Synergism of Holmium Orthovanadate/Phosphorus-Doped Carbon Nitride Nanocomposite: Nonenzymatic Electrochemical Detection of Hydrogen Peroxide.

Developing efficient and robust electrode materials for electrochemical sensors is critical for real-time analysis. In this paper, a hierarchical holmium vanadate/phosphorus-doped graphitic carbon nitride (HoVO4/P-CN) nanocomposite is synthesized and used as an electrode material for electrochemical detection of hydrogen peroxide (H2O2). The HoVO4/P-CN nanocomposite exhibits superior electrocatalytic activity at a peak potential of -0.412 V toward H2O2 reduction in alkaline electrolytes while compared with other reported electrocatalysts. The HoVO4/P-CN electrochemical platform operated under the optimized conditions shows excellent analytical performance for H2O2 detection with a linear concentration range of 0.009-77.4 µM, a high sensitivity of 0.72 µA µM-1 cm-2, and a low detection limit of 3.0 nΜ. Furthermore, the HoVO4/P-CN-modified electrode exhibits high selectivity, remarkable stability, good repeatability, and satisfactory reproducibility in detecting H2O2. Its superior performance can be attributed to a large specific surface area, high conductivity, more active surface sites, unique structure, and synergistic action of HoVO4 and P-CN to benefit enhanced electrochemical activity. The proposed HoVO4/P-CN electrochemical platform is effectively applied to ascertain the quantity of H2O2 in food and biological samples. This work outlines a promising and effectual strategy for the sensitive electrochemical detection of H2O2 in real-world samples.

Influence of Fe Doping on the Electrochemical Performance of a ZnO-Nanostructure-Based Electrode for Supercapacitors.

ZnO is a potential candidate for providing an economic and environmentally friendly substitute for energy storage materials. Therefore, in this work, Fe-doped ZnO nanostructures prepared using the microwave irradiation procedure were investigated for structural, morphological, magnetic, electronic structural, specific surface area and electrochemical properties to be used as electrodes for supercapacitors. The X-ray diffraction, high-resolution transmission electron microscopy images, and selective-area electron diffraction pattern indicated that the nanocrystalline structures of Fe-doped ZnO were found to possess a hexagonal wurtzite structure. The effect of Fe doping in the ZnO matrix was observed on the lattice parameters, which were found to increase with the dopant concentration. Rods and a nanosheet-like morphology were observed via FESEM images. The ferromagnetic nature of samples is associated with the presence of bound magnetic polarons. The enhancement of saturation magnetization was observed due to Fe doping up to 3% in correspondence with the increase in the number of bound magnetic polarons with an Fe content of up to 3%. This behavior is observed as a result of the change in the oxidation state from +2 to +3, which was a consequence of Fe doping ranging from 3% to 5%. The electrode performance of Fe-doped ZnO nanostructures was studied using electrochemical measurements. The cyclic voltammetry (CV) results inferred that the specific capacitance increased with Fe doping and displayed a high specific capacitance of 286 F·g-1 at 10 mV/s for 3% Fe-doped ZnO nanostructures and decreased beyond that. Furthermore, the stability of the Zn0.97Fe0.03O electrode, which was examined by performing 2000 cycles, showed excellent cyclic stability (85.0% of value retained up to 2000 cycles) with the highest specific capacitance of 276.4 F·g-1, signifying its appropriateness as an electrode for energy storage applications.

Improvement of Supercapacitor Performance of In Situ Doped Laser-Induced Multilayer Graphene via NiO.

Herein, we have reported a novel strategy for improving the electrochemical performance of laser-induced graphene (LIG) supercapacitors (SCs). The LIG was prepared using a CO2 laser system. The polyimide polymer was the source material for the fabrication of the LIG. The doping process was performed in situ using the CO2 laser, which works as a rapid thermal treatment to combine graphene and NiO particles. NiO was used to improve the capacitance of graphene by combining an electric double-layer capacitor (EDLC) with the pseudo-capacitance effect. The high-resolution transmission electron microscopy, energy-dispersive X-ray spectroscopy, and Raman spectroscopy showed that the structure of the LIG is multilayered and waved. The HRTEM image proves the distribution of NiO fine particles with sizes of 5-10 nm into the graphene layers. The electrochemical performance of the as-prepared LIG was tested. The effect of the combination of the two materials (oxide and carbon) was investigated at different concentrations. The LIG showed a specific capacitance of 69 Fg-1, which increased up to 174 Fg-1 for the NiO-doped LIG. The stability investigations showed that the electrodes were very stable for more than 1000 cycles. This current study establishes an innovative method to improve the electrochemical properties of LIG.

