ZusammenfassungDas Wasserstoffatom (H) stellt ein einzigartiges System für Tests der Quanten-Elektrodynamik dar. Aufgrund seiner einfachen Struktur und genauen theoretischen Beschreibung liefert es außerdem wichtige Daten für die Bestimmung der RydbergKonstante R ∞ und des Proton-Ladungsradius r p im Rahmen der globalen Anpassung fundamentaler Konstanten durch das Committee on Data for Science and Technology (CODATA). Im Jahre 2010 kam das sogenannte "proton size puzzle" auf, eine Diskrepanz von sieben Standardabweichungen zwischen CODATA und dem zehn mal genauer gemessenen Wert von r p in myonischem Wasserstoff (µ -p, [1, 2] AbstractThe hydrogen atom (H) is a unique system for tests of quantum electrodynamics (QED). Due to its simplicity and accurate theoretical description, it also provides key input data for the determination of the Rydberg constant R ∞ and the proton root mean square (r.m.s.) charge radius r p in the global adjustment of fundamental constants [4] by the Committee on Data for Science and Technology (CODATA). In the year 2010, the "proton size puzzle" emerged, which refers to a discrepancy of seven standard deviations between CODATA and a ten times more accurate measurement of r p in muonic hydrogen (µ -p, [1, 2]). Proposed solutions for this puzzle cover a wide range of scenarios, up to physics beyond the standard model [3]. This thesis reports on a novel scheme for high resolution spectroscopy of dipole allowed 2S -nP transitions in H, using a cryogenic beam of H atoms that are prepared in the meta-stable 2S F =0 1/2 state by state selective optical excitation. Such measurements can be used for a new determination of R ∞ and r p from H spectroscopy, shedding new light on the "proton size puzzle". The scheme has been applied to spectroscopy of the 2S-4P transition first, yielding: These values are as accurate as the ones determined from the aggregate world data of precision H spectroscopy (15 measurements) that enter the CODATA adjustment. While a discrepancy of 3.8 combined standard deviations is found to the latter, the presented results agree with the measurements in µ -p. The 2S-4P experiment is essentially unaffected by the systematic effects dominating the uncertainties in the previous most precise determinations of R ∞ using dipole forbidden two photon transitions in H. Instead, the main systematic effects are the first order Doppler effect, canceled by the use of an active fiber-based retroreflector (AFR) developed in this thesis, and line shape distortions due to quantum interference (QI) of neighboring atomic resonances. The latter effect has come to the attention of the precision spectroscopy community only recently [8,9]. Apparent QI line shifts have been studied experimentally, yielding the first direct observation in precision spectroscopy of largely separated atomic resonances. The observed shifts of up to ± 51 kHz are six times larger than the proton size discrepancy for the 2S-4P transition. They are brought under control by a suitable line shape model function, derived and...

Development of the optical frequency comb has revolutionised metrology and precision spectroscopy due to its ability to provide a precise and direct link between microwave and optical frequencies 1,2 . A novel application of frequency comb technology that leverages both the ultrashort duration of each laser pulse and the exquisite phase coherence of a train of pulses is the generation of frequency combs in the extreme ultraviolet (XUV) via high harmonic generation (HHG) in a femtosecond enhancement cavity 3,4 . Until now, this method has lacked sufficient average power for applications, which has also hampered efforts to observe phase coherence of the high-repetition rate pulse train produced in the extremely nonlinear HHG process. Hence, the existence of a frequency comb in the XUV has not been confirmed. We have overcome both challenges. Here, we present generation of >200 µW per harmonic reaching 50 nm (20 µW after harmonic separation), and the observation of single-photon spectroscopy signals for both an argon transition at 82 nm and a neon transition at 63 nm. The absolute frequency of the argon transition has been determined via direct frequency comb spectroscopy. The resolved 10-MHz linewidth of the transition, limited by the transverse temperature of the argon atoms, is unprecedented in this spectral region and places a stringent upper limit on the linewidth of individual comb teeth. Due to the lack of continuous wave lasers, these frequency combs are currently the only promising avenue towards extending ultrahigh precision spectroscopy to below the 100-nm spectral region with a wide range of applications that include spectroscopy of electronic transitions in molecules 5 , experimental tests of bound state and many body quantum electrodynamics in He + and He 6,7 , development of next-generation "nuclear" clocks 8,9,10 , and searches for spatial and temporal variation of fundamental constants 11,12 using the enhanced sensitivity of highly charged ions 13,14 .Techniques developed to control a train of ultrashort pulses in the frequency domain have led to rapid advancements not only in ultrahigh precision metrology 1 , but also in generation of attosecond pulses for time-resolved studies 15 . This symbiotic relationship between time and frequency techniques continues with the development of the XUV frequency combs where HHG, a standard technique for attosecond physics, is utilized to produce phase coherent XUV radiation. In conventional HHG, a single infrared pulse generates a burst of attosecond pulses separated by half cycles of the driving laser field, resulting in the odd harmonic spectrum shown in Fig 1. In contrast, in intracavity HHG, a phase-coherent infrared pulse train is used to produce a train of such bursts that repeat at the repetition frequency of the fundamental comb. This new temporal structure is responsible for the much finer frequency comb within each harmonic order. We anticipate that high precision characterization of the HHG process enabled by the XUV frequency comb will once again pr...

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