Wenderoth, Martin

[["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Nature Communications"],["dc.bibliographiccitation.volume","11"],["dc.contributor.author","Sinterhauf, Anna"],["dc.contributor.author","Traeger, Georg A."],["dc.contributor.author","Momeni Pakdehi, Davood"],["dc.contributor.author","Schädlich, Philip"],["dc.contributor.author","Willke, Philip"],["dc.contributor.author","Speck, Florian"],["dc.contributor.author","Seyller, Thomas"],["dc.contributor.author","Tegenkamp, Christoph"],["dc.contributor.author","Pierz, Klaus"],["dc.contributor.author","Schumacher, Hans Werner"],["dc.contributor.author","Wenderoth, Martin"],["dc.date.accessioned","2021-04-14T08:27:37Z"],["dc.date.available","2021-04-14T08:27:37Z"],["dc.date.issued","2020"],["dc.description.sponsorship","Open-Access-Publikationsfonds 2020"],["dc.identifier.doi","10.1038/s41467-019-14192-0"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/17320"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/82350"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-399"],["dc.notes.intern","Merged from goescholar"],["dc.relation.eissn","2041-1723"],["dc.relation.orgunit","Fakultät für Physik"],["dc.rights","CC BY 4.0"],["dc.rights.uri","http://creativecommons.org/licenses/by/4.0/"],["dc.title","Substrate induced nanoscale resistance variation in epitaxial graphene"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.artnumber","15283"],["dc.bibliographiccitation.firstpage","1"],["dc.bibliographiccitation.journal","Nature Communications"],["dc.bibliographiccitation.lastpage","7"],["dc.bibliographiccitation.volume","8"],["dc.contributor.author","Willke, Philip"],["dc.contributor.author","Kotzott, Thomas"],["dc.contributor.author","Pruschke, Thomas"],["dc.contributor.author","Wenderoth, Martin"],["dc.date.accessioned","2018-11-07T10:23:54Z"],["dc.date.available","2018-11-07T10:23:54Z"],["dc.date.issued","2017"],["dc.description.abstract","Transport experiments in strong magnetic fields show a variety of fascinating phenomena like the quantum Hall effect, weak localization or the giant magnetoresistance. Often they originate from the atomic-scale structure inaccessible to macroscopic magnetotransport experiments. To connect spatial information with transport properties, various advanced scanning probe methods have been developed. Capable of ultimate spatial resolution, scanning tunnelling potentiometry has been used to determine the resistance of atomic-scale defects such as steps and interfaces. Here we combine this technique with magnetic fields and thus transfer magnetotransport experiments to the atomic scale. Monitoring the local voltage drop in epitaxial graphene, we show how the magnetic field controls the electric field components. We find that scattering processes at localized defects are independent of the strong magnetic field while monolayer and bilayer graphene sheets show a locally varying conductivity and charge carrier concentration differing from the macroscopic average."],["dc.description.sponsorship","Open-Access-Publikationsfonds 2017"],["dc.identifier.doi","10.1038/ncomms15283"],["dc.identifier.isi","000400561800001"],["dc.identifier.pmid","28469282"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/14628"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/42553"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","PUB_WoS_Import"],["dc.publisher","Nature Publishing Group"],["dc.relation.issn","2041-1723"],["dc.relation.orgunit","Fakultät für Physik"],["dc.rights","CC BY 4.0"],["dc.title","Magnetotransport on the nano scale"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","113044"],["dc.bibliographiccitation.issue","11"],["dc.bibliographiccitation.journal","New Journal of Physics"],["dc.bibliographiccitation.volume","23"],["dc.contributor.author","Kotzott, Thomas"],["dc.contributor.author","Bouhassoune, Mohammed"],["dc.contributor.author","Prüser, Henning"],["dc.contributor.author","Weismann, Alexander"],["dc.contributor.author","Lounis, Samir"],["dc.contributor.author","Wenderoth, Martin"],["dc.date.accessioned","2022-01-11T14:05:53Z"],["dc.date.available","2022-01-11T14:05:53Z"],["dc.date.issued","2021"],["dc.description.abstract","Abstract We investigate single Ge and Ag impurities buried below a Cu(100) surface using low temperature scanning tunneling microscopy. The interference patterns in the local density of states are surface scattering signatures of the bulk impurities, which result from 3D Friedel oscillations and the electron focusing effect. Comparing the isoelectronic d scatterer Ag and the sp scatterer Ge allows to distinguish contributions from impurity scattering and the host. Energy-independent effective scattering phase shifts are extracted using a plane wave tight-binding model