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Postdoc position available at the University Par ... (No replies)

federica.agostini
7 years ago
federica.agostini 7 years ago
A postdoctoral researcher position is available at the Laboratoire de Chimie Physique (LCP http://www.lcp.u-psud.fr/) of the University Paris-Sud (Orsay, south of Paris, France). The position is already available, for two years, and we have the possibility of hiring until the end of the year.
 
The project places itself within a collaboration between the LCP (under the supervision of Federica Agostini and David Lauvergnat) and the Institute of Molecular Sciences of Orsay (ISMO http://www.ismo.u-psud.fr/, under the supervision of Sabine Morisset and Nathalie Rougeau).
We are looking for candidates for a strong background in chemical physics and/or theoretical chemistry. The project will involve a large part of theoretical and code development. Therefore, we look for candidates with good analytical skills and with experience in programming (Fortran, bash, C/C++, phython). Knowledge of English is required; knowledge of French is not mandatory.
 
Please find below a brief description of the project.
 
For further information, please, do not hesitate to contact me ([email protected]).
 
Best regards,
 
Federica Agostini
 
PROJECT DESCRIPTION
 
The reaction of ground-state oxygen O(3P) with ethylene [1] encloses all the relevant and most challenging features of excited-state dynamical phenomena. Upon collision with energetic oxygen atoms, reaction paths involving electronic excited states are opened. Due to the ultrafast motion of the nuclei, transient products are short-lived, but important to determine in order to predict all possible channels for relaxation of the excited states to the ground state. For a full-dimensional excited-state simulation of the process, it is essential to capture the coupling among electronic states with different spin multiplicity, i.e., intersystem crossings, along with standard avoided crossings and conical intersections among singlet states (internal conversions). This project aims at developing a theoretical and computational tool allowing for quasiclassical simulations of the reaction of atomic oxygen in the triplet state with ethylene. The coupled-trajectory mixed quantum-classical (CT-MQC) algorithm, recently [2, 3] developed in the framework of the exact factorization of the electron-nuclear wavefunction [4], will be employed, as it has been shown to capture features of the coupled electron-nuclear motion involving electronic excited states that are usually missed by standard methods [5]. In parallel, the performance of time-dependent density functional theory as electronic structure method used to predict available electronic states and to capture intersystem crossings will be thoroughly investigated. 
 
[1] B. Fu, Y.-C. Han, J. M. Bowman, L. Angelucci, N. Balucani, F. Leonori, and P. Casavecchia, Proc. Nat. Ac. Sci. 109, 9733 (2012). 
[2] S. K. Min, F. Agostini, and E. K. U. Gross, Phys. Rev. Lett. 115, 073001 (2015).
[3] F. Agostini, S. K. Min, A. Abedi, and E. K. U. Gross, J. Chem. Theory Comput. 12, 2127 (2016).
[4] A. Abedi, F. Agostini, Y. Suzuki, and E. K. U. Gross, Phys. Rev. Lett. 110, 263001 (2013).
[5] S. K. Min, F. Agostini, I. Tavernelli, and E. K. U. Gross, J. Phys. Chem. Lett. 8, 3048 (2017). 



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Ab initio (from electronic structure) calculation of complex processes in materials