Optical spectroscopy, magnetic g tensors, and decoherence studies of magnetic dipole transitions of Er3+ at C3i-symmetry lattice sites in Y2O3 at 1.5 µm

Jan 7, 2025
16 pages
Published in:
  • Phys.Rev.B 111 (2025) 4, 045119
  • Published: Jan 7, 2025
DOI:

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Abstract: (APS)
When introduced as dopants into Y2O3, Er3+ ions replace Y3+ ions at two crystallographic sites of C2 and C3i point symmetries. The C3i site is particularly interesting, given that the inversion symmetry prohibits static electric-dipole moments and electric-dipole transitions, resulting in 1.5 µm optical transitions characterized by purely magnetic-dipole properties. Employing Er3+I15/24I13/24 transitions, we examined the inherent C3i site of Er3+ in Y2O3 for its potential in quantum information science and spectral hole burning applications. Our approach involved absorption and site-selective fluorescence spectroscopy to discern Er3+ energy levels and revealed an excited-state lifetime of 14.6 ms. High-resolution laser spectroscopy at 3.7 K indicated an inhomogeneous linewidth of 1.3 GHz in our sample. Orientation-dependent Zeeman laser absorption spectroscopy facilitated the determination of the full g tensors for both the ground and excited states, confirming the C3i site assignment. Furthermore, it identified a suitable magnetic field direction for mitigating decoherence, a finding corroborated through two-pulse photon echo spectroscopy. Our study presents photon echo coherent transient measurements related to magnetic-dipole-allowed rare-earth ion transitions at the C3i site. The observed decoherence, attributed to spectral diffusion arising from Er3+-Er3+ magnetic-dipole interactions, underscores the complex spin dynamics at play in systems with multiple inequivalent dopant sites. Coupled with the practicality of telecom laser wavelengths, our investigation highlights the promise of magnetic-dipole transitions in advancing quantum information science and spectral hole burning applications.