Abstract

The Stark splitting of the second excited level of atomic hydrogen (with principal quantum number $n=3$) has been measured by pulsed laser spectroscopy in order to determine small electric fields by optical means. Doppler-free excitation with two counterpropagating laser beams at $205\phantom{\rule{0.3em}{0ex}}\mathrm{nm}$ allows us to measure the $n=3$ Stark spectra either by an optogalvanic signal after ionization by a third laser photon or by detection of the Balmer-$\ensuremath{\alpha}$ fluorescence photons emitted by the excited atoms. Three different cases of laser polarization have been investigated in order to evaluate the possibilities and limitations of this one-step laser excitation method for electric field determination, especially at field strengths below $200\phantom{\rule{0.3em}{0ex}}\mathrm{V}∕\mathrm{cm}$. The method provides the best field sensitivity achieved with lower excited levels that can be reached directly by two-photon absorption from the ground state (in contrast to the more sensitive Rydberg levels). For this purpose, an advanced tunable pulsed uv laser with narrow bandwidth almost at the Fourier limit has been used. The high spectral resolution allowed us to deduce electric field strengths as small as $50\phantom{\rule{0.3em}{0ex}}\mathrm{V}∕\mathrm{cm}$ from the frequency shift between two selected isolated Stark components. As a main advantage, this simple analysis of the measured spectra does not rely on knowledge of the line intensities which may be strongly affected by the measuring conditions.

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