Light-field driven charge motion links semiconductor technology to electric fields with attosecond temporal control. Motivated by ultimate-speed electron-based signal processing, strong-field excitation has been identified viable for the ultrafast manipulation of a solid’s electronic properties but found to evoke perplexing post-excitation dynamics. Here, we report on single-photon-populating the conduction band of a wide-gap dielectric within approximately one femtosecond. We control the subsequent Bloch wavepacket motion with the electric field of visible light. The resulting current allows sampling optical fields and tracking charge motion driven by optical signals. Our approach utilizes a large fraction of the conduction-band bandwidth to maximize operating speed. We identify population transfer to adjacent bands and the associated group velocity inversion as the mechanism ultimately limiting how fast electric currents can be controlled in solids. Our results imply a fundamental limit for classical signal processing and suggest the feasibility of solid-state optoelectronics up to 1 PHz frequency.

The first nuclear excited state in 229Th possesses the lowest excitation energy of all currently known nuclear levels. The energy difference between the ground- and first-excited (isomeric) state (denoted with 229mTh) amounts only to ≈8.2 eV (≈151.2 nm), which results in several interesting consequences: Since the excitation energy is in the same energy range as the binding energy of valence electrons, the lifetime of 229mTh is strongly influenced by the electronic structure of the Th atom or ion. Furthermore, it is possible to potentially excite the isomeric state in 229Th with laser radiation, which led to the proposal of a nuclear clock that could be used to search for new physics beyond the standard model. In this article, we will focus on recent technical developments in our group that will help to better understand the decay mechanisms of 229mTh, focusing primarily on measuring the radiative lifetime of the isomeric state.

We demonstrate a Petahertz bandwidth single-photon photoconductive switch by populating the conduction band in dielectrics with attosecond vacuum-ultraviolet (VUV) light pulses. Femtosecond pulse-driven currents reveal intra- and inter-band conduction band carrier dynamics.

We demonstrate an attosecond one-photon photoconductive switch by injecting conduction band carriers in dielectrics using vacuum-ultraviolet light pulses. Femtosecond pulse- driven currents reveal intra- and inter-band conduction band carrier dynamics.