Chen Li, Zhang Jiahua, Zhao Haifeng, Wang Xiaojun
Key Laboratory of Excited State Processes, Changchun Institute of Optics, Fine Mechanics and Physics, Chinese Academy of Sciences, 16 Eastern South-Lake Road, Changchun 130033, China.
J Nanosci Nanotechnol. 2008 Mar;8(3):1326-9.
Tubular micrometer-sized ZnS:Mn2+ constructed by fluffy nanostructures were fabricated in the mixed solutions of water and ethanol in a fixed volume ratio with the aid of ethylenediamine. In the X-ray diffraction pattern, the products obtained in the presence and absence of ethylenediamine show the wurtzite and sphalerite phases, respectively. Field-emission scanning electron microscopic images reveal the evolution process from nanowires to fluffy ZnS:Mn2+ to microtubes with the reaction times of 2, 4, and 8 hours at 100 degrees C, and the basal nanowires are below 10 nm in diameter. Photoluminescence and photoluminescence excitation spectra were investigated. The results suggest that the wurtzite phase, instead of the sphalerite phase ZnS:Mn2+ is luminescence-active for the 4T1 -6A1 transition of the Mn2+ in the ZnS host. The excitation spectra monitored at orange emission bands exhibit sharp peaks at 320, 326 and 327 nm with increasing reaction times of 2, 4, and 8 hours, respectively, indicating the energy transfer from ZnS host to Mn2+ ions, and the blue-shifts compared with the band gap absorption of the bulk counterpart (344 nm) are also observed due to the quantum confinement effects. The formation mechanism of the wurtzite one-dimensional nanostructures at such a low temperature is proposed based on a molecular template mechanism involving the bidentate coordinating ligand, ethylenediamine, and the possible formation mechanism of novel tubular structure are also discussed.
通过蓬松纳米结构构建的管状微米级ZnS:Mn2+是在水和乙醇按固定体积比混合的溶液中借助乙二胺制备的。在X射线衍射图谱中,有无乙二胺存在下获得的产物分别呈现纤锌矿相和闪锌矿相。场发射扫描电子显微镜图像揭示了在100℃下反应2小时、4小时和8小时时从纳米线到蓬松ZnS:Mn2+再到微管的演变过程,且基础纳米线直径低于10nm。研究了光致发光和光致发光激发光谱。结果表明,纤锌矿相而非闪锌矿相的ZnS:Mn2+对于ZnS基质中Mn2+的4T1-6A1跃迁具有发光活性。在橙色发射带监测的激发光谱分别在反应时间为2小时、4小时和8小时时在320nm、326nm和327nm处呈现尖锐峰,表明从ZnS基质到Mn2+离子的能量转移,并且由于量子限域效应,与块状对应物的带隙吸收(344nm)相比还观察到蓝移。基于涉及双齿配位配体乙二胺的分子模板机制提出了如此低温下纤锌矿一维纳米结构的形成机制,并且还讨论了新型管状结构可能的形成机制。