Abstract
Materials and molecular systems exhibiting long-lived electronic coherence can facilitate coherent transport, opening the door to efficient charge and energy transport beyond traditional methods. Recently, signatures of a possible coherent, recurrent electronic motion were identified in femtosecond pump-probe spectroscopy experiments on a binuclear platinum complex, where a persistent periodic beating in the transient absorption signal's anisotropy was observed. In this study, we investigate the excitonic dynamics that underlie the suspected electronic coherence for a series of binuclear platinum complexes exhibiting a range of interplatinum distances. Results suggest that the long-lived coherence can only result when competitive electronic couplings are in balance. At longer Pt-Pt distances, the electronic couplings between the two halves of the binuclear system weaken, and exciton localization and recombination is favored on short time scales. For short Pt-Pt distances, electronic couplings between the states in the coherent superposition are stronger than the coupling with other excitonic states, leading to long-lived coherence. (Equation Presented).
Original language | English |
---|---|
Pages (from-to) | 1932-1939 |
Number of pages | 8 |
Journal | Journal of Physical Chemistry A |
Volume | 121 |
Issue number | 9 |
DOIs | |
State | Published - Mar 9 2017 |
Externally published | Yes |
Funding
This work was supported by the Ultrafast Initiative of the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, through Argonne National Laboratory under Contract No. DE-AC02-06CH11357. The development of time-dependent electronic structure methods is supported by the National Science Foundation (CHE-1565520 to X.L.). Computations were facilitated through the use of advanced computational, storage, and networking infrastructure provided by the Hyak supercomputer system at the University of Washington, funded by the Student Technology Fee. D.B.L. and P.J.L. are grateful for support by the State of Washington through the University of Washington Clean Energy Institute. S.E.B.-X. and L.X.C. are grateful for the support from the National Science Foundation (CHE-1363007 to L.X.C). F.N.C. was supported by the National Science Foundation (CHE-1362942).
Funders | Funder number |
---|---|
Office of Basic Energy Sciences | |
State of Washington | |
Ultrafast Initiative | |
University of Washington Clean Energy Institute | CHE-1363007, CHE-1362942 |
National Science Foundation | 1362942, CHE-1565520 |
U.S. Department of Energy | |
Office of Science | |
Argonne National Laboratory | DE-AC02-06CH11357 |
University of Washington |