3
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Nonlinear infrared polaritonic interaction between cavities mediated by molecular vibrations at ultrafast time scale

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Strong coupling enables delocalized intercavity nonlinearity by combining the photon delocalization and molecular anharmonicity.

          Abstract

          Realizing nonlinear interactions between spatially separated particles can advance molecular science and technology, including remote catalysis of chemical reactions, ultrafast processing of information in infrared (IR) photonic circuitry, and advanced platforms for quantum simulations with increased complexity. Here, we achieved nonlinear interactions at ultrafast time scale between polaritons contained in spatially adjacent cavities in the mid-IR regime, altering polaritons in one cavity by pumping polaritons in an adjacent one. This was done by strong coupling molecular vibrational modes with photon modes, a process that combines characteristics of both photon delocalization and molecular nonlinearity. The dual photon/molecule character of polaritons enables delocalized nonlinearity—a property that neither molecular nor cavity mode would have alone.

          Related collections

          Most cited references27

          • Record: found
          • Abstract: found
          • Article: not found

          Tilting a ground-state reactivity landscape by vibrational strong coupling

          Many chemical methods have been developed to favor a particular product in transformations of compounds that have two or more reactive sites. We explored a different approach to site selectivity using vibrational strong coupling (VSC) between a reactant and the vacuum field of a microfluidic optical cavity. Specifically, we studied the reactivity of a compound bearing two possible silyl bond cleavage sites—Si–C and Si–O, respectively—as a function of VSC of three distinct vibrational modes in the dark. The results show that VSC can indeed tilt the reactivity landscape to favor one product over the other. Thermodynamic parameters reveal the presence of a large activation barrier and substantial changes to the activation entropy, confirming the modified chemical landscape under strong coupling.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            Nonlinear optics of normal-mode-coupling semiconductor microcavities

              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              All-optical polariton transistor

                Bookmark

                Author and article information

                Journal
                Sci Adv
                Sci Adv
                SciAdv
                advances
                Science Advances
                American Association for the Advancement of Science
                2375-2548
                May 2021
                07 May 2021
                : 7
                : 19
                : eabf6397
                Affiliations
                [1 ]Materials Science and Engineering Program, UC San Diego, La Jolla, CA 92093, USA.
                [2 ]Department of Chemistry and Biochemistry, UC San Diego, La Jolla, CA 92093, USA.
                Author notes
                [* ]Corresponding author. Email: w2xiong@ 123456ucsd.edu
                Author information
                http://orcid.org/0000-0002-9055-7931
                http://orcid.org/0000-0001-7663-6978
                http://orcid.org/0000-0003-4287-784X
                http://orcid.org/0000-0002-7702-0187
                Article
                abf6397
                10.1126/sciadv.abf6397
                8104880
                33962949
                c9237cb0-edb5-41cf-9d91-12efe16f0d5d
                Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).

                This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license, which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.

                History
                : 09 November 2020
                : 19 March 2021
                Funding
                Funded by: doi http://dx.doi.org/10.13039/100000001, National Science Foundation;
                Award ID: DMR1848215
                Categories
                Research Article
                Research Articles
                SciAdv r-articles
                Chemical Physics
                Chemistry
                Chemistry
                Custom metadata
                Mariane Belen

                Comments

                Comment on this article