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Scanning Tunneling Microscopy (scanning + tunneling_microscopy)
Selected AbstractsAtomic Structure and Electrical Properties of In(Te) Nanocontacts on CdZnTe(110) by Scanning Probe MicroscopyADVANCED FUNCTIONAL MATERIALS, Issue 2 2010Gili Cohen-Taguri Abstract Understanding complex correlations between the macroscopic device performance (largely dependent on the character of the metal,semiconductor contact) and the metallurgy of contact formation on the atomic level in cadmium zinc telluride (CdZnTe) radiation detectors remains a formidable challenge. In this work, an effort towards bridging that macro,nano knowledge gap is made by conducting a series of controlled experiments aimed at correlating electrical properties of the In contact to n-type CdZnTe(110) surface with the step-by-step process of contact formation. This can only be achieved by using high spatial resolution techniques, capable of conducting highly localized measurements on the nano- and sub-nanoscale, such as scanning probe microscopy. Scanning tunneling microscopy is used in situ to monitor the behavior of various In atom coverages on an atomically flat and ordered CdZnTe surface under well-controlled molecular beam epitaxial conditions in ultra-high vacuum. Electrical derivatives of atomic force microscopy are used to measure the electrical contact properties, such as contact potential difference and spreading resistance in torsion resonance tunneling mode. It is concluded that In atoms preferentially reacted with Te atomic-rows already at room temperature, forming nanometric patches of indium,telluride Schottky-type contacts. The methods developed in this study, in terms of both nanocontact fabrication and characterization (especially in terms of electrical properties) should benefit basic and applied research of any metal,semiconductor system. [source] Computation of STM images of carbon nanotubesINTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, Issue 4-5 2003P. Lambin Abstract Scanning tunneling microscopy (STM) is the only probing technique that allows for the investigation of both the topography and the electronic structure of carbon nanosystems at a subnanometer resolution. The interpretation of the STM images of carbon nanostructures involves complications that are normally absent in the study of planar crystalline surfaces. The complications typically appear from a number of quantum effects responsible for distortions in the microscope image of a nano-object. Because of these difficulties, computer simulation plays an extremely important role in the analysis of experimental data. In the current article, we report on two theoretical approaches developed for aiding in the interpretation and understanding of the formation of the STM image of a nanotube: first, the quantum mechanical dynamics of a wave packet, which allows for the modeling of the flow of the tunneling current between a tip and a nanotube supported by a substrate; and, second, a tight-binding perturbation theory that allows for the explicit calculation of realistic STM images and scanning tunneling spectra of carbon nanostructures. An atlas of computed STM images is provided for a series of 27 single-wall nanotubes with diameter around 1.3 nm. © 2003 Wiley Periodicals, Inc. Int J Quantum Chem, 2003 [source] Development of graphene layers by reduction of graphite fluoride C2F surfacePHYSICA STATUS SOLIDI (B) BASIC SOLID STATE PHYSICS, Issue 11-12 2009A. V. Okotrub Abstract We studied a possibility of reduction of the surface of graphite fluoride obtained by fluorination of highly oriented pyrolytic graphite (HOPG) by a gaseous mixture of BrF3 and Br2. X-ray diffraction (XRD) revealed a layered structure of the fluorinated product being a second-stage intercalate due to a presence of bromine molecules between the fluorinated graphite layers. Scanning tunneling microscopy and spectroscopy showed that the "old" surface of graphite fluoride (exposed to the ambient air) has the graphite-like structure, while the fresh cleaved surface is non-conductive. Therefore, the outer layers of graphite fluoride can be reduced by water present in the laboratory atmosphere. The sample was treated by H2O vapor to confirm that. The reduction was controlled by Raman spectroscopy using intensity of the 1360 and 1580,cm,1 bands. The energy dependent photoelectron spectroscopy was used for estimation of thickness of the reduction layer, which was found, does not exceed 2,3 graphite layers. The obtained results indicate the possibility of synthesis of graphene