An experimental and theoretical study on the electronic and structural properties of CdSe@TiO2 nanotube arrays.

In this work, the effects of the structural (crystallite size, stress) and electronic parameters (band gap, lifetime) on the photoelectrocatalysis and electron transport over CdSe electrodeposited inside TiO2-nanotubes (CdSe@TiO2NT) were investigated. Density functional theory (DFT) calculations of TiO2 were used to elucidate the electronic band structure and to correlate with experimental values. CdSe was grown by pulsed electrodeposition into previous and late thermal-treated TiO2NT (Sample-PTT and Sample-LTT, respectively) without blocking the nanotube's entrance. The Rietveld refinement method was used to obtain information from crystallographic data of each photoelectrode. The lattice strains calculated from the Rietveld analysis for Sample-PTT and Sample-LTT were 0.472 and 0.540, and the average volume of the TiO2-anatase unit cell increased from 133.235(0) Å3 to 136.950(6) Å3, respectively. Sample-PTT exhibited higher experimental electron lifetime, larger than 1.0 order of magnitude compared to Sample-LTT photoanodes. The band structures and DOS obtained by computational modelling showed theoretical band gap values of 2.54 eV and 2.75 eV, which were close to the experimental values. All studies evidenced a strong dependence of the electronic properties of the CdSe@TiO2 samples on their morphology, and, consequently, on their photoelectrochemical activity in water splitting.

Electron scattering by methanol and ethanol: a joint theoretical-experimental investigation.

We present a joint theoretical-experimental study on electron scattering by methanol (CH(3)OH) and ethanol (C(2)H(5)OH) in a wide energy range. Experimental differential, integral and momentum-transfer cross sections for elastic electron scattering by ethanol are reported in the 100-1000 eV energy range. The experimental angular distributions of the energy-selected electrons are measured and converted to absolute cross sections using the relative flow technique. Moreover, elastic, total, and total absorption cross sections for both alcohols are calculated in the 1-500 eV energy range. A complex optical potential is used to represent the dynamics of the electron-alcohol interaction, whereas the scattering equations are solved iteratively using the Padé's approximant technique. Our calculated data agree well with those obtained using the Schwinger multichannel method at energies up to 20 eV. Discrepancies at high energies indicate the importance of absorption effects, included in our calculations. In general, the comparison between our theoretical and experimental results, as well as with other experimental data available in the literature, also show good agreement. Nevertheless, the discrepancy between the theoretical and experimental total cross sections at low incident energies suggests that the experimental cross sections measured using the transmission technique for polar targets should be reviewed.