Negative thermal expansion and phase transition of low-temperature Mg2NiH4

Abstract

The negative thermal expansion (NTE) phenomenon is of great significance in fabricating zero thermal expansion (ZTE) materials to avoid thermal shock during heating and cooling. NTE is observed in limited groups of materials, e.g., metal cyanides, oxometallates, and metal-organic frameworks, but has not been reported in the family of metal hydrides. Herein, a colossal and continuous negative thermal expansion is firstly developed in the low-temperature phases of LT1- and LT2-Mg2NiH4 between 488 K and 733 K from in-situ transmission electron microscope (TEM) video, with the volume contraction reaching 18.7% and 11.3%, respectively. The mechanisms for volume contraction of LT1 and LT2 phases are elucidated from the viewpoints of phase transformation, magnetic transition, and dehydrogenation, which is different from common NTE materials containing flexible polyhedra units in the structure. The linear volume shrinkage of LT2 in the temperature of 488–553 K corresponds to the phase transition of LT2→HT with a thermal expansion coefficient of –799.7 × 10–6 K–1 revealed by in-situ synchrotron powder X-ray diffraction. The sudden volume contraction in LT1 between 488 and 493 K may be caused by the rapid dehydrogenation of LT1 to Mg2Ni. The revealed phenomenon in single composite material with different structures would be significant for preparing zero thermal expansion materials by tuning the fraction of LT1 and LT2 phases.

Keywords

• Negative thermal expansion
• Mg2NiH4
• Phase transformation
• In situ TEM
• In situ XRD