Johannes Biskupek

Selective Sputtering and Atomic Resolution Imaging of Atomically Thin Boron Nitride Membranes

We report on the preparation, atomic resolution imaging, and element selective damage mechanism in atomically thin boron nitride membranes. Flakes of less than 10 layers are prepared by mechanical cleavage and are thinned down to single layers in a high-energy electron beam. At our beam energies, we observe a highly selective sputtering of only one of the elements and predominantly at the exit surface of the specimen, and then subsequent removal of atoms next to a defect. Triangle-shaped holes appear in accordance with the crystallographic orientation of each layer. Defects are compared to those observed in graphene membranes. The observation of clean single-layer membranes shows that hexagonal boron nitride is a further material (in addition to graphene) that can exist in a quasi-two-dimensional allotrope without the need for a substrate.

Self-assembly of a sulphur-terminated graphene nanoribbon within a single-walled carbon nanotube

The ability to tune the properties of graphene nanoribbons (GNRs) through modification of the nanoribbons width and edge structure widens the potential applications of graphene in electronic devices. Although assembly of GNRs has been recently possible, current methods suffer from limited control of their atomic structure, or require the careful organization of precursors on atomically flat surfaces under ultra-high vacuum conditions. Here we demonstrate that a GNR can self-assemble from a random mixture of molecular precursors within a single-walled carbon nanotube, which ensures propagation of the nanoribbon in one dimension and determines its width. The sulphur-terminated dangling bonds of the GNR make these otherwise unstable nanoribbons thermodynamically viable over other forms of carbon. Electron microscopy reveals elliptical distortion of the nanotube, as well as helical twist and screw-like motion of the nanoribbon. These effects suggest novel ways of controlling the properties of these nanomaterials, such as the electronic band gap and the concentration of charge carriers.

Transmission electron microscopy at 20 kV for imaging and spectroscopy

The electron optical performance of a transmission electron microscope (TEM) is characterized for direct spatial imaging and spectroscopy using electrons with energies as low as 20 keV. The highly stable instrument is equipped with an electrostatic monochromator and a C(S)-corrector. At 20 kV it shows high image contrast even for single-layer graphene with a lattice transfer of 213 pm (tilted illumination). For 4 nm thick Si, the 200 reflections (271.5 pm) were directly transferred (axial illumination). We show at 20 kV that radiation-sensitive fullerenes (C(60)) within a carbon nanotube container withstand an about two orders of magnitude higher electron dose than at 80 kV. In spectroscopy mode, the monochromated low-energy electron beam enables the acquisition of EELS spectra up to very high energy losses with exceptionally low background noise. Using Si and Ge, we show that 20 kV TEM allows the determination of dielectric properties and narrow band gaps, which were not accessible by TEM so far. These very first results demonstrate that low kV TEM is an exciting new tool for determination of structural and electronic properties of different types of nano-materials.

Size, Structure, and Helical Twist of Graphene Nanoribbons Controlled by Confinement in Carbon Nanotubes

Carbon nanotubes (CNTs) act as efficient nanoreactors, templating the assembly of sulfur-terminated graphene nanoribbons (S-GNRs) with different sizes, structures, and conformations. Spontaneous formation of nanoribbons from small sulfur-containing molecules is efficiently triggered by heat treatment or by an 80 keV electron beam. S-GNRs form readily in CNTs with internal diameters between 1 and 2 nm. Outside of this optimum range, nanotubes narrower than 1 nm do not have sufficient space to accommodate the 2D structure of S-GNRs, while nanotubes wider than 2 nm do not provide efficient confinement for unidirectional S-GNR growth, thus neither can support nanoribbon formation. Theoretical calculations show that the thermodynamic stability of nanoribbons is dependent on the S-GNR edge structure and, to a lesser extent, the width of the nanoribbon. For nanoribbons of similar widths, the polythiaperipolycene-type edges of zigzag S-GNRs are more stable than the polythiophene-type edges of armchair S-GNRs. Both the edge structure and the width define the electronic properties of S-GNRs which can vary widely from metallic to semiconductor to insulator. The encapsulated S-GNRs exhibit diverse dynamic behavior, including rotation, translation, and helical twisting inside the nanotube, which offers a mechanism for control of the electronic properties of the graphene nanoribbon via confinement at the nanoscale.

