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Multidimensional femtosecond coherence spectroscopy for study of the carrier dynamics in photonics materials

Lap Van Dao, My Thi Tra Do, Peter Hannaford

Published Jan 1, 2004• 0 citations
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Abstract

We present a new multidimensional spectroscopy technique based on femtosecond spectrally resolved 2colour 3-pulse photon echoes for investigating of the carriers dynamics in the photonic materials such as semiconductor doped glass and porous silicon. The use of different colours and polarisations for the pump and probe pulses together with spectral analysis of the photon echo signals allows separation of the dynamics of electrons and holes.

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Accounts of Chemical Research•Mar 26, 2009•97 citations
We present a new multidimensional spectroscopy technique based on femtosecond spectrally resolved 2colour 3-pulse photon echoes for investigating of the carriers dynamics in the photonic materials such as semiconductor doped glass and porous silicon. The use of different colours and polarisations for the pump and probe pulses together with spectral analysis of the photon echo signals allows separation of the dynamics of electrons and holes.
Coherent optical phenomena such as the optical Stark effect, Rabi flopping, photon echo and quantum beating which are well-known in atomic spectroscopy can also be observed in semiconductors by using femtosecond laser pulses. On these short time scales, the quantum coherence of the optical excitations in the solid do not only influence the optical properties but change at the same time the relaxation and dephasing kinetics. The quasi-classical Boltzmann kinetics has to be replaced by quantum kinetics. Coherence leads to the appearance of memory in the scattering integrals. For femtosecond four-wave mixing and pump-and-probe spectroscopy the use of quantum kinetics for LO-phonon and for carrier-carrier scattering will be reviewed.
The nonlinear polarization close to the band gap of GaAs is studied by spectrally and temporally resolved four-wave mixing. Excitonic and free carrier contributions both excited within the bandwidth of the 100 fs pulses are distinguished for the first time. The excitonic part dominates at carrier densities below 1016{10}^{16}1016 ${\mathrm{cm}}^{\mathrm{\ensuremath{-}}3}$. At higher density, nonthermalized free carriers give rise to an additional component resonant to the pulse that shows a photon-echo-like time behavior. Monte Carlo simulations including the coherent polarization and the scattering dynamics of the carriers account for the data.
Multidimensional analysis of coherent signals is commonly used in nuclear magnetic resonance to study correlations among spins. These techniques were recently extended to the femtosecond regime and applied to chemical, biological and semiconductor systems. In this work, we apply a two-dimensional correlation spectroscopy technique which employs double-quantum-coherence to investigate many-body effects in a semiconductor quantum well. The signal is detected along the direction k(1)+ k(2)- k(3), where k(1), k(2) and k(3) are the pulse wave vectors in chronological order. We show that this signal is particularly sensitive to many-body correlations which are missed by time-dependent Hartree-Fock approximation. The correlation energy of two-exciton can be probed with a very high resolution arising from a two-dimensional correlation spectrum, where two-exciton couplings spread the cross peaks along both axes of the 2D spectrum to create a characteristic highly resolved pattern. This level of detail is not available from conventional one-dimensional four-wave mixing or other two-dimensional correlation spectroscopy signals such as the photo echo (-k(1)+ k(2)+ k(3)).
Semiconductor nanocrystals are a novel class of materials intermediate between the molecular and solid state forms of matter. Their homogenous linewidths and electronic structure are of considerable interest for the understanding of the physics of quantum confinement. In this work we study the electronic and vibrational dephasing dynamics in InP nanocrystals using femtosecond three pulse photon echo (3PPE) experiments1 complemented by nanosecond transient hole-burning (HB) spectroscopy.2 The echo decay is explained by taking into account the multi-level electronic structure as observed in the hole-burning experiment.
Over the past 15 years, researchers have extended the multidimensional techniques which originated with NMR in the 1970s to infrared and visible coherent spectroscopy. These advances have dramatically enhanced the temporal resolution from the microsecond to the femtosecond regime. NMR spectroscopists have developed principles for the design of pulse sequences that enhance selected spectral features and reveal desired dynamical events. Extending these principles to the optical regime offers numerous opportunities for narrowing the line shapes in specific directions, unraveling weak cross-peaks from otherwise congested spectra, and controlling the interferences between quantum pathways. We can achieve these enhancements by shaping the spectral and temporal profiles of the pulses. Pulse polarization shaping may lead to unique probes of time-dependent chirality. In this Account, we compare two types of signals. The first, the photon echo, is generated in the direction -k(1) + k(2) + k(3), and the second, double quantum coherence, is detected at +k(1) + k(2) - k(3). Here k(1), k(2), and k(3) are the wave vectors of the three incoming pulses in chronological order. We illustrate the novel information extracted from these signals by simulations of three physical systems. In the first system, spectra of GaAs semiconductor quantum wells provide a direct look at many-body electron correlation effects. We directly observe specific projections of the many-electron wave function, which we can use to test the quality of various levels of computational techniques for electronic structure. Secondly, the spectra of photosynthetic aggregates reveal couplings between chromophores, quantum coherence signatures of chromophore entanglement, and energy-transfer pathways. Using some fundamental symmetries of pulse polarization configurations of nonlinear signals, we can construct superpositions of signals designed to better distinguish among various coherent and incoherent exciton transport pathways and amplify subtle variations among different species of the Fenna-Matthews-Olson (FMO) antenna complex. Both of the first two applications require femtosecond pulses of light in the visible range. The third application demonstrates how resonant core spectroscopy may be used to generate core excitations that are highly localized at selected atoms. Such signals can monitor the motions of valence electron wavepackets in real space with atomic spatial resolution. These future X-ray applications will require attosecond bright X-ray sources, which are currently being developed in several labs. Common principles underlie these techniques in coherent spectroscopy for spins, valence electrons, and core electronic excitations, spanning frequencies from radiowaves to hard X-rays.