Investigation of the crystallization process in 2 nm CdSe quantum dots

被引:109
作者
Chen, XB [1 ]
Samia, ACS [1 ]
Lou, YB [1 ]
Burda, C [1 ]
机构
[1] Case Western Reserve Univ, Ctr Chem Dynam & Nanomat Res, Dept Chem, Cleveland, OH 44106 USA
关键词
D O I
10.1021/ja0458219
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Investigation of the growth of CdSe nanocrystals (similar to 160 atoms) to the uniquely stable size of 2 nm allows the monitoring of the crystallization process in semiconductor quantum dots. By using a combination of optical techniques, high-resolution transmission electron microscopy (HRTEM), and powder X-ray diffractometry (XRD), new phenomena were explored during the CdSe nanocrystal growth process, which involved significant morphological reconstruction and crystallization of the initially formed amorphous nanoparticles. During the crystallization, the absorption onset of the CdSe quantum dots blue shifted toward higher energies at 3 eV (414 nm), while the photoluminescence red shifted to lower energies. Furthermore, an apparent increasing Stokes shift was observed during the formation of small CdSe nanoparticles. On the other hand, the photoluminescence excitation spectra showed constant features over the reaction time. Additionally, results from HRTEM and XRD studies show that the CdSe nanoparticles were amorphous at early reaction stages and became better crystallized after longer reaction times, while the particle size remained the same during the crystallization process. These observations demonstrate the important role of the surface on the optical properties of small CdSe quantum dots and facilitated the spectroscopic monitoring of the crystallization process in quantum dots.
引用
收藏
页码:4372 / 4375
页数:4
相关论文
共 34 条
[1]   Nanocrystals: Building blocks for modern materials design [J].
Alivisatos, AP .
ENDEAVOUR, 1997, 21 (02) :56-60
[2]   Perspectives on the physical chemistry of semiconductor nanocrystals [J].
Alivisatos, AP .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (31) :13226-13239
[3]   LUMINESCENCE PROPERTIES OF CDSE QUANTUM CRYSTALLITES - RESONANCE BETWEEN INTERIOR AND SURFACE LOCALIZED STATES [J].
BAWENDI, MG ;
CARROLL, PJ ;
WILSON, WL ;
BRUS, LE .
JOURNAL OF CHEMICAL PHYSICS, 1992, 96 (02) :946-954
[4]   Dielectric dispersion measurements of CdSe nanocrystal colloids: Observation of a permanent dipole moment [J].
Blanton, SA ;
Leheny, RL ;
Hines, MA ;
GuyotSionnest, P .
PHYSICAL REVIEW LETTERS, 1997, 79 (05) :865-868
[5]   The relaxation pathways of CdSe nanoparticles monitored with femtosecond time-resolution from the visible to the IR: Assignment of the transient features by carrier quenching [J].
Burda, C ;
Link, S ;
Mohamed, M ;
El-Sayed, M .
JOURNAL OF PHYSICAL CHEMISTRY B, 2001, 105 (49) :12286-12292
[6]   Absorption and luminescence of the surface states in ZnS nanoparticles [J].
Chen, W ;
Wang, ZG ;
Lin, ZJ ;
Lin, LY .
JOURNAL OF APPLIED PHYSICS, 1997, 82 (06) :3111-3115
[7]  
CHEN W, 2000, HDB NANOSTRUCTURED M, V4, P325
[8]   Coherency strain effects on the optical response of core/shell heteronanostructures [J].
Chen, XB ;
Lou, YB ;
Samia, AC ;
Burda, C .
NANO LETTERS, 2003, 3 (06) :799-803
[9]   Band-edge exciton in quantum dots of semiconductors with a degenerate valence band: Dark and bright exciton states [J].
Efros, AL ;
Rosen, M ;
Kuno, M ;
Nirmal, M ;
Norris, DJ ;
Bawendi, M .
PHYSICAL REVIEW B, 1996, 54 (07) :4843-4856
[10]   Quantum-confined stark effect in single CdSe nanocrystallite quantum dots [J].
Empedocles, SA ;
Bawendi, MG .
SCIENCE, 1997, 278 (5346) :2114-2117