We report a very simple and novel approach to produce anodic TiO2 nanotube arrays with highly defined and ordered tube openings. It is based on carrying out anodization through a slowly soluble photoresist coating. This eliminates the formation of undesired initiation layers on the tube tops and protects them to a certain extent from etching by the electrolyte.
Ti–Ni–Si glassy alloy supercapacitors, devices that store electric charge on their TiO2 surfaces that contain many nanometer‐sized cavities, display many advantages over other power‐source technologies. The use of de‐alloying and anodic oxidization methods has made possible the synthesis of a TiO2 surface accessible to electron trapping. Until recently, no studies have addressed the “dry” electric storage in light glassy alloys. Our device realizes AC electric storage from 193 to 453 K with a voltage variation from 10 to 150 V, and DC capacitance of ～4.8 F (～52.8 kF/cm3), on the basis of electric double layers, deep electronic trapping sites and Shottky barriers. Further gains could be attained with surface optimization.
MgZnO‐based ultraviolet avalanche photodetectors (APDs) have been fabricated from Au/MgO/Mg0.44Zn0.56O/MgO/Au Schottky structures. The carrier avalanche multiplication is realized via an impact ionization process occurring in the MgO layer under relatively large electric field. The APDs exhibit an avalanche gain of 587 at 31 V bias, and the response speed of the APDs is in the order of microseconds.
Thin amorphous tantalum films are prepared on Si(111) substrates in a metallic glassy state. The amorphous monoatomic state of the film is characterized by X‐ray diffraction studies. The glassy state leads to a negative t emperature c oefficient of the r esistivity (TCR) for low sample temperatures <200 K which is attributed to incipient localization. Above 200 K a positive TCR is observed as expected for a normal Boltzmann transport regime. Upon heating the Si substrate to 1200 K TaSi2 is formed out of the amorphous tantalum film and the silicon substrate. The TaSi2 layer is crystalline as evident from X‐ray diffraction data.
We demonstrate the fabrication of a solid state heterojunction photovoltaic device with solution‐processed graphene oxide (GO) and n‐Si. Partially reduced GO with a high optical gap (2.8 eV) was spin‐coated on the n‐Si substrate and a heterojunction device was fabricated with the structure of Au/pr‐GO/n‐Si. In the fabricated device, incident light was transmitted through the thin GO film to reach the junction interface, generating photoexciton, and thereby a photovoltaic action was observed. By means of a built‐in electric potential at the GO/n‐Si junction, photoexcited electrons and holes can be separated, transported and collected at the electrodes.
Optically transparent and high‐quality hybrid ZnO nanoparticle and anthracene embedded polyphenylsiloxane (PPS) glass films were spin‐coated on quartz substrates. A strong Förster resonant energy transfer (FRET) process was indicated by the observation of quenching of the ZnO emission and an enhancement of the anthracene emission at room temperature. The efficiency of this energy transfer between ZnO and the S1 vibronic states of the anthracene molecules can be optimized to exceed 90%.
We propose a theory of thin film photovoltaics in which one of the polycrystalline films is made of a pyroelectric material grains such as CdS. That film is shown to generate strong polarization improving the device open circuit voltage. Implications and supporting facts for the major photovoltaic types based on CdTe and CuIn(Ga)Se2 absorber layers are discussed.
We demonstrate the self‐catalyst growth of vertically aligned InAs nanowires on bare Si(111) by droplet epitaxy. The growth conditions of indium droplets suitable for nucleation and growth of nanowires have been identified. We have then realized vertically aligned and non‐tapered InAs nanowires on bare Si(111) substrates through optimal indium droplets. It was found that the lateral dimensions and density of nano‐wires are defined by the indium droplets. This technique unravels a controllable, cost‐effective and time‐efficient route to fabricating functional monolithic hybrid structures of InAs nanowires on silicon.
Lead carbonate chloride, Pb2CO3Cl2, known as mineral phosgenite, is introduced as a novel SRS‐active carbonate crystal with tetragonal symmetry. Under picosecond one‐micron laser pumping Raman‐induced χ(3)‐nonlinear generation in the near‐IR is observed. All recorded high‐order Stokes and anti‐Stokes sidebands are identified and attributed to two SRS‐promoting vibration modes with ωSRS1 ≈ 1062 cm–1 and ωSRS2 ≈ 86 cm–1.
