A modular scanning tunneling microscope with an interchangeable elastic closed cell and external actuators

We introduce a novel modular cell based scanning tunneling microscope with external piezoelectric actuators. A tip and a sample are contained in a closed interchangeable cell, consisting of a stiff top plate and a bottom part, fastened together by an elastic material. The bottom part, containing a scanning tip, is fastened to a base unit while the top plate, containing a sample, is capable of scanning motion by external piezoelectric actuators mounted in the same base unit. The actuators are pre-loaded by the deformation of the elastic material of the cell, giving an increased stability. This design is expected to simplify the scanning tunneling microscope (STM) operation in difficult environments greatly by enclosing only the tip and sample in a small cell-module, which is pluggable to a scanning mechanism and other supportive functionalities. A frequency characterization and an image scan showing atomic resolution of highly oriented graphite in air, at room temperature, is presented.     

Ordered thin films of alkyloxy-substituted benzaldehydes on a graphite surface studied by scanning tunneling microscopy

The molecular assembly of three different trialkyloxy-substituted benzaldehydes on graphite has been studied using scanning tunneling microscopy (STM). It is found that these benzaldehydes, which do not have intermolecular hydrogen bonding, could form a lamella arrangement in which the headgroups are aligned side by side. The effect due to the alkyl chain length on the lamella structure is also presented. Received: 21 January 2002 / Accepted: 22 March 2002 / Published online: 10 September 2002 RID="*" ID="*"Corresponding author. Fax: +86-10/6255-7908     

Observation of Si(1 0 0) surfaces annealed in hydrogen gas ambient by scanning tunneling microscopy

We investigated the cleaning process of Si(1 0 0) surfaces by annealing in H₂ gas ambient following chemical treatments by scanning tunneling microscopy. We observed the monohydride Si structure: Si(1 0 0):2 × 1-H on the surfaces annealed at 1000 °C in 2.5 × 10⁴ Pa H₂ gas ambient without conspicuous contaminants. On the sample annealed for 10 min or longer times, well-defined Si(1 0 0) structures with alternating S_A and S_B steps were observed, whereas the initial roughness still remained on the surfaces annealed for only 5 min.     

An externally cooled beetle type scanning tunneling microscope for imaging in cryogenic liquids

We describe a variable temperature cryogenic scanning tunneling microscope designed for imaging and research in cryogenic liquids. It has an external Dewar type large scale cooling system with a temperature control range of roughly 85-110 K using pressure controlled liquid nitrogen cooling. The liquid nitrogen is kept in a closed chamber surrounding the STM and maintained at a pressure to suit the chosen temperature. Several gases have triple points in this temperature range and can therefore be liquified, such as argon, methane, silane and germane. The STM is based on a beetle type design built into a small cube vacuum chamber to fit into the cooling dewar. The system has been used for atomic resolution of highly oriented graphite submerged in a methane liquid at a temperature of 100 K.     

Oxidation of graphene on Ru(0 0 0 1) studied by scanning tunneling microscopy

The oxidation of graphene layer on Ru(0 0 0 1) has been investigated by means of scanning tunneling microscopy. Graphene overlayer can be formed by decomposing ethyne on Ru(0 0 0 1) at a temperature of about 1000 K. The lattice mismatch between the graphene overlayer and the substrate causes a moiré pattern with a superstructure in a periodicity of about 30 Å. The oxidation of graphene/Ru(0 0 0 1) was performed by exposure the sample to O₂ gas at 823 K. The results showed that, at the initial stage, the oxygen intercalation between the graphene and the Ru(0 0 0 1) substrate takes place at step edges, and extends on the lower steps. The oxygen intercalation decouples the graphene layer from the Ru(0 0 0 1) substrate. More oxygen intercalation yields wrinkled bumps on the graphene surface. The oxidation of graphene, or the removal of carbon atoms can be attributed to a process of the combination of the carbon atoms with atomic oxygen to form volatile reaction products. Finally, the Ru(0 0 0 1)-(2 × 1)O phase was observed after the graphene layer is fully removed by oxidation.     

