Scalable synthesis of Sb(III)Sb(V)O4 nanorods from Sb2O5 powder via solvothermal processing

Scalable Sb(III)Sb(V)O₄ nanorods from Sb₂O₅ powder were prepared using solvothermal route. XRD and HRTEM demonstrate that the nanorods are single-crystal orthorhombic-Sb₂O₄ phase with several micrometers long and 200-300 nm diameter size. XPS result further shows that the antimony cations in the nanorods are composed of three valence and five valence antimony ions. The emission of the nanorods appears around 450 nm wavelength. The formation mechanism of the Sb(III)Sb(V)O₄ nanorods was discussed in detail.     

Synthesis, structure, and photoluminescence of Zn2SnO4 single-crystal nanobelts and nanorings

A large quantity of single-crystal Zn₂SnO₄ (ZTO) nanobelts is synthesized by using a thermal evaporation method. The lengths of the nanobelts are up to several hundreds of micrometers, and the average width and thickness are about 400 and 30 nm, respectively. Some ring-like nanobelts, called nanorings here, are also observed. The nanobelts are characterized in detail with scanning electron microscope, X-ray powder diffraction, transmission electron microscope, high-resolution transmission electron microscope and selected area electron diffraction. Possible growth mechanisms for the ZTO nanobelts and nanorings are proposed. In addition, the photoluminescence spectrum (PL) of the nanobelts at room temperature shows a stable broad blue-green emission around the 400-600 nm wavelengths with a maximum center at 490 nm. The strong PL emission of the nanobelts may find potential applications in nano-scale optoelectronic devices.     

Growth and mechanism of titania nanowires

Anatase and rutile-phase titania nanowires have been prepared via an efficient molten salt-assisted and novel pyrolysis route, respectively. The growth of anatase nanowires is parallel to [010] direction. The anatase titanium oxide nanowires are obtained by exchange reaction between Na₂TiO₃ and HCl, whereas the formation of rutile titania nanowires is conventional vapor-liquid-solid growth mechanism.     

Raman spectroscopic and photoluminescence study of single-crystalline SnO2 nanowires

Single-crystalline SnO₂ nanowires with sizes of 4-14 nm in diameter and 100-500 nm in length were produced in a molten salt approach by using hydrothermal synthesized precursor. Structural characters of the nanowires were examined by X-ray diffraction and high-resolution electron transmission microscopy. Raman, photoluminescence and X-ray photoelectron spectra of the samples were examined under heat treatments. Three new Raman modes at 691, 514 and 358 cm⁻¹ were recorded and assigned. The former two are attributed to activation of original Raman-forbidden A_2uLO mode and the third is attributed to defects in small-sized nanowires. A strong photoluminescence is observed at about 600 nm, the temperature effects is examined and the origin of the PL process is discussed via X-ray photoelectron spectra.     

Low-temperature transport properties of individual SnO2 nanowires

Stannic oxide (SnO₂) nanowires have been prepared by Chemical vapor deposition (CVD). The low-temperature transport properties of a single SnO₂ nanowire have been studied. It is found that the transport of the electrons in the nanowires is dominated by the Efros-Shklovskii variable-range hopping (ES-VRH) process due to the enhanced Coulomb interaction in this semiconducting nanowire. The temperature dependence of the resistance follows the relation lnR∼T^−1/2. On the I-V and dI/dV curves of the nanowire a Coulomb gap-like structure at low temperatures appears.     

Synthesis of ZnS nanorods by annealing precursor ZnS nanoparticles in NaCl flux

ZnS nanorods were fabricated by annealing precursor ZnS nanoparticles, which were prepared by one-step, solid-state reaction of ZnCl₂ and Na₂S through grinding by hand at ambient temperature, in NaCl flux. The as-prepared ZnS nanorods have diameters of 40-80 nm, and lengths up to several micrometers. The structural features and chemical composition of the nanorods were investigated by X-ray diffraction (XRD), transmission electron microscopy (TEM), selected area electron diffraction (SAED), high-resolution transmission electron microscopy (HRTEM), and Raman spectra.     

