arXiv · 2202.12682
Charge-state dependent vibrational relaxation in a single-molecule junction
Abstract
The interplay between nuclear and electronic degrees of freedom strongly influences molecular charge transport. Herein, we report on transport through a porphyrin dimer molecule, weakly coupled to graphene electrodes, that displays sequential tunneling within the Coulomb-blockade regime. The sequential transport is initiated by current-induced phonon absorption and proceeds by rapid sequential transport via a non-equilibrium vibrational distribution. We demonstrate this is possible only when the vibrational dissipation is slow relative to sequential tunneling rates, and obtain a lower bound for the vibrational relaxation time of 8 ns, a value that is dependent on the molecular charge state.
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Xinya Bian, Zhixin Chen, Jakub K. Sowa, Charalambos Evangeli, Bart Limburg, Jacob L. Swett, Jonathan Baugh, G. Andrew D. Briggs, Harry L. Anderson, Jan A. Mol, James O. Thomas. 2022-02-25. Charge-state dependent vibrational relaxation in a single-molecule junction. https://doi.org/10.1103/physrevlett.129.207702
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