layers on dielectric fluorinated graphite matrix. [source] Scanning tunneling microscopy of monoatomic gold chains on vicinal Si(335) surface: experimental and theoretical studyPHYSICA STATUS SOLIDI (B) BASIC SOLID STATE PHYSICS, Issue 2 2005M. Krawiec Abstract We study electronic and topographic properties of the Si(335) surface, containing Au wires parallel to the steps. We use scanning tunneling microscopy (STM) supplemented by reflection of high energy electron diffraction (RHEED) technique. The STM data show the space and voltage dependent oscillations of the distance between STM tip and the surface which can be explained within one band tight binding Hubbard model. We calculate the STM current using nonequilibrium Keldysh Green function formalism. (© 2005 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Current,Voltage Characteristics of a Homologous Series of Polycyclic Aromatic HydrocarbonsCHEMISTRY - A EUROPEAN JOURNAL, Issue 26 2007Thilo Böhme Dr. Abstract A novel alkyl-substituted polycyclic aromatic hydrocarbon (PAH) with D2h symmetry and 78 carbon atoms in the aromatic core (C78) was synthesized, thereby completing a homologous series of soluble PAH compounds with increasing size of the aromatic , system (42, 60, and 78 carbon atoms). The optical band gaps were determined by UV/Vis and fluorescence spectroscopy in solution. Scanning tunneling microscopy (STM) and spectroscopy (STS) revealed diode-like current versus voltage (I,V) characteristics through individual aromatic cores in monolayers at the interface between the solution and the basal plane of graphite. The asymmetry of the current,voltage (I,V) characteristics increases with the increasing size of the aromatic core, and the concomitantly decreasing HOMO,LUMO gap. This is attributed to resonant tunneling through the HOMO of the adsorbed molecule, and an asymmetric position of the molecular species in the tunnel junction. Consistently, submolecularly resolved STM images at negative substrate bias are in good agreement with the calculated pattern for the electron densities of the HOMOs. The analysis provides the basis for tailoring rectification with a single molecule in an STM junction. [source] Two-Dimensional Self-Assembly of a Porphyrin,Polypyridyl Ruthenium(II) Hybrid on HOPG Surface through Metal,Ligand InteractionsCHEMPHYSCHEM, Issue 9 2010Aimei Gao Dr. Abstract The synthesis and self-assembly behavior of porphyrin,polypyridyl ruthenium(II) hybrid, which consists of a flexible alkyl chain attached with two conjugated moieties is described. The electronic absorption spectrum and emission spectra show that the [C8 -TPP-(ip)Ru(phen)2](ClO4)2, abbreviated as (C8ip)TPPC has optical properties. Scanning tunneling microscopy (STM) studies found that the ,,, interaction and metal,ligand interaction allow (C8ip)TPPC to form self-assembled structure and have an edge-on orientation on the highly oriented pyrolytic graphite (HOPG) surface. The multidentate structure in (C8ip)TPPC molecules act as linkers between the molecules and form metal,ligand coordination, which forces the assembly process in the direction of stable columnar arrays. In addition, although the sample was stored for two months in ambient conditions, STM experiments showed that the order of (C8ip)TPPC self-assembly only slightly decreased which indicates that the self-assembled monolayer is stable. This work demonstrates that introducing a metal-ligand in the porphyrin-polypyridyl compound is a useful strategy to obtain novel surface assemblies. [source] Nanocrystalline boron-doped diamond films, a mixture of BCS-like and non-BCS-like superconducting grainsPHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 9 2010F. Dahlem Abstract Scanning tunneling topography and spectroscopy are performed below 100,mK on granular nanocrystalline boron-doped diamond (BDD) films. We found the superconductivity behavior to follow mainly the granular features of the BDD films. The temperature dependence of the local differential conductance spectra shows our nanocrystalline BDD films as made of grains with a supercondutivity either BCS-like or non-BCS-like. Such a distribution is not discernible in transport measurements, which present a sharp macroscopic superconducting transition at a temperature of a few Kelvins. Our local scanning tunneling microscopies also confirm the good coupling between these grains: only a few opaque interfaces are detected. Such a transparency of intergrain interfaces is responsible for a proximity effect in weakly superconductive grains and an inverse proximity effect in strongly