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Photophysics of a Copper Phenanthroline Elucidated by Trajectory and Wavepacket-based Quantum Dynamics: A Synergetic Approach

Lookup NU author(s): Professor Thomas Penfold



This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0).


On-the-fly excited state molecular dynamics is an attractive method for studying non-equilibrium processes in excited states and is beginning to emerge as a mature approach much like its ground state counterparts. In contrast to quantum wavepacket dynamics methods, it negates the need for modelling potential energy surfaces, which usually confine nuclear motion within a reduced number of vibrational modes. In addition, on-the-fly molecular dynamics techniques are easily combined with the atomistic description of the solvents (through the QM/MM approach) allowing to explicitly address the effect of the environment. Herein, we study the nonadiabatic relaxation of photoexcited [Cu(dmp)2]+ (dmp = 2,9-dimethyl-1,10-phenanthroline) using QM/MM Trajectory Surface Hopping (TSH). We show that the decay of the initially excited singlet state into the lowest singlet (S1) state occurs within 100 fs, in agreement with previous experiments, and is slightly influenced by the nature of the solvent. Using principal component analysis (PCA), we also identify the dominant normal modes activated during the excited state decay, which are then used to design the vibrational Hamiltonian for quantum wavepacket dynamics simulations.

Publication metadata

Author(s): Capano G, Penfold TJ, Chergui M, Tavernelli I

Publication type: Article

Publication status: Published

Journal: Physical Chemistry Chemical Physics

Year: 2017

Volume: 19

Issue: 30

Pages: 19590-19600

Print publication date: 14/08/2017

Online publication date: 23/03/2017

Acceptance date: 21/03/2017

Date deposited: 24/03/2017

ISSN (print): 1463-9076

ISSN (electronic): 1463-9084

Publisher: Royal Society of Chemistry


DOI: 10.1039/C7CP00436B


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