Two-dimensional spectroscopy is an extension of conventional spectroscopic methods that characterises resonant systems as a function of two frequency variables. We use this technique to improve on the characterisation of atomic media along the lines discussed in the preceding chapter. On a microscopic level, the most important physical process for two-dimensional spectroscopy is the transfer of coherence between different transitions. We introduce the basics of the technique and discuss a few specific examples to outline its potential. Fundamentals Motivation and principle Motivation The preceding chapter showed how light drives the internal dynamics of resonant atomic media and how the measurement of optical anisotropies allows us to monitor these dynamics. The experiments discussed in the preceding chapter, however, can provide only limited information about the system. Most physical systems have more degrees of freedom than we can observe by measurements on transmitted light. As another limitation, we have primarily considered atoms that evolve under their internal Hamiltonian, only weakly perturbed by the probe laser beam. The example of light-induced spin nutation showed that the dynamics of optically pumped atoms differ significantly from those of a free atom. Although it is possible to observe spin nutation for systems with more than two ground-state sublevels, such an experiment suffers from the damping that accompanies optical pumping. The damping drives the system rapidly to an equilibrium, too fast for detailed dynamical observations.
Two-dimensional spectroscopy is an extension of conventional spectroscopic methods that characterises resonant systems as a function of two frequency variables. We use this technique to improve on the characterisation of atomic media along the lines discussed in the preceding chapter. On a microscopic level, the most important physical process for two-dimensional spectroscopy is the transfer of coherence between different transitions. We introduce the basics of the technique and discuss a few specific examples to outline its potential. Fundamentals Motivation and principle Motivation The preceding chapter showed how light drives the internal dynamics of resonant atomic media and how the measurement of optical anisotropies allows us to monitor these dynamics. The experiments discussed in the preceding chapter, however, can provide only limited information about the system. Most physical systems have more degrees of freedom than we can observe by measurements on transmitted light. As another limitation, we have primarily considered atoms that evolve under their internal Hamiltonian, only weakly perturbed by the probe laser beam. The example of light-induced spin nutation showed that the dynamics of optically pumped atoms differ significantly from those of a free atom. Although it is possible to observe spin nutation for systems with more than two ground-state sublevels, such an experiment suffers from the damping that accompanies optical pumping. The damping drives the system rapidly to an equilibrium, too fast for detailed dynamical observations.
In all preceding chapters, we have tried to separate the effect of the light on the atoms from the reverse effect, the modification of the light by the atomic medium. In most cases this allows an explicit solution of the equations of motion and provides stable stationary states. In recent years, another approach to the interaction between light and matter has appeared, which emphasises strong coupling between the two. It uses the interactions as a tool to study general aspects of nonlinear dynamics. This chapter provides an introduction to this field, without trying to give a complete summary. Overview Resonant vapours as optically nonlinear media Mutual interactions So far, we have considered the effect of the laser on the atomic medium separately from the measurement of microscopic dynamics by the polarisation selective detection of transmitted light. In this approximation, the pump laser drives the atoms without suffering significant attenuation or polarisation changes. Conversely, the probe beam, which monitors the optical properties of the atomic medium, changes the microscopic state of the atoms only infinitesimally. This approach guarantees, e.g., that the response of the medium to the probe beam is linear. As stressed before, this assumption of one-sided interactions is always an approximation, since the conservation of energy and angular momentum make it impossible to change either of the two partial systems without compensating changes in the other part.
Abstract Resonance scattering techniques are very useful for high-resolution atomic spectroscopy. The applicability of these techniques has been much extended, particularly through the rapid development of tunable-laser technology. The use of a narrow-band tunable laser, acting on a collimated atomic beam, gives a direct method enabling, for example, hyperfine structure and isotope shift studies. The intensity of lasers allows stepwise excitations to be performed, and with the two-photon absorption technique, Doppler-free measurements on thermal gases are also possible. By using pulsed lasers, time-resolved measurements yielding radiative life-times and structural information can be performed. The basic resonance scattering methods can be combined with radiofrequency and coherence techniques to yield a resolution, limited only by the uncertainty relation. Optical double resonance and level-crossing techniques, not requiring a narrow-band light source, have been extensively used. Several examples of the application of resonance scattering methods are given.