superconducting grains. [source] Low-energy irradiation effects of gas cluster ion beamsELECTRONICS & COMMUNICATIONS IN JAPAN, Issue 2 2008Shingo Houzumi Abstract A cluster-ion irradiation system with cluster-size selection has been developed to study the effects of the cluster size for surface processes using cluster ions. A permanent magnet with a magnetic field of 1.2 T is installed for size separation of large cluster ions. Trace formations at HOPG surface by the irradiation with size-selected Ar-cluster ions under an acceleration energy of 30 keV were investigated by scanning tunneling microscopy. Generation behavior of the craterlike traces is strongly affected by the number of constituent atoms (cluster size) of the irradiating cluster ion. When the incident cluster ion is composed of 100 to 3000 atoms, craterlike traces are observed on the irradiated surfaces. In contrast, such traces are not observed at all with the irradiation of the cluster ions composed of over 5000 atoms. Such behavior is discussed on the basis of the kinetic energy per constituent atom of the cluster ion. To study GCIB irradiation effects on macromolecules, GCIB was irradiated on DNA molecules absorbed on graphite surface. Using GCIB irradiation, many more DNA molecules were sputtered away compared with the monomer-ion irradiation. © 2008 Wiley Periodicals, Inc. Electron Comm Jpn, 91(2): 40,45, 2008; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/eej.10031 [source] Orientation and Arrangement of Octaruthenium Supramolecules with Alkyl Chains on GraphiteEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 35 2007Dong-Lin Shieh Abstract The self-assemblies of octaruthenium grid-type supramolecules, {[Ru2(CO)4(NH2C16H33)2](,-O2CCO2)}4, on highly oriented pyrolytic graphite (HOPG) in air and in 1-phenyloctane were studied by scanning tunneling microscopy (STM). The surface supramolecules are arranged into rows in which the metal cores are linearly packed and the alkyl chains are parallel to the surface. With the aid of theoretical calculations in the framework of density functional theory, the electronic origin of the tunneling in the measured STM images is discussed. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007) [source] Rigid Bisphenanthrolines: Synthesis, Structure and Self-Assembly at a Solid,Liquid Interface,EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 14 2006Michael Schmittel Abstract Several rigid linear bisphenanthrolines with and without bulky groups at the bisimine sites were synthesized. For three representatives, the solid-state structures were elucidated. Their potential for self-assembled monolayers was explored by scanning tunneling microscopy (STM) at the solid,liquid interface, and the resulting architectures were found to be promising candidates for templating metal-ion nanopatterns. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006) [source] Improving the ON/OFF Ratio and Reversibility of Recording by Rational Structural Arrangement of Donor,Acceptor MoleculesADVANCED FUNCTIONAL MATERIALS, Issue 5 2010Ying Ma Abstract Organic molecules with donor,acceptor (D,A) structure are an important type of material for nanoelectronics and molecular electronics. The influence of the electron donor and acceptor units on the electrical function of materials is a worthy topic for the development of high-performance data storage. In this work, the effect of different D,A structures (namely D,,,A,,,D and A,,,D,,,A) on the electronic switching properties of triphenylamine-based molecules is investigated. Devices based on D,,,A,,,D molecules exhibit excellent write,read,erase characteristics with a high ON/OFF ratio of up to 106, while that based on A,,,D,,,A molecules exhibit irreversible switching behavior with an ON/OFF ratio of about (3.2,×,101),(1,×,103). Moreover, long retention time of the high conductance state and low threshold voltage are observed for the D,A switching materials. Accordingly, stable and reliable nanoscale data storage is achieved on the thin films of the D,A molecules by scanning tunneling microscopy. The influence of the arrangement of the D and A within the molecular backbone disclosed in this study will be of significance for improving the electronic switching properties (ON/OFF current ratio and reversibility) of new molecular systems, so as to achieve more efficient data storage through appropriate design strategies. [source] Electric-Field-Assisted Nanostructuring of a Mott InsulatorADVANCED FUNCTIONAL MATERIALS, Issue 17 2009Vincent Dubost Abstract Here, the first experimental evidence for a strong