4.7 Article

Investigation of plasmon relaxation mechanisms using nonadiabatic molecular dynamics

期刊

JOURNAL OF CHEMICAL PHYSICS
卷 157, 期 21, 页码 -

出版社

AIP Publishing
DOI: 10.1063/5.0127435

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资金

  1. Guangdong Shenzhen Joint Key Fund [2019B1515120045]
  2. NSFC [22073007, 12088101]
  3. Shenzhen Basic Research Fund [JCYJ20190813164805689]
  4. Sino-German mobility program [M-0215]
  5. Hong Kong Quantum AI Lab
  6. LDRD Early Career program of Los Alamos National Laboratory
  7. Humboldt Research Award (Germany)
  8. Center for Integrated Nanotechnology (CINT) at Los Alamos National Laboratory (LANL)
  9. U.S. Department of Energy and Office of Basic Energy Sciences User Facility
  10. National Nuclear Security Administration of U.S. Department of Energy [89233218CNA000001]

向作者/读者索取更多资源

This study uses the Trajectory Surface Hopping (TSH) nonadiabatic molecular dynamics algorithm to simulate plasmon relaxation in Au-20 clusters, taking atomistic details into account. The simulation results show that the relaxation time is about 2.7 ps, and the lifetime of the phonon-induced plasmon dephasing process is approximately 10.4 fs.
Hot carriers generated from the decay of plasmon excitation can be harvested to drive a wide range of physical or chemical processes. However, their generation efficiency is limited by the concomitant phonon-induced relaxation processes by which the energy in excited carriers is transformed into heat. However, simulations of dynamics of nanoscale clusters are challenging due to the computational complexity involved. Here, we adopt our newly developed Trajectory Surface Hopping (TSH) nonadiabatic molecular dynamics algorithm to simulate plasmon relaxation in Au-20 clusters, taking the atomistic details into account. The electronic properties are treated within the Linear Response Time-Dependent Tight-binding Density Functional Theory (LR-TDDFTB) framework. The relaxation of plasmon due to coupling to phonon modes in Au-20 beyond the Born-Oppenheimer approximation is described by the TSH algorithm. The numerically efficient LR-TDDFTB method allows us to address a dense manifold of excited states to ensure the inclusion of plasmon excitation. Starting from the photoexcited plasmon states in Au-20 cluster, we find that the time constant for relaxation from plasmon excited states to the lowest excited states is about 2.7 ps, mainly resulting from a stepwise decay process caused by low-frequency phonons of the Au-20 cluster. Furthermore, our simulations show that the lifetime of the phonon-induced plasmon dephasing process is & SIM;10.4 fs and that such a swift process can be attributed to the strong nonadiabatic effect in small clusters. Our simulations demonstrate a detailed description of the dynamic processes in nanoclusters, including plasmon excitation, hot carrier generation from plasmon excitation dephasing, and the subsequent phonon-induced relaxation process. Published under an exclusive license by AIP Publishing.

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