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Metal Junctions (metal + junction)
Selected AbstractsBacteriorhodopsin-Monolayer-Based Planar Metal,Insulator,Metal Junctions via Biomimetic Vesicle Fusion: Preparation, Characterization, and Bio-optoelectronic Characteristics,ADVANCED FUNCTIONAL MATERIALS, Issue 8 2007D. Jin Abstract A reliable and reproducible method for preparing bacteriorhodopsin (bR)-containing metal,biomolecule,monolayer-metal planar junctions via vesicle fusion tactics and soft deposition of Au top electrodes is reported. Optimum monolayer and junction preparations, including contact effects, are discussed. The electron-transport characteristics of bR-containing membranes are studied systematically by incorporating native bR or artificial bR pigments derived from synthetic retinal analogues, into single solid-supported lipid bilayers. Current,voltage (I,V) measurements at ambient conditions show that a single layer of such bR-containing artificial lipid bilayers pass current in solid electrode/bilayer/solid electrode structures. The current is passed only if retinal or its analogue is present in the protein. Furthermore, the preparations show photoconductivity as long as the retinal can isomerize following light absorption. Optical characterization suggests that the junction photocurrents might be associated with a photochemically induced M-like intermediate of bR. I,V measurements along with theoretical estimates reveal that electron transfer through the protein is over four orders of magnitude more efficient than what would be estimated for direct tunneling through 5,nm of water-free peptides. Our results furthermore suggest that the light-driven proton-pumping activity of the sandwiched solid-state bR monolayer contributes negligibly to the steady-state light currents that are observed, and that the orientation of bR does not significantly affect the observed I,V characteristics. [source] Experimental Approaches for Controlling Current Flowing through Metal,Molecule,Metal Junctions,ADVANCED MATERIALS, Issue 10 2006E. Tran Abstract Two experimental approaches that enable control of current flow through metal,molecules,metal junctions are described. A number of studies using two-electrode metal,molecules,metal junctions have shown that the current between the electrodes depends on the structures of the incorporated molecules. When a tunneling mechanism dominates electron transport through organic molecules, the molecules behave similar to resistors with resistivities that can be controlled by changing the structure. Incorporation of molecules with increasing conjugation into Hg-based junctions increases the current flow dramatically. Alternatively, by using four-electrode electrochemical junctions that allow the potential of the electrodes to be controlled with respect to the energy levels of the incorporated molecules, it is possible to change the mechanism of electron transfer and produce abrupt increases in the current flow. These signals, analogous to solid-state diodes, are particularly significant for molecular electronics. Electrochemical junctions also permit prediction of the value of the applied potential at which the current will start taking off and to identify the mechanism of charge transport. New and recently published results obtained using junctions based on Hg electrodes in an "electrochemical" mode show that two junctions incorporating redox centers by different interactions behave as current switches, with the current flow dominated by different charge-transport mechanisms. [source] Molecular Transport Junctions: Clearing Mists,ADVANCED MATERIALS, Issue 1 2007M. Lindsay Abstract Recent progress in the measurement and modeling of transport in molecular junctions has been very significant. Tunnel transport in the Landauer,Imry regime is now broadly understood for several systems, although a detailed understanding of the role of contact geometry is still required. We overview some clear indications from recent research and note the quite reasonable agreement between measured and calculated conductance in metal,molecule,metal junctions. The next challenge lies in obtaining a microscopic understanding of charge transport that involves reduction or oxidation of molecules. [source] Experimental Approaches for Controlling Current Flowing through Metal,Molecule,Metal Junctions,ADVANCED MATERIALS, Issue 10 2006E. Tran Abstract Two experimental approaches that enable control of current flow through metal,molecules,metal junctions are described. A number of studies using two-electrode metal,molecules,metal junctions have shown that the current between the electrodes depends on the structures of the incorporated molecules. When a tunneling mechanism dominates electron transport through organic molecules, the molecules behave similar to resistors with resistivities that can be controlled by changing the structure. Incorporation