Fantastical Excited State Optimized Structures and Where to Find Them
Justin J. Talbot, Juan E. Arias-Martinez, Stephen J. Cotton, and, Martin Head-Gordon

TL;DR
This paper reveals that some optimized excited state structures in quantum chemistry are artifacts caused by electronic state couplings and avoided crossings, and are not physically observable, as demonstrated through ab initio calculations and nonadiabatic dynamics.
Contribution
It introduces a diagnostic criterion based on harmonic frequencies to identify non-observable excited state minima caused by electronic couplings.
Findings
Fantastical excited state structures have unphysically high harmonic frequencies.
Such structures have extremely short lifetimes, on the order of femtoseconds.
Their occurrence indicates nearby avoided crossings or conical intersections.
Abstract
The quantum chemistry community has developed analytic forces for approximate electronic excited states to enable walking on excited state potential energy surfaces (PES). One can thereby computationally characterize excited state minima and saddle points. Always implicit in using this machinery is the fact that an excited state PES only exists within the realm of the Born-Oppenheimer approximation, where the nuclear and electronic degrees of freedom separate. This work demonstrates through ab initio calculations and simple nonadiabatic dynamics that some excited state minimum structures are fantastical: they appear to exist as stable configurations only as a consequence of the PES construct, rather than being physically observable. One such case is the S2 excited state of phosphine and a second case are local minima of a number of states of tris(bipyridine)ruthenium(II). Each…
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Taxonomy
TopicsMolecular Junctions and Nanostructures · Advanced Chemical Physics Studies · Spectroscopy and Quantum Chemical Studies
