High-Pressure Structural Transformation Pathway and Electronic Properties of AgGaTe₂: Ab Initio Evolutionary Structural Searching

Abstract

We have used systematic ab initio evolutionary structural searching to uncover the high-pressure transformation pathway of a promising thermoelectric material, AgGaTe2. The global structures of the ternary Ag–Ga–Te system have been predicted up to 100 GPa. The known chalcopyrite phase at ambient pressure is validated by the searching method. The B3-like structure with the space group (s.g.) of P4̅m 2 exhibits a metastable one at a low-pressure range. The first structural phase transition is calculated at about 4 GPa, processing the I4̅2 d phase to a B1-like phase (s.g. Pmma). Other predicted structures, Pmn21 and Pm phases, are potentially coexisting phases up to 30 GPa because of the slightly different enthalpy. This finding reasonably explains the ambiguous results in the previous experiments. The high-pressure phase beyond 30 GPa is proposed to be a short-range alloy of bcc-Te and B2-AgGa rather than a cation-disordered B2-like phase. The band gap of the I4̅2 d phase is increased with increasing pressure, while the metastable P4̅m 2 phase is a narrow band gap semiconductor. The electron–phonon coupling of the metallic phases of ternary IB-IIIA-VIA2 compounds is derived for the first time in AgGaTe2. They exhibit superconductors with a maximum T c of 2.4 K in the Pmma phase at 6 GPa. The findings of this work not only provide a clear explanation of the high-pressure transformation pathway of AgGaTe2 but also suggest promising electronic properties guiding further applications, especially in a thermometric device, of this material under high pressure.

Pressure‐Induced Effects on BaPbO3: A Prospectively Valuable Material for Piezoelectric Applications via DFT

“…When materials undergo high pressure, there is a possibility of deformation or phase variation within their structure. [ 43–47 ] To evaluate the structural stability and determine potential phase transitions under varying pressures denoted as “P” ranging from 0 GPa to 80 GPa in Equations (1–5), the material stability criteria, based on elastic constants, is utilized. [ 48 ] $$$$\begin{equation}({{C}_{44}},\;{{C}_{11}},\;{\mathrm{and}}\;{\mathrm{B}}) > 0\end{equation}$$$$ $$$$\begin{equation} ({{C}_{11}} - {{C}_{12}}) > 0\end{equation}$$$$ $$$$\begin{equation}\left( {\frac{{\left( {{{{\mathrm{C}}}_{11}} + 2{{{\mathrm{C}}}_{12}}} \right)}}{3} + \frac{{\mathrm{P}}}{3}} \right) > 0\end{equation}$$$$ $$$$\begin{equation}{{{\mathrm{C}}}_{44}} - {\mathrm{P}} > 0\end{equation}$$$$ $$$$\begin{equation}\left( {\frac{{\left( {{{{\mathrm{C}}}_{11}} - {{{\mathrm{C}}}_{12}}} \right)}}{2} - {\mathrm{P}}} \right) > 0\end{equation}$$$$…”

“…[40][41][42] When materials undergo high pressure, there is a possibility of deformation or phase variation within their structure. [43][44][45][46][47] To evaluate the structural stability and determine potential phase transitions under varying pressures denoted as "P" ranging from 0 GPa to 80 GPa in Equations (1-5), the material stability criteria, based on elastic constants, is utilized. [48] (C 44 , C 11 , and B) > 0…”

First-principles study of 2H-Mo2C-based MXenes under biaxial strain as Li-battery anodes

“…Through modulation of strain, materials can exhibit remarkable mechano–electrochemical coupling due to their adaptable properties, by mechanically altering their atomic structures. 27–32 This has the potential to open significant opportunities for achieving exceptional energy-storage capabilities. For instance, according to Yu et al , the presence of local strain at carbon–MoS 2 interfaces with different properties can regulate the energetic pathways in LIBs.…”