Measuring the weak mixing angle with the P2 experiment at MESA

The P2 experiment in Mainz aims to measure the weak mixing angle in electron- proton scattering to a precision of 0.13 %. In order to suppress uncertainties due to proton structure and contributions from box graphs, both a low average momentum transfer $Q^2$ of $4.5\cdot 10^{-3}$ GeV$^2/c^2$ and a low beam energy of 155 MeV are chosen. In order to collect the enormous statistics required for this measurement, the new Mainz Energy Recovery Superconducting Accelerator (MESA) is being constructed. These proceedings describe the motivation for the measurement, the experimental and accelerator challenges and how we plan to tackle them.Comment: Proceedings of the PhiPsi15, Sep. 23-26, 2015, Hefei, Chin

Cavity-Enhanced Few-Cycle Mid-IR Pulses for Field-Resolved Spectroscopy

Up to tenfold power enhancement of waveform-stable few-cycle pulses is demonstrated in a minimally-dispersive resonator (22-37 THz). This enables spectroscopy of molecular samples based on impulsive excitation and electro-optic sampling at 66 m interaction length

Cavity-enhanced field-resolved spectroscopy

Femtosecond enhancement cavities1 are key to applications including high-sensitivity linear2–4 and nonlinear5,6 gas spectroscopy, as well as efficient nonlinear optical frequency conversion7–10. Yet, to date, the broadest simultaneously enhanced bandwidths amount to <20% of the central optical frequency8,9,11–15. Here, we present an ultrabroadband femtosecond enhancement cavity comprising gold-coated mirrors and a wedged-diamond-plate input coupler, with an average finesse of 55 for optical frequencies below 40 THz and exceeding 40 in the 120–300 THz range. Resonant enhancement of a 50-MHz-repetition-rate offset-free frequency comb spanning 22–40 THz results in a waveform-stable ultrashort circulating pulse with a spectrum supporting a Fourier limit of 1.6 cycles, enabling time-domain electric-field-resolved spectroscopy of molecular samples with temporally separated excitation and molecular response16. The contrast between the two is improved by taking advantage of destructive interference at the input coupler. At an effective interaction length with a gas of up to 81 m, this concept promises parts-per-trillion-level ultrabroadband electric-field-resolved linear and nonlinear spectroscopy of impulsively excited molecular vibrations