electromechanical coupling in the Mott insulator GaTa4Se8 that allows highly reproducible nanoscaled writing by means of scanning tunneling microscopy (STM) is reported. The local electric field across the STM junction is observed to have a threshold value above which the clean (100) surface of GaTa4Se8 becomes mechanically instable: at voltage biases >1.1,V, the surface suddenly inflates and comes in contact with the STM tip, resulting in nanometer-sized craters. The formed pattern can be indestructibly "read" by STM at a lower voltage bias, thus allowing 5,Tdots inch,2 dense writing/reading at room temperature. The discovery of the electromechanical coupling in GaTa4Se8 might give new clues in the understanding of the electric pulse induced resistive switching recently observed in this stoichiometric Mott insulator. [source] Selective Formation of Bi-Component Arrays Through H-Bonding of Multivalent Molecular ModulesADVANCED FUNCTIONAL MATERIALS, Issue 8 2009Luc Piot Abstract Here, the formation of discrete supramolecular mono- and bi-component architectures from novel and multivalent molecular modules bearing complementary recognition moieties that are prone to undergo multiple H-bonds, such as 2,6-di(acetylamino)pyridine and uracil residues, is described. These nanostructured H-bonded arrays, including dimeric and pentameric species, are thoroughly characterized in solution by NMR, in the solid state by FT-IR, and at the solid,liquid interface by means of scanning tunneling microscopy. The employed strategy is extremely versatile as it relies on the tuning of the valency, size, and geometry of the molecular modules; thus, it may be of interest for the bottom-up fabrication of nanostructured functional materials with sub-nanometer precision. [source] Tetrathiafulvalene-, 1,5-Dioxynaphthalene-, and Cyclobis(paraquat- p -phenylene)-based [2]Rotaxanes with Cyclohexyl and Alkyl Chains as Spacers: Synthesis, Langmuir,Blodgett Films, and Electrical Bistability,ADVANCED FUNCTIONAL MATERIALS, Issue 5 2007X. Guo Abstract The synthesis and characterization of two new (TTF-DNP-CBPQT4+) [2]rotaxanes 1 and 2 is reported, based on tetrathiafulvalene (TTF), 1,5-dioxynaphthalene (DNP), and cyclobis(paraquat- p -phenylene) (CBPQT4+) with cyclohexyl and alkyl chains as the spacers. Multilayer Langmuir,Blodgett (LB) films of [2]rotaxanes 1 and 2 are prepared. Conducting atomic force microscopy, scanning tunneling microscopy, and two-terminal junction device studies indicate that the LB films of [2]rotaxanes 1 and 2 show electrical bistability behavior. By comparing with the TTF-DNP-CBPQT4+ [2]rotaxanes reported by Stoddart et,al. previously, the present results imply that proper modification of the chemical structures of the TTF unit and the spacer have negligible effect on the electrical bistability behavior of these TTF-DNP-CBPQT4+ [2]rotaxanes. These findings will allow for the design and preparation of new multifunctional TTF-DNP-CBPQT4+ [2]rotaxanes in the future. [source] Observation of Structural and Conductance Transition of Rotaxane Molecules at a Submolecular Scale,ADVANCED FUNCTIONAL MATERIALS, Issue 5 2007M. Feng Abstract Rotaxane molecules have attracted considerable interest because of their good performance in both molecular electronic devices and nanoscale data-storage media. Low-temperature scanning tunneling microscopy is used to investigate the structure and conductance of single H2 rotaxane molecules on a buffer-layered Au(111) substrate at 77,K. It is demonstrated that the conductance switching in rotaxane-based, solid-state devices is an inherent property of the rotaxane molecules. These results provide evidence that the conductance switching might arise from the movement of the cyclobis(paraquat- p -phenylene) ring along the rod section of the dumbbell-shaped backbone of the rotaxane molecule. [source] Evidence for Band-Like Transport in Graphene-Based Organic MonolayersADVANCED MATERIALS, Issue 3 2010Daniel Käfer Evidence for a band-like, lateral transport of electrons through the cores of HBC-thiolates, forming a highly ordered self-assembled monolayer (SAM) containing a very regular array of HBC-cores, is provided based on a detailed analysis of temperature-dependent scanning tunneling microscopy (STM) data recorded for islands of aromatic SAMs immersed in an insulating matrix. [source] Self-Assembled Pb Nanostructures on Si(111) Surfaces: From Nanowires to NanoringsADVANCED MATERIALS, Issue 45 2009Rui Wu Abstract A template-directed growth method for metals is described in which ordered arrays of super-long single-crystalline