Area-selectively sputtering the RuO2 nanorods array

The RuO₂ nanorods array is grown selectively on the SiO₂-patterned sapphire (SA) wafers using reactive sputtering. The area-selectivity is attributed to an early nucleation of RuO₂ and its fast surface coverage on SA (1 0 0) and (0 1 2), in contrast to the sluggish nucleation on glassy SiO₂ in the initial sputtering period. The growth domain is explored by investigating the temperature windows at sputtering power 40, 50, and 60 W. The low-temperature bound is limited by the mobility of precursors on SiO₂ surface, which enables the precursors to depart before aggregating into a large size to smear the non-growth region. The high-temperature bound is set by the horizontal growth which enlarges the rod width and deteriorates its one-dimensional feature. The temperature window shrinks with increasing sputtering power. The X-ray photoelectron spectra indicate the as-sputtered rod surface is ruthenium rich. The X-ray diffraction analysis shows that RuO₂ growth on SA (1 0 0) and (0 1 2) follows the epitaxial relations between RuO₂ and SA crystals.     

Photo-catalytic H2 evolution over a series of Keggin-structure heteropoly blue sensitized Pt/TiO2 under visible light irradiation

We report the visible light-induced hydrogen generation over a series of Keggin-structure heteropoly blue (HPB) anions (PW₁₂O₄₀³⁻, phosphotungstic blue (PTB), GeW₁₂O₄₀⁴⁻ (GTB), SiW₁₂O₄₀⁴⁻ (STB), BW₁₂O₄₀⁵⁻ (BTB)) sensitized Pt/TiO₂ photo-catalysts. The sensitization of TiO₂ by HPB was certified using photo-electrochemical measurements and UV-vis absorption spectra. PTB showed the most pronounced sensitization effect for TiO₂ in those HPB anions and Pt/TiO₂-PTB showed the highest hydrogen generation activity. The sensitization of TiO₂ was significantly dependent on the reduction potential of HPA, which was determined by the kind of central atom in HPA.     

Growth of high-density Ru- and RuO2-composite nanodots on atomic-layer-deposited Al2O3 film

Growth of Ru- and RuO₂-composite (ROC) nanodots on atomic-layer-deposited Al₂O₃ film has been studied for the first time using ion-beam sputtering followed by post-deposition annealing (PDA). X-ray photoelectron spectroscopy analyses reveal that RuO₂ and Ru co-exist before annealing, and around 10% RuO₂ is reduced to metallic Ru after PDA at 900 °C for 15 s. Scanning electron microscopy measurements show that well-defined spherical ROC nanodots are not formed till the PDA temperature is raised to 900 °C. The mean diameter of the nanodots enlarges with increasing PDA temperature whereas the nanodot density decreases, which is attributed to coalescence process between adjacent nanodots. It is further illustrated that the resulting nanodot size and density are weakly dependent on the annealing time, but are markedly influenced by the decomposition of RuO₂. In this article, the ROC nanodots with a high density of 1.6 × 10¹¹ cm⁻², a mean diameter of 20 nm with a standard deviation of 3.0 nm have been achieved for the PDA at 900 °C for 15 s, which is promising for flash memory application.     

Surface characterization of the Zn-Ni-Al2O3 nanocomposite coating fabricated under ultrasound condition

Zn-Ni-Al₂O₃ nanocomposite coating, which was fabricated by eletrodeposition technique with the aid of ultrasound, was investigated by scanning electron microscopy (SEM), energy dispersive X-ray (EDX) analysis and X-ray photoelectron spectroscopy (XPS). The results reveal that 7.2 wt.% nano-alumina particles uniformly dispersed in the matrix of the composite coating. The XPS analyses demonstrate that the outermost layer of Zn-Ni-Al₂O₃ coating was composed of nano-alumina and Zn(OH)₂, while the transition layer between the outermost layer and the Zn-Ni matrix consisted of nano-alumina, metallic Zn, ZnO and metallic Ni. In order to investigate the influences of ultrasonic agitation and the incorporation of nano-alumina on the composition and surface structure of Zn-Ni matrix, the comparison studies of Zn-Ni-Al₂O₃ nanocomposite coating with Zn-Ni coatings fabricated with and without ultrasound were conducted. The results indicate that ultrasonic agitation resulted in a decrease of Ni content in the Zn-Ni matrix and an increase of the thickness of surface oxide layer; while the incorporation of nano-α-Al₂O₃ increased the Ni content in the Zn-Ni matrix.     