Investigations of Structural, Magnetic, and Electrochemical Properties of NiFe2O4 Nanoparticles as Electrode Materials for Supercapacitor Applications.

Magnetic nanoparticles of NiFe2O4 were successfully prepared by utilizing the sol-gel techniques. The prepared samples were investigated through various techniques such as X-ray diffraction (XRD), transmission electron microscopy (TEM), dielectric spectroscopy, DC magnetization and electrochemical measurements. XRD data analysed using Rietveld refinement procedure inferred that NiFe2O4 nanoparticles displayed a single-phase nature with face-centred cubic crystallinity with space group Fd-3m. Average crystallite size estimated using the XRD patterns was observed to be ~10 nm. The ring pattern observed in the selected area electron diffraction pattern (SAED) also confirmed the single-phase formation in NiFe2O4 nanoparticles. TEM micrographs confirmed the uniformly distributed nanoparticles with spherical shape and an average particle size of 9.7 nm. Raman spectroscopy showed characteristic bands corresponding to NiFe2O4 with a shift of the A1g mode, which may be due to possible development of oxygen vacancies. Dielectric constant, measured at different temperatures, increased with temperature and decreased with increase in frequency at all temperatures. The Havrilliak-Negami model used to study the dielectric spectroscopy indicated that a NiFe2O4 nanoparticles display non-Debye type relaxation. Jonscher's power law was utilized for the calculation of the exponent and DC conductivity. The exponent values clearly demonstrated the non-ohmic behaviour of NiFe2O4 nanoparticles. The dielectric constant of the nanoparticles was found to be >300, showing a normal dispersive behaviour. AC conductivity showed an increase with the rise in temperature with the highest value of 3.4 × 10-9 S/cm at 323 K. The M-H curves revealed the ferromagnetic behaviour of a NiFe2O4 nanoparticle. The ZFC and FC studies suggested a blocking temperature of ~64 K. The saturation of magnetization determined using the law of approach to saturation was ~61.4 emu/g at 10 K, corresponding to the magnetic anisotropy ~2.9 × 104 erg/cm3. Electrochemical studies showed that a specific capacitance of ~600 F g-1 was observed from the cyclic voltammetry and galvanostatic charge-discharge, which suggested its utilization as a potential electrode for supercapacitor applications.

Fabrication of High-Performance Asymmetric Supercapacitors Using Rice Husk-Activated Carbon and MnFe2O4 Nanostructures.

To meet the growing demand for efficient and sustainable power sources, it is crucial to develop high-performance energy storage systems. Additionally, they should be cost-effective and able to operate without any detrimental environmental side effects. In this study, rice husk-activated carbon (RHAC), which is known for its abundance, low cost, and excellent electrochemical performance, was combined with MnFe2O4 nanostructures to improve the overall capacitance of asymmetric supercapacitors (ASCs) and their energy density. A series of activation and carbonization steps are involved in the fabrication process for RHAC from rice husk. Furthermore, the BET surface area for RHAC was determined to be 980 m2 g-1 and superior porosities (average pore diameter of 7.2 nm) provide abundant active sites for charge storage. Additionally, MnFe2O4 nanostructures were effective pseudocapacitive electrode materials due to their combined Faradic and non-Faradic capacitances. In order to assess the electrochemical performance of ASCs extensively, several characterization techniques were employed, including galvanostatic charge -discharge, cyclic voltammetry, and electrochemical impedance spectroscopy. Comparatively, the ASC demonstrated a maximum specific capacitance of ~420 F/g at a current density of 0.5 A/g. The as-fabricated ASC possesses remarkable electrochemical characteristics, including high specific capacitance, superior rate capability, and long-term cycle stability. The developed asymmetric configuration retained 98% of its capacitance even after 12,000 cycles performed at a current density of 6A/g, demonstrating its stability and reliability for supercapacitors. The present study demonstrates the potential of synergistic combinations of RHAC and MnFe2O4 nanostructures in improving supercapacitor performance, as well as providing a sustainable method of using agricultural waste for energy storage.