A Universal Scheme to Convert Aromatic Molecular Monolayers into Functional Carbon Nanomembranes

Free-standing nanomembranes with molecular or atomic thickness are currently explored for separation technologies, electronics, and sensing. Their engineering with well-defined structural and functional properties is a challenge for materials research. Here we present a broadly applicable scheme to create mechanically stable carbon nanomembranes (CNMs) with a thickness of ~0.5 to ~3 nm. Monolayers of polyaromatic molecules (oligophenyls, hexaphenylbenzene, and polycyclic aromatic hydrocarbons) were assembled and exposed to electrons that cross-link them into CNMs; subsequent pyrolysis converts the CNMs into graphene sheets. In this transformation the thickness, porosity, and surface functionality of the nanomembranes are determined by the monolayers, and structural and functional features are passed on from the molecules through their monolayers to the CNMs and finally on to the graphene. Our procedure is scalable to large areas and allows the engineering of ultrathin nanomembranes by controlling the composition and structure of precursor molecules and their monolayers.

Transformations of Carbon Adsorbates on Graphene Substrates under Extreme Heat

We describe new phenomena of structural reorganization of carbon adsorbates as revealed by in situ atomic-resolution transmission electron microscopy (TEM) performed on specimens at extreme temperatures. In our investigations, a graphene sheet serves as both a quasi-transparent substrate for TEM and as an in situ heater. The melting of gold nanoislands deposited on the substrate surface is used to evaluate the local temperature profile. At annealing temperatures around 1000 K, we observe the transformation of physisorbed hydrocarbon adsorbates into amorphous carbon monolayers and the initiation of crystallization. At temperatures exceeding 2000 K the transformation terminates in the formation of a completely polycrystalline graphene state. The resulting layers are bounded by free edges primarily in the armchair configuration.

Interactions and Reactions of Transition Metal Clusters with the Interior of Single-Walled Carbon Nanotubes Imaged at the Atomic Scale

Clusters of transition metals, W, Re, and Os, upon encapsulation within a single-walled carbon nanotube (SWNT) exhibit marked differences in their affinity and reactivity with the SWNT, as revealed by low-voltage aberration-corrected high-resolution transmission electron microscopy (AC-HRTEM). Activated by an 80 keV electron beam, W reacts only weakly with the SWNT, Re creates localized defects on the sidewall, and Os reacts readily causing extensive defect formation and constriction of the SWNT sidewall followed by total rupture of the tubular structure. AC-HRTEM imaging at the atomic level of structural transformations caused by metal-carbon bonding of π- and σ-character demonstrates what a crucial role these types of bonds have in governing the interactions between the transition metal clusters and the SWNT. The observed order of reactivity W < Re < Os is independent of the metal cluster size, shape, or orientation, and is related to the metal to nanotube bonding energy and the amount of electronic density transferred between metal and SWNT, both of which increase along the triad W, Re, Os, as predicted by first-principles density functional theory calculations. By selecting the appropriate energy of the electron beam, the metal-nanotube interactions can be controlled (activated or precluded). At an electron energy as low as 20 keV, no visible transformations in the nanotube in the vicinity of Os-clusters are observed.

Optimization of STEM tomography acquisition — A comparison of convergent beam and parallel beam STEM tomography

In this paper two imaging modes in a state-of-the-art scanning transmission electron microscope (STEM) are compared: conventional STEM with a convergent beam (referred to as nanoprobe) and STEM with a parallel beam (referred to as microprobe). The effect and influence of both modes with respect to their depth of field are investigated. Tomograms of a human white blood cell (hemophagocytes) are acquired, aligned, and evaluated. It is shown that STEM using a parallel beam produces tomograms with fewer distortions and artifacts that allows resolving finer features. Microprobe STEM tomography is advantageous especially in life science, when semi-thin sections (approximately 0.5 microm thick) of biological samples are imaged at relatively low magnification with a large field of view.

Planar semipolar (101¯1) GaN on (112¯3) sapphire

We report on the growth of planar semipolar (101¯1) GaN on (112¯3) prepatterned sapphire. This is a method that allows the growth of semipolar oriented (101¯1) GaN on large scale. Using x-ray diffraction only the peaks of the desired (101¯1) plane could be observed. Scanning electron, transmission electron, and atomic force microscopy measurements show an atomically flat surface. Further investigations using photoluminescence spectroscopy show spectra that are dominated by the near band edge emission. The high crystal quality is furthermore confirmed by the small full width at half maximum values of x-ray rocking curve measurements of less than 400 arcsec.

Effect of nanoscale surface morphology on the phase stability of 3C-AlN films on Si(111)

In this work, we report on the stabilization of 3C-AlN polytype by molecular-beam epitaxy (MBE) on 3C-SiC∕Si(111) pseudosubstrates. The main purpose of the present studies is to analyze the mechanisms forcing the epitaxy of the 3C-AlN at typical MBE conditions. The forces driving the cubic polytype formation have been considered including supersaturation, macroscopic stress, interfacial energy, and interface morphology. We conclude that the growth of 3C-AlN phase can be stabilized on the “rough” 3C-SiC(111) surface by the polytype replication due to the lateral character of the nucleation and the reduction in the total energy of the film provided by periodical undulations of the template surface.