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      Visually constructing the chemical structure of a single molecule by scanning Raman picoscopy

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          Abstract

          The strong spatial confinement of a nanocavity plasmonic field has made it possible to visualize the inner structure of a single molecule and even to distinguish its vibrational modes in real space. With such ever-improved spatial resolution, it is anticipated that full vibrational imaging of a molecule could be achieved to reveal molecular structural details. Here we demonstrate full Raman images of individual vibrational modes at the ångström level for a single Mg-porphine molecule, revealing distinct characteristics of each vibrational mode in real space. Furthermore, by exploiting the underlying interference effect and Raman fingerprint database, we propose a new methodology for structural determination, which we have called ‘scanning Raman picoscopy’, to show how such ultrahigh-resolution spectromicroscopic vibrational images can be used to visually assemble the chemical structure of a single molecule through a simple Lego-like building process.

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          Most cited references44

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          Principles of Fluorescence Spectroscopy

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            Chemical mapping of a single molecule by plasmon-enhanced Raman scattering.

            Visualizing individual molecules with chemical recognition is a longstanding target in catalysis, molecular nanotechnology and biotechnology. Molecular vibrations provide a valuable 'fingerprint' for such identification. Vibrational spectroscopy based on tip-enhanced Raman scattering allows us to access the spectral signals of molecular species very efficiently via the strong localized plasmonic fields produced at the tip apex. However, the best spatial resolution of the tip-enhanced Raman scattering imaging is still limited to 3-15 nanometres, which is not adequate for resolving a single molecule chemically. Here we demonstrate Raman spectral imaging with spatial resolution below one nanometre, resolving the inner structure and surface configuration of a single molecule. This is achieved by spectrally matching the resonance of the nanocavity plasmon to the molecular vibronic transitions, particularly the downward transition responsible for the emission of Raman photons. This matching is made possible by the extremely precise tuning capability provided by scanning tunnelling microscopy. Experimental evidence suggests that the highly confined and broadband nature of the nanocavity plasmon field in the tunnelling gap is essential for ultrahigh-resolution imaging through the generation of an efficient double-resonance enhancement for both Raman excitation and Raman emission. Our technique not only allows for chemical imaging at the single-molecule level, but also offers a new way to study the optical processes and photochemistry of a single molecule.
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              Nanoscale chemical analysis by tip-enhanced Raman spectroscopy

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                Author and article information

                Journal
                Natl Sci Rev
                Natl Sci Rev
                nsr
                National Science Review
                Oxford University Press
                2095-5138
                2053-714X
                November 2019
                08 November 2019
                08 November 2019
                : 6
                : 6
                : 1169-1175
                Affiliations
                [1] Hefei National Laboratory for Physical Sciences at the Microscale and Synergetic Innovation Center of Quantum Information and Quantum Physics, University of Science and Technology of China , Hefei 230026, China
                Author notes
                Corresponding author. E-mail: yiluo@ 123456ustc.edu.cn
                Corresponding author. E-mail: zcdong@ 123456ustc.edu.cn
                Corresponding author. E-mail: jghou@ 123456ustc.edu.cn

                Equally contributed to this work.

                Article
                nwz180
                10.1093/nsr/nwz180
                8291412
                34691995
                ff716008-1eeb-4147-8be0-4b0ace4f619f
                © The Author(s) 2019. Published by Oxford University Press on behalf of China Science Publishing & Media Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 11 October 2019
                : 06 November 2019
                : 07 November 2019
                Page count
                Pages: 7
                Funding
                Funded by: National Key R&D Program of China
                Award ID: 2016YFA0200600
                Award ID: 2017YFA0303500
                Funded by: National Natural Science Foundation of China 10.13039/501100001809
                Funded by: Chinese Academy of Sciences 10.13039/501100002367
                Categories
                Research Article
                Chemistry

                scanning raman picoscopy,tip-enhanced raman spectroscopy,structure determination,vibrational mode imaging,interference effect

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