metal nanowires with atomic-level-controlled width, thickness (height), and surface location are prepared by molecular beam epitaxy. Their subsequent examination by in situ scanning tunneling microscopy is also outlined. A phase-separated stripe pattern composed of alternately a Ge-rich incommensurate phase and a ,3,×,,3 phase is first obtained by Ge deposition on Si(111) substrates. Further deposition of Pb on this patterned surface leads to a well-ordered array of super-long Pb nanowires. Using the same mechanism, superconducting Pb nanorings can also be fabricated. In this review of our recent work, these Pb single-crystalline nanowires and nanorings are shown to serve as an ideal platform for the study of superconductivity in reduced dimensionalities. Furthermore, because the widths and spatial distributions of two phases can be precisely controlled by the Ge coverage and substrate temperature, and because a metal will always selectively nucleate on one of two phases, this template-directed growth method can be applied to a wide range of metals. [source] The Quest for Nanoscale Magnets: The example of [Mn12] Single Molecule MagnetsADVANCED MATERIALS, Issue 43 2009Guillaume Rogez Abstract Recent advances on the organization and characterization of [Mn12] single molecule magnets (SMMs) on a surface or in 3D are reviewed. By using nonconventional techniques such as X-ray magnetic circular dichroism (XMCD) and scanning tunneling microscopy (STM), it is shown that [Mn12]-based SMMs deposited on a surface lose their SMM behavior, even though the molecules seem to be structurally undamaged. A new approach is reported to get high-density information-storage devices, based on the 3D assembling of SMMs in a liquid crystalline phase. The 3D nanostructure exhibits the anisotropic character of the SMMs, thus opening the way to address micrometric volumes by two photon absorption using the pump-probe technique. We present recent developments such as µ-SQUID, magneto-optical Kerr effect (MOKE), or magneto-optical circular dichroism (MOCD), which enable the characterization of SMM nanostructures with exceptional sensitivity. Further, the spin-polarized version of the STM under ultrahigh vacuum is shown to be the key tool for addressing not only single molecule magnets, but also magnetic nano-objects. [source] Reversible Conductance Switching of Single Diarylethenes on a Gold Surface,ADVANCED MATERIALS, Issue 11 2006N. Katsonis Light-controlled conductance switching of diarylethenes attached to Au(111) is reported (see figure). First, scanning tunneling microscopy is used to demonstrate reversible photoswitching for individual molecules. Second, reversible switching in self-assembled monolayers is established by means of optical spectroscopy. [source] Scanning Probe Studies of Porphyrin Assemblies and Their Supramolecular Manipulation at a Solid,Liquid InterfaceADVANCED MATERIALS, Issue 24 2003J.A.A.W. Elemans Dynamic self-assembly and metal,ligand coordination processes of porphyrin hexamers on a solid,liquid interface have been visualized with scanning tunneling microscopy. The organization of these hexamers into stable and highly organized arrays of "edge-on" or "face-on" oriented molecules can be controlled by the addition of different ditopic axial ligands (see Figure). [source] Theory of tip-dependent imaging of adsorbates in the STM: CO on Cu(111)INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, Issue 6 2006D. Drakova Abstract The processes of local electron injection or extraction in the scanning tunneling microscopy (STM) and spectroscopy (STS) lead to the creation of short-lived excited states localized at the electrode surfaces. The dynamic relaxation of the transient negative or positive ion resonances, due to both local and long-range interactions, is the clue to the understanding of numerous phenomena in STM/STS ranging from the "anomalously" large tip height corrugation amplitudes on clean metal surfaces to the observation of quantum mirages and features in the STS, which are not observed with the help of other surface spectroscopies. Quantum nanodynamics theory (QND) has been applied to calculate the interaction potential of a single CO molecule with the Cu(111) surface, with a transient negative ion resonance formed when an electron is injected from the tip, and the tunneling conductance on the clean and CO covered Cu(111) surface using a clean metal tip Al/Al(111) and a Pt(111) tip with an adsorbed CO molecule at the apex. Within QND and three-dimensional scattering theory, regarding the tunneling as an excited-state