Structural, Optical, Magnetic and Electrochemical Properties of CeXO2 (X: Fe, and Mn) Nanoparticles.

CeXO2 (X: Fe, Mn) nanoparticles, synthesized using the coprecipitation route, were investigated for their structural, morphological, magnetic, and electrochemical properties using X-ray diffraction (XRD), field emission transmission electron microscopy (FE-TEM), dc magnetization, and cyclic voltammetry methods. The single-phase formation of CeO2 nanoparticles with FCC fluorite structure was confirmed by the Rietveld refinement, indicating the successful incorporation of Fe and Mn in the CeO2 matrix with the reduced dimensions and band gap values. The Raman analysis supported the lowest band gap of Fe-doped CeO2 on account of oxygen non-stoichiometry. The samples exhibited weak room temperature ferromagnetism, which was found to be enhanced in the Fe doped CeO2. The NEXAFS analysis supported the results by revealing the oxidation state of Fe to be Fe2+/Fe3+ in Fe-doped CeO2 nanoparticles. Further, the room temperature electrochemical performance of CeXO2 (X: Fe, Mn) nanoparticles was measured with a scan rate of 10 mV s-1 using 1 M KCL electrolyte, which showed that the Ce0.95Fe0.05O2 electrode revealed excellent performance with a specific capacitance of 945 FÖ¼·g-1 for the application in energy storage devices.

Structural growth of zinc oxide nanograins on carbon cloth as flexible electrochemical platform for hydroxychloroquine detection.

Pharmaceutical pollution that imposes a health threat worldwide is making accurate and rapid detection crucial to prevent adverse effects. Herein, binder-free zinc oxide nanograins on carbon cloth (ZnO NGs@CC) have been synthesized hydrothermally and employed to fabricate a flexible electrochemical sensor for the quantification of hydroxychloroquine (HCQ) that is typical pharmaceutical pollution. The characteristics of ZnO NGs@CC were investigated by various in-depth electron microscopic, spectroscopic and electroanalytical approaches. Compared with the pristine CC platform, the ZnO NGs@CC platform exhibits superior electrochemical performance in detecting HCQ with a large oxidation current at a low over-potential of +0.92 V with respect to the Ag/AgCl (Sat. KCl) reference electrode. With the support of desirable characteristics, the fabricated ZnO NGs@CC-based electrochemical sensor for HCQ detection displays good performances in terms of wide sensing range (0.5-116 µM), low detection limit (0.09 µM), high sensitivity (0.279 µA µM-1 cm-2), and strong selectivity. By the resulting 3D hierarchical nanoarchitecture, ZnO NGs@CC has progressive structural advantages that led to its excellent electrochemical performance in sensing applications. Furthermore, the electrochemical sensor is employed to detect HCQ in biological and environmental samples and also achieves good recovery rates. Thus, the designed ZnO NGs@CC demonstrates admirable electrochemical activity toward HCQ real-time monitoring and would be an excellent electrochemical platform for HCQ sensing.

Structural, Magnetic, and Electrical Properties of CoFe2O4 Nanostructures Synthesized Using Microwave-Assisted Hydrothermal Method.