Subharmonic gap structure in superconducting scanning tunneling microscope junctions

We observe a subharmonic gap structure (SGS) and the Josephson effect in superconducting scanning tunneling microscope junctions with resistances below 100 kΩ. The magnitude of the n=2 SGS is shown to scale with the square of the junction normal state conductance, in agreement with theory. We show by analyzing the Josephson effect in these junctions that the superconducting phase dynamics are strongly affected by thermal fluctuations. We estimate the linewidth of the Josephson oscillations due to phase fluctuations, a quantity that may be important in modern theories of the subgap structure. While phase fluctuations may smear the SGS current onsets, we conclude that the sharpness of these onsets in our data is not limited by fluctuations.     

Adsorption of cobalt phthalocyanine on a Si(1 0 0) surface with Bi-line structures as evaluated by scanning tunneling microscopy

We report the reaction dynamics of cobalt phthalocyanine (CoPc) molecules with Bi-line structures (BLSs) on a Si(1 0 0) surface, investigated using scanning tunneling microscopy (STM). When CoPc molecules were deposited on a Si(1 0 0) surface with BLSs at room temperature, single-spot protrusions were observed in the STM image instead of four-spot images corresponding to CoPcs flat molecular structure. Moreover, domains with a c(4 × 4) periodicity appeared on the terraces of the Si(1 0 0) surface. This indicates that CoPc molecules may have decomposed on the surface by catalytic reaction with Bi atoms.     

Defects in III–V semiconductor surfaces

This work reports the measurement of the nano-scale physical properties of surface vacancies and the extraction of the types and concentrations of dopant atoms and point defects inside compound semiconductors, primarily by cross-sectional scanning tunneling microscopy on cleavage surfaces of III–V semiconductors. The results provide the basis to determine the physical mechanisms governing the interactions, the formation, the electronic properties, and the compensation effects of surface as well as bulk point defects and dopant atoms. Received: 10 May 2001 / Accepted: 23 July 2001 / Published online: 3 April 2002     

Imaging of ferroelectric vinylidene fluoride and trifluoroethylene copolymer films by scanning tunneling microscopy

In this paper, we reported the possibility to image non-conducting P(VDF-TrFE) copolymer films by STM. The films had the thickness of ∼25.0 nm and were spin-coated onto Au or graphite substrates. For films deposited on Au substrates, STM images showed grain structures of ∼100 nm, much larger than the grains of bare Au substrate. With increased scan rate, the film surface was damaged by STM tip and extreme protrusions and holes were observed. For films deposited on graphite substrates, we only obtained an image of very flat plane and could not observe the topography of the film surface. It seemed that the tip had pierced through the uppermost P(VDF-TrFE) layers and only imaged the layers nearest to the substrate. Asymmetrical current-voltage curves were observed from copolymer films deposited on HOPG. Experimental results were discussed.     

Quasi-one-dimensional In atomic chains on Si(1 1 1) at low temperature studied by reflection high-energy positron diffraction and scanning tunneling microscopy

We have investigated a quasi-one-dimensional structure of Si(1 1 1)-8 × 2-In surface using reflection high-energy positron diffraction (RHEPD) and scanning tunneling microscopy (STM). From the RHEPD rocking curve analyses, we confirmed the formation of the In hexagon structure proposed by González et al. [C. González, F. Flores, J. Ortega, Phys. Rev. Lett. 96 (2006) 136101]. Furthermore, we found that the empty-state STM image at 44 K is consistent with that calculated with the optimum hexagon structure by the RHEPD analyses.     

