Attosecond transient absorption of a bound wave packet coupled to a smooth continuum

We investigate the possibility to use transient absorption of a coherent bound electron wave packet in hydrogen as an attosecond pulse characterization technique. In recent work we have shown that photoionization of such a coherent bound electron wave packet opens up for pulse characterization with unprecedented temporal accuracy — independent of the atomic structure — with maximal photoemission at all kinetic energies given a wave packet with zero relative phase [Pabst and Dahlstr"om, Phys. Rev. A, 94, 13411 (2016)]. Here, we perform numerical propagation of the time-dependent Schr"odinger equation and analytical calculations based on perturbation theory to show that the energy-resolved maximal absorption of photons from the attosecond pulse does not uniquely occur at zero relative phase of the initial wave packet. Instead, maximal absorption occurs at different relative wave packet phases, distributed as a non-monotonous function with a smooth $-\pi \mathrm{/}2$ shift across the central photon energy (given a Fourier-limited Gaussian pulse). Similar results are found also in helium. Our finding is surprising because it implies that the energy-resolved photoelectrons are not mapped one-to-one with the energy-resolved absorbed photons of the attosecond pulse.