What is it about?

Due to the good thermal-mechanical and luminescence properties, Yb:YAG ceramics are suitable as thin-disk lasers; however, their efficiency is limited by the presence of Yb2+ ions, which entail parasitic energy transfer from Yb3+ to Yb2+. This article focuses on the Yb2+ formation in Yb:YAG ceramics prepared by solid-state reaction sintering. The samples were prepared by air annealing, the oxidation of the material leads to recharging Yb2+ ion to its trivalent state. The activation energy was determined by Jander to be Ea(D) = 2.7 ± 0.2 eV, which is in good agreement with the activation energy for oxygen diffusion in the YAG lattice. It was concluded that the recharging of Yb2+ ion to its trivalent state in YAG ceramics is limited by the oxygen self-diffusion through the grain volume, and the oxygen vacancy alone and/or together with the presence of antisites can be proposed as Yb2+ charge compensation mechanism in the YAG ceramics, unlike the YbAG single crystals, where tetravalent impurities are responsible for charge compensation.

Featured Image

Why is it important?

The garnet ceramics of Yb:YAG were synthesized by vacuum reaction sintering at high temperature, the time-dependence of Yb2+ concentration was investigated by air annealing in a special furnace. After vacuum sintering, the absorption spectra of the Yb:YAG ceramics contained four absorption bands which disappeared under air annealing and correspond to the absorption of the Yb2+ ions and the F+ colour centres, moreover, the absorption bands of Yb3+ slightly increased in intensity. A longer air annealing led to a decrease in the Yb2+ amount, whereas a higher temperature sped up the oxidation velocity. Only 0.25 at% of Yb ions existed in the divalent state before oxidation. The Yb2+ time-dependence was described by the Jander model, allowing to conclude that the Yb2+ to Yb3+ oxidation process is limited by the diffusion of oxidative agents. The EG of Yb2+ oxidation was Ea(D) = 2.7 ± 0.2 eV, which corresponds to the activation energy EG for volume oxygen diffusion in the YAG lattice. We concluded that the Yb2+ oxidation in the Yb:YAG ceramics is limited by oxygen diffusion, meaning that oxygen vacancies and/or oxygen vacancies with antisites compensate for the Yb2+ charge, in contrast to the YbAG single crystal where tetravalent impurities are responsible for it.

Perspectives

The formation of Yb2+ ions is an important part of the energy loss process due to the energy transfer in the Yb3+-Yb2+ pairs, therefore, understanding the nature of Yb2+ charge compensation mechanism would allow decreasing the occurrence of this parasitic process in laser materials. To our knowledge, few works related to the Yb2+-Yb3+ ions valence transformation process have been published [14,15], and a detailed mechanism of Yb2+ ions charge compensation has not yet been proposed due to the lack of supporting information.

Mykhailo Chaika
Institute of Low Temperature and Structure Research

Read the Original

This page is a summary of: Dynamics of Yb2+ to Yb3+ ion valence transformations in Yb:YAG ceramics used for high-power lasers, Optical Materials, March 2020, Elsevier,
DOI: 10.1016/j.optmat.2020.109774.
You can read the full text:

Read

Contributors

The following have contributed to this page