Pulsed electron paramagnetic resonance (EPR) and pulsed electron‐nuclear double resonance (ENDOR) techniques have been applied to study the environment of luminescent Ce3+ ions in garnet based scintillator powders and ceramics. The presence of aluminum and gallium isotopes with large nuclear magnetic and quadrupole moments in the nearest neighborhood of the Ce3+ ion allows for the use of the hyperfine and quadrupole interactions with these ions for determination of the unpaired electron spatial distribution and the definition of the electric field gradient at the aluminum and gallium sites. Pulsed EPR and ENDOR techniques made it possible to study the coherent properties of the Ce3+ spin system in garnet powders and ceramics, which is important for spin manipulation on Ce3+ centers.
Electron paramagnetic resonance (EPR) spectra of Ce3+, Yb3+, Cr3+, and Gd3+ impurity ions in yttrium aluminum garnet Y3Al5O12 (YAG) ceramics were detected and identified at frequency of 94 GHz. The advantage of measuring the EPR spectra in the high-frequency range compared to the standard EPR technique is shown, which makes it possible to separate the EPR spectra characterized by different anisotropic g-factors and also to isolate the EPR signals due to the splitting of the fine structure for centers with high-spin states. In ceramics with a high content of magnetic Gd3+ ions, EPR and electron spin echo (ESE) spectra of multi-ionic gadolinium complexes were observed, and EPR spectra of complexes with the maximum number of exchange-coupled gadolinium ions are seen at low temperatures. The temperature dependences of the EPR spectra indicates ferromagnetic ordering of exchange-coupled complexes of gadolinium.
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