Magnetic nanostructures of CoFe2O4 were synthesized via a microwave-assisted hydrothermal route. The prepared nanostructures were investigated using X-ray diffraction (XRD), field emission electron microscopy (FE-SEM), energy dispersive X-ray (EDX) spectroscopy, high-resolution transmission electron microscopy (HR-TEM), selective area electron diffraction (SAED) pattern, DC magnetization, and dielectric spectroscopy measurements. The crystal structure studied using HR-TEM, SAED, and XRD patterns revealed that the synthesized nanostructures had a single-phase nature and ruled out the possibility of any secondary phase. The lattice parameters and unit cell volume determined from the XRD data were found to be 8.4821 Å and 583.88 Å3. The average crystallite size (~7.0 nm) was determined using Scherrer's equation. The FE-SEM and TEM micrographs revealed that the prepared nanostructures had a spherical shape morphology. The EDX results showed that the major elements present in the samples were Co, Fe, and O. The magnetization (M) versus temperature (T) measurements specified that the CoFe2O4 nanostructures showed ferromagnetic ordering at room temperature. The blocking temperature (TB) determined using the M-T curve was found to be 315 K. The magnetic hysteresis (M-H) loop of the CoFe2O4 nanostructures recorded at different temperatures showed the ferromagnetic behavior of the CoFe2O4 nanostructures at temperatures of 200 K and 300 K, and a superparamagnetic behavior at 350 K. The dielectric spectroscopy studies revealed a dielectric constant (ε') and loss tangent (tanδ) decrease with the increase in the frequency, as well as demonstrating a normal dispersion behavior, which is due to the Maxwell-Wagner type of interfacial polarization. The values of ε' and tanδ were observed to increase with the increase in the temperature.

Structural, Morphological, Optical and Magnetic Studies of Cu-Doped ZnO Nanostructures.

In the present work, Cu-doped ZnO nanostructures (Cu% = 0, 1, 5) have been prepared using microwave-assisted chemical route synthesis. The synthesized nanostructures were investigated through structural, morphological, optical, and magnetic characterizations. The results of the X-ray diffraction (XRD), high resolution transmission electron microscopy (HR-TEM), and selective area electron diffraction (SAED) patterns confirmed that all of the samples exhibit the single-phase polycrystalline hexagonal crystal structure. The XRD results infer a decrease in the lattice parameters (a/c) by increasing the Cu% doping into ZnO. The field emission scanning electron microscopy (FE-SEM) and energy dispersive x-ray (EDX) spectroscopic measurements revealed the formation of nanostructures, showing the major elemental presence of Zn and O in the samples. The photoluminescence (PL) spectra exhibited photoemission in the UV and blue-green regions. With the increase in the Cu%, the photoemission in the UV region is reduced, while it is enhanced in the blue-green region. Raman spectra of the Cu-doped ZnO nanostructures displayed a blue shift of the E2High mode and an increase in the peak intensity of E1(LO), indicating the doping of Cu ion in the ZnO lattice. The dc magnetization measurements demonstrated the ferromagnetic behavior of all of the samples with an enhanced ferromagnetic character with increasing Cu%.

Zinc Oxide/Phosphorus-Doped Carbon Nitride Composite as Potential Scaffold for Electrochemical Detection of Nitrofurantoin.

Herein, we present an electrocatalyst constructed by zinc oxide hexagonal prisms/phosphorus-doped carbon nitride wrinkles (ZnO HPs/P-CN) prepared via a facile sonochemical method towards the detection of nitrofurantoin (NF). The ZnO HPs/P-CN-sensing platform showed amplified response and low-peak potential compared with other electrodes. The exceptional electrochemical performance could be credited to ideal architecture, rapid electron/charge transfer, good conductivity, and abundant active sites in the ZnO HPs/P-CN composite. Resulting from these merits, the ZnO HPs/P-CN-modified electrode delivered rapid response (2 s), a low detection limit (2 nM), good linear range (0.01-111 µM), high sensitivity (4.62 µA µM-1 cm2), better selectivity, decent stability (±97.6%), and reproducibility towards electrochemical detection of NF. We further demonstrated the feasibility of the proposed ZnO HPs/P-CN sensor for detecting NF in samples of water and human urine. All the above features make our proposed ZnO HPs/P-CN sensor a most promising probe for detecting NF in natural samples.

Role of Cr Doping on the Structure, Electronic Structure, and Electrochemical Properties of BiFeO3 Nanoparticles.