Cr-doping induced ferromagnetic behavior in antiferromagnetic EuTiO3 nanoparticles

We have synthesized a series of high quality EuTi_1−xCr_xO₃ (x = 0.0, 0.02, and 0.04) nanoparticles by simple sol-gel technique. The averaged grain size of these obtained nanoparticles displays no obvious change with Cr-doping and is about 100 nm. The structural and magnetic properties of EuTi_1−xCr_xO₃ (x = 0.0, 0.02, and 0.04) samples were detailedly investigated. It is found that the G-antiferromagnetic (G-AFM) ordering of pure EuTiO₃ can be significantly modified with slight Cr-doping, and finally the ferromagnetic behavior is enhanced for EuTi_1−xCr_xO₃ system with Cr-doping.     

SnO2 / In2O3 one-dimensional nano-core-shell structures: Synthesis, characterization and photoluminescence properties

SnO₂/In₂O₃ one-dimensional nano-core-shell structures have been synthesized at 1350 ^°C by thermal evaporation of the mixture of metal Sn, Fe(NO₃)₃ powders and In particles. The as-synthesized products have been characterized by energy-dispersive X-ray spectroscopy, selected-area electron diffraction and high-resolution transmission electron microscopy. Microstructure characterization indicates the orientation relationship between core and shell is , . The formation mechanism of this nano-core-shell structure can be attributed to the cover of In₂O₃ on the surface of SnO₂ nanochains. The photoluminescence properties of the nano-core-shell structures have been measured. The PL spectrum shows some difference with the result from pure SnO₂ and In₂O₃ nanostructure that be deemed to relate to interface defects in SnO₂/In₂O₃ nano-core-shell structure.     

Photoluminescence from amorphous silica nanowires synthesized using TiN/Ni/SiO2/Si and TiN/Ni/Si substrates

Photoluminescence characteristics of amorphous silica nanowires (a-SiONWs) grown on TiN/Ni/Si and TiN/Ni/SiO₂ substrates have been studied. A-SiONWs grown on TiN/Ni/Si substrates show a Si-rich composition compared to those grown from TiN/Ni/SiO₂/Si. The emission characteristics of the nanowires were found to depend on the type of substrate. By annealing the a-SiONWs grown on TiN/Ni/Si in air, emission bands shift from blue to green bands. It is likely that silicon to oxygen ratio is an important factor in deciding the types of defects and emission bands of amorphous silica nanowires.     

Effects of organic acids on the size-controlled synthesis of rutile TiO2 nanorods

Size-controlled synthesis of pure rutile-phase TiO₂ nanorods was carried out by a hydrothermal method using different organic acids as modifiers, and metatitanic acid and concentrated sulfuric acid as raw materials. The synthesized rutile TiO₂ nanorods were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). The effects of organic acid modifiers on the sizes of rutile TiO₂ nanorods were investigated. It was found that the steric effect occurred by the organic modifiers and non-polarity of organic acids were beneficial to the formation of small-sized rutile TiO₂ nanorods. The strongly coordinative interaction between the carboxyl (or hydroxyl) group of the modifier and the surface of TiO₂ nanoparticles effectively inhibited the crystal growth.     

