TY - JOUR
T1 - High-Temperature Polymorphism and Band-Gap Evolution in BaZrS3
AU - Jaiswal, Ankit
AU - Sakharov, Konstantin A.
AU - Lekina, Yulia
AU - Kamonsuangkasem, Krongthong
AU - Tomm, Yvonne
AU - Wei, Fengxia
AU - White, Timothy J.
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024
Y1 - 2024
N2 - Barium zirconium trisulfide (BZS) is a three-dimensional (3D) perovskite with optoelectronic properties suitable for photovoltaic (PV) and light-emitting diode (LED) applications that is conventionally reported in the orthorhombic Pnma (62) symmetry. Synchrotron X-ray diffraction, thermal analysis, and Raman and absorption spectroscopy revealed three high-temperature polymorphs that appear when BZS is heated in air prior to complete oxidation (BaZrS3 + 5O2 → BaSO4 + ZrO2 + 2SO2↑) at 700 °C with the approximate stability ranges: BaZrS3 IV Pnma (62) T < 400 °C BaZrS3 III Cmcm (63) 400 °C ≤ T ≤ 500 °C BaZrS3 II 14/mcm (140) 500 °C ≤ T ≤ 700 °C Differential scanning calorimetry (DSC) revealed exothermic features accompanying the IV → III and III → II phase changes. Furthermore, the direct band gap varied inversely with temperature with distinct energies for each polymorph (1.84 eV ≤ IV ≤ 1.65 eV; 1.65 eV ≤ III ≤ 1.54 eV; 1.54 eV ≤ II ≤ 1.52 eV). Raman spectroscopy found that polymorphic changes up to 600 °C were reversible with bands characteristic of BaZrS3 IV entirely restored upon cooling to room temperature (RT). This more complete understanding of BSZ polymorphism provides a basis for producing crystallochemical variants with enhanced optoelectronic properties under ambient conditions.
AB - Barium zirconium trisulfide (BZS) is a three-dimensional (3D) perovskite with optoelectronic properties suitable for photovoltaic (PV) and light-emitting diode (LED) applications that is conventionally reported in the orthorhombic Pnma (62) symmetry. Synchrotron X-ray diffraction, thermal analysis, and Raman and absorption spectroscopy revealed three high-temperature polymorphs that appear when BZS is heated in air prior to complete oxidation (BaZrS3 + 5O2 → BaSO4 + ZrO2 + 2SO2↑) at 700 °C with the approximate stability ranges: BaZrS3 IV Pnma (62) T < 400 °C BaZrS3 III Cmcm (63) 400 °C ≤ T ≤ 500 °C BaZrS3 II 14/mcm (140) 500 °C ≤ T ≤ 700 °C Differential scanning calorimetry (DSC) revealed exothermic features accompanying the IV → III and III → II phase changes. Furthermore, the direct band gap varied inversely with temperature with distinct energies for each polymorph (1.84 eV ≤ IV ≤ 1.65 eV; 1.65 eV ≤ III ≤ 1.54 eV; 1.54 eV ≤ II ≤ 1.52 eV). Raman spectroscopy found that polymorphic changes up to 600 °C were reversible with bands characteristic of BaZrS3 IV entirely restored upon cooling to room temperature (RT). This more complete understanding of BSZ polymorphism provides a basis for producing crystallochemical variants with enhanced optoelectronic properties under ambient conditions.
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U2 - 10.1021/acs.inorgchem.4c03895
DO - 10.1021/acs.inorgchem.4c03895
M3 - Article
AN - SCOPUS:85211618618
SN - 0020-1669
JO - Inorganic Chemistry
JF - Inorganic Chemistry
ER -