Morphology, atomic composition and photoelectric properties of the microrelief InP-electrolyte interface

Morphology and atomic composition of anisotropically etched surfaces of InP have been studied by Auger electron spectroscopy (AES) and scanning electron microscopy (SEM). The photoelectric properties and the voltage-capacitance characteristics of the InP-electrolyte interface have been investigated. A correlation between these properties and the surface morphology and atomic composition was shown. The highest photosensitivity was found for flat stoichiometric surfaces with an optimal transition layer between the oxide and the semiconductor and a low content of In in its oxide.     

低能电子显微术及其应用

低能电子显微术是新发展起来的一种显微探测技术。它的特点是利用低能（１－３０ｅＶ）电子的弹性背散射使表面实空间实时成像，具有高的横向（１５ｎｍ）和纵向（原子级）分辩率，且易与低能电子衍射及其他电子显微术相结合。近年来它已有效地应用于金属和半导体表面的形貌观测、表面相变、吸附、反应及生长过程的研究。     

Investigating the surface morphology and magnetic contrast of epitaxial ferromagnetic structures

The surface morphology of nickel thin films is investigated via atomic force microscopy. The multistage film growth mechanism is found to be dependent on substrate temperature and film thickness. It is shown that conduction electron scattering from the irregularities of the outer and inner surfaces of structures are influenced by the surface morphology and determined by an integrated contribution of the surface’s fluctuation density spectrum. The morphology influence can be decreased under certain growth conditions so that the residual mean free path of conduction electrons can reach 1000 nm, exceeding the film thickness. Epitaxial nanostructures with high electron mobility have been fabricated. Investigation of their magnetic structure has shown that their magnetic domain dimensions are less than the residual mean free path of electrons determined by the surface morphology.     

Nanoscale depth-resolved cathodoluminescence spectroscopy of ZnO surfaces and metal interfaces

The electronic properties of ZnO surfaces and interfaces has until recently been relatively unexplored. We have used a complement of ultrahigh vacuum scanning electron microscope (SEM)-based, depth-resolved cathodoluminescence spectroscopy (DRCLS), temperature-dependent charge transport, trap spectroscopy, and surface science techniques to probe the electronic and chemical properties of clean surfaces and interfaces on a nanometer scale. DRCLS reveals remarkable nanoscale correlations of native point defect distributions with surface and sub-surface defects calibrated with capacitance trap spectroscopies, atomic force microscopy, and Kelvin probe force microscopy. The measurement of these near-surface states associated with native point defects in the ZnO bulk and those induced by interface chemical bonding is a powerful extension of cathodoluminescence spectroscopy that provides a guide to understanding and controlling ZnO electronic contacts.     

Atomic structure of alkali halide surfaces

The atomic structure of surfaces of alkali halide crystals has been revealed by means of high-resolution dynamic force microscopy. True atomic resolution is demonstrated both on steps surrounding islands or pits, and on a chemically mixed crystal. We have directly observed the enhanced interaction at low-coordinated sites by force microscopy. The growth of NaCl films on metal surfaces and radiation damage in a KBr surface is discussed based on force microscopy results. The damping of the tip oscillation in dynamic force microscopy might provide insight into dissipation processes on the atomic scale. Finally, we present atomically resolved images of wear debris found after scratching a KBr surface. PACS 68.37.-d; 68.37.Ps; 75.55.Fv     

Directed assembly of nanostructured carbon materials on to patterned polymer surfaces

Directed assembly of single-walled carbon nanomaterials on to polymer surfaces has been achieved. The approach relies on selective interactions of the polymer functionalities with the surface structures present on the carbon materials. The successful immobilization of the carbon structures was confirmed by scanning electron microscopy, atomic force microscopy, and Raman spectroscopy. By generating patterned polymer surfaces with chemically distinct components through the control of polymer–polymer or polymer–substrate interactions, directed assembly of single-walled carbon nanohorns and single-walled nanotubes was demonstrated. This new type of carbon assembly might open up new avenues in the construction of functional polymer/carbon composites and flexible nanocarbon nano-electronics.     