Determining the spin polarization of surfaces by spin-polarized scanning tunneling spectroscopy

During the last few years, spin-polarized scanning tunneling microscopy and spectroscopy has been developed as a reliable tool to image surface magnetic domain structures of bulk materials as well as thin films and nanostructured systems. In principle, this technique also allows for the determination of the energy-resolved spin polarization of the sample P_S(E) with nanometer resolution, information which might play a crucial role in understanding systems like, for example, non-magnetic adatoms on magnetic surfaces. A main problem in quantifying P_S(E), however, arises from the fact that, in contrast to planar junctions, the tip–sample distance generally varies with the magnitude and direction of the surface magnetization, since the distance is controlled indirectly by the tunneling current that is itself spin-polarized. We employ a simple model of the tunneling process to investigate this issue and show that a normalization of the dI/dU spectra with the total conductance I/U is insufficient to correct for their distance dependence. Received: 2 September 2002 / Accepted: 2 September 2002 / Published online: 5 March 2003 RID="*" ID="*"Corresponding author. Fax: +49-40/42838-5311, E-mail: kubetzka@physnet.uni-hamburg.de     

Atomic structure of the non‐polar GaN($ \bar 2 $110) surface by cross‐sectional scanning tunneling microscopy

The ( 110) plane of gallium nitride, exposed by cleaving a GaN single crystal under ultra‐high vacuum conditions, has been atomically resolved for the first time, using cross‐sectional scanning tunneling microscopy. The spatial period length supports a (1 × 1) unit mesh size, i.e., the absence of a reconstruction. The contrast observed in the experimental data is well explained by the atomic arrangement expected for a truncated‐bulk structure. (© 2009 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Optical oscillation modes of plasmon particles observed in direct space by phase-contrast near-field microscopy

Light distributions near resonant metal nanoparticles are recorded by a scattering-type scanning near-field optical microscope (s-SNOM), for the first time with a sub-particle-size resolution (<10 nm) and with simultaneous amplitude and phase contrast. The images depict the optical oscillation patterns of single plasmon particles. Examples are presented of particles excited in dominantly dipolar and quadrupolar modes, and also of closely spaced particles sustaining a gap mode. The gap mode can provide enhanced optical fields in nanometric spots for non-linear and single-molecule spectroscopy applications. Received: 20 June 2001 / Revised version: 3 August 2001 / Published online: 19 September 2001     

Coherent scattering phenomena in apertureless scanning near-field fluorescence microscopy

We study near-field fluorescence images of samples composed of aggregates of 100 nm dye-doped latex spheres. These images have been performed by a reflection Apertureless Scanning Near-field Optical Microscope (A-SNOM). We show that the near-field distribution in fluorescence A-SNOM images arises from coherent scattering phenomena between all spheres. This is a consequence of the coherent nature of the fluorescence emission of each single sphere. The results shown here are significant for all fluorescent samples characterised by a nonnegligible topography.     

Fabrication and scanning tunneling microscopy studies of the Si(1 1 1)-(√31 × √31)-In surface

We report on the fabrication of single phase of the Si(1 1 1)-(√31 × √31)-In reconstruction surface, observed by scanning tunneling microscopy (STM) at room temperature. By depositing specific amounts of indium atoms while heating the Si(1 1 1)-(7 × 7) substrate at a critical temperature, the single phase of Si(1 1 1)-(√31 × √31)-In surfaces could be routinely obtained over the whole surface with large domains. This procedure is certified by our high-resolution STM images in the range of 5-700 nm. Besides, the high resolution STM images of the Si(1 1 1)-(√31 × √31)-In surface were also presented.     

High temperature STM/STS investigations of resonant image states on Au(1 1 1)

Scanning tunneling microscopy (STM) and spectroscopy (STS) were used to study the electronic structure of Au(1 1 1) surface in the range of 2-5.5 eV above the Fermi level. In this paper, we concentrate firstly on the position of the upper band gap edge (BE) existing in [1 1 1] direction in Au(1 1 1) and secondly on the position of the resonant image potential surface state (RIS) located in the bulk states approximately 1.1 eV above BE. The experiment was carried out in UHV at two temperatures 294 K and 580 K. Our high temperature STS (HT-STS) results clearly show the presence of RIS and BE local maxima at both temperatures. What is more, a slight shift towards the Fermi level of BE and RIS was observed. Those shifts were the consequence of the change of [1 1 1] band gap and lowering gold work function due to the thermal extension of interatomic distances. Finally, estimation of the work function was given at 294 K and 580 K.     

