Thermal ionization mass spectrometry (TIMS) has been
extensively
employed for the assessment of plutonium (Pu) isotopes in nuclear
forensics and environmental monitoring. Recently, great efforts have
been made to improve the ionization efficiency (IE) of Pu to achieve
better accuracy and precision for trace-level analysis. Herein, the
thermal ionization enhancement effect for plutonium of graphene oxide
(GO) was investigated and the corresponding mechanism was discussed.
The GO layers were homogeneously mounted on the filament’s
central surface to promote pg-level Pu ion emission. With the excellent
structural property of GO, a greatly promoted ionization efficiency
of 0.44% for Pu was obtained, and the initial ionization temperature
for Pu was remarkably reduced from 1610 to 1390 °C. Average boosts
in IE compared to the classical double-filament mode and graphite-loaded
single-filament mode were 1640 and 520%, respectively. The analytical
accuracy and precision based on the GO-loaded single-filament mode
were validated using Pu isotopic certified reference materials. This
work demonstrates the excellent property of GO as an ion source additive
for Pu ionization, as it provided an interface for the promotion of
energy transfer and Pu carbide formation. The operation of GO loading
is quite simple and can be finished within 5 min. This rapid filament
carburization approach has great potential for improving the measurement
precision of trace-level plutonium isotopes and can be applied in
nuclear safeguards, nuclear forensics, and environmental monitoring.