and reveal similar values for both species. A comparison with ab initio calculations suggests incoherent sp scattering processes at the Ge impurity. As both scatterers are spectrally homogeneous, scanning tunneling spectroscopy of the interference patterns yields real-space signatures of the bulk electronic structure. We find a kink around zero bias for both species that we assign to a renormalization of the band structure due to many-body effects, which can be described with a Debye self-energy and a surprisingly high electron–phonon coupling parameter λ . We propose that this might originate from bulk propagation in the vicinity of the surface."],["dc.description.abstract","Abstract We investigate single Ge and Ag impurities buried below a Cu(100) surface using low temperature scanning tunneling microscopy. The interference patterns in the local density of states are surface scattering signatures of the bulk impurities, which result from 3D Friedel oscillations and the electron focusing effect. Comparing the isoelectronic d scatterer Ag and the sp scatterer Ge allows to distinguish contributions from impurity scattering and the host. Energy-independent effective scattering phase shifts are extracted using a plane wave tight-binding model and reveal similar values for both species. A comparison with ab initio calculations suggests incoherent sp scattering processes at the Ge impurity. As both scatterers are spectrally homogeneous, scanning tunneling spectroscopy of the interference patterns yields real-space signatures of the bulk electronic structure. We find a kink around zero bias for both species that we assign to a renormalization of the band structure due to many-body effects, which can be described with a Debye self-energy and a surprisingly high electron–phonon coupling parameter λ . We propose that this might originate from bulk propagation in the vicinity of the surface."],["dc.description.sponsorship","Open-Access-Publikationsfonds 2021"],["dc.identifier.doi","10.1088/1367-2630/ac3681"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/97768"],["dc.notes.intern","DOI-Import GROB-507"],["dc.relation.eissn","1367-2630"],["dc.relation.orgunit","IV. Physikalisches Institut"],["dc.rights","CC BY 4.0"],["dc.title","Scanning tunneling spectroscopy of subsurface Ag and Ge impurities in copper"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.artnumber","2000473"],["dc.bibliographiccitation.issue","13"],["dc.bibliographiccitation.journal","Advanced Materials Interfaces"],["dc.bibliographiccitation.volume","7"],["dc.contributor.author","Wit, Bareld"],["dc.contributor.author","Bunjes, Ole"],["dc.contributor.author","Wenderoth, Martin"],["dc.contributor.author","Ropers, Claus"],["dc.date.accessioned","2020-05-29T09:51:18Z"],["dc.date.available","2020-05-29T09:51:18Z"],["dc.date.issued","2020"],["dc.description.abstract","Abstract The structure of a physisorbed sub‐monolayer of 1,2‐bis(4‐pyridyl)ethylene (bpe) on epitaxial graphene is investigated by low‐energy electron diffraction and scanning tunneling microscopy. Additionally, nonequilibrium heat‐transfer between bpe and the surface is studied by ultrafast low‐energy electron diffraction. Bpe arranges in an oblique unit cell which is not commensurate with the substrate. Six different rotational and/or mirror domains, in which the molecular unit cell is rotated by 28 ± 0.1° with respect to the graphene surface, are identified. The molecules are weakly physisorbed, as evidenced by the fact that they readily desorb at room temperature. At liquid nitrogen temperature, however, the layers are stable and time‐resolved experiments can be performed. The temperature changes of the molecules and the surface can be measured independently through the Debye–Waller factor of their individual diffraction features. Thus, the heat flow between bpe and the surface can be monitored on a picosecond timescale. The time‐resolved measurements, in combination with model simulations, show the existence of three relevant thermal barriers between the different layers. The thermal boundary resistance between the molecular layer and graphene is found to be 2 ± 1 × 10−8 K m2 W−1."],["dc.description.abstract","Physisorbed sub‐monolayers of 1,2‐bis(4‐pyridyl)ethylene on graphene are thoroughly characterized. Moreover, nonequilibrium heat dissipation from the molecular layer into the surface is investigated. The structure of the substrate enables simultaneous measurement of the temperature of the molecules and the surface. From this, the thermal boundary resistance between the molecules and graphene can be determined. image"],["dc.description.sponsorship","European Research Council http://dx.doi.org/10.13039/501100000781"],["dc.description.sponsorship","Deutsche Forschungsgemeinschaft