ABSTRACT
We have developed a new category of sensor for measurement of the (240)Pu/(239)Pu mass ratio from aqueous solution samples with advantages over existing methods. Aqueous solution plutonium samples were evaporated and encapsulated inside of a gold foil absorber, and a superconducting transition-edge-sensor microcalorimeter detector was used to measure the total reaction energy (Q-value) of nuclear decays via heat generated when the energy is thermalized. Since all of the decay energy is contained in the absorber, we measure a single spectral peak for each isotope, resulting in a simple spectral analysis problem with minimal peak overlap. We found that mechanical kneading of the absorber dramatically improves spectral quality by reducing the size of radioactive inclusions within the absorber to scales below 50 nm such that decay products primarily interact with atoms of the host material. Due to the low noise performance of the microcalorimeter detector, energy resolution values of 1 keV fwhm (full width at half-maximum) at 5.5 MeV have been achieved, an order of magnitude improvement over α-spectroscopy with conventional silicon detectors. We measured the (240)Pu/(239)Pu mass ratio of two samples and confirmed the results by comparison to mass spectrometry values. These results have implications for future measurements of trace samples of nuclear material.
ABSTRACT
The (229)Th nucleus possesses the lowest-energy nuclear isomeric state. Two widely accepted indirect measurements of the transition energy place it within reach of existing laser capabilities. Direct searches for the isomer deexcitation have proven elusive despite extensive effort over the past couple of decades. There is now a growing interest in finding this unique transition because of its potential applications in nuclear, atomic, condensed matter, and optical physics, quantum information, metrology, and cosmology, including the development of a new type of clock based on this nuclear transition. In this Letter we report the first direct observation of the deexcitation of the lowest-lying isomeric state in (229)Th. By collecting (229)Th recoils following the alpha decay of (233)U into MgF(2) plates and measuring the subsequent light emission, we have isolated the isomer deexcitation and measured the transition's half-life to be 6±1 h. Through comparison measurements with (235m)U isomer, we found that the observed (229m)Th deexcitation signal originates from photon emission rather than internal conversion electron emission. This discovery lays the groundwork for optical and laser spectroscopy of (229m)Th nuclear isomer and the development of a (229)Th nuclear clock.