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Updated: Jul 12, 2026

Orientational Transition in a Liquid Crystal Triggered by the Thermodynamic Growth of Interfacial Wetting Sheets
Published on: May 15, 2017
Pressure-induced phase transitions in LiNH2
Raja S Chellappa1, Dhanesh Chandra, Maddury Somayazulu
1Materials Science & Engineering Division, Department of Chemical & Metallurgical Engineering (MS 388), University of Nevada, Reno, Nevada 89557, USA. rchellappa@ciw.edu
Abstract:
In situ high-pressure Raman spectroscopy studies on LiNH2 (lithium amide) have been performed at pressures up to 25 GPa. The pressure-induced changes in the Raman spectra of LiNH2 indicates a phase transition that begins at approximately 12 GPa is complete at approximately 14 GPa from ambient-pressure alpha-LiNH2 (tetragonal, I) to a high-pressure phase denoted here as beta-LiNH2. This phase transition is reversible upon decompression with the recovery of the alpha-LiNH2 phase at approximately 8 GPa. The N-H internal stretching modes (nu([NH2]-)) display an increase in frequency with pressure, and a new stretching mode corresponding to high-pressure beta-LiNH2 phase appears at approximately 12.5 GPa. Beyond approximately 14 GPa, the N-H stretching modes settle into two shouldered peaks at lower frequencies. The lattice modes show rich pressure dependence exhibiting multiple splitting and become well-resolved at pressures above approximately 14 GPa. This is indicative of orientational ordering [NH2]- ions in the lattice of the high-pressure beta-LiNH2 phase.
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A substance melts or freezes at a temperature called its melting point and boils or condenses at its boiling point. These temperatures depend on pressure. High pressure favors the denser form of the substance, so typically, high pressure...