@article{VarykhalovShikinGudatetal.2005, author = {Varykhalov, Andrei and Shikin, A. M. and Gudat, Wolfgang and Moras, P. and Grazioli, C. and Carbone, C. and Rader, Oliver}, title = {Probing the ground state electronic structure of a correlated electron system by quantum well states: Ag/ Ni(111)}, issn = {0031-9007}, year = {2005}, abstract = {The ground state electronic properties of the strongly correlated transition metal Ni are usually not accessible from the excitation spectra measured in photoelectron spectroscopy. We show that the bottom of the Ni d band along [111] can be probed through the energy dependence of the phase of quantum-well states in Ag/Ni(111). Our model description of the quantum-well energies measured by angle-resolved photoemission determines the bottom of the Lambda(1) d band of Ni as 2.6 eV, in full agreement with standard local density theory and at variance with the values of 1.7-1.8 eV from direct angle-resolved photoemission experiments of Ni}, language = {en} } @article{VarykhalovRaderGudat2005, author = {Varykhalov, Andrei and Rader, Oliver and Gudat, Wolfgang}, title = {Structure and quantum-size effects in a surface carbide : W(110)/C-R(15 X 3)}, issn = {1098-0121}, year = {2005}, abstract = {Results of the combined investigation of atomic and electronic structure of the W(110)/C-R(15x3) surface carbide are reported. A variety of experimental techniques has been involved such as scanning tunneling microscopy (STM), low-energy electron diffraction, x-ray photoelectron spectroscopy, and angle-resolved photoemission (ARPES). Distance-dependent STM measurements show a nontrivial geometrical behavior in the topography data, demonstrating five different patterns representing the superstructure at different values of the tip-surface separation. Atomic resolution was achieved at lower tunneling gap resistance. An unexpected spatial asymmetry in the distribution of the local density of states across the surface unit cell has been observed as well. Photoelectron spectroscopy of C1s and W4f core levels clarifies the nature of the chemical bonding in the system. The band mapping with ARPES provides information on the wave- vector dependence of the electronic states. Notable quantum size and superlattice effects were discovered in the dispersion of the valence-band states. The experimental data suggests an apparent one-dimensional character of the electronic structure. Lateral quantization and umklapp scattering are proposed as explanation. Finally, based on photoemission and STM measurements, an improved crystallographic model of the tungsten surface carbide is introduced}, language = {en} } @article{VarykhalovGudatAdamchuketal.2006, author = {Varykhalov, Andrei and Gudat, Wolfgang and Adamchuk, V. K. and Rader, Oliver}, title = {Magic numbers in two-dimensional self-organization of C-60 molecules}, doi = {10.1103/Physrevb.73.241404}, year = {2006}, abstract = {Employing the chemically passive carbon reconstruction W(110)/C-R(15x3) as substrate for deposition of C-60 molecules, we have discovered by scanning tunneling microscopy two-dimensional self-assembly of fullerenes into uniform molecular nanoclusters with "magic" numbers. Our photoemission measurements determine van der Waals forces as the dominating interaction in this self-organizing two-dimensional molecular gas. Based on this, a theoretical determination of the cluster structures in the framework of the Girifalco model gives perfect agreement with the experiment}, language = {en} } @misc{VarykhalovFreyseAguileraetal.2020, author = {Varykhalov, Andrei and Freyse, Friedrich and Aguilera, Irene and Battiato, Marco and Krivenkov, Maxim and Marchenko, Dmitry and Bihlmayer, Gustav and Blugel, Stefan and Rader, Oliver and Sanchez-Barriga, Jaime}, title = {Effective mass enhancement and ultrafast electron dynamics of Au(111) surface state coupled to a quantum well}, series = {Zweitver{\"o}ffentlichungen der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe}, journal = {Zweitver{\"o}ffentlichungen der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe}, number = {1}, issn = {1866-8372}, doi = {10.25932/publishup-54989}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-549892}, pages = {11}, year = {2020}, abstract = {We show that, although the equilibrium band dispersion of the Shockley-type surface state of two-dimensional Au(111) quantum films grown on W(110) does not deviate from the expected free-electron-like behavior, its nonequilibrium energy-momentum dispersion probed by time- and angle-resolved photoemission exhibits a remarkable kink above the Fermi level due to a significant enhancement of the effective mass. The kink is pronounced for certain thicknesses of the Au quantum well and vanishes in the very thin limit. We identify the kink as induced by the coupling between the Au(111) surface