Optical multidimensional coherent spectroscopy is a powerful tool for studying structure and dynamics in complex systems, such as semiconductors. In optical two-dimensional coherent spectroscopy (2DCS), where the spectrum is presented in a two-dimensional (2D) plane with two frequency axes, an important advantage is the ability to isolate quantum pathways by unfolding a one-dimensional spectrum onto a 2D plane. For many systems, however, the quantum pathways are only partially separated in a 2D spectrum. In order to completely isolate the quantum pathways, we extend 2DCS into a third dimension to generate three-dimensional (3D) spectra in which the spectrum is further unfolded. A 3D spectrum provides complete and well-isolated information of the third-order optical response of the system. The information can be used to fully characterize the quantum pathways and to determine the system’s Hamiltonian. Quantitative knowledge of the Hamiltonian enables prediction and control of quantum processes. For instance, such information is essential for deterministic control and improved performance of coherent control schemes.
This thesis studies the interaction between two-and three-level systems and strong, coherent radio-frequency (rf) electrom agnetic fields.The investigations were carried out in both the frequency domain, where steady state properties are examined, and the time domain, where transient behaviours are studied.The two-and three-level systems studied arise from the nuclear spin I = 1 triplet within the 3 A ground state of the nitrogen-vacancy (N-V) centre in diamond.The nuclear magnetic resonance (NMR) is detected optically using a coherent optical-rf double resonance Raman heterodyne technique.Owing to the unique features of both the nuclear spin triplet and the detection technique, many interesting experimental results have been obtained.The thesis is comprised of four parts.Part 1 includes Chapters 1 to 3, which provides introductory accounts.The two-level system concept and associated theoretical treatments in the density matrix formalism are introduced in Chapter 1.The theory is given in a very general form and is developed later in relevant chapters for specific situations.Chapter 2 gives an introduction to the N-V centre and its electronic and hyperfine energy levels.The Raman heterodyne technique and the experimental details are described in Chapter 3.In Part 2, consisting of Chapters 4 and 5, the nuclear magnetic transition of interest is characterized.Chapter 4 describes various coherent transient observations including nutation, free-induction-decay (FID), spin echo, spin locking, delayed FID, and rotary echo, from which important parameters such as the transition strength, population decay time T 1? and dephasing time T2 can be deduced.The dependence of these parameters upon the wave function mixing due to the level anti-crossing is discussed in Chapter 5.Part 3 is the most significant part of the thesis and consists of Chapters 6 to 9. In these chapters the interaction of a two-and three-level system with electromagnetic fields are studied in the frequency domain using pump-probe spectroscopy.This technique involves driving the systems with a strong (pump) field and monitoring it with a separate (probe) field.The absorption and dispersion profiles of a driven two-level system probed by a weak field are discussed in Chapter 6. Topics include the dynamic "Stark" effect and amplification without inversion.When the probe intensity is increased from weak to strong, multiphoton transitions and multiphoton gain without inversion are observed.These effects are described in Chapter 7. When the pump and probe fields interact separately with two transitions which share one common level the two-level system is extended to a three-level one.The power broadening of the Autler-Townes spectrum in such a three-level system is the topic presented in Chapter 8. Chapter 9 considers the case where there are two strong fields and a weak probe field.The discussion is in terms of the dressed state picture and it is shown that the dressed state can be also dressed.Experimental results of the transient nutation in dressed states are presented in part 4 which consists of Chapter 10.The dressed states transition strength is determined for the first time experimentally.Finally, Chapter 11 presents a summary of this thesis.
After the discussion of ionic solids we shift our attention to atomic vapours. Here, we discuss the dynamics of microscopic order within the angular momentum substates under the influence of light and magnetic fields. For this purpose, we combine optical pumping as outlined in Chapter 5 to prepare the ordered states, and polarisation-selective detection introduced in Chapter 6 for its observation. In contrast to the introductory sections, we no longer discuss these dynamics as mathematical models, but for specific physical systems, using experimental data to illustrate the theoretical description. The systems we use for this illustration are vapours of alkali metal atoms, in particular sodium. These one-electron systems allow the most direct application of the theoretical models developed above. In addition, we concentrate on electronic ground states, whose long lifetimes permit long observation times and correspondingly precise observations. Experimental arrangement General considerations Laser-induced dynamics This chapter surveys the coherent evolution of coherences between angular momentum sublevels. Optical pumping excites this microscopic order, and it evolves under the influence of external magnetic fields and the laser radiation. The primary goal of this section is to show how the mathematical models developed in the preceding sections apply to real physical systems. We discuss how the observed signals arise and by which parameters the experimenter can control the dynamics of these systems.