SAW devices which are outfitted with an appropriate functional layer are highly promising candidates for small, reliable and cheap gas sensors that can operate at high temperatures and hence measure the composition of exhaust gases very close to the place of their origin. This work contributes to the development of such sensors by exploring the underlying acousto-electric sensor effect.

Heterojunction solar cells were fabricated by electrochemical deposition of p-type, cuprous oxide (Cu2O) absorber on sputtered, n-type ZnO layer. X-ray diffraction measurements revealed that the as-deposited absorber consists mainly of Cu2O, but appreciable amounts of metallic Cu and cupric oxide (CuO) are also present. These undesired oxidation states are incorporated during the deposition process and have a detrimental effect on the photovoltaic properties of the cells. The open circuit voltage (VOC), short circuit current density (jSC), fill factor (FF) and power conversion efficiency (η) of the as-deposited cells are 0.37 V, 3.71 mA/cm2, 35.7% and 0.49%, respectively, under AM1.5G illumination. We show that by thermal annealing in vacuum, at temperatures up to 300 °C, compositional purity of the Cu2O absorber could be obtained. A general improvement of the heterojunction and bulk materials quality is observed, reflected upon the smallest influence of the shunt and series resistance on the transport properties of the cells in dark and under illumination. Independent of the annealing temperature, transport is dominated by the space-charge layer generation-recombination current. After annealing at 300 °C the solar cell parameters could be significantly improved to the values of: VOC = 0.505 V, jSC = 4.67 mA/cm2, FF = 47.1% and η = 1.12%.

ABSTRACTThis contribution presents the correlation between structural, morphological, and fluorescence properties as well as device performance of nanocomposite solar cells comprising two low‐band gap polymers, poly[[9‐(1‐octylnonyl)−9H‐carbazole‐2,7‐diyl]‐2,5‐thiophenediyl‐2,1,3‐benzothiadiazole‐4,7‐diyl‐2,5‐thiophenediyl] (PCDTBT) and poly[2,1,3‐benzothiadiazole‐4,7‐diyl‐2,5‐thiophenediyl(9,9‐dioctyl‐9H‐9‐silafluorene‐2,7‐diyl)−2,5‐thiophenediyl] (PSiF‐DBT) and copper indium sulfide (CIS). It shows that, in analogy to organic solar cells, the device efficiency is strongly determined by different polymer structures leading to a different packing of the polymer chains and consequently to diverse morphologies. X‐ray diffraction investigation indicates increased semicrystallinity in PSiF‐DBT compared with the nitrogen analogue PCDTBT. The photoluminescence (PL) quenching of this polymer indicates that the higher photogeneration achieved in PSiF‐DBT based films can be correlated to a favorable donor‐acceptor phase separation. Transmission electron microscopy studies of PCDTBT:CIS blended films suggest the formation of polymer agglomerates in the layer resulting in a decreased PL quenching efficiency. For the considered polymer:CIS system, the combination of these effects leads to an enhanced overall device efficiency. © 2013 Wiley Periodicals, Inc. J. Polym. Sci. Part B: Polym. Phys. 2013, 51, 1400–1410

In this work, we report on the fabrication, characterization, and photovoltaic properties of sputter-deposited, thin film heterojunctions combining p-type cupric oxide (CuO) absorber with n-type ZnO. The structural investigation reveals highly crystalline, columnar growth of the layers and confirms that the absorber's phase is purely CuO, with only negligible traces of Cu2O. The optical characterization yields for CuO an indirect bandgap of 1.2 eV and a direct optical transition at approximately 3 eV. The short circuit current, open circuit voltage, fill factor, and power conversion efficiency of the heterojunction solar cells were extracted as a function of the CuO thickness under AM1.5 G (1 kW/m2) illumination. From the observed dependencies, we conclude that the photovoltaic performance is compromised by a restricted carrier collection efficiency, caused by the small carrier lifetime in CuO. Indeed, the carrier population is found to decay with time constants of 40 and 460 ps. A maximum power conversion efficiency of 0.08% was obtained for the solar cell with CuO thickness of 500 nm.

We present a single step and an electrochemical synthesis of vertically aligned ZnO nanorod (NR) arrays, directly on transparent aluminium-doped zinc oxide (AZO) electrodes. The NRs grow from mild, aqueous-based solution at low temperature, with no need for catalysts or additional seed layer. The use of textured AZO as substrate allows for highly effective growth of hexagonally faceted, single-crystalline ZnO NRs along the wurtzite c-axis . The matching of the crystal lattices initiates a self-seeding route, thus the inherent growth habit of the AZO crystallites advances the vertical growth and alignment of NRs. Moreover, the thickness-dependant grain size of the AZO layer provides a valuable feature for tuning the diameter of ZnO NRs grown atop. In the absence of any seed mediator, the interfacial quality is expected to improve significantly. This should enhance the thermal and electrical transport throughout the whole nanostructured transparent electrode. The NR growth was investigated under systematic manipulation of the synthesis variables in order to optimize growth conditions for highly aligned, single-crystalline NRs with a large aspect ratio and a good optical quality. The structure and optical property of the AZO/ZnO NR ensembles were characterized by atomic force microscopy, scanning electron microscopy, X-ray diffraction, photoluminescence, and ultraviolet-visible transmission spectroscopy.

Nanoparticulate WO(3) films were prepared using microwave plasma synthesis and studied with respect to the electrical conductivity in dependence of ambient conditions. The WO(3) films with a monoclinic structure were made from cluster-assembled nanoparticles (diameter 3 nm) by means of dispersion and spin-coating. Above 100 °C a thermally activated decrease of the electrical resistance due to oxygen vacancy donors is found. A reversible increase of the electrical resistance R due to oxygen uptake is observed. The decrease of R in response to reducing H(2)S in the ppm range is studied in dependence of temperature and pre-annealing conditions.