state and emergent quantum-well states which probe directly the buried gold-tungsten interface. The signatures of the coupling are further revealed by our time-resolved measurements which show that surface state and quantum-well states thermalize together behaving as dynamically locked electron populations. In particular, relaxation of hot carriers following laser excitation is similar for both surface state and quantum-well states and much slower than expected for a bulk metallic system. The influence of quantum confinement on the interplay between elementary scattering processes of the electrons at the surface and ultrafast carrier transport in the direction perpendicular to the surface is shown to be the reason for the slow electron dynamics.}, language = {en} } @article{VarykhalovFreyseAguileraetal.2020, author = {Varykhalov, Andrei and Freyse, Friedrich and Aguilera, Irene and Battiato, Marco and Krivenkov, Maxim and Marchenko, Dmitry and Bihlmayer, Gustav and Blugel, Stefan and Rader, Oliver and Sanchez-Barriga, Jaime}, title = {Effective mass enhancement and ultrafast electron dynamics of Au(111) surface state coupled to a quantum well}, series = {Physical Review Research}, volume = {2}, journal = {Physical Review Research}, number = {1}, publisher = {American Physical Society}, address = {Ridge, NY}, issn = {0031-9007}, doi = {10.1103/PhysRevResearch.2.013343}, pages = {1 -- 9}, year = {2020}, abstract = {We show that, although the equilibrium band dispersion of the Shockley-type surface state of two-dimensional Au(111) quantum films grown on W(110) does not deviate from the expected free-electron-like behavior, its nonequilibrium energy-momentum dispersion probed by time- and angle-resolved photoemission exhibits a remarkable kink above the Fermi level due to a significant enhancement of the effective mass. The kink is pronounced for certain thicknesses of the Au quantum well and vanishes in the very thin limit. We identify the kink as induced by the coupling between the Au(111) surface state and emergent quantum-well states which probe directly the buried gold-tungsten interface. The signatures of the coupling are further revealed by our time-resolved measurements which show that surface state and quantum-well states thermalize together behaving as dynamically locked electron populations. In particular, relaxation of hot carriers following laser excitation is similar for both surface state and quantum-well states and much slower than expected for a bulk metallic system. The influence of quantum confinement on the interplay between elementary scattering processes of the electrons at the surface and ultrafast carrier transport in the direction perpendicular to the surface is shown to be the reason for the slow electron dynamics.}, language = {en} } @phdthesis{Varykhalov2005, author = {Varykhalov, Andrei}, title = {Quantum-size effects in the electronic structure of novel self-organized systems with reduced dimensionality}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-5784}, school = {Universit{\"a}t Potsdam}, year = {2005}, abstract = {The Thesis is focused on the properties of self-organized nanostructures. Atomic and electronic properties of different systems have been investigated using methods of electron diffraction, scanning tunneling microscopy and photoelectron spectroscopy. Implementation of the STM technique (including design, construction, and tuning of the UHV experimental set-up) has been done in the framework of present work. This time-consuming work is reported to greater detail in the experimental part of this Thesis. The scientific part starts from the study of quantum-size effects in the electronic structure of a two-dimensional Ag film on the supporting substrate Ni(111). Distinct quantum well states in the sp-band of Ag were observed in photoelectron spectra. Analysis of thickness- and angle-dependent photoemission supplies novel information on the properties of the interface. For the first time the Ni(111) relative band gap was indirectly probed in the ground-state through the electronic structure of quantum well states in the adlayer. This is particularly important for Ni where valence electrons are strongly correlated. Comparison of the experiment with calculations performed in the formalism of the extended phase accumulation model gives the substrate gap which is fully consistent with the one obtained by ab-initio LDA calculations. It is, however, in controversy to the band structure of Ni measured directly by photoemission. These results lend credit to the simplest view of photoemission from Ni, assigning early observed contradictions between theory and experiments to electron correlation effects in the final state of photoemission. Further, nanosystems of lower dimensionality have been studied. Stepped surfaces W(331) and W(551) were used as