The influence of sulfur adsorption on the step structure of vicinal Mo(100): a LEED and STM study

The effect of sulfur adsorption on the step structure of vicinal Mo(100) surfaces has been studied with scanning tunneling microscopy (STM) and low energy electron diffraction (LEED). STM was used for low densities of steps on a nominally flat (100) surface. LEED was used to study the more highly and regularly stepped (910), (911), and (28,4,1) oriented surfaces. Steps and the sulfur adsorbate were found to have a strong interaction. The presence and orientation of steps on the surface governed the formation of ordered domains of sulfur, and sulfur modified the structure of the steps on the surface. Both techniques show that monatomic steps predominate on the clean surfaces. When sulfur was adsorbed on the surfaces, however, steps coalesced to form groups of steps, double atomic height steps, and multiple height steps, depending on sulfur coverage and initial step density. The results are discussed in the framework of the theory of equilibrium crystal shape and provide information on how the Mo step-step interactions are affected by sulfur adsorption.     

Methods for the Modification and Characterization of Oxide Surfaces

This paper presents a general overview of the chemical modificationof oxide surfaces with particular emphasis on the silanization/hydrosilationmethod. A number of materials have been synthesized that have hydrophobic,hydrophilic, chiral and liquid crystal surfaces. The most frequently usedoxide in these materials is silica with chromatography as the primaryapplication for the chemically modified oxide surfaces. Also presented is anoverview of a number of methods used to characterize modified oxide surfacessuch as elemental analysis, diffuse reflectance infrared Fourier transformspectroscopy, solid-state NMR, electron spectroscopy for chemical analysis,scanning electron microscopy and atomic force microscopy. The particularadvantages of each method for the characterization of modified oxidematerials are discussed.     

Surface morphology and surface chemical states of epitaxial Pb(Zr0.95Ti0.05)O3 thin films grown on SrTiO3(100) by sputter deposition

0.95 Ti_0.05)O₃ thin films of an orthorhombic perovskite structure were obtained on SrTiO₃(100) substrates by radio frequency sputter deposition. The surface morphology of the films was investigated with atomic force microscopy, scanning electron microscopy, and reflection electron microscopy. It is shown that the film surfaces are rather bumpy. There are undulations of about 400 nm in length in an in-plane direction. The mean roughness perpendicular to the surface is 39.6 nm, for the film thickness of 0.45 μm. The surface roughening was probably caused by island-shaped nucleation and growth during the film growth. It has also been found that some gorges and a number of small pits remain at the film surfaces. The surface chemical states of the films were characterized by using X-ray photoelectron spectroscopy. A Pb enrichment layer and a large amount of adsorbed oxygen have been found at the surfaces of the films. Near the film surface Pb and Zr exist mainly in the forms of, besides Pb(Zr,Ti)0₃, metal Pb, metal Zr, oxygen-chemisorbed Pb, and various lead oxides. In addition, a small amount of lead, whose binding energy of Pb 4f_7/2 is much lower than that of metal Pb, was observed at the film surfaces, but its chemical state is unknown up to now. Received: 2 June 1997/Accepted: 22 September 1997     

Influence of the grain-size and chemical composition of a MgO coating on the structure-phase state and elemental composition of the ground layer formed on an electric steel surface

The surface morphology, phase state and elemental composition, and substructure of the ground layer of anisotropic electric steel (AES) samples have been studied via scanning electron microscopy, atomic force microscopy, transmission electron microscopy, electron probe microanalysis, and x-ray diffractometry. High-temperature annealing of MgO coatings with different grain-size distributions and chemical compositions was found to lead to formation of a single-phase layer of forsterite (Mg₂SiO₄) on the AES surface. It has been revealed that the morphology and substructure of a forsterite layer depend on the grain-size distribution and chemical composition of magnesium oxide and the conditions used in preparation of MgO suspensions. When added to MgO suspensions, TiO₂ and Na₂B₄O₇ impurities promote formation of a denser coating substructure. The increased mixing speed used in suspension preparation improves the surface homogeneity of a ground layer only if a suspension contains MgO grains of different size.     

General regularities of interaction between halogens and surface of fcc metals

Main peculiarities of chemical interaction between halogens and fcc metals have been analyzed and results for chemical reaction on copper and silver surfaces as the most studied ones are discussed. General information about the structure of adsorbed layers on metal surfaces is presented. It has been shown that halogenation occurs in two stages. First, a monolayer of chemisorbed halogen atoms is formed, and then metal halide starts to grow, forming a continuous halide film on the surface. The chlorination of silver is indicated (on the basis of the spectroscopic data) as a unique case due to the possible chlorine dissolution into the substrate bulk. It has also been shown that the use of low-energy electron diffraction is usually ineffective for identification of incommensurate lattices at the stage of monolayer and halide film structure formation. To study incommensurate surface structures and halide nucleation processes on atomic scale, probe microscopy and methods for detecting local structure are necessary.     