http://dx.doi.org/10.13039/501100001659"],["dc.identifier.doi","10.1002/admi.202000473"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/66022"],["dc.language.iso","en"],["dc.notes.intern","DeepGreen Import"],["dc.relation","SFB 1073: Kontrolle von Energiewandlung auf atomaren Skalen"],["dc.relation","SFB 1073 | Topical Area C | C04 Untersuchung und Kontrolle photochemischer Reaktionen durch lokale optische Anregung im Rastertunnelmikroskop"],["dc.relation.issn","2196-7350"],["dc.relation.issn","2196-7350"],["dc.rights","This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited."],["dc.title","Structure and Nonequilibrium Heat‐Transfer of a Physisorbed Molecular Layer on Graphene"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.artnumber","055009"],["dc.bibliographiccitation.issue","5"],["dc.bibliographiccitation.journal","New Journal of Physics"],["dc.bibliographiccitation.volume","15"],["dc.contributor.affiliation","Sürgers, C;"],["dc.contributor.affiliation","Wenderoth, M;"],["dc.contributor.affiliation","Löser, K;"],["dc.contributor.affiliation","Garleff, J K;"],["dc.contributor.affiliation","Ulbrich, R G;"],["dc.contributor.affiliation","Lukas, M;"],["dc.contributor.affiliation","v Löhneysen, H;"],["dc.contributor.author","Suergers, Christoph"],["dc.contributor.author","Wenderoth, Martin"],["dc.contributor.author","Loeser, K."],["dc.contributor.author","Garleff, J. K."],["dc.contributor.author","Ulbrich, Rainer G."],["dc.contributor.author","Lukas, M."],["dc.contributor.author","v Loehneysen, H."],["dc.date.accessioned","2018-11-07T09:24:41Z"],["dc.date.available","2018-11-07T09:24:41Z"],["dc.date.issued","2013"],["dc.date.updated","2022-02-10T10:17:24Z"],["dc.description.abstract","The (111)-2x1 surface of in situ cleaved heavily P-or B-doped Si is investigated by scanning tunnelling microscopy and spectroscopy at room temperature and at low temperature. P atoms have been identified on different sites of the Si(111)-2x1 surface by their characteristic voltage-dependent contrast for positive as well as negative buckling of the pi-bonded chains. The distributions of dopants per surface area and of nearest-neighbour distances are found to be in agreement with a random arrangement of dopants in Si up to doping levels well above the metal-insulator transition. In addition, P atoms have been identified by their depth-dependent contrast down to the third layer beneath the surface with a volume density in agreement with the bulk doping density. The random electronic disorder supports the view of an Anderson transition driven by disorder close to the critical concentration or critical uniaxial stress."],["dc.identifier.doi","10.1088/1367-2630/15/5/055009"],["dc.identifier.eissn","1367-2630"],["dc.identifier.fs","599177"],["dc.identifier.isi","000318968300003"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/10562"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/29884"],["dc.language.iso","en"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.publisher","IOP Publishing"],["dc.relation.issn","1367-2630"],["dc.relation.orgunit","Fakultät für Physik"],["dc.rights","CC BY 3.0"],["dc.rights.uri","http://creativecommons.org/licenses/by/3.0/"],["dc.title","Electronic disorder of P- and B-doped Si at the metal-insulator transition investigated by scanning tunnelling microscopy and electronic transport"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.status","published"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.artnumber","10108"],["dc.bibliographiccitation.journal","Nature Communications"],["dc.bibliographiccitation.volume","7"],["dc.contributor.author","Kloth, Philipp"],["dc.contributor.author","Kaiser, Katharina"],["dc.contributor.author","Wenderoth, Martin"],["dc.date.accessioned","2018-11-07T10:21:13Z"],["dc.date.available","2018-11-07T10:21:13Z"],["dc.date.issued","2016"],["dc.description.abstract","The miniaturization of future electronic devices is intimately connected to the ability to control electric fields on the atomic scale. In a nanoscopic system defined by a limited number of charges, the combined dynamics of bound and free charges become important. Here we present a model system based on the electrostatic interaction between a metallic tip of a scanning tunnelling microscope and a GaAs(110) semiconductor surface. The system is driven out of equilibrium by optical excitation, which provides ambipolar free charge carriers, and by an optically induced unipolar tunnel current. This combination enables the active control of the density and spatial distribution of free and bound charge in the space-charge region, that is, modifying the screening processes. Temporal fluctuations of single dopants are modified, meaning we are able to control the noise