Tailored pump-probe transient spectroscopy with time-dependent density-functional theory: controlling absorption spectra

TL;DR

This paper explores the use of tailored pump pulses in transient spectroscopy to control and enhance absorption features, using theoretical analysis and TDDFT simulations, despite significant computational challenges.

Contribution

It introduces a theoretical framework and computational approach for using shaped pulses to manipulate absorption spectra in complex systems.

Findings

Tailored pump pulses can theoretically excite systems into light-absorbing states.

Non-equilibrium response functions can be analyzed with simple models and TDDFT.

Numerical and theoretical challenges limit practical implementation.

Abstract

Recent advances in laser technology allow us to follow electronic motion at its natural time-scale with ultra-fast time resolution, leading the way towards attosecond physics experiments of extreme precision. In this work, we assess the use of tailored pumps in order to enhance (or reduce) some given features of the probe absorption (for example, absorption in the visible range of otherwise transparent samples). This type of manipulation of the system response could be helpful for its full characterization, since it would allow us to visualize transitions that are dark when using unshaped pulses. In order to investigate these possibilities, we perform first a theoretical analysis of the non-equilibrium response function in this context, aided by one simple numerical model of the Hydrogen atom. Then, we proceed to investigate the feasibility of using time-dependent density-functional theory as a means to implement, theoretically, this absorption-optimization idea, for more complex atoms or molecules. We conclude that the proposed idea could in principle be brought to the laboratory: tailored pump pulses can excite systems into light-absorbing states. However, we also highlight the severe numerical and theoretical difficulties posed by the problem: large-scale non-equilibrium quantum dynamics are cumbersome, even with TDDFT, and the shortcomings of state-of-the-art TDDFT functionals may still be serious for these out-of-equilibrium situations.