanoparticles were analyzed from BET. It has been revealed that SnO2 nanoparticles have surface area is 47.8574m2/g and the pore size is 10.5nm. Moreover, hydrogen gas sensor made of SnO2 nanoparticles showed good sensitivity and faster response for the hydrogen gas. This method is template-less and surfactant-free which circumvents rigorous reaction work-up for the former removal, reaction temperature and reaction time compared to hydrothermal synthesis and pertinent to many other oxide materials.

Sonochemical Assisted Solvothermal Synthesis of Gallium Oxynitride Nanosheets and their Solar-Driven Photoelectrochemical Water-Splitting Applications.

Gallium oxynitride (GaON) nanosheets for photoelectrochemical (PEC) analysis are synthesized via direct solvothermal approach. Their FE-SEM revealed nanosheets morphology of GaON prepared at a reaction time of 24 hours at 180 °C. The elemental composition and mapping of Ga, O and N are carried out through electron dispersive X-ray spectroscopy (EDX). The cubic structure of GaON nanosheets is elucidated by X-ray diffraction (XRD)analysis. The X-ray Photoelectron Spectroscopy (XPS) further confirms Ga, O and N in their respective ratios and states. The optical properties of GaON nanosheets are evaluated via UV-Visible, Photoluminescence (PL) and Raman spectroscopy’s. The band gap energy of ~1.9 eV is calculated from both absorption and diffused reflectance spectroscopy’s which showed stronger p-d repulsions in the Ga (3d) and N (2p) orbitals. This effect and chemical nitridation caused upward shift of valence band and band gap reduction. The GaON nanosheets are investigated for PEC studies in a standard three electrode system under 1 Sun irradiation in 0.5 M Na2SO4. The photocurrent generation, oxidation and reduction reactions during the measurements are observed by Chronoampereometry, linear sweep Voltametry (LSV) and Cyclic Voltametry (CV) respectively. Henceforward, these GaON nanosheets can be used as potential photocatalyts for solar water splitting.

Sonochemical assisted synthesis of RGO/ZnO nanowire arrays for photoelectrochemical water splitting

This article presented the synthesis of a hybrid nanoarchitecture material composed of reduced graphene oxide (RGO) multiple sheets and ZnO nanowire arrays (NWAs) formed on an arbitrary ZnO coated fluorine doped tin oxide (FTO) substrates via pulse sonication and hydrothermal approach. The NWAs have high aspect-ratio, high density, apt positioning and well-ordered formation. FESEM images demonstrated that RGO layers have been effectively intercalated between and on the accessible surfaces of the ZnO NWAs. The diameter of ZnO nanowires is 80-150nm and length about 1-2μm. Raman spectrum of hybrid material exhibited characteristic D and suppressed G peaks for graphene and E2 mode at 437cm-1 for ZnO NWAs. UV-visible spectrum indicated slight red shift towards visible range after formation of RGO/ZnO NWAs heterostructure. The Photoelectrochemical results indicated higher current densities for RGO/ZnO NWAs heterostructure due to water oxidation reaction at the working electrode compared to pristine ZnO NWAs.

Shape Controlled Synthesis of Copper Vanadate Platelet Nanostructures, Their Optical Band Edges, and Solar-Driven Water Splitting Properties

We report the morphological and size tailored rational and facile synthesis of copper vanadate nanostructures via sonication assisted sol gel method. Field emission scanning electron microscopy (FESEM), indicated irregular and nanoflakes morphologies for the as synthesized copper vanadate (CV-120) and copper vanadate calcined at 250 °C (CV-250). The semispherical platelets shaped morphology revealed for the copper vanadate calcined at 550 °C (CV-500). The XRD patterns confirm the monoclinic and triclinic crystal phases for CV-250 and CV-500, respectively. The optical properties of CV-250 and CV-500 via UV-DRS showed significant absorption in the visible regime at λ = 565 nm and 670 nm with band gap 2.2 eV and 1.84 eV, respectively as calculated from Kubelka-Munk (KM) equation via Tauc’s plot. The values of band edge positions of CV-250 and CV-550 straddle with the hydrogen (HER) and oxygen evolution reaction (OER) potentials. The photoelectrodes of CV-250 and CV-500 fabricated by adsorption desorption method to test their photoelectrochemical (PEC) water splitting performance in the three-electrode cell. The onset photocurrent potential is observed at ~0.42 V, which reached to saturation at 1.05 V. The photocurrent density at saturation is ~0.65 mA/cm2 for CV-250 and CV-500, respectively.