BiFe1−xCrxO3, (0 ≤ x ≤ 10) nanoparticles were prepared through the sol−gel technique. The synthesized nanoparticles were characterized using various techniques, viz., X-ray diffraction, high-resolution field emission scanning electron microscopy (HRFESEM), energy dispersive spectroscopy (EDS), UV−Vis absorption spectroscopy, photoluminescence (PL), dc magnetization, near-edge X-ray absorption spectroscopy (NEXAFS) and cyclic voltammetry (CV) measurements, to investigate the structural, morphological, optical, magnetic and electrochemical properties. The structural analysis showed the formation of BiFeO3 with rhombohedral (R3c) as the primary phase and Bi25FeO39 as the secondary phase. The secondary phase percentage was found to reduce with increasing Cr content, along with reductions in crystallite sizes, lattice parameters and enhancement in strain. Nearly spherical shape morphology was observed via HRFESEM with Bi, Fe, Cr and O as the major contributing elements. The bandgap reduced from 1.91 to 1.74 eV with the increase in Cr concentration, and PL spectra revealed emissions in violet, blue and green regions. The investigation of magnetic field (H)-dependent magnetization (M) indicated a significant effect of Cr substitution on the magnetic properties of the nanoparticles. The ferromagnetic character of the samples was found to increase with the increase in the Cr concentration and the increase in the saturation magnetization. The Fe (+3/+4) was dissolved in mixed-valence states, as found through NEXAFS analysis. Electrochemical studies showed that 5%-Cr-doped BFO electrode demonstrated outstanding performance for supercapacitors through a specific capacitance of 421 F g−1 measured with a scan rate of 10 mV s−1. It also demonstrated remarkable cyclic stability through capacitance retention of >78% for 2000 cycles.

Influence of Fe and Cu Co-Doping on Structural, Magnetic and Electrochemical Properties of CeO2 Nanoparticles.

The nanoparticles of CeO2, Ce0.98Fe0.02O2, and Ce0.78Fe0.02Cu0.20O2 were synthesized using the co-precipitation-synthesis technique. The effect of co-doping of Fe and Cu on structural, optical, and magnetic properties as well as specific capacitance have been studied using X-ray diffraction (XRD), scanning-electron microscopy (SEM), UV-visible spectroscopy, Raman spectroscopy, dc magnetization, and electrochemical measurements at room temperature. The results of the XRD analysis infer that all the samples have a single-phase nature and exclude the formation of any extra phase. Particle size has been found to reduce as a result of doping and co-doping. The smallest particle size was obtained to be 5.59 nm for Ce0.78Fe0.02Cu0.20O2. The particles show a spherical-shape morphology. Raman active modes, corresponding to CeO2, were observed in the Raman spectra, with noticeable shifting with doping and co-doping indicating the presence of defect states. The bandgap, calculated using UV-Vis spectroscopy, showed relatively low bandgap energy (1.7 eV). The dc magnetization results indicate the enhancement of the magnetic moment in the samples, with doping and co-doping. The highest value of saturation magnetization (1.3 × 10-2 emu/g) has been found for Ce0.78Fe0.02Cu0.20O2 nanoparticles. The electrochemical behavior studied using cyclic-voltammetry (CV) measurements showed that the Ce0.98Fe0.02O2 electrode exhibits superior-specific capacitance (~532 F g-1) along with capacitance retention of ~94% for 1000 cycles.

Binder-Free Electrode Based on ZnO Nanorods Directly Grown on Aluminum Substrate for High Performance Supercapacitors.

Herein, for the first time, the growth of ZnO nanorods directly on aluminum (Al) substrate via a low temperature (80 °C) wet chemical method, and used as binder-free electrode for supercapacitors were reported. XRD pattern and HRTEM images showed that high crystalline nanorods grown on Al substrate with c-axis orientation. Morphological studies revealed that the nanorods possessed well defined hexagon phase with length and diameter of ~2 µm and 100-180 nm, respectively. Raman spectrum of ZnO nanorods showed that the characteristic E2H mode corresponds to the vibration associated with the oxygen atoms of ZnO. The optical properties of ZnO nanorods studied using Room-temperature PL spectra revealed a near-band-edge (NBE) peak at ~388 nm emission and deep level (DLE) at ~507 nm. Electrochemical measurements showed that ZnO nanorods on Al substrate exhibited remarkably enhanced performance as electrode for supercapacitors with a value of specific capacitance of 394 F g-1 measured with scan rate of 20 mV s-1. This unique nanorods structures also exhibited excellent stability of >98% capacitance retention for 1000 cycles that were measured at 1A g-1. The presented easy and cost-effective method might open up the possibility for the mass production of binder-free electrodes for efficient electrochemical energy storage devices.