problem, we provide the explanation of the tip-dependent STM image of a single CO molecule on Cu(111). The appearance of the CO molecule as an indentation, using a clean metal tip and as a protrusion with a tip terminated by a CO molecule, is understood as a result of tunneling through two competing channels. Tunneling via adsorbate-induced ion resonances enhances the tunneling conductance. In contrast, tunneling via metal ion resonances only leads to attenuation of the conductance in the presence of the adsorbate. The current in the vicinity of the adsorbed CO molecule is reduced when a clean metal tip is used; i.e., CO appears dark in the STM image, because metal ion resonances on Cu(111) derive from the surface states with image state components coupling to plasmons and are therefore very diffuse. With a CO-terminated tip, the major current channel is, for symmetry reasons, from the 2,-derived orbital of the tip CO molecule, via the diffuse 2,-derived orbital of the CO molecule on the sample, hence adsorbed CO appears bright. © 2005 Wiley Periodicals, Inc. Int J Quantum Chem, 2006 [source] Metal Objects Mapping After Small Charge Explosions.JOURNAL OF FORENSIC SCIENCES, Issue 3 2006A Study on AISI 304Cu Steel with Two Different Grain Sizes ABSTRACT: Evidence of exposure of a metal component to a small charge explosion can be detected by observing microstructural modifications; they may be present even if the piece does not show noticeable overall plastic deformations. Particularly, if an austenitic stainless steel (or another metal having a face-centered cubic structure and a low stacking fault energy) is exposed to an explosive shock wave, high-speed deformation induces primarily mechanical twinning, whereas, in nonexplosive events, a lower velocity plastic deformation first induces slip. The occurrence of mechanical twins can be detected even if the surface is damaged or oxidized in successive events. In the present research, optical metallography (OM) and scanning electron microscopy (SEM), and scanning tunneling microscopy (STM) were used to detect microstructural modifications caused on AISI 304Cu steel disks by small-charge explosions. Spherical charges of 54.5 or 109 g TNT equivalent mass were used at explosive-to-target distances from 6.5 to 81.5 cm, achieving peak pressures from 160 to 0.5 MPa. Explosions induced limited or no macro-deformation. Two alloy grain sizes were tested. Surface OM and SEM evidenced partial surface melting, zones with recrystallization phenomena, and intense mechanical twinning, which was also detected by STM and X-ray diffraction. In the samples' interior, only twins were seen, up to some distance from the explosion impinged surface and again, at the shortest charge-to-sample distances, in a thin layer around the reflecting surface. For forensic science locating purposes after explosions, the maximum charge-to-target distance at which the phenomena disappear was singled out for each charge or grain size and related to the critical resolved shear stress for twinning. [source] Preparation, characterization, and electrical properties of dual-emissive Langmuir-Blodgett films of some europium-substituted polyoxometalates and a platinum polyyne polymerJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 4 2010Li Liu Abstract A new series of organometallic/inorganic composite Langmuir-Blodgett (LB) films consisting of a rigid-rod polyplatinyne polymer coordinated with 2,7-bis(buta-1,3-diynyl)-9,9-dihexylfluorene (denoted as PtP) as the ,-conjugated organometallic molecule, an europium-substituted polyoxometalate (POM; POM = Na9EuW10O36, K13[Eu(SiW11O39)2] and K5[Eu(SiW11O39)(H2O)2]) as the inorganic component, and an amphiphilic behenic acid (BA) as the auxiliary film-forming agent were prepared. Structural and photophysical characterization of these LB films were achieved by ,,A isotherms, absorption and photoluminescence spectra, atomic force microscopy imaging, scanning tunneling microscopy, and low-angle X-ray diffraction. Our experimental results indicate that stable, well-defined, and well-organized Langmuir and LB films are formed in pure water and POM subphases, and the presence of Eu-based POM in the subphase causes an area expansion. It is proposed that a lamellar layered structure exists for the PtP/BA/POM LB film in which the POM and PtP molecules can lay down with the interfacial planes. Luminescence spectra of the prepared hybrid LB films show that near-white emission spectra can be obtained due to the dual-emissive nature of the mixed PtP/POM blends. These Pt-polyyne-based LB films displayed interesting electric conductivity behavior. Among them, PtP/BA/POM 13-layer films showed a good electrical response, with the tunneling current up to ±100 nA when the voltage was monitored between ,1 and 7 V. