Liu C X, Liu J Y, Dou K
Key Laboratory of Excited State Processes, Changchun Institute of Optics, Fine Mechanics and Physics, Chinese Academy of Sciences, Changchun 130033, P R China.
J Nanosci Nanotechnol. 2005 Sep;5(9):1552-6. doi: 10.1166/jnn.2005.328.
ZnS: Mn2+ nanocrystals embedded in Pyrex glasses were spectrally studied using EPR and photoluminescence techniques. Photoluminescence (PL) and excitation (PLE) spectra revealed that manganese impurities can be classified as two types of luminescent centers, i.e., occupying substitutional sites (Mn2+)sub or interstitial sites (Mn2+)int. Three types of manganese sites of (Mn2+)sub, (Mn2+)int, and Mn clusters were identified by the EPR spectra. An increase of the g1 factor and hyperfine structure (HFS) constant with decreasing sizes of nanocrystals was observed. The increase was attributed to a hybridization of the s-p state of ZnS and the d state of manganese ions enhanced by quantum confinement effects or surface states.
采用电子顺磁共振(EPR)和光致发光技术对嵌入派热克斯玻璃中的硫化锌:锰离子(ZnS: Mn2+)纳米晶体进行了光谱研究。光致发光(PL)和激发(PLE)光谱表明,锰杂质可分为两种类型的发光中心,即占据替代位点(Mn2+)sub或间隙位点(Mn2+)int。通过EPR光谱确定了(Mn2+)sub、(Mn2+)int和锰簇三种类型的锰位点。观察到随着纳米晶体尺寸减小,g1因子和超精细结构(HFS)常数增加。这种增加归因于量子限制效应或表面态增强了硫化锌的s-p态与锰离子d态的杂化。