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Abstract The exceptionally low-energy²²⁹Th nuclear isomeric state is expected to provide several new and powerful applications^1,2, including the construction of a robust and portable solid-state nuclear clock³, perhaps contributing to a redefinition of the second⁴, exploration of nuclear superradiance^5,6and tests of fundamental physics^7–10. Further, analogous to the capabilities of traditional Mössbauer spectroscopy, the sensitivity of the nucleus to its environment can be used to realize laser Mössbauer spectroscopy and, with it, new types of strain and temperature sensors^3,11and a new probe of the solid-state environment^12,13, all with excellent sensitivity. However, current models for examining the nuclear transition in a solid require the use of a high-bandgap, vacuum ultraviolet (VUV) transmissive host, severely limiting the applicability of these techniques. Here we report the first, to the authors’ knowledge, demonstration of laser-induced conversion electron Mössbauer spectroscopy (CEMS) of the²²⁹Th isomer in a thin ThO₂sample whose bandgap (approximately 6 eV) is considerably smaller than the nuclear isomeric state energy (8.4 eV). Unlike fluorescence spectroscopy of the²²⁹Th isomeric transition, this technique is compatible with materials whose bandgap is less than the nuclear transition energy, opening a wider class of systems to study and the potential of a conversion-electron-based nuclear clock.