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Electron Spin Resonance Study on Local Structure of Manganese Ions Doped in Gamma-Aluminum Oxynitride Phosphors

机译:电子自旋共振研究γ-铝氧氮化磷掺杂锰离子的局域结构

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References(12) 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 3d electrons with the 55Mn nucleus of spin I=5/2. The six peaks are attributed to the allowed transitions (ΔMI=0) between hyperfine splitting states of Ms=±1/2. The five doublets are interpreted as the forbidden transitions (ΔMI=±1) between the hyperfine splitting states. The spectral feature of γ-AlON: Mn resembles with the ESR spectrum of Mn2+ doped MgAl2O4 spinel, in which Mn2+ ions are substituted for tetrahedral Mg2+ sites. Since γ-AlON is also of the spinel structure, it is suggested that Mn2+ ions occupy tetrahedral Al3+ sites. We further chased the effect of Mg2+ co-doping on ESR spectra of Mn2+ ions in γ-AlON, in order to elucidate the luminescence enhancement in γ-AlON: Mn, Mg. It turned out that the Mg2+ co-doping increases Mn2+ ions at tetrahedral Al3+ sites.
机译:参考文献(12)我们使用电子自旋共振(ESR)实验研究了γ氮氧化铝磷光体(γ-AlON:Mn)中掺杂的锰离子的局部结构。在γ-AlON:Mn的ESR光谱中出现六个尖峰,以及五个弱双峰。这些结构是由3d电子与自旋I = 5/2的55Mn核的超精细相互作用引起的。六个峰归因于Ms =±1/2的超精细分裂状态之间的允许跃迁(ΔMI= 0)。五个双峰被解释为超精细分裂状态之间的禁止跃迁(ΔMI=±1)。 γ-AlON:Mn的光谱特征类似于掺杂Mn2 +的MgAl2O4尖晶石的ESR光谱,其中Mn2 +离子代替了四面体Mg2 +部位。由于γ-AlON也是尖晶石结构,因此建议Mn2 +离子占据Al4 +的四面体。为了阐明γ-AlON中的发光增强:Mn,Mg,我们进一步追踪了Mg2 +共掺杂对γ-AlON中Mn2 +离子的ESR谱的影响。结果表明,Mg2 +共掺杂使四面体Al3 +位上的Mn2 +离子增加。

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