Technetium–carbon nanophases
are obtained by thermal
decomposition
of pertechnetates with large organic cations under an argon atmosphere.
Parallel carbonization of organic cations (hexamethyleneiminium and
triphenylguanidinium), which occurs during the thermal decomposition
of their pertechnetates, leads to the formation of X-ray amorphous
solid products. An X-ray absorption fine structure study revealed
that they have a crystal structure containing technetium–carbon
bonds with a length of 1.76 Å. After subsequent annealing treatment
at 1073–1673 K, the synthesized technetium–carbon phase
has a cubic lattice with an a of 4.01 ± 0.03
Å. The products of thermal decomposition of the same perrhenates
are also X-ray amorphous; however, unlike that of pertechnetates,
the distance between rhenium and carbon atoms in them is significantly
greater (2.14 Å). After subsequent annealing, they have a hexagonal
lattice. The electrochemical properties of technetium–carbon
nanophases prepared by thermal decomposition of pertechnetates with
large organic cations are different from the properties of those prepared
with metallic technetium. The oxidation of technetium carbide to its
oxides at the electrode surface observed in the first anodic scan
of cyclic voltammograms can be used for the deposition of noble metal
nanoclusters under open-circuit conditions to prepare composite catalysts
for the hydrogen evolution reaction. Nanotechnetium in the amorphous
carbon matrix can also be a prospective material for reactor transmutation
of technetium to stable isotopically pure ruthenium-100.