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The radionuclide thorium-229 features an isomer with an exceptionally low excitation energy that enables direct laser manipulation of nuclear states. It constitutes one of the leading candidates for use in next-generation optical clocks
1
–
3
. This nuclear clock will be a unique tool for precise tests of fundamental physics
4
–
9
. Whereas indirect experimental evidence for the existence of such an extraordinary nuclear state is substantially older
10
, the proof of existence has been delivered only recently by observing the isomer’s electron conversion decay
11
. The isomer’s excitation energy, nuclear spin and electromagnetic moments, the electron conversion lifetime and a refined energy of the isomer have been measured
12
–
16
. In spite of recent progress, the isomer’s radiative decay, a key ingredient for the development of a nuclear clock, remained unobserved. Here, we report the detection of the radiative decay of this low-energy isomer in thorium-229 (
229m
Th). By performing vacuum-ultraviolet spectroscopy of
229m
Th incorporated into large-bandgap CaF
2
and MgF
2
crystals at the ISOLDE facility at CERN, photons of 8.338(24) eV are measured, in agreement with recent measurements
14
–
16
and the uncertainty is decreased by a factor of seven. The half-life of
229m
Th embedded in MgF
2
is determined to be 670(102) s. The observation of the radiative decay in a large-bandgap crystal has important consequences for the design of a future nuclear clock and the improved uncertainty of the energy eases the search for direct laser excitation of the atomic nucleus.
The authors report on the radiative decay of a low-energy isomer in thorium-229 (
229m
Th), which has consequences for the design of a future nuclear clock and eases the search for direct laser excitation of the atomic nucleus.