Synthesis of bismuth nanocap arrays on quartz substrates and their surface plasmon resonance properties

Bismuth nanocap arrays have been prepared by vacuum depositing Bi films onto the surfaces of self-assembled monolayer arrays of SiO₂ nanoparticles. The surface morphologies, structures, and optical properties of the obtained samples have been characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), atomic force microscope (AFM), X-ray diffraction (XRD), and ultraviolet–visible–near infrared (UV–vis–NIR) spectrophotometer. TEM and AFM images indicated that the SiO₂/Bi composite nanoparticles were incompletely encapsulated and their surfaces were relatively rough. UV–vis–NIR absorption spectra showed that Bi nanocap arrays had strong and tunable surface plasmon resonance peaks in the visible and near infrared regions, which were dependent dramatically on the relative ratio of the SiO₂ core diameter to the Bi cap thickness.     

Features of atomic processes at the formation of a wetting layer and nucleation of three-dimensional Ge islands on Si(111) and Si(100) surfaces

The intermediate stages of the formation of a Ge wetting layer on Si(111) and Si(100) surfaces under quasiequilibrium grow conditions have been studied by means of scanning tunneling microscopy. The redistribution of Ge atoms and relaxation of mismatch stresses through the formation of surface structures of decreased density and faces different from the substrate orientation have been revealed. The sites of the nucleation of new three-dimensional Ge islands after the formation of the wetting layer have been analyzed. Both fundamental differences and common tendencies of atomic processes at the formation of wetting layers on Si(111) and Si(100) surfaces have been demonstrated. The density of three-dimensional nuclei on the Si(111) surface is determined by changed conditions for the surface diffusion of Ge adatoms after change in the surface structure. Transition to three-dimensional growth on the Si(100) surface is determined by the nucleation of single {105} faces on the rough Ge(100) surface.     

Effects of KOH etching on the properties of Ga-polar n-GaN surfaces

The effects of a KOH treatment on the properties of n-type GaN surfaces and associated Au/n-GaN contacts have been investigated by X-ray photoelectron spectroscopy, atomic force microscopy, reflection high-energy-electron diffraction, current–voltage and electron-beam-induced current characterization. Ga-polar surfaces grown by molecular beam epitaxy and metal–organic chemical vapour deposition were compared. A decrease in electron barrier height and an increase in non-radiative recombination properties of Au/n-GaN contacts were found with KOH treatment, correlated with an increase of surface Ga vacancies, an increase in surface N–H₂ content and a decrease in surface C contamination. A 0.3-eV shift in the Ga3d peak position towards the valence band and a reduction in the dislocation contrast were observed for the case of molecular-beam-epitaxy-grown GaN only, demonstrating that surface Ga vacancies and threading dislocations play only a limited role in defining the resultant metal/GaN contact properties. Accordingly, the surface atomic content and the resulting surface states, following KOH treatment, should be taken into consideration when appraising the electrical properties of n-GaN surfaces and the performance of associated metallic contacts.     

UHV-HREM and diffraction of surfaces

Characterization of the structure of surfaces is very important in order to develop a fundamental understanding of the electronic, mechanical and chemical properties of a material. While transmission electron microscopy imaging (TEM) and diffraction (TED) techniques are capable of providing surface structural information at the atomic level, such data would be suspect if obtained under conventional vacuum conditions (10^-6–10^-8 Torr). Ultrahigh vacuum (UHV) conditions are imperative during both preparation and observation of clean surfaces/interfaces. Conventional TEM techniques are very powerful for UHV-TEM investigations; however, the marriage of surface science and conventional TEM to yield an UHV-TEM is a complex task. These complexities and some of the results obtained using UHV-TEM and UHV-TED techniques for surfaces i.e. solid-vacuum interfaces will be illustrated.     

