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- W4200318583 abstract "Flat lying physisorbates on surfaces can be expected to be lifted by heating. The details of this lattice expansion depend on the competition between two mechanisms. On the one hand, the interaction potential of each atom with the substrate is anharmonic and constitutes the reason for lifting. On the other hand, the internal bending stiffness of the planar adsorbate reduces its tendency to lift with temperature. Here we show that this competition can be investigated in a simplified molecular-dynamics simulation which considers only the vertical motion of the atoms of the adsorbate in respective model potentials. For two prototypical systems, i.e., graphene and 1,4,5,8-naphthalene-tetracarboxylic acid dianhydride (NTCDA) on Ag(111), we observe lifting by 0.04 AA{} (graphene) and 0.06 AA{} (NTCDA) between zero and room temperature. For the latter system, the impact of the temperature-dependent geometrical and vibrational properties on the occurring interface state (IS) is discussed. By introducing a local electron-phonon interaction model, we combine the indirect dependence of the IS on the average binding distance with direct coupling to the vibrational modes and obtain good agreement with the experimental results." @default.
- W4200318583 created "2021-12-31" @default.
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- W4200318583 date "2021-12-06" @default.
- W4200318583 modified "2023-10-05" @default.
- W4200318583 title "Graphene and NTCDA adsorbed on Ag(111): Temperature-dependent binding distance and phonon coupling to the interface state" @default.
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- W4200318583 doi "https://doi.org/10.1103/physrevb.104.245403" @default.
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