Nucleation and Growth of Silver Sulfide Nanoparticles

被引:61
|
作者
Leon-Velazquez, Madeline S. [1 ]
Irizarry, Roberto [1 ]
Castro-Rosario, Miguel E. [1 ]
机构
[1] Univ Puerto Rico, Dept Chem, Chem Imaging Ctr, Mayaguez, PR 00680 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2010年 / 114卷 / 13期
关键词
QUANTUM-DOTS; IN-SITU; TRANSPORT-PROPERTIES; SELF-ORGANIZATION; AG2S; NANOCRYSTALS; PARTICLES; MECHANISM; CLUSTERS; LUMINESCENCE;
D O I
10.1021/jp911238a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Real time UV-visible absorption measurements of stopped flows of AgNO3 and (NH4)(2)S are used to study the nucleation and growth of silver sulfide nanoparticles (Ag2S NP). Ag2S NP in the size range of 2 to 10 nm are formed a few seconds after the flow containing the reactants stops. The absorbance near the band edge of the semiconductor nanoparticle is used to monitor the number of particles formed with time and study the nucleation process. Transmission electron microscopy measurements are used to correlate particle size and the indirect band gap energy, determined from the onset of light absorption. A linear relation is established between Ag2S NP particle size and indirect band gap energy. The nucleation and growth process are not well separated in time. The initial nucleation and growth rates are found to increase with initial [AgNO3](o)/[(NH4)(2)S](o) ratios larger than 1. Silver-rich sulfides are proposed to be involved in the nucleation stage and growth process of Ag2S NP. Density functional calculations are consistent with that interpretation: Ag3S+ is found to have a lower energy than the Ag2S and AgSH molecules or the AgS- and Ag2SH+ ions. The results are discussed in terms of classic nucleation theory and the possible growth mechanisms are discussed.
引用
收藏
页码:5839 / 5849
页数:11
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