Samenvatting
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.
Originele taal-2 | Engels |
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Pagina's (van-tot) | 898-904 |
Aantal pagina's | 7 |
Tijdschrift | Nature Nanotechnology |
Volume | 18 |
Nummer van het tijdschrift | 8 |
DOI's | |
Status | Gepubliceerd - aug. 2023 |
Bibliografische nota
Funding Information:We acknowledge financial support from the MaxWater initiative of the Max Planck Society. We thank X. Jia and H. Wang for carrying out preliminary experiments, M. Grechko and D.-W. Scholdei for assisting with the Fourier transform infrared measurements, and M.-J. van Zadel and F. Gericke for constructing the sample holder. X.Y. is grateful for support from the China Scholarship Council. K.J.T. acknowledges funding from the European Union’s Horizon 2020 research and innovation programme under grant agreement number 804349 (ERC StG CUHL), RYC fellowship number RYC-2017-22330 and IAE project PID2019-111673GB-I00. A.P. acknowledges support from the European Commission under the EU Horizon 2020 MSCA-RISE-2019 programme (project 873028 HYDROTRONICS) and from the Leverhulme Trust under grant RPG-2019-363. N.K. acknowledges support from a Humboldt fellowship. The Flatiron Institute is a division of the Simons Foundation. We thank L. Reading-Ikkanda (Simons Foundation) for help with figure preparation.