Because of the common oxidation states
of group IV elements (+2
or +4) and group VI elements (−2), 1:1 and 1:2 are two typical
stoichiometries found in the IV–VI compounds. Particularly,
in the Pb–Te binary system, the 1:1 stoichiometric PbTe is
believed to be the only stable compound. Herein, using evolutionary
algorithms, density functional theory, a laser-heated diamond anvil
cell, and synchrotron X-ray diffraction experiments, we discovered
a novel Pb–Te compound with an unexpected stoichiometry of
3:2 above 20 GPa. This tetragonal Pb
3
Te
2
is
the one of the very few cation-rich compounds that has ever been discovered
in the entire IV–VI binary system. Further analyses based on
electron density distribution, electron localization function, and
Bader charge have shown that this newly discovered compound has a
mixed character of chemical bonding with a decreased ionicity. By
further calculating the electron–phonon interaction, Pb
3
Te
2
is predicted to exhibit a superconducting transition
at low temperatures. The discovery of Pb
3
Te
2
paves the way for further explorations of other novel cation-rich
IV–VI group compounds.