Self-assembled one-pot synthesis of red luminescent CdS:Mn/Mn(OH)2 nanoparticles

被引:18
|
作者
Marandi, M. [1 ]
Taghavinia, N. [1 ,2 ]
Zad, A. Iraji [1 ,2 ]
Mahdavi, S. M. [1 ]
机构
[1] Sharif Univ Technol, Dept Phys, Tehran 14588, Iran
[2] Sharif Univ Technol, Inst Nanosci & Nanotechnol, Tehran 14588, Iran
关键词
CdS:Mn; Nanoparticles; Luminescence; Core-shell;
D O I
10.1016/j.jlumin.2008.06.014
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We report a novel method of growing red luminescent (635 nm) Mn-doped CdS (CdS:Mn) nanoparticles capped by an inorganic shell of Mn(OH)(2), CdSO4, Na2S2O3 and Mn(NO3)(2) were used as the precursors, and thioglycerol (C3H8O2S) was employed as the capping agent and also the catalyst of the reaction. Using these materials resulted in very slow rate of the reaction and particles growth. The self-assembled one-pot process was performed at pH of 8 and Mn:Cd ratio of 10. and took about 10 days for completion. CdS:Mn nanoparticles are slowly formed in the first day of the process; however, the luminescence is weak. After 7 days, the solution turns white turbid through the formation of additional particles, which precipitate on the walls on the next day. At this stage, a relatively strong red luminescence at 635 nm appears from transparent solution of the CdS:Mn nanoparticles. The white deposit on the walls turns to dark-brown color and luminescence increases on the 9th day. Finally, the CdS:Mn nanoparticles agglomerate and precipitate out of the solution on 10th day. X-ray diffraction and optical spectroscopy showed crystalline phase CdS nanoparticles with an average size of 3.6 nm. We explain the luminescence enhancement based on the formation of a Mn(OH)2 shell on the surface of the CdS:Mn nanoparticles during the precipitation stage. This can passivate the S dangling bonds located on the particles surface. As the surface Cd sites are previously capped with thioglycerol molecules, a complete surface passivation is achieved and results in emergence of high-intensity luminescence. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1980 / 1984
页数:5
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