posted on 2016-12-21, 13:03authored byJürgen Evers, Leonhard Möckl, Gilbert Oehlinger, Ralf Köppe, Hansgeorg Schnöckel, Oleg Barkalov, Sergey Medvedev, Pavel Naumov
SiO2 exhibits
a high-pressure–high-temperature polymorphism, leading to an
increase in silicon coordination number and density. However, for
the related compound SiS2 such pressure-induced behavior
has not been observed with tetrahedral coordination yet. All four
crystal structures of SiS2 known so far contain silicon
with tetrahedral coordination. In the orthorhombic, ambient-pressure
phase these tetrahedra share edges and achieve only low space filling
and density. Up to 4 GPa and 1473 K, three phases can be quenched
as metastable phases from high-pressure high-temperature to ambient
conditions. Space occupancy and density are increased first by edge
and corner sharing and then by corner sharing alone. The structural
situation of SiS2 up to the current study resembles that
of SiO2 in 1960: Then, in its polymorphs only Si–O4 tetrahedra were known. But in 1961, a polymorph with rutile
structure was discovered: octahedral Si-O6 coordination
was established. Now, 50 years later, we report here on the transition
from 4-fold to 6-fold coordination in SiS2, the sulfur
analogue of silica.