M. Kitaura, Ai Harima, R. Xie, T. Takeda, N. Hirosaki, A. Ohnishi, M. Sasaki
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引用次数: 5
摘要
利用电子自旋共振(ESR)实验研究了γ -AlON: Mn氧氮化铝荧光粉中掺杂锰离子的局部结构。γ -AlON: Mn的ESR谱出现6个尖峰,外加5个弱重偶态。这些结构是由三维电子与自旋I = 5/2的55mn原子核的超精细相互作用引起的。这6个峰归因于M s =(cid:156) 1/2的超细分裂态之间允许的跃迁(Δ M I = 0)。这五个重态被解释为超精细分裂态之间的禁止跃迁(Δ M I =(cid:156) 1)。γ -AlON: Mn的光谱特征与Mn 2 +掺杂mgal2o4尖晶石的ESR光谱相似,其中Mn 2 +离子取代了四面体的Mg 2 +位点。由于γ -AlON也具有尖晶石结构,表明Mn 2 +离子占据了四面体Al 3 +的位置。我们进一步追踪了Mg +共掺杂对γ -AlON中Mn 2 +离子ESR谱的影响,以阐明γ -AlON: Mn, Mg中的发光增强。结果表明,mg2 +共掺杂增加了四面体Al 3 +位上的Mn 2 +离子。
Electron Spin Resonance Study on Local Structure of Manganese Ions Doped in Gamma-Aluminum Oxynitride Phosphors
We have studied the local structure of manganese ion doped in gamma aluminum oxynitride phosphors ( γ -AlON: Mn) using electron spin resonance (ESR) experiment. Six sharp peaks appear in ESR spectra of γ -AlON: Mn, together with five weak doublets. These structures are caused by the hyperfine interaction of 3 d electrons with the 55 Mn nucleus of spin I = 5/2. The six peaks are attributed to the allowed transitions (Δ M I = 0) between hyperfine splitting states of M s =(cid:156) 1/2. The five doublets are interpreted as the forbidden transitions (Δ M I =(cid:156) 1) between the hyperfine splitting states. The spectral feature of γ -AlON: Mn resembles with the ESR spectrum of Mn 2 + doped MgAl 2 O 4 spinel, in which Mn 2 + ions are substituted for tetrahedral Mg 2 + sites. Since γ -AlON is also of the spinel structure, it is suggested that Mn 2 + ions occupy tetrahedral Al 3 + sites. We further chased the effect of Mg 2 + co-doping on ESR spectra of Mn 2 + ions in γ -AlON, in order to elucidate the luminescence enhancement in γ -AlON: Mn, Mg. It turned out that the Mg 2 + co-doping increases Mn 2 + ions at tetrahedral Al 3 + sites.