Cantilever magnetometry has been used to measure the upper critical magnetic field H c2 of the quasi-one dimensional molecular organic superconductor (TMTSF) 2 ClO 4 . From simultaneous resistivity and torque magnetization experiments conducted under precise field alignment, H c2 at low temperature is shown to reach 5T, nearly twice the Pauli paramagnetic limit imposed on spin singlet superconductors. These results constitute the first thermodynamic evidence for a large H c2 in this system and provide support for spin triplet pairing in this unconventional superconductor.
To study the mechanism of metal- and nonmetal-ion-doped
TiO2, TiO2 codoped with carbon and molybdenum
prepared
by a hydrothermal method following calcination post-treatment is chosen
as the study object. The prepared samples are characterized by X-ray
diffractmeter, Raman spectroscopy, X-ray photoelectron spectroscopy,
and Brunauer–Emmett–Teller measurement. It is found
that the doped carbon exists in the form of deposited carbonaceous
species on the surface of TiO2, and molybdenum substitutes
for titanium in the lattice and exists as the Mo6+ state.
All the prepared samples have comparable large surface areas. The
photocatalytic activities are tested by degradation of rhodamine-B
and acetone under visible light irradiation. The results show that
the codoped sample has the best performance in the degradation of
both RhB and acetone. Briefly, the enhanced photocatalytic activity
of codoped TiO2 is the synergistic effect of C and Mo.
Mo substitutes in the Ti site in the lattice for the formation of
the doping energy level, and C exists as carbonaceous species on the
surface of the TiO2, which can absorb visible light. The
synergetic effects of C and Mo not only enhance the adsorption of
visible light but also promote the separation of photogenerated electrons
and holes, which consequently contribute to the best photodegradation
efficiency of organic pollutants under visible-light irradiation.
UV–vis diffuse reflectance spectra and photoluminescence spectra
of the prepared samples and fluorescence of terephthalic acid for
the detection of hydroxide radical are employed to verify the proposed
mechanism.
We have successfully fabricated well-ordered silicon nanowire (SiNW) arrays of smooth surface by using a low-cost and facile Ag-assisted chemical etching technique. We have experimentally found that the reflectance can be significantly suppressed (<1%) over a wide solar spectrum (300-1000 nm) in the as-grown samples. Also, based on our bundled model, we have used rigorous coupled-wave analysis to simulate the reflectance in SiNW arrays, and found that the calculated results are in good agreement with the experimental data. From a further simulation study on the light absorption in SiNW arrays, we have obtained a photocurrent enhancement of up to 425% per unit volume of material as compared to crystalline Si, implying that effective light trapping can be realized in the as-grown samples. In addition, we have demonstrated experimentally and theoretically that the as-grown samples have an omnidirectional high-efficiency antireflection property.
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