Showing posts with label D. N. Basov. Show all posts
Showing posts with label D. N. Basov. Show all posts

Tuesday, July 27, 2021

Abstract-Quantitative terahertz emission nanoscopy with multiresonant near-field probes

 

Fabian Mooshammer, Markus Plankl, Thomas Siday, Martin Zizlsperger, Fabian Sandner, Rocco Vitalone, Ran Jing, Markus A. Huber, D. N. Basov, and Rupert Huber



https://www.osapublishing.org/viewmedia.cfm?r=1&rwjcode=ol&uri=ol-46-15-3572&seq=0

By sampling terahertz waveforms emitted from InAs surfaces, we reveal how the entire, realistic geometry of typical near-field probes drastically impacts the broadband electromagnetic fields. In the time domain, these modifications manifest as a shift in the carrier-envelope phase and emergence of a replica pulse with a time delay dictated by the length of the cantilever. This interpretation is fully corroborated by quantitative simulations of terahertz emission nanoscopy based on the finite element method. Our approach provides a solid theoretical framework for quantitative nanospectroscopy and sets the stage for a reliable description of subcycle, near-field microscopy at terahertz frequencies.

© 2021 Optical Society of America

Tuesday, June 30, 2020

Abstract-Collective modes and terahertz near-field response of superconductors


Zhiyuan Sun, M. M. Fogler, D. N. Basov, and Andrew J. Millis
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We theoretically study the low-energy electromagnetic response of Bardeen-Cooper-Schrieffer–type superconductors focusing on propagating collective modes that are observable with terahertz near-field optics. The interesting frequency and momentum range is ω<2Δ and q<1/ξ, where Δ is the gap and ξ is the coherence length. We show that it is possible to observe the superfluid plasmons, amplitude (Higgs) modes, Bardasis-Schrieffer modes, and Carlson-Goldman modes using the terahertz near-field technique, although none of these modes couple linearly to far-field radiation. Coupling of terahertz near-field radiation to the amplitude mode requires particle-hole symmetry breaking, while coupling to the Bardasis-Schrieffer mode does not and is typically stronger. For parameters appropriate to layered superconductors of current interest, the Carlson-Goldman mode appears in the near-field reflection coefficient as a weak feature in the subterahertz frequency range. In a system of two superconducting layers with nanometer-scale separation, an acoustic phase mode appears as the antisymmetric density fluctuation mode of the system. This mode produces well-defined resonance peaks in the near-field terahertz response and has strong anticrossings with the Bardasis-Schrieffer and amplitude modes, enhancing their response. In a slab consisting of many layers of quasi-two-dimensional superconductors, realized for example in samples of high-Tc cuprate compounds, many branches of propagating Josephson plasmon modes are found to couple to the terahertz near-field radiation.
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Tuesday, September 11, 2018

Abstract-Imaging the nanoscale phase separation in vanadium dioxide thin films at terahertz frequencies


H. T. Stinson, A. Sternbach, O. Najera, R. Jing, A. S. Mcleod, T. V. Slusar, A. Mueller, L. Anderegg, H. T. Kim, M. Rozenberg,  D. N. Basov

https://www.nature.com/articles/s41467-018-05998-5

Vanadium dioxide (VO2) is a material that undergoes an insulator–metal transition upon heating above 340 K. It remains debated as to whether this electronic transition is driven by a corresponding structural transition or by strong electron–electron correlations. Here, we use apertureless scattering near-field optical microscopy to compare nanoscale images of the transition in VO2 thin films acquired at both mid-infrared and terahertz frequencies, using a home-built terahertz near-field microscope. We observe a much more gradual transition when THz frequencies are utilized as a probe, in contrast to the assumptions of a classical first-order phase transition. We discuss these results in light of dynamical mean-field theory calculations of the dimer Hubbard model recently applied to VO2, which account for a continuous temperature dependence of the optical response of the VO2 in the insulating state.