Are you an EPFL student looking for a semester project?
Work with us on data science and visualisation projects, and deploy your project as an app on top of Graph Search.
Concept
Vibronic coupling
Summary
Vibronic coupling (also called nonadiabatic coupling or derivative coupling) in a molecule involves the interaction between electronic and nuclear vibrational motion. The term "vibronic" originates from the combination of the terms "vibrational" and "electronic", denoting the idea that in a molecule, vibrational and electronic interactions are interrelated and influence each other. The magnitude of vibronic coupling reflects the degree of such interrelation.
In theoretical chemistry, the vibronic coupling is neglected within the Born–Oppenheimer approximation. Vibronic couplings are crucial to the understanding of nonadiabatic processes, especially near points of conical intersections. The direct calculation of vibronic couplings used to be uncommon due to difficulties associated with its evaluation, but has recently gained popularity due to increased interest in the quantitative prediction of internal conversion rates, as well as the development of cheap but rigorous ways to analytically calculate the vibronic couplings, especially at the TDDFT level.
Vibronic coupling describes the mixing of different electronic states as a result of small vibrations.
The evaluation of vibronic coupling often involves complex mathematical treatment.
The form of vibronic coupling is essentially the derivative of the wave function. Each component of the vibronic coupling vector can be calculated with numerical differentiation methods using wave functions at displaced geometries. This is the procedure used in MOLPRO.
First order accuracy can be achieved with forward difference formula:
Second order accuracy can be achieved with central difference formula:
Here, is a unit vector along direction . is the transition density between the two electronic states.
Evaluation of electronic wave functions for both electronic states are required at N displacement geometries for first order accuracy and 2*N displacements to achieve second order accuracy, where N is the number of nuclear degrees of freedom. This can be extremely computationally demanding for large molecules.
Official source
About this result
This page is automatically generated and may contain information that is not correct, complete, up-to-date, or relevant to your search query. The same applies to every other page on this website. Please make sure to verify the information with EPFL's official sources.