Jonas Rodewald

A universal matter-wave interferometer with optical ionization gratings in the time domain

Matter-wave interferometry with atoms1 and molecules2 has attracted a rapidly growing interest throughout the last two decades both in demonstrations of fundamental quantum phenomena and in quantum-enhanced precision measurements. Such experiments exploit the non-classical superposition of two or more position and momentum states which are coherently split and rejoined to interfere3-11. Here, we present the experimental realization of a universal near-field interferometer built from three short-pulse single-photon ionization gratings12,13. We observe quantum interference of fast molecular clusters, with a composite de Broglie wavelength as small as 275 fm. Optical ionization gratings are largely independent of the specific internal level structure and are therefore universally applicable to different kinds of nanoparticles, ranging from atoms to clusters, molecules and nanospheres. The interferometer is sensitive to fringe shifts as small as a few nanometers and yet robust against velocity-dependent phase shifts, since the gratings exist only for nanoseconds and form an interferometer in the time-domain.

Photofragmentation Beam Splitters for Matter-Wave Interferometry

Extending the range of quantum interferometry to a wider class of composite nanoparticles requires new tools to diffract matter waves. Recently, pulsed photoionization light gratings have demonstrated their suitability for high mass matter-wave physics. Here, we extend quantum interference experiments to a new class of particles by introducing photofragmentation beam splitters into time-domain matter-wave interferometry. We present data that demonstrate this coherent beam splitting mechanism with clusters of hexafluorobenzene and we show single-photon depletion gratings based both on fragmentation and ionization for clusters of vanillin. We propose that photofragmentation gratings can act on a large set of van der Waals clusters and biomolecules which are thermally unstable and often resilient to single-photon ionization.

New avenues for matter-wave-enhanced spectroscopy

We present matter-wave interferometry as a tool to advance spectroscopy for a wide class of nanoparticles, clusters and molecules. The high sensitivity of de Broglie interference fringes to external perturbations enables measurements in the limit of an individual particle absorbing only a single photon on average, or even no photon at all. The method allows one to extract structural and electronic information from the loss of the interference contrast. It is minimally invasive and works even for dilute ensembles.

Refined model for Talbot–Lau matter-wave optics with pulsed photodepletion gratings

We analyze time-domain Talbot–Lau interferometry of organic cluster beams that are exposed to pulsed photodepletion gratings in the vacuum ultraviolet. We focus particularly on the analysis of the complex (phase and absorption) character of the optical elements. The discussion includes the role of wavefront distortions due to mirror imperfections on the nanometer level and the effect of finite coherence in the diffraction gratings. This improved understanding of the interferometer allows us to extract new information on optical properties of anthracene and ferrocene clusters and to define conditions for future matter-wave experiments.