Modifying the physicochemical and electrical properties of tantalite and columbite surfaces under conditions of electrochemical treatment and high-voltage nanosecond pulses

Structural and chemical modifications of tantalite and columbite surfaces, induced by treating the minerals with anolyte—a product derived via the electrolysis of aqueous solutions—and high-voltage electromagnetic pulses, are studied by means of X-ray photoelectron spectroscopy, scanning electron microscopy, energy-dispersive spectroscopy, atomic force microscopy, and electrophoretic light scattering. The mechanical properties of the surfaces are characterized via Vickers microhardness testing. Treating the minerals with anolyte removes iron-containing surface films and leads to considerable conversion of surface-confined Fe(II) species into Fe(III), increasing the differences between the physicochemical and electrical properties of these rare earth minerals. The nonthermal impact of high-voltage pulses results in effective surface softening, a reduction in microhardness, and the disintegration of mineral particles, yielding surface micro- and nanosized phases enriched with iron and oxygen.     

Towards the demonstration of actuator properties of a single carbon nanotube

Owing to its huge elastic modulus, good conductivity and large free surface area per mass, a single carbon single-walled nanotube (SWNT) should present optimal intrinsic actuation properties. Our aim is to demonstrate the viability of such a single nanotube-based actuator (“nano-actuator”). To achieve this goal, the primary focus was on how to obtain and manipulate an isolated and suspended SWNT. Several strategies have been attempted to produce such nanotubes (NTs), among them the “stamping” of tubes on functionalised substrates, or the direct growth of tubes from an oxide catalyst layer on a pre-designed substrate. Characterisation of these structures was carried out by atomic force microscopy, scanning electron microscopy and transmission electron microscopy. Manipulation of NT on flat surfaces was first demonstrated, before attempts were made to probe the suspended NTs. The final and most important step will be the use of an atomic force microscope to probe the deformation of the nanotube which should occur under a bias voltage in an electrochemical cell.     

Steps, ledges and kinks on the surfaces of platinum nanoparticles of different shapes

Platinum nanoparticles with a high percentage of cubic-, tetrahedral- and octahedral-like shapes, respectively, have been synthesized by a shape-controlling technique that we developed recently [Ahmadi et al., Science 272 (June 1996) 1924]. High resolution transmission electron microscopy (HRTEM) is used here to directly image the atomic scale structures of the surfaces of these particles with different shapes. The truncated shapes of these particles are mainly defined by the {100}, {111}, and {110} facets, on which numerous atom-high surface steps, ledges and kinds have been observed. This atomic-scale fine structure of the surfaces of these particles is expected to play a critical role in their catalytic activity and selectivity.     

Adsorption and valence electronic states of nitric oxide on metal surfaces

Among fundamental diatomic molecules, the adsorption of carbon monoxide (CO) and nitric oxide (NO) on metal surfaces has been a subject of intensive research in the surface science community, partly owing to its relevance to heterogeneous catalysis used for environmental control. Compared to the rather well-defined adsorption mechanism of CO, that of NO is less understood because the adsorption results in much more complex reactions. The complexity is ascribed to the open-shell structure of valence electrons, making the molecule readily interact with the metal surface itself as well as with co-adsorbed molecules. Furthermore, the interaction crucially depends on the local structure of the surface. Therefore, to elucidate the interaction at the molecular scale, it is essential to study the valence state as well as the bonding geometry for individual NO molecules placed in a well-defined environment on the surface. Scanning tunneling microscopy (STM) is suitable for this purpose. In this review, we summarize the knowledge about the interaction of NO with metal surfaces, mainly focused on the valence electronic states, followed by recent studies using STM and atomic force microscopy (AFM) at the level of individual molecules.     

Superhydrophobic wind turbine blade surfaces obtained by a simple deposition of silica nanoparticles embedded in epoxy

Samples of wind turbine blade surface have been covered with a superhydrophobic coating made of silica nanoparticles embedded in commercial epoxy paint. The superhydrophobic surfaces have a water contact angle around 152°, a hysteresis less than 2° and a water drop sliding angle around 0.5°. These surfaces are water repellent so that water drops cannot remain motionless on the surface. Examination of coated and uncoated surfaces with scanning electron microscopy and atomic force microscopy, together with measurements of water contact angles, indicates that the air trapped in the cavity enhances the water repellency similarly to the lotus leaf effect. Moreover, this new coating is stable under UVC irradiation and water pouring. The production of this nanoscale coating film being simple and low cost, it can be considered as a suitable candidate for water protection of different outdoor structures.