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Electron cooling in graphene enhanced by plasmon–hydron resonance
Evidence is accumulating for the crucial role of a solid’s free electrons in the dynamics of solid–liquid interfaces. Liquids induce electronic polarization and drive electric currents as they flow; electronic excitations, in turn, participate in hydrodynamic friction. Yet, the underlying solid–liqu...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10427419/ https://www.ncbi.nlm.nih.gov/pubmed/37349505 http://dx.doi.org/10.1038/s41565-023-01421-3 |
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author | Yu, Xiaoqing Principi, Alessandro Tielrooij, Klaas-Jan Bonn, Mischa Kavokine, Nikita |
author_facet | Yu, Xiaoqing Principi, Alessandro Tielrooij, Klaas-Jan Bonn, Mischa Kavokine, Nikita |
author_sort | Yu, Xiaoqing |
collection | PubMed |
description | Evidence is accumulating for the crucial role of a solid’s free electrons in the dynamics of solid–liquid interfaces. Liquids induce electronic polarization and drive electric currents as they flow; electronic excitations, in turn, participate in hydrodynamic friction. Yet, the underlying solid–liquid interactions have been lacking a direct experimental probe. Here we study the energy transfer across liquid–graphene interfaces using ultrafast spectroscopy. The graphene electrons are heated up quasi-instantaneously by a visible excitation pulse, and the time evolution of the electronic temperature is then monitored with a terahertz pulse. We observe that water accelerates the cooling of the graphene electrons, whereas other polar liquids leave the cooling dynamics largely unaffected. A quantum theory of solid–liquid heat transfer accounts for the water-specific cooling enhancement through a resonance between the graphene surface plasmon mode and the so-called hydrons—water charge fluctuations—particularly the water libration modes, which allows for efficient energy transfer. Our results provide direct experimental evidence of a solid–liquid interaction mediated by collective modes and support the theoretically proposed mechanism for quantum friction. They further reveal a particularly large thermal boundary conductance for the water–graphene interface and suggest strategies for enhancing the thermal conductivity in graphene-based nanostructures. |
format | Online Article Text |
id | pubmed-10427419 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104274192023-08-17 Electron cooling in graphene enhanced by plasmon–hydron resonance Yu, Xiaoqing Principi, Alessandro Tielrooij, Klaas-Jan Bonn, Mischa Kavokine, Nikita Nat Nanotechnol Article Evidence is accumulating for the crucial role of a solid’s free electrons in the dynamics of solid–liquid interfaces. Liquids induce electronic polarization and drive electric currents as they flow; electronic excitations, in turn, participate in hydrodynamic friction. Yet, the underlying solid–liquid interactions have been lacking a direct experimental probe. Here we study the energy transfer across liquid–graphene interfaces using ultrafast spectroscopy. The graphene electrons are heated up quasi-instantaneously by a visible excitation pulse, and the time evolution of the electronic temperature is then monitored with a terahertz pulse. We observe that water accelerates the cooling of the graphene electrons, whereas other polar liquids leave the cooling dynamics largely unaffected. A quantum theory of solid–liquid heat transfer accounts for the water-specific cooling enhancement through a resonance between the graphene surface plasmon mode and the so-called hydrons—water charge fluctuations—particularly the water libration modes, which allows for efficient energy transfer. Our results provide direct experimental evidence of a solid–liquid interaction mediated by collective modes and support the theoretically proposed mechanism for quantum friction. They further reveal a particularly large thermal boundary conductance for the water–graphene interface and suggest strategies for enhancing the thermal conductivity in graphene-based nanostructures. Nature Publishing Group UK 2023-06-22 2023 /pmc/articles/PMC10427419/ /pubmed/37349505 http://dx.doi.org/10.1038/s41565-023-01421-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Yu, Xiaoqing Principi, Alessandro Tielrooij, Klaas-Jan Bonn, Mischa Kavokine, Nikita Electron cooling in graphene enhanced by plasmon–hydron resonance |
title | Electron cooling in graphene enhanced by plasmon–hydron resonance |
title_full | Electron cooling in graphene enhanced by plasmon–hydron resonance |
title_fullStr | Electron cooling in graphene enhanced by plasmon–hydron resonance |
title_full_unstemmed | Electron cooling in graphene enhanced by plasmon–hydron resonance |
title_short | Electron cooling in graphene enhanced by plasmon–hydron resonance |
title_sort | electron cooling in graphene enhanced by plasmon–hydron resonance |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10427419/ https://www.ncbi.nlm.nih.gov/pubmed/37349505 http://dx.doi.org/10.1038/s41565-023-01421-3 |
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