Low-temperature preparation of F-doped TiO2 film and its photocatalytic activity under solar light

A novel and simple method for preparing F-doped anatase TiO₂ (defined as FTO) film with high photocatalytic activity was developed using titanium-n-butoxide and NH₄F as TiO₂ and fluorine precursors under mild condition, i.e. low temperature (lower than 373 K) and ambient pressure. The prepared samples were characterized by XRD, SEM, X-ray photoelectron spectroscopy (XPS), diffuse reflectance spectrum (DRS), photoluminescence spectrum (PL) and TG-DSC analysis. The photocatalytic activity was evaluated by decomposing X-3B under artificial solar light. The results showed that the crystallinity of TiO₂ was improved by F-doping. F⁻ ions can prevent the grain growth, and the transformation of anatase to rutile phase was also inhibited. The doped fluorine atoms existed in two chemical forms, and the ones incorporated into TiO₂ lattice might take a positive role in photocatalysis. Compared with surface fluorination samples, FTO film exhibited better photocatalytic activity. The high photocatalytic activity of FTO may due to extrinsic absorption through the creation of oxygen vacancies rather than the excitation of the intrinsic absorption band of bulk TiO₂. Furthermore, the FTO can be recycled with little photocatalytic activity depression. Without any further treatment besides rinsing, after 6 recycle utilization, the photocatalytic activity of FTO film was still higher than 79%.     

Magnetic properties of large-area one-dimensional WO2 and MoO2 nanorods

Large-area one-dimensional (1D) monoclinic WO₂ and MoO₂ nanorods in the space group P2₁/c were synthesized by reactive thermal evaporation. The as-synthesized 1D WO₂ and MoO₂ nanorods become soft magnetic materials at 10 K, implying that structural or magnetic transitions occur. There are large differences in saturation magnetization, the coercive field, and remanence between the 1D WO₂ and MoO₂ nanorods, although both 1D nanorods have a similar shape.     

Synthesis of PEO/4Hb-TaS2 layered nanocomposite

Single-phase layered nanocomposite containing 4Hb-TaS₂ and poly(ethylene oxide) [PEO] has been first synthesized by using the exfoliation-adsorption technique. It has been characterized by powder X-ray diffraction (XRD) and electrical dc resistivity measurements. As the product exhibited lattice expansions along the stacking direction, PEO was intercalated into 4Hb-TaS₂ galleries.     

One-dimensional structures of Bi2O3 synthesized via metalorganic chemical vapor deposition process

We have demonstrated the synthesis of one-dimensional (1D) structures of bismuth oxide (Bi₂O₃) by a reaction of a trimethylbismuth (TMBi) and oxygen (O₂) mixture at 450 °C. Scanning electron microscopy showed that the product consisted of 1D materials with width or diameters less than 1 μm and lengths up to several tens of micrometers. The X-ray energy dispersive spectroscopy revealed that the materials contained elements of Bi and O. The results of X-ray diffraction and selected area electron diffraction pattern indicated that the obtained Bi₂O₃ were crystalline with monoclinic structure.     

Electronic transport properties and Microstructures of TiO2:Co magnetic semiconductors

TiO₂:Co thin films of high Co concentration were investigated by the high resolution transmission electron microscopy, physical property measurement system and energy dispersive X-ray. The as-deposited films are amorphous magnetic semiconductors and we did not find any Co metal particles in them. The electronic transport process in the low-temperature range below 80 K could be described by the spin-dependent variable-range-hopping process. However, after the samples were annealed at 300 °C, large amounts of Co metal particles were observed to connect each other and the films show a metallic behavior. The origin of ferromagnetism of the thin films is also discussed.     

Photoelectron spectroscopy of nanocrystalline anatase TiO2 films

Nanocrystalline TiO₂ (anatase) films were prepared using either colloidal suspensions or a sol-gel route. The electronic structure of these films was analyzed using X-ray photoelectron spectroscopy (XPS) and ultraviolet photoelectron spectroscopy (UPS). Apart from pristine films, films containing defects introduced by annealing under ultra-high vacuum conditions or by ion bombardment were investigated. Generally, annealing in the temperature range up to 720 K results in no significant changes in the XPS and UPS spectra as compared to the pristine state, indicating that the amount of defect formation is too low to be observable by these techniques. On the other hand, ion irradiation causes the appearance of distinct defect states; these could be identified in agreement with previous data from photoemission studies on rutile and anatase single crystals. From UPS, a valence-band width of ∼4.6 eV was determined for the nanocrystalline anatase films.