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Vladimir P. Oleshko

Publications and source records attributed to Vladimir P. Oleshko.

2 recordsLinked to original sources

Unraveling atomic-resolution valence electron energy-loss spectroscopic imaging in a single-crystal CaNb2O6

Despite advancements in electron optics and spectrometer design over the past twenty years, atomic-resolution valence-electron energy-loss spectroscopy imaging remains challenging due to the delocalization of inelastic electron scattering. In this study, we used an energy-filtered spectrometer equipped with a hybrid-pixel direct electron detector and spherical aberration-corrected scanning transmission electron microscopy to analyze many-electron excitations and interband transitions in a single-crystal calcium niobate, CaNb2O6, with spatial resolution ranging from the nanometers to the atomic scale. In the low-loss region above the bandgap at about 3.8 eV, we observed volume plasmons, around 6 eV and 15 eV energy loss, as well as a mix of strongly correlated plasmons and excitons, known as plexcitons, at approximately 7.3 eV energy loss. Additionally, we employed an on-axis EELS setup for atomic-resolution zero-loss peak (ZLP) imaging and visualized energy- and atom-resolved images of plexcitons and VPs, which showed contrast reversal relative to high-angle annular dark-field images. To investigate elastic contrast preservation, we also analyzed the effect of the collection angle and minimized its influence to produce delocalized VP images. In fact, the ZLP and VEELS images obtained using the weak-beam setup demonstrate that, in both cases, the contrast resembles Z-contrast. Moreover, we found that [NbO6] octahedra directly contributed to the lateral maps of interband transitions in the range from 3.2 eV to 3.5 eV energy loss. These findings demonstrate that Cs-STEM-EELS, which examines atomic-scale contrast associated with low-energy losses, can be a powerful tool for visualizing the structure, bonding, and electronic properties of complex crystalline nanostructures, including individual atomic sites, interstitial sites, and point defects.

cond-mat.mtrl-sci↗

Atomic reconstruction and moiré patterns in transition metal dichalcogenide van der Waals heterostructures

Van der Waals layered materials, such as transition metal dichalcogenides (TMDs), are an exciting class of materials with weak interlayer bonding which enables one to create van der Waals heterostructures (vdWH). Recent work has shown that control of the twist angle between layers can have a dramatic effect on vdWH properties. For TMD vdWH, twist angle has been treated solely through the use of rigid-lattice moiré patterns. No atomic reconstruction, i.e. any rearrangement of atoms within the individual layers, has been reported experimentally to date. Here we demonstrate that vdWH of MoSe2/WSe2 and MoS2/WS2 at twist angles less than 1° undergo significant atomic level reconstruction leading to discrete commensurate domains divided by narrow domain walls, rather than a smoothly varying rigid-lattice moiré pattern as has been assumed in prior work. Using conductive atomic force microscopy (CAFM), we show that the stacking orientation of the two TMD crystals has a profound impact on the atomic reconstruction, consistent with recent theoretical work on graphene/graphene and MoS2/MoS2 structures and experimental work on graphene bilayers and hBN/graphene vdWH. Transmission electron microscopy (TEM) provides additional evidence of atomic reconstruction in MoSe2/WSe2 structures and demonstrates the transition between a rigid-lattice moiré pattern for large angles and atomic reconstruction for small angles. We use density functional theory to calculate the band structures of the commensurate reconstructed domains and find that the modulation of the relative electronic band edges is consistent with the CAFM results and photoluminescence spectra from reconstructed vdWH. The presence of atomic reconstruction in TMD heterostructures and the observed impact on nanometer-scale electronic properties provides fundamental insight into the behavior of this important class of heterostructures.

cond-mat.mtrl-sci↗