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The properties of thin organic films offer many challenging opportunities for science and technology. A crucial requirement for the advancement of molecular film technology is the selective characterization and modification on an atomic level. Local proximal probes like Scanning Tunneling Microscopy (STM) or Atomic Force Microscopy (AFM) bear certainly the potential for this purpose. So far, however, mainly adsorbed organic molecules lying flat on a smooth substrate have been imaged with near atomic resolution. Here, we demonstrate the ability of STM to selectively image self-assembled monolayers of long-chain molecules (hexanethiol) oriented upright on the substrate Au(111) with molecular resolution. Upon proper choice of the tunneling parameters we can image the molecular head-group anchored at the substrate and/or the molecular tail group.  相似文献   
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We have measured and interpreted the ultraviolet (HeI) and X‐ray photoelectron spectra and the metastable impact electron spectra (MIES) from aluminum–organic‐stabilized platinum–colloids and colloid networks, deposited on silicon substrates and characterized by X‐ray photoelectron spectroscopy, scanning Auger electron microscopy and transmission electron microscopy. MIES, in particular, gives information on the electronic structure of the spacer molecules interconnecting the colloids. In addition, changes in the electronic structure of the platinum clusters that are induced by different spacer molecules were identified by means of X‐ray absorption near‐edge structure measurements at the platinum LIII‐edge of these materials. This combination of techniques was also employed to follow the chemical changes that occur upon heating of the network in situ. It turns out that the thermal decomposition of the network is driven by the disintegration of the spacer molecules. Moreover, less sintering of the colloidal particles occurs in the networked systems than in unconnected particles. Most of the networked platinum–particles are still present in their original shape even after the destruction of spacer molecules. This observation could be linked to the encapsulation of these platinum particles into an (Al? O) protecting shell. Copyright © 2003 John Wiley & Sons, Ltd.  相似文献   
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We present azimuthal angle correlations of intermediate transverse momentum (1-4 GeV/c) hadrons from dijets in Cu+Cu and Au+Au collisions at square root sNN=62.4 and 200 GeV. The away-side dijet induced azimuthal correlation is broadened, non-Gaussian, and peaked away from Delta phi=pi in central and semicentral collisions in all the systems. The broadening and peak location are found to depend upon the number of participants in the collision, but not on the collision energy or beam nuclei. These results are consistent with sound or shock wave models, but pose challenges to Cherenkov gluon radiation models.  相似文献   
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A series of photochromic derivatives based on the trans‐10b,10c‐dimethyl‐10b,10c‐dihydropyrene (DHP, “closed form”) skeleton has been synthesized and their photoisomerization leading to the corresponding cyclophanediene (CPD, “open form”) isomers has been investigated by UV/Vis and 1H NMR spectroscopies. Substitution of the DHP core with electron‐withdrawing pyridinium groups was found to have major effects on the photoisomerization efficiency, the most remarkable examples being to enhance the quantum yield of the opening reaction and to allow fast and quantitative conversions at much lower radiant energies. This effect was rationalized by theoretical calculations. We also show that the reverse reaction, that is, going from the open form to the closed form, can be electrochemically triggered by oxidation of the CPD unit and that the photo‐opening properties of pyridine‐substituted DHPs can be efficiently tuned by protonation, the system behaving as a multi‐addressable molecular switch. These multi‐addressable photochromes show promise for the development of responsive materials.  相似文献   
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We used a simple chemical synthesis route to deposit nanorod-like cobalt oxide thin films on different substrates such as stainless steel (ss), indium tin oxide (ITO), and microscopic glass slides. The morphology of the films show that the films were uniformly spread having a nanorod-like structure with the length of the nanorods shortened on ss substrates. The electrochemical properties of the films deposited at different time intervals were studied using cyclic voltammetry (CV), galvanostatic charge–discharge (GCD), and electrochemical impedance spectroscopy (EIS). The film deposited after 20 cycles on ss gave the highest specific capacity of 67.6 mAh g?1 and volumetric capacity of 123 mAh cm?3 at a scan rate 5 mV s?1 in comparison to 62.0 mAh g?1 and 113 mAh cm?3 obtained, respectively, for its counterpart on ITO. The film electrode deposited after 20 cycles on ITO gave the best rate capability and excellent cyclability with no depreciation after 2000 charge–discharge cycles.  相似文献   
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We consider closed manifolds that admit a metric locally isometric to a product of symmetric planes. For such manifolds, we prove that the Euler characteristic is an obstruction to the existence of flat structures, confirming an old conjecture proved by Milnor in dimension 2. In particular, the Chern conjecture follows in these cases. The proof goes via a new sharp Milnor–Wood inequality for Riemannian manifolds that are locally a product of hyperbolic planes. Furthermore, we analyze the possible flat vector bundles over such manifolds. Over closed Hilbert–Blumenthal modular varieties, we show that there are finitely many flat structures with nonzero Euler number and none of them corresponds to the tangent bundle. Some of the main results were announced in [M. Bucher, T. Gelander, Milnor–Wood inequalities for manifolds locally isometric to a product of hyperbolic planes, C. R. Acad. Sci. Paris Ser. I 346 (2008) 661–666].  相似文献   
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