Growth kinetics and metastability of monodisperse tetraoctylammonium bromide capped gold nanocrystals

被引:85
作者
Saunders, AE
Sigman, MB
Korgel, BA [1 ]
机构
[1] Univ Texas, Texas Mat Inst, Dept Chem Engn, Austin, TX 78712 USA
[2] Univ Texas, Ctr Nano & Mol Sci & Technol, Austin, TX 78712 USA
关键词
D O I
10.1021/jp036272g
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
Small-angle X-ray scattering (SAXS) was used to measure the time-dependent evolution of the size and size distribution of tetraoctylammonium-stabilized gold nanocrystals formed by arrested precipitation. The initial growth mechanism was varied by controlling the addition of reducing agent to the ionic gold precursor solution. Slow addition gives high Au-0 monomer supersaturation and provides discrete nucleation and growth events and a narrowing of the particle size distribution over short reaction times. Rapid addition of reducing agent leads to broad initial particle size distributions that begin to narrow only after the first few hours of the reaction. After 24 h, the nanocrystals grow to 52 Angstrom in diameter with a very narrow size distribution regardless of the initial growth kinetics. Analysis of the reaction and transport rates reveal that nanocrystal growth is limited by the surface reaction rate of monomer addition to the crystal surface. The final size appears to be thermodynamically metastable, with the system free energy, which includes the gold surface tension and the tetraoctylammonium binding energy, reaching a local minimum. Nanocrystal size is also found to vary inversely with the binding strength of the capping ligand present during growth, allowing the mean particle diameter to be tuned to between 1.7 and 5.2 nm.
引用
收藏
页码:193 / 199
页数:7
相关论文
共 43 条
[21]  
Lifshin E., 1999, XRAY CHARACTERIZATIO
[22]   Digestive ripening, nanophase segregation and superlattice formation in gold nanocrystal colloids [J].
Lin, X. M. ;
Sorensen, C. M. ;
Klabunde, K. J. .
JOURNAL OF NANOPARTICLE RESEARCH, 2000, 2 (02) :157-164
[23]   Growth of single crystal nanowires in supercritical silicon solution from tethered gold particles on a silicon substrate [J].
Lu, XM ;
Hanrath, T ;
Johnston, KP ;
Korgel, BA .
NANO LETTERS, 2003, 3 (01) :93-99
[24]   Properties of CdSe nanocrystal dispersions in the dilute regime: Structure and interparticle interactions [J].
Mattoussi, H ;
Cumming, AW ;
Murray, CB ;
Bawendi, MG ;
Ober, R .
PHYSICAL REVIEW B, 1998, 58 (12) :7850-7863
[25]   Heating-induced evolution of thiolate-encapsulated gold nanoparticles: A strategy for size and shape manipulations [J].
Maye, MM ;
Zheng, WX ;
Leibowitz, FL ;
Ly, NK ;
Zhong, CJ .
LANGMUIR, 2000, 16 (02) :490-497
[27]   Kinetics of II-VI and III-V colloidal semiconductor nanocrystal growth: "Focusing" of size distributions [J].
Peng, XG ;
Wickham, J ;
Alivisatos, AP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1998, 120 (21) :5343-5344
[28]   Nearly monodisperse and shape-controlled CdSe nanocrystals via alternative routes: Nucleation and growth [J].
Peng, ZA ;
Peng, XG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (13) :3343-3353
[29]   Digestive ripening of thiolated gold nanoparticles: The effect of alkyl chain length [J].
Prasad, BLV ;
Stoeva, SI ;
Sorensen, CM ;
Klabunde, KJ .
LANGMUIR, 2002, 18 (20) :7515-7520
[30]   Digestive-ripening agents for gold nanoparticles: Alternatives to thiols [J].
Prasad, BLV ;
Stoeva, SI ;
Sorensen, CM ;
Klabunde, KJ .
CHEMISTRY OF MATERIALS, 2003, 15 (04) :935-942