Low temperature growth of ZnO nanotubes for fluorescence quenching detection of DNA.

In this work, large-scale and single-crystalline ZnO nanotubes were fabricated by a simple technique from an aqueous solution at a low temperature of 65 °C. According to detailed morphology, structural and compositional analyses showed that the ZnO nanotubes [diameter ~200 nm (wall thickness ~50 nm); length ~1 µm] have single-crystallite with wurtzite structure. As-prepared ZnO nanotubes showed an effective fluorescence quenching for the detection of calf thymus DNA. In particular, increasing DNA concentrations (5-50 µM) into the fixed concentration of ZnO nanotubes (50 µM) progressively quenched the intrinsic fluorescence of nanotubes, which showed that the nanotubes fluorescence was efficiently quenched upon binding to DNA. At the highest ZnO-DNA molar ratios of 1:1.8, around 50.1 % of fluorescence quenching of DNA was observed. Significance of this study provides simple, cost-effective, and low temperature synthesis of ZnO nanotubes revealed better fluorescence property toward a platform of DNA sensor. ZnO nanotubes with diameter of ~200 nm (wall thickness ~50 nm) and length of about 1 µm prepared at low temperature (65 °C) showed fluorescence was efficiently quenched upon binding to DNA. In particular, around 50.1 % of DNA fluorescence quenching at the highest ZnO-DNA molar ratios of 1:1.8 was observed.

Novel Biomimatic Synthesis of ZnO Nanorods Using Egg White (Albumen) and Their Antibacterial Studies.

Zinc oxide (ZnO) is well-recognized as a biocompatible multifunctional material with outstanding properties as well as low toxicity and biodegradability. In this work, a simple and versatile technique was developed to prepare highly crystalline ZnO nanorods by introducing egg white to a bio-inspired approach. X-ray diffraction (XRD) and selected area electron diffraction (SAED) pattern results indicated that the ZnO nanorods have single phase nature with the wurtzite structure. Field emission scanning electron microscopy (FESEM) and Transmission electron microscopy (TEM) results showed the nanometer dimension of the nanorods. Raman, FTIR, and TGA/DTA analyses revealed the formation of wurtzite ZnO. The antibacterial properties of ZnO nanorods were investigated using both Gram-positive and Gram-negative microorganisms. These studies demonstrate that ZnO nanorods have a wide range of antibacterial activities toward various microorganisms that are commonly found in environmental settings. Survival ratio of bacteria decreased with increasing powder concentration, i.e., increase in antibacterial activity. The antibacterial activity of the ZnO nanorods toward Pseudomonas aeruginosa was stronger than that of Escherichia coli and Staphylococcus aureus. Surprisingly, the antibacterial activity did not require specific UV activation using artificial lamps, rather activation was achieved under ambient lighting conditions. Overall, the experimental results suggest that ZnO nanorods could be developed as antibacterial agents against a wide range of microorganisms to control and prevent the spreading and persistence of bacterial infections. This research introduces a new concept to synthesize ZnO nanorods by using egg white as a biological template for various applications including food science, animal science, biochemistry, microbiology and medicine.

Relationship Between Structural, Morphological, Optical and Magnetic Properties of Transition Metal (TM)-Doped ZnO Nanostructures Prepared by Microwave-Hydrothermal.

In this work, pure and 3% TM (Co, Ni, and Cu)-doped ZnO nanostructures were prepared by microwave-hydrothermal method. The striking similarities between changes in the lattice volume, bandgap energy, morphology and saturation magnetization indicated a strong correlation between these properties. XRD, SAED and HRTEM analyses revealed that all the TM-doped ZnO nano-structures have wurtzite structure and no secondary phase was detected. FESEM and TEM results confirmed a higher aspect ratio and highly crystalline nature of nanostructures. Raman spectra revealed that no defect related mode was observed which indicated that the nanostructures have high quality and negligible defects. The value of bandgap was found to decrease with the increase in atomic number of TM dopants. RTFM was observed in all the TM-doped ZnO nanostructures and the value of Ms and Mr were decreased with TM dopants.

