Emerging brain-inspired computing needs phase-change materials of the next generation with lower energy consumption and wider temperature range. Gallium tellurides appear to be promising candidates enable to achieve the necessary requirements.
Vitreous
germanium disulfide GeS2 and diselenide GeSe2 belong to canonical chalcogenide glasses extensively studied
over the past half century. Their high-temperature orthorhombic polymorphs
are congruently melting compounds, and the tetrahedral crystal and
glass structure is largely preserved in the melt. In contrast, the
ditelluride counterpart is absent in the Ge–Te phase diagram,
which shows only a single compound, monotelluride GeTe. Phase-change
materials based on GeTe have become a technologically important class
of solids, and their structure and properties are also widely studied.
Surprisingly, very scarce information is available for alloys having
GeTe2 stoichiometry. Using a fast quenching procedure in
silica capillaries, high-energy X-ray diffraction, and Raman spectroscopy
supported by first-principles simulations, we show that bulk glassy
GeTe2 differs substantially from the lighter GeX2 members, revealing 46% of trigonal germanium, 31% of three-fold
coordinated tellurium, and only 20% of edge-sharing tetrahedra or
pyramids. The fraction of homopolar Ge–Ge bonds is low; however,
the population of dominant Te–Te dimers and Te
n
oligomers, n ≤ 10, appears
to be significant. The complex structural and chemical topology of
g-GeTe2 is directly related to the thermodynamic metastability
of germanium ditelluride, schematically represented by the following
reaction: GeTe2 ⇄ GeTe + Te. Disproportionation
is complete above liquidus in the temperature range of semiconductor–metal
transition, and the dense metallic GeTe2 liquid, mostly
consisting of five-fold coordinated Ge species, exhibits high fluidity,
strong fragility (m = 99 ± 5), and presumably
a fast structural transformation rate combined with low atomic mobility
in the vicinity of the glass transition temperature, favorable for
reliable long-term data retention in nonvolatile memories. The observed
and predicted characteristic features make GeTe2 a promising
precursor for the next generation of phase-change materials, especially
coupled with additional metal doping, depolymerizing the tetrahedral
interconnected glass network and accelerating (sub)nanosecond crystallization.
Binary Ge–Te
and ternary Ge–Sb–Te systems
belong to flagship phase-change materials (PCMs) and are used in nonvolatile
memory applications and neuromorphic computing. The working temperatures
of these PCMs are limited by low-T glass transition
and crystallization phenomena. Promising high-T PCMs
may include gallium tellurides; however, the atomic structure and
transformation processes for amorphous Ga–Te binaries are simply
missing. Using high-energy X-ray diffraction and Raman spectroscopy
supported by first-principles simulations, we elucidate the short-
and intermediate-range order in bulk glassy Ga
x
Te1–x
, 0.17 ≤ x ≤ 0.25, following their thermal, electric, and
optical properties, revealing a semiconductor–metal transition
above melting. We also show that a phase change in binary Ga–Te
is characterized by a very unusual nanotectonic compression with the
high internal transition pressure reaching 4–8 GPa, which appears
to be beneficial for PCM applications increasing optical and electrical
contrast between the SET and RESET states and decreasing power consumption.
Phase-change materials based on tellurides are widely used for optical storage (DVD and Blu-ray disks), non-volatile random access memories and for development of neuromorphic computing. Narrow-gap tellurides are intrinsically limited...
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