of molecules with increasing conjugation into Hg-based junctions increases the current flow dramatically. Alternatively, by using four-electrode electrochemical junctions that allow the potential of the electrodes to be controlled with respect to the energy levels of the incorporated molecules, it is possible to change the mechanism of electron transfer and produce abrupt increases in the current flow. These signals, analogous to solid-state diodes, are particularly significant for molecular electronics. Electrochemical junctions also permit prediction of the value of the applied potential at which the current will start taking off and to identify the mechanism of charge transport. New and recently published results obtained using junctions based on Hg electrodes in an "electrochemical" mode show that two junctions incorporating redox centers by different interactions behave as current switches, with the current flow dominated by different charge-transport mechanisms. [source] Molecular rectification in metal,bridge molecule,metal junctionsPHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 4 2010Yaqing Liu Abstract Molecular bridged nanocontacts allow direct electrical addressing of electroactive molecules, which is of interest for the development of molecular based electronic devices. In the present paper, the electroactive molecule 6-ferrocenyl-1-hexanethiol (Fc-HT) was integrated into metal,bridge,metal (MBM) junctions assembled in a scanning tunneling microscope (STM) setup. A diode-like behavior was observed from the current/bias (It/Vb) signal through Au (substrate)/Fc-HT/Au (tip) junction, which presented an asymmetric current response due to the resonant tunneling between metal electrode and ferrocenylthiol molecules. With gate electrode modulation, the enhancement of the tunneling current can be controlled, which allows to tune the direction of the current rectification. Our investigations demonstrated that ferrocenylthiol bridged MBM nanostructure has potential applications in the future design of higher-order heterojunctions components in combination with electrochemical logic gates. [source] Role of interfaces on the direct tunneling and the inelastic tunneling behaviors through metal/alkylsilane/silicon junctionsPHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 6 2006D. K. Aswal Abstract We studied the influence of the end group of the alkylsilane molecule used in Self Assembled Monolayer (SAM) in Silicon/SAM/Metal junctions. By Inelastic Electron Tunneling spectroscopy (IETS), we showed the formation of a covalent bond between the molecules and the gold electrode in the case of a thiol terminated alkylsilane. By electrical characterizations, we demonstrated that the thiol group at the interface avoids diffusion of gold into the molecule even for a 3 carbons chain. For this short molecule, we observed pure tunnel conduction with barrier height at the monolayer/Si and monolayer/Au interfaces found to be respectively 2.14 and 2.56 eV. These values were obtained using Simmons equation with an effective mass parameter m * = 0.16me (me = mass of the electron). This extends the demonstration of the excellent tunnel dielectric behavior of these organic monolayers down to 3 carbon atoms with a thiol/Au bond at the interface. (© 2006 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Electrochemically Assisted Fabrication of Metal Atomic Wires and Molecular Junctions by MCBJ and STM-BJ Methods,CHEMPHYSCHEM, Issue 13 2010Dr. Jing-Hua Tian Abstract Atomic wires (point contacts) and molecular junctions are two fundamental units in the fields of nanoelectronics and devices. This Minireview introduces our recent approaches aiming to develop versatile methods to fabricate and characterize these unique metallic and molecular structures reliably. Electrochemical methods are coupled with mechanically controllable break junction (EC-MCBJ) or scanning tunneling microscopy (STM) break junction (EC-STMBJ) methods to fabricate metallic point contacts and metal/molecule/metal junctions. With the designed electrodeposition method, the metal of interest (e.g. Au, Cu, Fe or Pd) is deposited in a controlled way on the original electrode pair, on a chip for MCBJ or on the STM tip, to make the metallic contact. Then, various metal atomic wires and molecular junctions can be fabricated and characterized systematically. Herein, we measured the quantized conductance through the construction of histograms of these metal atomic point contacts and of single molecules including benzene-1,4-dithiol (BDT), ferrocene-bisvinylphenylmethyl dithiol (Fc-VPM), 4,4,-bipyridine (BPY), 1,2-di(pyridin-4-yl)ethene (BPY-EE), and 1,2-di(pyridin-4-yl)ethane (BPY-EA). Finally, we briefly discussed the future of EC-MCBJ and EC-STM for nanoelectronics and devices, for example, for the formation of heterogeneous metal-based atomic point contacts and molecular junctions. [source] |