of the system. It is found that free charge carriers suppress the noise level in field-controlled, nanoscopic systems."],["dc.description.sponsorship","[CRC1073]; [C4]"],["dc.identifier.doi","10.1038/ncomms10108"],["dc.identifier.isi","000369018600001"],["dc.identifier.pmid","26728867"],["dc.identifier.purl","https://resolver.sub.uni-goettingen.de/purl?gs-1/12893"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/42049"],["dc.notes.intern","Merged from goescholar"],["dc.notes.status","zu prüfen"],["dc.notes.submitter","Najko"],["dc.relation","SFB 1073: Kontrolle von Energiewandlung auf atomaren Skalen"],["dc.relation","SFB 1073 | Topical Area C | C04 Untersuchung und Kontrolle photochemischer Reaktionen durch lokale optische Anregung im Rastertunnelmikroskop"],["dc.relation.issn","2041-1723"],["dc.relation.orgunit","Fakultät für Physik"],["dc.rights","CC BY 4.0"],["dc.title","Controlling the screening process of a nanoscaled space charge region by minority carriers"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.peerReviewed","yes"],["dc.type.subtype","original_ja"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.artnumber","3"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","Communications Chemistry"],["dc.bibliographiccitation.volume","5"],["dc.contributor.author","Bunjes, Ole"],["dc.contributor.author","Paul, Lucas A."],["dc.contributor.author","Dai, Xinyue"],["dc.contributor.author","Jiang, Hongyan"],["dc.contributor.author","Claus, Tobias"],["dc.contributor.author","Rittmeier, Alexandra"],["dc.contributor.author","Schwarzer, Dirk"],["dc.contributor.author","Ding, Feng"],["dc.contributor.author","Siewert, Inke"],["dc.contributor.author","Wenderoth, Martin"],["dc.date.accessioned","2022-02-01T10:31:12Z"],["dc.date.available","2022-02-01T10:31:12Z"],["dc.date.issued","2022"],["dc.description.abstract","Abstract Atomic scale studies of the anchoring of catalytically active complexes to surfaces may provide valuable insights for the design of new catalytically active hybrid systems. In this work, the self-assembly of 1D, 2D and 3D structures of the complex fac -Re(bpy)(CO) 3 Cl (bpy = 2,2′-bipyridine), a CO 2 reduction catalyst, on the Ag(001) surface are studied by a combination of low-temperature scanning tunneling microscopy and density functional theory calculations. Infrared and sum frequency generation spectroscopy confirm that the complex remains chemically intact under sublimation. Deposition of the complexes onto the silver surface at 300 K leads to strong local variations in the resulting surface coverage on the nanometer scale, indicating that in the initial phase of deposition a large fraction of the molecules is desorbing from the surface. Low coverage regions show a decoration of step edges aligned along the crystal’s symmetry axes <110>. These crystallographic directions are found to be of major importance to the binding of the complexes to the surface. Moreover, the interaction between the molecules and the substrate promotes the restructuring of surface steps along these directions. Well-aligned and decorated steps are found to act as nucleation point for monolayer growth (2D) before 3D growth starts."],["dc.description.sponsorship","Open-Access-Publikationsfonds 2021"],["dc.identifier.doi","10.1038/s42004-021-00617-9"],["dc.identifier.pii","617"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/98802"],["dc.language.iso","en"],["dc.notes.intern","DOI-Import GROB-517"],["dc.relation","SFB 1073: Kontrolle von Energiewandlung auf atomaren Skalen"],["dc.relation","SFB 1073 | Topical Area C: Photonen- und elektronengetriebene Reaktionen"],["dc.relation","SFB 1073 | Topical Area C | C01 Hydrid-Anordnungen für die Untersuchung photo-induzierter mehrstufiger katalytischer Prozesse"],["dc.relation","SFB 1073 | Topical Area C | C04 Untersuchung und Kontrolle photochemischer Reaktionen durch lokale optische Anregung im Rastertunnelmikroskop"],["dc.relation","SFB 1073 | Topical Area C | C07 Kontrolle Reaktivität hydridischer Photokatalysatoren"],["dc.relation.eissn","2399-3669"],["dc.rights","CC BY 4.0"],["dc.rights.uri","https://creativecommons.org/licenses/by/4.0"],["dc.title","Ordering a rhenium catalyst on Ag(001) through molecule-surface step interaction"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.artnumber","033047"],["dc.bibliographiccitation.issue","3"],["dc.bibliographiccitation.journal","New Journal of Physics"],["dc.bibliographiccitation.volume","22"],["dc.contributor.author","Schröder, Benjamin"],["dc.contributor.author","Bunjes, Ole"],["dc.contributor.author","Wimmer, Lara"],["dc.contributor.author","Kaiser, Katharina"],["dc.contributor.author","Traeger, Georg