Self-assembled monolayers of radical molecules physisorbed on HOPG(0 0 0 1) substrate studied by scanning tunnelling microscopy and electron paramagnetic resonance techniques

In this paper, we present a combined STM and EPR study on the adsorption and self-organization of monolayers formed from 2-(14-Carboxytetradecyl)-2-ethyl-4,4-dimethyl-3-oxazolidinyloxy (16DS) and 4′,4′-Dimethylspiro(5α-cholestane-3,2′-oxazolidin)-3′-yloxy (CSL) adsorbed on a highly oriented pyrolitic graphite HOPG(0 0 0 1) substrate. Both 16DS and CSL molecules are persistent free radicals containing a paramagnetic doxyl group. The STM measurements of 16DS on HOPG(0 0 0 1) were performed at the liquid-solid interface while the studies of CSL on HOPG(0 0 0 1) were carried out under ultrahigh vacuum conditions. It was found that the 16DS molecules on the HOPG(0 0 0 1) surface form a highly-ordered monolayer with a domain structure. The high-resolution STM images show structural details of 16DS molecules on HOPG(0 0 0 1) revealing the paramagnetic doxyl group. In contrast, CSL molecules on HOPG(0 0 0 1) form a well-ordered monolayer without domain structure. The EPR results indicate that both compounds deposited on HOPG(0 0 0 1) substrate are not reduced and retain their paramagnetic character. We believe that the molecular systems described can be used in single spin detection experiments using an electron spin noise-scanning tunnelling microscopy (ESN-STM) technique. In particular, the possibility of obtaining contrast spin signals from the paramagnetic and diamagnetic parts of molecules increases the significance of our results.     

Scanning tunneling microscopy observation of initial growth of Sn and Ge1−xSnx layers on Ge(0 0 1) substrates

We have investigated the initial growth of Sn and Ge_1−xSn_x layers on Ge(0 0 1) surface by using scanning tunneling microscopy. After the growth of a 0.035 ML-thick Sn layer at room temperature, Sn clusters lining vertically to a dimer row was observed. In the case of the 0.035-0.018 ML-thick Sn growth at 250 °C, the characteristic surface reconstruction with the step-edge undulation like a comb was observed. In the growth of a Ge_0.994Sn_0.006 layer at 250 °C, the multilayer polynuclear growth with a lot of two-dimensional small domain was observed. These surface reconstructions should be accounted for by the large compressive stress induced in the surface layer due to the incorporation of Sn atoms.     

Electrochemical behaviour of gold modified with contaminated TMP amine adlayers studied by STM, CV, EPR

Scanning tunnelling microscopy (STM), cyclic voltammetry (CV) and electron paramagnetic resonance spectroscopy (EPR) were used to investigate the influence of the TMP amine derivative on Au (1 1 1). The STM results show that the gold surface covered by the adlayer of the TMP derivative is easily modified (holes formation) after increasing the bias voltage to 0.5 V. The CV and EPR results show the electrochemical origin of observed STM topography changes. It is suggested that TMP could be oxidized to the nitroxyl TEMPO radical which adsorbs on Au in the form of an oxoammonium cation. Such an oxoammonium cation at the potential of 0.5 V forms a permanent complex of gold and the nitroxyl radical which could be easily desorbed during STM imaging.     

Atomic scale characterization of oxygen adsorbates on Al(111) by scanning tunneling microscopy

We present atomic scale STM pictures of clean and oxygen containing Al(111) surfaces. Little influence of the surface oxygen on the topography of the surfaces is found. Three different oxygen species can be distinguished. One of them is associated with adsorbed oxygen and found to grow in small islands upon adsorption at 300 K. Characteristic hexagonal nuclei, created upon annealing of a dilute oxygen adlayer, represent the second one. By comparison with existing spectroscopic data these are assigned to nuclei of a surface oxide.