Oxygen-Vacancy-Driven Persistent Luminescence in Mn(2+)-Doped MgGeO(3): Insights from X-Ray Absorption Fine Structure Spectroscopy

锰(2+)掺杂MgGeO(3)中氧空位驱动的持续发光:来自X射线吸收精细结构光谱的启示

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Abstract

Mn(2+)-doped MgGeO(3) (MMGO) is a near-infrared-emitting persistent luminescence (PersL) phosphor. Its low luminescence decay has been linked to vacancies within the MgGeO(3) host, likely associated with Ge, although no direct correlations have been confirmed. In this study, the Ge K-edge X-ray absorption fine structure (XAFS) spectroscopy is employed to investigate a series of MMGO submicron-sized particles with varying afterglow durations. These samples are synthesized using a recently developed hydrothermal method, where it is found that the PersL duration is related to the annealing temperature and the presence of codopants. It is first demonstrated that the XAFS spectra obtained using an in-house XAFS spectrometer are comparable in quality to those acquired at synchrotron facilities. Analysis of the local Ge environment of the MMGO shows that the PersL duration is directly related to the Ge-O coordination number. Additionally, the introduction of Li(+) extends the PersL duration of MMGO but does not alter the Ge-O coordination. The findings provide insights into the structural mechanisms driving luminescence and highlight the capability of in-house XAFS systems to deliver high-quality data for advanced materials research.

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