A"],["dc.contributor.author","Kotzott, Thomas"],["dc.contributor.author","Ropers, Claus"],["dc.contributor.author","Wenderoth, Martin"],["dc.date.accessioned","2020-05-13T10:58:36Z"],["dc.date.available","2020-05-13T10:58:36Z"],["dc.date.issued","2020"],["dc.description.abstract","We investigate photocurrents driven by femtosecond laser excitation of a (sub)-nanometer tunnel junction in an ultrahigh vacuum low-temperature scanning tunneling microscope (STM). The optically driven charge transfer is revealed by tip retraction curves showing a current contribution for exceptionally large tip-sample distances, evidencing a strongly reduced effective barrier height for photoexcited electrons at higher energies. Our measurements demonstrate that the magnitude of the photo-induced electron transport can be controlled by the laser power as well as the applied bias voltage. In contrast, the decay constant of the photocurrent is only weakly affected by these parameters. Stable STM operation with photoelectrons is demonstrated by acquiring constant current topographies. An effective non-equilibrium electron distribution as a consequence of multiphoton absorption is deduced by the analysis of the photocurrent using a one-dimensional potential barrier model."],["dc.identifier.doi","10.1088/1367-2630/ab74ac"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/65298"],["dc.language.iso","en"],["dc.relation","SFB 1073: Kontrolle von Energiewandlung auf atomaren Skalen"],["dc.relation","SFB 1073 | Topical Area C | C04 Untersuchung und Kontrolle photochemischer Reaktionen durch lokale optische Anregung im Rastertunnelmikroskop"],["dc.relation.issn","1367-2630"],["dc.rights","CC BY 4.0"],["dc.title","Controlling photocurrent channels in scanning tunneling microscopy"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dc.type.subtype","original_ja"],["dc.type.version","published_version"],["dspace.entity.type","Publication"]]

[["dc.bibliographiccitation.firstpage","2000421"],["dc.bibliographiccitation.issue","1"],["dc.bibliographiccitation.journal","physica status solidi (b)"],["dc.bibliographiccitation.volume","258"],["dc.contributor.author","Dziuba, Thomas"],["dc.contributor.author","Pietsch, Ina-Marie"],["dc.contributor.author","Stark, Máté"],["dc.contributor.author","Traeger, Georg A."],["dc.contributor.author","Gegenwart, Philipp"],["dc.contributor.author","Wenderoth, Martin"],["dc.date.accessioned","2021-04-14T08:32:18Z"],["dc.date.available","2021-04-14T08:32:18Z"],["dc.date.issued","2020"],["dc.description.abstract","The search for materials with novel and unusual electronic properties is at the heart of condensed matter physics as well as the basis to develop conceptual new technologies. In this context, the correlated honeycomb transition metal oxides have attracted large attention for both, being a possible experimental realization of the theoretically predicted magnetic Kitaev exchange and the theoretical prospect of topological nontriviality. Mott‐insulating Na2IrO3 is prototypical among these materials, characterized by crystal field splitting, spin–orbit coupling, and Hubbard repulsion being on similar energy scales. Herein, a combined electrical transport and scanning tunneling spectroscopy (STS) study of the surface of sodium iridate cleaved and in situ investigated under ultrahigh vacuum is reported. Temperature‐dependent transport measurements prove the existence of surface conductance with a surprisingly high and temperature‐independent conductivity. STS shows a variety of different spectra. Most importantly, a significant density of states is found within the bandgap of sodium iridate at the surface. Based on the local spectroscopic information, multiple conductive channels with differing nature being simultaneously apparent in this material are discussed."],["dc.description.abstract","Na2IrO3 is a spin–orbit Mott insulator for which novel and unconventional magnetic and electronic properties are predicted. A combined transport and scanning tunneling spectroscopy study on cleaved surfaces under ultrahigh vacuum condition shows clear signatures of high surface conductance and V‐shaped bandgap closing. image © 2020 WILEY‐VCH Verlag GmbH \\u0026 Co. KGaA, Weinheim"],["dc.description.sponsorship","Deutsche Forschungsgemeinschaft http://dx.doi.org/10.13039/501100001659"],["dc.identifier.doi","10.1002/pssb.202000421"],["dc.identifier.uri","https://resolver.sub.uni-goettingen.de/purl?gro-2/83876"],["dc.language.iso","en"],["dc.notes.intern","DOI Import GROB-399"],["dc.relation.eissn","1521-3951"],["dc.relation.issn","0370-1972"],["dc.rights","This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited."],["dc.title","Surface Conductivity of the Honeycomb Spin–Orbit Mott Insulator Na2IrO3"],["dc.type","journal_article"],["dc.type.internalPublication","yes"],["dspace.entity.type","Publication"]]