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 879,888, 2010 [source] Adlayer structure of octa-alkoxy-substituted copper(II) phthalocyanine on Au(111) by electrochemical scanning tunneling microscopyMICROSCOPY RESEARCH AND TECHNIQUE, Issue 1 2008Li Wang Abstract Electrochemical scanning tunneling microscopy (ECSTM) has been used to examine the adlayer of octa-alkoxy-substituted copper(II) phthalocyanines (CuPc(OC8H17)8) on Au(111) in 0.1 M HClO4, where the molecular adlayer was prepared by spontaneous adsorption from a benzene solution containing this molecule. Topography STM scans revealed long-range ordered, interweaved arrays of CuPc(OC8H17)8 with coexistent rectangular and hexagonal symmetries. High-quality STM molecular resolution yielded the internal molecular structure and the orientation of CuPc(OC8H17)8 admolecules. These STM results could shed insight into the method of generating ordered molecular assemblies of phthalocyanine molecules with long-chained substitutes on metal surface. Microsc. Res. Tech., 2008. © 2007 Wiley-Liss, Inc. [source] Vertically aligned diamond nanowires: Fabrication, characterization, and application for DNA sensingPHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 9 2009Nianjun Yang Abstract In this review, we introduce a novel procedure to fabricate vertically aligned diamond nanowires with controlled geometrical properties like length and distance between wires by use of nanodiamond particles as a hard mask and by use of reactive ion etching. We summarize the characterizations of nanowires by atomic force microscopy and scanning tunneling microscopy as well as electrochemical techniques. In the last section, we show biofunctionalization of nucleic acid molecules on diamond nanowires using electrochemically bond nitrophenyl molecules as linker for deoxyribonucleic acid (DNA) sensing. The tip biofunctionalization and performance of as-prepared DNA sensors are discussed in detail. [source] Mechanisms of semiconductor nanostructure formationPHYSICA STATUS SOLIDI (A) APPLICATIONS AND MATERIALS SCIENCE, Issue 1 2003R. S. Goldman Abstract We have examined the formation mechanisms of a variety of semiconductor nanostructures, including phase separation-induced alloy nanostructures and strain-induced self-assembled quantum dots. Using data from cross-sectional scanning tunneling microscopy, in conjunction with X-ray reciprocal space maps, we have developed new models for self-ordering of InAs/GaAs quantum dot superlattices and spontaneous lateral phase separation in InAlAs alloys. These models are likely to be applicable to a wide range of heteroepitaxial semiconductor nanostructures. [source] Influence of substrate and temperature on the shape of deposited Fe, Co, and FeCo nanoparticlesPHYSICA STATUS SOLIDI (B) BASIC SOLID STATE PHYSICS, Issue 5 2010Wolfgang Rosellen Abstract In situ scanning tunneling measurements have been carried out on mass-filtered supported Fe, Co, and FeCo alloy nanoparticles with diameters between 4 and 14,nm. These nanoparticles are prepared from the gas phase using a continuously working cluster source and are subsequently deposited on bare W(110) and Ni(111)/W(110) surfaces. The size and the crystallographic structure before deposition are determined by high resolution transmission electron microscopy (HRTEM), the height of the nanoparticles on the substrate by scanning tunneling microscopy (STM). Depending on the substrate the particles do not maintain their spherical shape after deposition. The melting at elevated temperatures results in an anisotropic elongation along the [001] direction of the W(110) substrate. STM illustration of large Co nanoparticles deposited on an atomically flat W(110)-surface. [source] Crystallographically oriented high resolution lithography of graphene nanoribbons by STM lithographyPHYSICA STATUS SOLIDI (B) BASIC SOLID STATE PHYSICS, Issue 4 2010G. Dobrik Abstract Due to its exciting physical properties and sheet-like geometry graphene is in the focus of attention both from the point of view of basic science and of potential applications. In order to fully exploit the advantage of the sheet-like geometry very high resolution, crystallographicaly controlled lithography has to be used. Graphene is a zero gap semiconductor, so that a field effect transistor (FET) will not have an "off" state unless a forbidden gap is created. Such a gap