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Valence and spin states of Fe were investigated in a glass of almandine (Fe3Al2Si3O12) composition to 91 GPa by X-ray emission spectroscopy and energy- and time-domain synchrotron Mössbauer spectroscopy in the diamond-anvil cell. Changes in optical properties, total spin moment and Mössbauer parameters all occur predominantly between 1 bar and ~30 GPa. Over this pressure range, the glass changes from translucent brown to opaque and black. The total spin moment of the glass derived from X-ray emission spectroscopy decreases by ~20%. The complementary Mössbauer spectroscopy approaches reveal consistent changes in sites corresponding to 80–90% Fe2+ and 10–20% Fe3+. The high-spin Fe2+ doublet exhibits a continuous decrease in isomer shift and increase in line width and asymmetry. A high-spin Fe3+ doublet with quadrupole splitting of ~1.2 mm/s is replaced by a doublet with quadrupole splitting of ~1.9 mm/s, a value higher than all previous measurements of high-spin Fe3+ and consistent with low-spin Fe3+. These observations suggest that Fe3+ in the glass undergoes a continual transition from a high-spin to a low-spin state between 1 bar and ~30 GPa. Almandine glass is not expected to undergo any abrupt transitions in electronic state at deep mantle pressures. [ABSTRACT FROM AUTHOR]

We explore alternative ways to Mössbauer spectroscopy such as nuclear forward scattering of synchrotron radiation, and synchrotron radiation perturbed angular correlation spectroscopy to reveal the elusive and long-sought hyperfine interactions in ε-Fe. We indicate that synchrotron radiation perturbed angular correlation spectroscopy is the most viable method. [ABSTRACT FROM AUTHOR]