TY - JOUR
T1 - Dominant mechanisms of thermo-mechanical properties of weberite-type RE3TaO7 (RE=La, Pr, Nd, Eu, Gd, Dy) tantalates toward multifunctional thermal/environmental barrier coating applications
AU - Chen, Lin
AU - Hu, Mingyu
AU - Wang, Jiankun
AU - Li, Baihui
AU - Feng, Jing
N1 - This study was supported by National Key Research and Development Program of China [No. 2022YFB3708600], the Top Innovative Talents of Graduate Students of Kunming University of Science and Technology, the Rare and Precious Metals Material Genetic Engineering Project of Yunnan Province [No. 202102AB080019–1].
Publisher Copyright:
© 2024
PY - 2024/5/15
Y1 - 2024/5/15
N2 - Weberite-type RE3TaO7 (RE=La, Pr, Nd, Eu, Gd, Dy) tantalates have been studied as multifunctional thermal/environmental barrier coating materials with working temperatures above 1500 K. This study proposes the dominant mechanisms of their thermo-mechanical properties. The relative ionicity of the RE-O bonds increased with increasing RE+3 ionic radius, which weakened the bond strength and led to decreases in Young's modulus and hardness. A model was proposed to derive the high-temperature thermal conductivity based on the relationship between the phonon thermal conductivity and temperature, and the thermal radiative conductivity was estimated. RE3TaO7 exhibited a lower thermal conductivity than other fluorite-related oxides because its weak bond strength could slow down the phonon speed and enhance the an-harmonic vibrations of the lattices. At low temperatures, the RE atomic weight was a better descriptor of the thermal conductivity than the RE+3 ionic radius, and which could aid in further regulating the thermal conductivity. The thermal expansion coefficients of the different axes were affected by both RE-O and Ta-O bonds when weak RE-O bonds dominated the linear thermal expansion. The low oxygen ion conductivity derived from the strong covalent Ta-O bonds, which increased the activation energy for oxygen hopping in lattices of RE3TaO7. This study elucidates the dominant mechanisms of properties from the characteristics of crystals and chemical bonds, which are significant for high-temperature applications of tantalates.
AB - Weberite-type RE3TaO7 (RE=La, Pr, Nd, Eu, Gd, Dy) tantalates have been studied as multifunctional thermal/environmental barrier coating materials with working temperatures above 1500 K. This study proposes the dominant mechanisms of their thermo-mechanical properties. The relative ionicity of the RE-O bonds increased with increasing RE+3 ionic radius, which weakened the bond strength and led to decreases in Young's modulus and hardness. A model was proposed to derive the high-temperature thermal conductivity based on the relationship between the phonon thermal conductivity and temperature, and the thermal radiative conductivity was estimated. RE3TaO7 exhibited a lower thermal conductivity than other fluorite-related oxides because its weak bond strength could slow down the phonon speed and enhance the an-harmonic vibrations of the lattices. At low temperatures, the RE atomic weight was a better descriptor of the thermal conductivity than the RE+3 ionic radius, and which could aid in further regulating the thermal conductivity. The thermal expansion coefficients of the different axes were affected by both RE-O and Ta-O bonds when weak RE-O bonds dominated the linear thermal expansion. The low oxygen ion conductivity derived from the strong covalent Ta-O bonds, which increased the activation energy for oxygen hopping in lattices of RE3TaO7. This study elucidates the dominant mechanisms of properties from the characteristics of crystals and chemical bonds, which are significant for high-temperature applications of tantalates.
KW - Mechanical properties
KW - Oxygen ion conductivity
KW - T/EBCs
KW - Tantalates
KW - Thermal conductivity
KW - Thermal expansion anisotropy
UR - http://www.scopus.com/inward/record.url?scp=85189104549&partnerID=8YFLogxK
U2 - 10.1016/j.actamat.2024.119857
DO - 10.1016/j.actamat.2024.119857
M3 - Journal article
AN - SCOPUS:85189104549
SN - 1359-6454
VL - 270
JO - Acta Materialia
JF - Acta Materialia
M1 - 119857
ER -