Doping dependent properties of Cr-doped ZnO nanostructures prepared by microwave irradiation.

In this work, undoped and Cr-doped single-crystalline ZnO nanorods were prepared by a facile microwave assisted solution method. X-ray diffraction (XRD) and transmission electron microscopy (TEM) results showed that Cr-doped ZnO was comprised of single phase nature with hexagonal wurtzite structure up to 5% Cr doping, however, secondary phase ZnCr2O4 appeared upon further increasing the Cr dopant concentration. Field emission scanning electron microscopy (FESEM) and TEM micrographs suggested that the undoped nanorods with an average length of -~2 µm and a diameter in the range of 150-200 nm, respectively were observed. Interestingly, the size of nanorods decreased with the increase of Cr concentration in ZnO. Optical studies depicted that the energy bandgap was decreased with the increase of Cr concentration. Raman scattering spectra of Cr-doped ZnO revealed the lower frequency shift of E2(high) phonon mode with the increase in concentration of Cr dopant, suggested the successful doping of Cr into Zn site in ZnO. Magnetic studies showed that Cr-doped ZnO exhibited room temperature ferromagnetism (RTFM) and the value of magnetization was continuously decreased with the increase in Cr doping.

Magnetic, optical and structural property studies of Mn-doped ZnO nanosheets.

We report the synthesis of pure and Mn doped ZnO in the form of nanosheets using a simple and single step procedure involving a microwave assisted chemical method. As prepared Mn-doped ZnO nanosheets were characterized using X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), ultra violet-visible (UV-Vis), Raman spectroscopy and magnetization measurements. The structural studies using XRD and TEM revealed the absence of Mn-related secondary phases and showed that Mn-doped ZnO comprise a single phase nature with wurtzite structure. FESEM and TEM micrographs show that the average diameter of Mn-ZnO assembled nanosheets is about approximately 50 nm, and the length of a Mn-doped ZnO nanosheet building block which is made up of thin mutilayered sheets is around approximately 300 nm. Concerning the Raman scattering spectra, the shift in peak position of E2 (high) mode toward low frequencies due to the Mn doping could be explained well by means of the spatial correlation model. Magnetic measurements showed that Mn-doped ZnO nanosheets exhibit ferromagnetic ordering at or above room temperature.

Structural and magnetic properties of Zn1-xcoxO nanorods prepared by microwave irradiation technique.

We have successfully synthesized large-scale aggregative flowerlike Zn1-xCo(x)O (0.0 < or = x < or = 0.07) nanostructures, consisting of many branches of nanorods at different orientations with diameter within 100-150 nm (tip diameter approximately 50 nm) and length of approximately 1 microm. The rods were prepared using Zinc nitrate, cobalt nitrate and KOH in 180 Watt microwave radiation for short time interval. The synthesized nanorods were characterized using X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), field emission transmission electron microscopy (FETEM) and DC magnetization measurements. XRD and TEM results indicate that the novel flowerlike nanostructures are hexagonal with wurtzite structure and Co ions were successfully incorporated into the lattice position of Zn ions in ZnO matrix. The selected area electron diffraction (SAED) pattern reveals that the nanorods are single crystal in nature and preferentially grow along [0 0 1] direction. Magnetic studies show that Zn1-xCo(x)O nanorods exhibit room temperature ferromagnetism. This novel nanostructure could be a promising candidate for a variety of future spintronic applications.

One step synthesis of rutile TiO2 nanoparticles at low temperature.

Sphere-like rutile TiO2 nanocrystals have been synthesized by sol-gel method followed by hydrolysis of titanium tetrachloride in deionized water in the presence of ammonium hydroxide as hydrolysis catalyst. The as-prepared TiO2 nanoparticles have single rutile phase with average diameter approximately 26.4 nm. The results show that the temperature has a great influence on the particle size distribution and also crystalline phase (rutile) of TiO2 nanoparticles is consistent with the temperature. Characterization of the as-prepared nanocrystalline powder was carried out by different techniques such as powder X-ray diffraction (XRD), field emission transmission electron microscopy (FE-TEM) and Raman spectroscopy.