Ordered anodic aluminum oxide (AAO) templates with pores <15 nm in diameter and an aspect ratio (length-to-diameter ratio) above 3 × 103 have been fabricated using a nonlithographic approach; specifically, by anodizing aluminum in an ethylene-glycol-containing sulfuric acid electrolyte. The pores are the smallest in diameter reported for a self-ordered AAO without pore aspect-ratio limitations and good ordering, which opens up the possibility of obtaining nanowire arrays in the quantum confinement regime that is of interest for efficient thermoelectric generators. The effect of the ethylene glycol addition on both the pore diameter and the ordering is evaluated and discussed. Moreover, 15-nm-diameter Bi2Te3 and poly(3-hexyl thiophene) (P3HT) nanowires have been prepared using these AAO templates. As known, Bi2Te3 is currently the most efficient thermoelectric bulk material for room-temperature operations and, according with theory, its Seebeck coefficient should be increased when it is confined to nanowires with diameters close to 10 nm. On the other hand, P3HT is one of the main candidates for integrating organic photovoltaic and thermoelectric devices, and its properties are also proposed to increase when it is confined to nanoscale structures, mainly due to molecular orientation effects.

Highly oriented [1 1 0] Bi2Te3 films were obtained by pulsed electrodeposition. The structure, composition, and morphology of these films were characterized. The thermoelectric figure of merit (zT), both parallel and perpendicular to the substrate surface, were determined by measuring the Seebeck coefficient, electrical conductivity, and thermal conductivity in each direction. At 300 K, the in-plane and out-of-plane figure of merits of these Bi2Te3 films were (5.6 ± 1.2)·10−2 and (10.4 ± 2.6)·10−2, respectively.

ZnO films have been grown on gold (111) by electrodeposition using two different OHsources, nitrate and peroxide, in order to obtain a comparative study between these films.The morphology, structural and optical characterization of the films were investigated depending on the solution used (nitrate and peroxide) and the applied potential. Scanning Electron Microscopy pictures show different morphologies in each case. X-Ray Diffraction confirms that the films are pure ZnO oriented along the (0002) direction.ZnO films have been studied by photoluminescence to identify the emission of defects in the visible range. A consistent model that explains the emissions for the different electrodeposited ZnO films is proposed. We have associated the green and yellow emissions to a transition from the donor OHto the acceptor zinc vacancies (V Zn -) and to interstitial oxygen (Oi 0 ), respectively. The orange-red emission is probably due to

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