Related Experiment Video
Updated: Aug 6, 2026

The Preparation and Properties of Thermo-reversibly Cross-linked Rubber Via Diels-Alder Chemistry
Published on: August 25, 2016
Compression behaviour of ErH3synthesized at non ambient conditions
Ajinkya P Khangal1,2, Nishant N Patel1, Ajay Kumar Kumar Mishra1,2
1High Pressure & Synchrotron Radiation Physics Division, Bhabha Atomic Resessarch Centre, Mumbai 400085, India.
None:
In recent times metal hydrides have reinvigorated the search for room-temperature superconductivity owing to their intriguing physical properties. Among these, rare earth hydrides are unique due to their unequivocal properties related to hydrogen storage, potential for ambient superconductivity, and switchable mirror technology. Towards this, we have synthesized higher erbium (Er) hydrides using pure Er metal and paraffin oil as an alternate hydrogen source by employing a laser heated diamond anvil cell. Thus, synthesized hydride has been investigated using the synchrotron-based angle dispersive x-ray diffraction (ADXRD) technique and Raman spectroscopy. At synthesized conditions (P= 36 GPa andT= 1800 K) the erbium hydride is found to be in a face centred cubic (fcc) structure with stoichiometry as ErH3. Its compression behaviour has been studied up to 40 GPa during both compression and decompression. On decompression, it transforms to hexagonal close packed (hcp) structure of ErH3at ∼5.2 GPa. The cubic phase is found to be partially recoverable on complete release of pressure. Equation of state for cubic phase has been established. The bulk modulus is determined to be 74 ± 4 GPa for the fcc phase. Furthermore, to study the possible chemical reaction of paraffin with Er and the effect of quasi hydrostaticity on its phase transition sequence, high pressure ADXRD measurements were carried out at room temperature. The detailed structural analysis establishes the phase transition sequence as hcp → hR24 (Sm-type structure) → dhcp beyond 9.6 GPa and across 23.8 GPa, respectively.
Related Concept Videos
NMR Spectroscopy of Benzene Derivatives
Stability of Substituted Cyclohexanes
The two chair conformations of cyclohexanes undergo rapid interconversion at room temperature. Both forms have identical energies and stabilities, each comprising equal amounts of the equilibrium mixture. Replacing a hydrogen atom with a functional group makes the two conformations energetically non-equivalent.
For example, in...
Nucleophilic Aromatic Substitution: Elimination–Addition
Radical Substitution: Allylic Bromination
E1 Reaction: Kinetics and Mechanism
Inductive Effects on Chemical Shift: Overview