ZnO thin films with a rippled surface structure were used as electron‐collecting layers of inverted organic photovoltaics (OPVs). Using additional ultrathin layers of ZnO and TiO2 fabricated using atomic layer deposition (ALD), not only the power‐conversion efficiency of the OPVs could be increased (up to 3.5%), but also the photovoltaic performance became nearly constant within 100 days without any additional encapsulations of the solar cells under ambient conditions.
The metastability of the bixbyite‐ and corundum‐type In2O3 polymorphs up to 33 GPa (at room temperature) is shown. While compressed (in diamond anvil cells) and laser‐heated, both polymorphs undergo a phase transition to the Rh2O3‐II‐type structure (space group Pbcn, No. 60). The direct transition from bixbyite to Rh2O3‐II structure has not yet been observed for any other oxide.
A facile metal catalyst free route to synthesize boron doped (0.6%–1.0%) carbon nanotubes via ceramic nanowires in which the formation of the nanowires (probably serving as templates), the carbon nanotubes and their doping all occur unanimously in the reaction, is presented.
Bulk polycrystalline La0.8Li0.2MnO3 is found to switch between a low‐resistance state and a high‐resistance state on thermal cycling. The low‐temperature, high‐resistance state exhibits strong electroresistance whereas the high‐temperature, low‐resistance state does not. The change in resistance between the two distinct states is of two orders of magnitude. It is proposed that the observed metastability may serve as the basis for resistive thermal‐switching devices.
Bi2Te3 doped p‐type Pb0.13Ge0.87Te samples were prepared by hot pressing. We report on very high power factor values of ～30 μW/cm K2 at 500 °C, as were determined from Seebeck coefficient and electrical resistivity measurements. From dilatometric characterization, the phase transition from the low temperature rhombohedral to the high temperature cubic NaCl structures, takes place at 373 °C. This transition is accompanied by a continuous and gradual change of the lattice parameters, as was observed by hot stage XRD, suggesting a good mechanical durability upon thermal cycling and operating in large thermal gradients.
We demonstrate here a simple but very effective approach to decorate anodically grown TiO2 nanotubes (NTs) uniformly with CdS and PbS quantum dots (QDs) deep inside the NT walls. This approach is based on SILAR (successive ionic layer adsorption and reaction) technique assisted with evacuation of the NTs. The basic idea of evacuation is to remove air pockets trapped inside the NTs so as to clear the passage for the penetration of QD precursors down the bottom of the NTs.
Steady‐state and time‐resolved photoluminescence of silicon nanoparticles dispersed in low‐polar liquids at above room temperature is studied. The roles of low‐polar liquids as well as mechanisms responsible for their temperature‐dependent photoluminescence are discussed. The thermal sensitivity of the photoluminescence is estimated and application of the nanoparticles as nanothermometers is proposed.
We present a computational study based on time‐dependent density functional theory of the optical absorption spectra of TiO2 nanowires sensitized with organic dye molecules. We concentrate on catechol and squaraine dyes. For those molecules, we compute adsorption geometries and energies and investigate the optical properties of the combined dye– nanowire system. We find that although the molecules have qualitatively different optical spectra in the gas phase, both lead to an enhancement of the absorption in the visible frequency range when adsorbed on a nanowire.
The possibility of multiferroicity arising from charge ordering in LuFe2O4 and structurally related rare earth ferrites is reviewed. Recent experimental work on macroscopic indications of ferroelectricity and microscopic determination of coupled spin and charge order indicates that this scenario does not hold. Understanding the origin of the experimentally observed charge and spin order will require further theoretical work. Other aspects of recent research in these materials, such as geometrical frustration effects, possible electric‐field‐induced transitions, or orbital order are also briefly treated.
Quasi‐aligned molybdenum oxide nanowires are synthesized on silicon substrate by a thermal evaporation method, at a low temperature of 550 °C without using any catalyst. The diameter of these nanowires is about 100 nm, with steps in the top to form a sharp tip. The field emission measurement shows that these nanowires have strong electron field emission abilities, with high field enhancement factor and a relatively low turn‐on field of 2.16 V µm–1, suggesting that these molybdenum oxide nanowire arrays might be promising candidates as field emitters.
