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Plasmon Geometric Phase and Plasmon Hall Shift

Li-kun Shi and Justin C. W. Song
Phys. Rev. X 8, 021020 – Published 17 April 2018
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Abstract

The collective plasmonic modes of a metal comprise a simple pattern of oscillating charge density that yields enhanced light-matter interaction. Here we unveil that beneath this familiar facade plasmons possess a hidden internal structure that fundamentally alters its dynamics. In particular, we find that metals with nonzero Hall conductivity host plasmons with an intricate current density configuration that sharply departs from that of ordinary zero Hall conductivity metals. This nontrivial internal structure dramatically enriches the dynamics of plasmon propagation, enabling plasmon wave packets to acquire geometric phases as they scatter. At boundaries, these phases accumulate allowing plasmon waves that reflect off to experience a nonreciprocal parallel shift. This plasmon Hall shift, tunable by Hall conductivity as well as plasmon wavelength, displaces the incident and reflected plasmon trajectories and can be readily probed by near-field photonics techniques. Anomalous plasmon geometric phases dramatically enrich the nanophotonics toolbox, and yield radical new means for directing plasmonic beams.

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  • Received 6 November 2017
  • Revised 22 February 2018

DOI:https://doi.org/10.1103/PhysRevX.8.021020

Published by the American Physical Society under the terms of the Creative Commons Attribution 4.0 International license. Further distribution of this work must maintain attribution to the author(s) and the published article’s title, journal citation, and DOI.

Published by the American Physical Society

Physics Subject Headings (PhySH)

Condensed Matter, Materials & Applied Physics

Synopsis

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Hidden Structure of Plasmons

Published 17 April 2018

Calculations of the current density within collective charge oscillations called plasmons reveal a complicated structure that could affect how plasmons reflect off a boundary.

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Authors & Affiliations

Li-kun Shi1 and Justin C. W. Song1,2,*

  • 1Institute of High Performance Computing, Agency for Science, Technology, and Research, Singapore 138632
  • 2Division of Physics and Applied Physics, Nanyang Technological University, Singapore 637371

  • *justinsong@ntu.edu.sg

Popular Summary

Much like photons are quantized oscillations of electromagnetic fields, plasmons are the collective oscillations of electrons and are found in all metals. Plasmons are essential in squeezing and enhancing the interaction between light and matter on the nanoscale, such as in bio-imaging, on-chip communication, and photodetection. There is intense interest in manipulating, exploiting, and probing plasmons in a variety of materials. However, on a fundamental physics level, plasmons in simple metals are typically thought to be devoid of structure, with a vanilla behavior that is well described by their dispersion and lifetime. We show that this naive perspective is far from complete. Our theoretical work demonstrates that plasmons in two-dimensional materials can possess hidden internal structure, which dramatically alters their dynamics and physical properties, such as scattering.

Deep subwavelength plasmons have wavelengths that are greatly compressed compared to the free-space wavelength of light. Conventionally, these plasmons can be described by their charge density and electric fields alone. Our results point to additional internal structure that comprises the local charge current density configuration in a metal, which can take on an intricate, nontrivial spatial pattern when a magnetic field is applied. When these plasmons scatter, their internal structure allows them to pick up nontrivial, tunable geometric phase shifts. This structure can even shift the trajectory by multiple plasmon wavelengths when the plasmon reflects off a boundary.

The internal structure of plasmons reveals uncharted territory for plasmonics, with new ways to manipulate their trajectories and a new playground in which to explore the geometry of quasiparticles.

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Vol. 8, Iss. 2 — April - June 2018

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