@article{Zhang2024, 
author = {Peixian Zhang and Yongqiang Qiao and Kaiyue Zhao and Qingjie Wang and Huan Zhao and Juan Guo and Erjun Liang and Tao Sun and Jiangwei Zhang and Qilong Gao},
title = {Synthesis, structure, and thermal expansion in CaZrF6 with two polymorphs},
year = {2024},
journal = {Nano Research},
volume = {17},
number = {9},
pages = {8618-8626},
keywords = {negative thermal expansion, polymorph, fluorides, lattice dynamics, first principles calculations},
url = {https://www.sciopen.com/article/10.1007/s12274-024-6832-x},
doi = {10.1007/s12274-024-6832-x},
abstract = {Due to the high structural flexibility and controllable thermal expansion, cubic double ReO3-type negative thermal expansion (NTE) fluorides provide a solution for solving the prominent phenomenon of thermal expansion mismatch between materials. However, the expensive raw materials and complex synthesis steps limit its practical application. In this work, we have designed a more advantageous method for the synthesis of NTE material CaZrF6, and it is expected to be generalized to the synthesis of other double ReO3-fluorides. Intriguingly, a new orthorhombic phase CaZrF6 has been synthesized via this method in a lower temperature. Unlike the strong isotropic NTE of the cubic phase CaZrF6, the orthorhombic phase shows the strong anisotropic positive thermal expansion (PTE). The combined analysis of temperature-dependent X-ray diffraction (XRD), Raman spectra, and first-principles calculations shows that the low frequency phonon vibration mode with negative Grüneisen parameter in cubic CaZrF6 are strongly correlated with the transverse thermal vibration of F atoms and dominates the NTE of the material.}
}