Optimal initiation of electronic excited state mediated intramolecular H-transfer in malonaldehyde by UV-laser pulses
Autor: | Susanta Mahapatra, S. Nagaprasad Reddy, Himanshi Singh, K. R. Nandipati, KandukuriMahesh Kumar |
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Rok vydání: | 2014 |
Předmět: | |
Zdroj: | The European Physical Journal D. 68 |
ISSN: | 1434-6079 1434-6060 |
DOI: | 10.1140/epjd/e2014-50486-6 |
Popis: | Optimally controlled initiation of intramolecular H-transfer in malonaldehyde is accomplished by designing a sequence of ultrashort (~80 fs) down-chirped pump-dump ultra violet (UV)-laser pulses through an optically bright electronic excited [S 2 (π π ∗)] state as a mediator. The sequence of such laser pulses is theoretically synthesized within the framework of optimal control theory (OCT) and employing the well-known pump-dump scheme of Tannor and Rice [D.J. Tannor, S.A. Rice, J. Chem. Phys. 83, 5013 (1985)]. In the OCT, the control task is framed as the maximization of cost functional defined in terms of an objective function along with the constraints on the field intensity and system dynamics. The latter is monitored by solving the time-dependent Schrodinger equation. The initial guess, laser driven dynamics and the optimized pulse structure (i.e., the spectral content and temporal profile) followed by associated mechanism involved in fulfilling the control task are examined in detail and discussed. A comparative account of the dynamical outcomes within the Condon approximation for the transition dipole moment versus its more realistic value calculated ab initio is also presented. |
Databáze: | OpenAIRE |
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