Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/86578
Title: Nanoscale phase engineering of niobium diselenide
Authors: Bischoff, Felix
Auwärter, Willi
Barth, Johannes V.
Schiffrin, Agustin
Fuhrer, Michael
Weber, Bent
Keywords: DRNTU::Science::Physics
Transition Metal Dichalcogenide
Niobium Diselenide
Issue Date: 2017
Source: Bischoff, F., Auwärter, W., Barth, J. V., Schiffrin, A., Fuhrer, M., & Weber, B. (2017). Nanoscale phase engineering of niobium diselenide. Chemistry of Materials, 29(23), 9907-9914. doi:10.1021/acs.chemmater.7b03061
Journal: Chemistry of Materials
Series/Report no.: Chemistry of Materials
Abstract: With the continuing miniaturization of semiconductor microelectronics, atomically thin materials are emerging as promising candidate materials for future ultrascale electronics. In particular, the layered transition metal dichalcogenides (TMDs) have attracted a significant amount of attention because of the variety of their electronic properties, depending on the type of transition metal and its coordination within the crystal. Here, we use low-temperature scanning tunneling microscopy (STM) for the structural and electronic phase engineering of the group V TMD niobium diselenide (NbSe2). By applying voltage pulses with an STM tip, we can transform the material crystal phase locally from trigonal prismatic (2H) to octahedral (1T), as confirmed by the concomitant emergence of a characteristic (√13 × √13)R13.9° charge density wave (CDW) order. At 77 K, atomic-resolution STM images of the junction with sublattice detail confirm the successful phase engineering of the material, as we resolve the difference in the Nb coordination evidenced by a slip of the top Se plane. Different 1T-CDW intensities suggest interlayer interactions to be present in 1T-NbSe2. Furthermore, a distinct voltage dependence suggests a complex CDW mechanism that does not just rely on a star-of-David reconstruction as in the case of other 1T-TMDs. Additionally, bias pulses cause surface modifications inducing local lattice strain that favors a one-dimensional charge order over the intrinsic 3 × 3 CDW at 4.5 K for 2H-NbSe2, which can be reversibly manipulated by STM.
URI: https://hdl.handle.net/10356/86578
http://hdl.handle.net/10220/48313
ISSN: 0897-4756
DOI: 10.1021/acs.chemmater.7b03061
Schools: School of Physical and Mathematical Sciences 
Rights: © 2017 American Chemical Society. This document is the Accepted Manuscript version of a Published Work that appeared in final form in Chemistry of Materials, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.chemmater.7b03061
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Journal Articles

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