Universität Wien

270170 VO Principles of Two-Dimensional Electronic Spectroscopy (2012S)

3.00 ECTS (2.00 SWS), SPL 27 - Chemie

Vorbesprechung: Fr. 30.03.2012 um 10:00
im Seminarraum des Instituts für Physikalische Chemie

Block: jeweils Fr. 16:00 bis 18:15 im
Seminarraum des Instituts für Physikalische Chemie
beginnend mit 20.04.2012 bis Semesterende.

Details

Language: English

Lecturers

Classes

Currently no class schedule is known.

Information

Aims, contents and method of the course

The Lectures will survey a broad class of coherent spectroscopic techniques and address tools and theoretical microscopic descriptions for the interpretation of non-linear observables in the study of complex molecules, biological systems, and selected semi-conductors. Experiments include excitation/probing with a sequence of laser-pulses with controllable inter-pulse relative phase, tuning-frequency and widths, and from the theoretical point-of-view, the development and design of formalisms suitable to cover molecular features such as electronic/nuclear motions) to establish, systematically, spectroscopy in polarization- (coherent regime) and population space (incoherent regime).
With the culmination of two-dimensional Fourier-Transform (FT) electronic spectroscopy (2D-ES), cutting edge experiments have emerged that probe molecular correlations on the 500 THz scale of the electronic transition dipole oscillation, thereby recording the diffracted molecular Four-Wave-Mixing - electrical field both under controlled phase at the amplitude level and along two frequency axes via double FT. In particular, the cross-peaks carrying the off-diagonal signals are directly sensitive to the presence of molecular quantum-interference and coherent phenomena. This has led, over the past few years, to exciting prototypical studies on electronic oscillators in biological light harvesting complexes and, in later experiments, to investigations on artificial aggregates by directly probing electronic coupling, quantum-oscillatory motion, and non-perturbative exciton dephasing.
From the theoretical point-of view, a correlation-function framework for computing NL optical signals will be introduced using superoperator techniques for describing the measurements via the evolution of the density-matrix in terms of the various Feynman quantum-pathways in Louville-space. Connection between multi-point correlation and optical response-functions will be established and the relationship between various FT-projections in multi-dimensional correlation spectroscopies will be surveyed. Very recent experimental highlights of 2D- spectroscopic science will be demonstrated from ground-breaking studies on excitonic (organic and semi-conductor) nanostructures, conjugated polymers, proteins, biological & synthetic aggregates , hydrogen bonded liquids and related bio-functional molecular systems

Assessment and permitted materials

Minimum requirements and assessment criteria

1) Density Operator, 2) Time-Dependent Perturbative Theory and Expansion, 3) Double-Sided Feynman Diagrams, 4) Line-Shapes-Microscopic Theory of Dephasing, 5) Microscopic Theory of Dephasing-Linear Response, NL-Response, Time-and Phase Resolved FourWaveMixing and Spectral Heterodyning 6) nD-Electronic Correlation Spectroscopies- Power and Beauty: Measuring the Third-Order response Function Directly Experiments in Best Light-Very Recent Applications

Examination topics

Reading list

: S. Mukamel, Principles of Nonlinear Optical Spectroscopy, Oxford University Press, New York (1995); Reviews: S. Mukamel, Annu.Rev.Phys.Chem. 51, 691 (2000); D. Abramavicius, B. Palmieri, D. V. Voronine, F. Sanda, and S. Mukamel Chem. Rev. 109, 2350 (2009); H. F. Kauffmann et al. Acc. of Chem. Research, 42 (9) 1364 (2009)
Special topics, cf. HFK, list of relevant publications

Association in the course directory

EF-1, EF-2, EF-3.

Last modified: Fr 31.08.2018 08:55