期刊文献+

PAMAM树形分子模板法原位制备CdS-ZnS核-壳结构量子点 被引量:5

In-situ Synthesis of CdS-ZnS Core-shell Structure Quantum Dots Inside PAMAM Dendrimer Templates
在线阅读 下载PDF
导出
摘要 以4.5代PAMAM树形分子(64个酯端基)为模板,在树形分子空腔内原位合成了CdS-ZnS核-壳结构量子点,并对其形貌和光学性能进行了表征.HRTEM观察发现量子点分散良好,尺寸均匀,平均粒径约为2.3 nm.UV-V is光谱证明ZnS外延生长在CdS核外,EDS能谱也证明了核壳结构的生成.适当厚度的ZnS壳层可使光致发光效率提高至31%.PAMAM树形分子包在CdS-ZnS核-壳结构量子点外,构成一层有机壳,有效地限制了粒子聚集,钝化了CdS量子点表面,提高了发光效率.另外,PAMAM树形分子良好的溶解性也赋予了量子点在不同极性溶剂中良好的溶解性,提高了其稳定性. CdS-ZnS core-shell structure quantum dots (QDs) were in-situ synthesized inside PAMAM dendrimer templates of generation 4.5 ( containing 64 ester end groups). The size distribution of the well-dispersed QDs was narrow and the average diameter was about 2. 3 nm as shown in HRTEM images. The red shift of the absorption spectra suggested the formation of the core-shell structure. Also the EDS confirmed that the QDs were comprised of CdS and ZnS. ZnS shell of appropriate thickness effectively eliminated the noradiactive centers and the PL efficiency was improved to 31%. An organic shell covering the CdS-ZnS core-shell QDs formed via the PAMAM dendrimers, which prevented the conglomeration of QDs, passivated the hanging bonds and improved the PL efficiency. Furthermore, the excellent solubility of PAMAM dendrimers in solvents with different polarities endowed the QDs good solubility and made the QDs more stable.
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2006年第5期793-796,共4页 Chemical Journal of Chinese Universities
基金 北京理工大学基础研究基金(批准号:BIT-UBF-200504E4203) 教育部跨世纪优秀人才培养计划基金资助
关键词 PAMAM树形分子 模板法 CdS-ZnS核-壳量子点 表面钝化 荧光效率 PAMAM dendrimer Template method CdS-ZnS core-shell QDs Surface passivation Photolu- minescence efficiency
  • 相关文献

参考文献3

二级参考文献22

  • 1[4]Marcel B. J., Mario M., Pater G. et al.. Science [J], 1998, 281: 2 013-2 015
  • 2[5]Nie S., Emory S. R.. Science[J], 1998, 281: 2 016-2 018
  • 3[6]Hasselbarth A., Eychmuller A., Eichberger R. et al.. J. Phys. Chem.[J], 1993, 97: 5 333-5 340
  • 4[7]Kim Y. J., Johnson R. C., Hupp J. T.. Nano. Letters[J], 2001, 1: 165
  • 5[8]Eychmuller A., Mews A., Weller H.. Chem. Phys. Lett.[J], 1993, 208: 59-62
  • 6Andreas, K.; Daniel, L. J. Electroanal. Chem. 1996, 418(1,2), 73.
  • 7Smyntyno, V.; Golovanov, V.; Kaciulis, S.; Mattogno, G;Righini, G. Sens. Actuators, B 1995, 24~25(1~3), 628.
  • 8Joseph, R.; Lakowicz, I. G.; Gregorz, P.; Catherine, J. M. J.Phys. Chem. B 2002, 106, 5365.
  • 9Kelly, S.; Leo, H.; Harry, J. P.; Catherine, J. M. Adv. Mater.1998, 10(14), 1083.
  • 10崔艳霞.[D].北京:北京理工大学,2003.

共引文献42

同被引文献55

引证文献5

二级引证文献13

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部