one-dimensional model systems and as templates for self-organization of Au nanoclusters. Photon energy dependent photoemission revealed a surface resonance which was never observed before on W(110) which is the base plane of the terrace microsurfaces. The dispersion E(k) of this state measured on stepped W(331) and W(551) with angle-resolved photoelectron spectroscopy is modified by a strong umklapp effect. It appears as two parabolas shifted symmetrically relative to the microsurface normal by half of the Brillouin zone of the step superlattice. The reported results are very important for understanding of the electronic properties of low-dimensional nanostructures. It was also established that W(331) and W(551) can serve as templates for self-organization of metallic nanostructures. A combined study of electronic and atomic properties of sub-monolayer amounts of gold deposited on these templates have shown that if the substrate is slightly pre-oxidized and the temperature is elevated, then Au can alloy with the first monolayer of W. As a result, a nanostructure of uniform clusters of a surface alloy is produced all over the steps. Such clusters feature a novel sp-band in the vicinity of the Fermi level, which appears split into constant energy levels due to effects of lateral quantization. The last and main part of this work is devoted to large-scale reconstructions on surfaces and nanostructures self-assembled on top. The two-dimensional surface carbide W(110)/C-R(15x3) has been extensively investigated. Photoemission studies of quantum size effects in the electronic structure of this reconstruction, combined with an investigation of its surface geometry, lead to an advanced structural model of the carbide overlayer. It was discovered that W(110)/C-R(15x3) can control self-organization of adlayers into nanostructures with extremely different electronic and structural properties. Thus, it was established that at elevated temperature the R(15x3) superstructure controls the self-assembly of sub-monolayer amounts of Au into nm-wide nanostripes. Based on the results of core level photoemission, the R(15x3)-induced surface alloying which takes place between Au and W can be claimed as driving force of self-organization. The observed stripes exhibit a characteristic one-dimensional electronic structure with laterally quantized d-bands. Obviously, these are very important for applications, since dimensions of electronic devices have already stepped into the nm-range, where quantum-size phenomena must undoubtedly be considered. Moreover, formation of perfectly uniform molecular clusters of C60 was demonstrated and described in terms of the van der Waals formalism. It is the first experimental observation of two-dimensional fullerene nanoclusters with "magic numbers". Calculations of the cluster potentials using the static approach have revealed characteristic minima in the interaction energy. They are achieved for 4 and 7 molecules per cluster. The obtained "magic numbers" and the corresponding cluster structures are fully consistent with the results of the STM measurements.}, subject = {Nanostruktur}, language = {en} } @article{ShikinVarykhalovPrudnikovaetal.2004, author = {Shikin, A. M. and Varykhalov, Andrei and Prudnikova, G. V. and Adamchuk, V. K. and Gudat, Wolfgang and Rader, Oliver}, title = {Photoemission from stepped W(110) : Initial or final state effect?}, issn = {0031-9007}, year = {2004}, abstract = {The electronic structure of the (110)-oriented terraces of stepped W(331) and W(551) is compared to the one of flat W(110) using angle-resolved photoemission. We identify a surface-localized state which develops perpendicular to the steps into a repeated band structure with the periodicity of the step superlattices. It is shown that a final-state diffraction process rather than an initial-state superlattice effect is the origin of the observed behavior and why it does not affect the entire band structure}, language = {en} } @article{SajediKrivenkovMarchenkoetal.2020, author = {Sajedi, Maryam and Krivenkov, Maxim and Marchenko, Dmitry and Varykhalov, Andrei and Sanchez-Barriga, Jaime and Rienks, Emile D. L. and Rader, Oliver}, title = {Absence of a giant Rashba effect in the valence band of lead halide perovskites}, series = {Physical review : B, Condensed matter and materials physics}, volume = {102}, journal = {Physical review : B, Condensed matter and materials physics}, number = {8}, publisher = {American Institute of Physics; American Physical Society (APS)}, address = {Woodbury, NY}, issn = {2469-9950}, doi = {10.1103/PhysRevB.102.081116}, pages = {6}, year = {2020}, abstract = {For hybrid organic-inorganic as well as all-inorganic lead halide perovskites a Rashba effect has been invoked to explain the high efficiency in energy conversion by prohibiting direct recombination. Both a bulk and surface Rashba effect have been predicted. In the valence band of methylammonium (MA) lead bromide a Rashba effect has been reported by angle-resolved photoemission and circular dichroism with giant values of 7-11 eV angstrom. We present band dispersion measurements of MAPbBr(3) and spin-resolved photoemission of CsPbBr3 to show that a large Rashba effect detectable by photoemission or circular dichroism does not exist and cannot be the origin of the high effciency.