The surface structures of copper phthalocyanine (CuPc) thin films deposited on sulphur-passivated and plane perylene-3,4,9,10-tetracarboxylic dianhydride (PTCDA)-covered InAs(100) surfaces have been studied by low energy electron diffraction (LEED) and van der Waals (vdW) intermolecular interaction energy calculations. The annealing to 300 o C and 450 o C of (NH4)2Sx-treated InAs(100) substrates produces a (1×1) and (2×1) S-passivated surface respectively. The CuPc deposition onto the PTCDA-covered InAs(100) surface leads to a ring-like diffraction pattern, indicating that the 2D ordered overlayer exists and the structure is dominantly determined by the intermolecular interactions rather than substrate-molecule interactions. However, no ordered LEED patterns were observed for the CuPc on S-passivated InAs(100) surface. The intermolecular interaction energy calculations have been carried out to rationalise this structural difference. In the case of CuPc unit cells on PTCDA layer, the planar layered CuPc structure is more stable than the α-herringbone structure, consistent with the experimental LEED results. For CuPc unit cells on a S-(1×1) layer, however, the α-herringbone structure is more stable than the planar layered structure, consistent with the absence of diffraction pattern. The results show that the lattice structure during the initial stages of thin film growth is influenced strongly by the intermolecular interactions at the interface.

No abstract

Supercapacitive properties of ruthenium oxide (RuO2) nanoparticles electrodeposited onto the indium tin oxide (ITO) nanopillars were investigated. Compared to conventional planar current collectors, this coaxially nanostructured current collector-electrode system can provide increased contact for efficient charge transport, and the internanopillar spacing allows easy access of electrolyte ions. The morphological and electrochemical properties depended on the thickness of the RuO2 layers, i.e., the number of electrodeposition cycles. A maximum specific capacitance, Csp, of 1235 F/g at a scan rate of 50 mV/s was achieved for the 30-cycle deposited RuO2-ITO nanopillars. The other capacitive properties such as electrochemical reversibility and Csp retention at high scan rates also improved greatly.

The α→β1 phase transition induced by annealing free-base phthalocyanine thin films grown by organic molecular-beam deposition has been studied by powder x-ray diffraction, electronic absorption spectroscopy, and Nomarski interference microscopy. The final β1 phase consists of two domains having a different orientation relative to the substrate surface. Starting with the α phase, by careful control of the annealing temperature, a series of intermediate states are observed consisting of coexisting α and β1 phases. At the beginning of the phase transition, only one domain is observed with the β1 crystal phase aligned with the (001) plane parallel to the substrate. As the transition proceeds, however, the amount of the other domain having the (201) plane parallel to the substrate increases rapidly. A mechanism is proposed for the transition that can account for all the experimental results.

No abstract