Related Experiment Video
Updated: May 31, 2026

Methods of Ex Situ and In Situ Investigations of Structural Transformations: The Case of Crystallization of Metallic Glasses
Published on: June 7, 2018
Iron dynamics in Al-Cu-Fe quasicrystals and approximants: Mössbauer and neutron experiments
Abstract:
We present new results on the iron dynamics in the icosahedral quasicrystal i-AlCuFe and two cubic approximants as well as the non-approximant Al-Cu-Fe cubic B2 phase. Conventional Mössbauer spectroscopy is used as well as, for the i-AlCuFe phase, high Doppler velocity Mössbauer spectroscopy and quasielastic neutron scattering for samples with different Fe isotope contents. We show that in the i-phase the Fe Lamb-Mössbauer recoilless fraction decreases below that predicted for lattice vibrations alone for temperatures above about 550 K. This decrease is correlated with the onset of a quasielastic signal seen in both Mössbauer and neutron backscattering spectroscopy, which indicates the presence above 550 K of Fe jump processes confined in a local cage. The timescale of the Fe jumps (660 ps at 1000 K) and their temperature dependence differ widely from those of Cu jumps in the same i-AlCuFe quasicrystal. From the temperature dependence of the quadrupole splitting of the (57)Fe Mössbauer spectrum, one can distinguish two kinds of Fe jumps, one starting at 550 K and the second above 800 K. In the two cubic approximants, a loss in the Fe recoilless fraction also occurs above 550 K, revealing the same kind of Fe dynamics as in the i-phase but the effect is smaller. On the other hand, no anomalous Fe dynamics (other than lattice vibrations) is detected in the B2-AlCuFe phase. Since the cubic approximants possess similar local configurations as the quasicrystal, we conclude that locally a Penrose tile description is appropriate. This shows that the detected Fe jumps can be interpreted in terms of phason-like local tiling flips.
More Related Videos
Related Concept Videos
Colors and Magnetism
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human eye.
Atomic Nuclei: Magnetic Resonance
Determination of Crystal Structures
Imperfections in Crystal Structure: Stoichiometric Point Defects
Ferromagnetism
Crystal Field Theory - Octahedral Complexes
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...