}, language = {en} } @article{RienksWimmerSanchezBarrigaetal.2019, author = {Rienks, Emile D. L. and Wimmer, S. and Sanchez-Barriga, Jaime and Caha, O. and Mandal, Partha Sarathi and Ruzicka, J. and Ney, A. and Steiner, H. and Volobuev, V. V. and Groiss, H. and Albu, M. and Kothleitner, G. and Michalicka, J. and Khan, S. A. and Minar, J. and Ebert, H. and Bauer, G. and Freyse, F. and Varykhalov, Andrei and Rader, Oliver and Springholz, G.}, title = {Large magnetic gap at the Dirac point in Bi2Te3/MnBi2Te4 heterostructures}, series = {Nature : the international weekly journal of science}, volume = {576}, journal = {Nature : the international weekly journal of science}, number = {7787}, publisher = {Nature Publ. Group}, address = {London}, issn = {0028-0836}, doi = {10.1038/s41586-019-1826-7}, pages = {423 -- 428}, year = {2019}, abstract = {Magnetically doped topological insulators enable the quantum anomalous Hall effect (QAHE), which provides quantized edge states for lossless charge-transport applications(1-8). The edge states are hosted by a magnetic energy gap at the Dirac point(2), but hitherto all attempts to observe this gap directly have been unsuccessful. Observing the gap is considered to be essential to overcoming the limitations of the QAHE, which so far occurs only at temperatures that are one to two orders of magnitude below the ferromagnetic Curie temperature, T-C (ref. (8)). Here we use low-temperature photoelectron spectroscopy to unambiguously reveal the magnetic gap of Mn-doped Bi2Te3, which displays ferromagnetic out-of-plane spin texture and opens up only below T-C. Surprisingly, our analysis reveals large gap sizes at 1 kelvin of up to 90 millielectronvolts, which is five times larger than theoretically predicted(9). Using multiscale analysis we show that this enhancement is due to a remarkable structure modification induced by Mn doping: instead of a disordered impurity system, a self-organized alternating sequence of MnBi2Te4 septuple and Bi2Te3 quintuple layers is formed. This enhances the wavefunction overlap and size of the magnetic gap(10). Mn-doped Bi2Se3 (ref. (11)) and Mn-doped Sb2Te3 form similar heterostructures, but for Bi2Se3 only a nonmagnetic gap is formed and the magnetization is in the surface plane. This is explained by the smaller spin-orbit interaction by comparison with Mn-doped Bi2Te3. Our findings provide insights that will be crucial in pushing lossless transport in topological insulators towards room-temperature applications.}, language = {en} } @article{KrivenkovMarchenkoSanchezBarrigaetal.2021, author = {Krivenkov, Maxim and Marchenko, Dimitry and S{\´a}nchez-Barriga, Jaime and Golias, Evangelos and Rader, Oliver and Varykhalov, Andrei}, title = {Origin of the band gap in Bi-intercalated graphene on Ir(111)}, series = {2D Materials}, volume = {8}, journal = {2D Materials}, number = {3}, publisher = {IOP Publ. Ltd.}, address = {Bristol}, issn = {2053-1583}, doi = {10.1088/2053-1583/abd1e4}, pages = {15}, year = {2021}, abstract = {Proximity to heavy sp-elements is considered promising for reaching a band gap in graphene that could host quantum spin Hall states. The recent report of an induced spin-orbit gap of 0.2 eV in Pb-intercalated graphene detectable by spin-resolved photoemission has spurred renewed interest in such systems (Klimovskikh et al 2017 ACS Nano 11, 368). In the case of Bi intercalation an even larger band gap of 0.4 eV has been observed but was assigned to the influence of a dislocation network (Warmuth et al 2016 Phys. Rev. B 93, 165 437). Here, we study Bi intercalation under graphene on Ir(111) and report a nearly ideal graphene dispersion without band replicas and no indication of hybridization with the substrate. The band gap is small (0.19 eV) and can be tuned by +/- 25 meV through the Bi coverage. The Bi atomic density is higher than in the recent report. By spin-resolved photoemission we exclude induced spin-orbit interaction as origin of the gap. Quantitative agreement of a photoemission intensity analysis with the measured band gap suggests sublattice symmetry breaking as one of the possible band gap opening mechanisms. We test several Bi structures by density functional theory. Our results indicate the possibility that Bi intercalates in the phase of bismuthene forming a graphene-bismuthene van der Waals heterostructure.}, language = {en} }