can be produced confining the electronic wave functions by etching narrow graphene nanoribbons (GNRs) typically of a few nanometers in width and with well defined crystallographic orientation. We developed the first lithographic method able to achieve GNRs that have both nanometer widths and well defined crystallographic orientation. The lithographic process is carried out by the local oxidation of the sample surface under the tip of a scanning tunneling microscopy (STM). Crystallographic orientation is defined by acquiring atomic resolution images of the surface to be patterned. The cutting of trenches with controlled depth and of a few nanometer in width, folding and manipulation of single graphene layers is demonstrated. The narrowest GNR cut by our method is of 2.5,nm width, scanning tunneling spectroscopy (STS) showed that it has a gap of 0.5,eV, comparable to that of germanium, which allows room temperature operation of graphene nanodevices. [source] Density functional study of graphene overlayers on SiCPHYSICA STATUS SOLIDI (B) BASIC SOLID STATE PHYSICS, Issue 7 2008Alexander Mattausch Abstract Despite the ongoing "graphene boom" of the last three years our understanding of epitaxial graphene grown on SiC substrate is only beginning to emerge. Along with experimental methods such as low energy electron diffraction (LEED), scanning tunneling microscopy (STM) and angle resolved photoemission spectroscopy (ARPES), ab initio calculations help to uncover the geometric and electronic structure of the graphene/SiC interface. In this chapter we describe the density-functional calculations we performed for single and double graphene layers on Si- and C-terminated 6H-SiC surfaces. Experimental data reveal a pronounced difference between the two surface terminations. On a Si-terminated surface the interface adopts a 6,3 × 6,3 unit cell whereas the C-face supports misoriented (turbostratic) graphene layers. It has been recently realized that, on the Si-face, the large commensurate cell is subdivided into patches of coherently matching to the substrate carbon atoms. In our calculations we assumed the "coherent match" geometry for the whole interface plane. This reduces the periodic unit to the ,3 × ,3R 30° cell but requires a substantial stretching of the graphene sheet. Although simplified, the model provides a qualitative picture of the bonding and of the interface electron energy spectrum. We find that the covalent bonding between the carbon layer and the substrate destroys the massless "relativistic" electron energy spectrum, the hallmark of a freestanding graphene. Hence the first carbon layer cannot be responsible for the graphene-type electron spectrum observed by ARPES and rather plays a role of a buffer between the substrate and the subsequent carbon sheets. The "true" graphene spectrum appears with the second carbon layer which exhibits a weak van der Waals bonding to the underlying structure. For Si-terminated substrate, we find that the Fermi level is pinned by the interface state at 0.45 eV above the graphene Dirac point, in agreement with experimental data. This renders the interface metallic. On the contrary, for a C-face the "coherent match" model predicts the Fermi level exactly at the Dirac point. However, this does not necessarily apply to the turbostratic graphene layers that normally grow on the C-terminated substrate. (© 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Inhomogeneous surface electronic properties and charge ordering in epitaxial Fe3O4 films on MgO(001)PHYSICA STATUS SOLIDI (B) BASIC SOLID STATE PHYSICS, Issue 12 2007A. Subagyo Abstract We report scanning tunneling microscopy (STM) study of surface electronic properties and charge ordering of epitaxially grown magnetite, Fe3O4, (001) films exhibiting high density of antiphase domain boundaries (APBs). STM measurements using a W tip reveal surface termination at B-sites. Fe ions with a 0.3 nm periodicity, i.e., a single atomic distance are observed. Current imaging tunneling spectroscopy reveals the alternation of two kinds of current peaks with a 0.6 nm periodicty indicating the presence of charge ordering consisted of Fe dimers with different charge states. STM measurements using a magnetic Ni tip provide higher contrast of the charge ordering. The APBs can modify the charge ordering as ordered and disordered areas are observed on adjacent domains separated by an APB. These strongly indicate that APBs can induce inhomogeneous properties on the surface of Fe3O4(001) films. (© 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] | |||||||||||||||||||