Transition of Growth Mode Controlled by the Density of Nuclei in Photocatalytic Synthesis of Ag Nanoparticles

被引:0
作者
Li Shuai [1 ]
Tao Qiang [1 ]
Zhang Qing-Yu [1 ]
机构
[1] Dalian Univ Technol, Sch Phys & Optoelect Technol, Key Lab Mat Modificat Laser Ion & Electron Beams, Dalian 116024, Liaoning, Peoples R China
关键词
Ag nanoparticles; photocatalytic synthesis; transition of growth mode; METAL NANOPARTICLES; OPTICAL-PROPERTIES; SILVER; FILMS; NANOSTRUCTURES; ENHANCEMENT; GENERATION; MECHANISM; SHAPE;
D O I
暂无
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Using the aqueous solution of AgNO3, the growth behavior of Ag nanoparticles synthesized by photocatalytic method is studied by controlling the chemical activity of TiO2 film. It is found that the Ag nanoparticles can grow up with two distinct growth modes, which correspond to the isotropic and anisotropic growth, respectively. When the concentration of AgNO3 is low, Ostwald ripening (OR) dominates the growth of Ag nanoparticles. If the concentration of AgNO3 exceeds a critical level, oriented attachment (OA) determines the Ag nanoparticles growing up into Ag nanoplates. The in-situ extinction spectra suggest that the Ag nuclei have the very similar features in the stage of nucleation before the growth of Ag nanoparticles is dominated by OR or OA mechanism. The transition of growth behavior is determined by the concentration of AgNO3 in the solution, or the local density of Ag primary nuclei. On the basis of experimental results and theoretical analysis, a physical model is suggested for the growth of Ag nanoparticles in the photocatalytic synthesis.
引用
收藏
页码:1567 / 1574
页数:8
相关论文
共 34 条
[1]   Aggregation-based crystal growth and microstructure development in natural iron oxyhydroxide biomineralization products [J].
Banfield, JF ;
Welch, SA ;
Zhang, HZ ;
Ebert, TT ;
Penn, RL .
SCIENCE, 2000, 289 (5480) :751-754
[2]   Enhancing Photochemical Activity of Semiconductor Nanoparticles with Optically Active Ag Nanostructures: Photochemistry Mediated by Ag Surface Plasmons [J].
Christopher, Phillip ;
Ingram, David B. ;
Linic, Suljo .
JOURNAL OF PHYSICAL CHEMISTRY C, 2010, 114 (19) :9173-9177
[3]   Surface-Enhanced Raman Excitation Spectroscopy of a Single Rhodamine 6G Molecule [J].
Dieringer, Jon A. ;
Wustholz, Kristin L. ;
Masiello, David J. ;
Camden, Jon P. ;
Kleinman, Samuel L. ;
Schatz, George C. ;
Van Duyne, Richard P. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (02) :849-854
[4]   Gold as a novel catalyst in the 21st century: Preparation, working mechanism and applications [J].
Haruta, M .
GOLD BULLETIN, 2004, 37 (1-2) :27-36
[5]   Controlling anisotropic nanoparticle growth through plasmon excitation [J].
Jin, RC ;
Cao, YC ;
Hao, EC ;
Métraux, GS ;
Schatz, GC ;
Mirkin, CA .
NATURE, 2003, 425 (6957) :487-490
[6]   The optical properties of metal nanoparticles: The influence of size, shape, and dielectric environment [J].
Kelly, KL ;
Coronado, E ;
Zhao, LL ;
Schatz, GC .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (03) :668-677
[7]   Plasmon-Enhanced Charge Carrier Generation in Organic Photovoltaic Films Using Silver Nanoprisms [J].
Kulkarni, Abhishek P. ;
Noone, Kevin M. ;
Munechika, Keiko ;
Guyer, Samuel R. ;
Ginger, David S. .
NANO LETTERS, 2010, 10 (04) :1501-1505
[8]  
LAI Wen-Zhong, 2010, ACTA PHYS CHIM SIN
[9]   Direction-Specific Interactions Control Crystal Growth by Oriented Attachment [J].
Li, Dongsheng ;
Nielsen, Michael H. ;
Lee, Jonathan R. I. ;
Frandsen, Cathrine ;
Banfield, Jillian F. ;
De Yoreo, James J. .
SCIENCE, 2012, 336 (6084) :1014-1018
[10]   Silver Nanorice Structures: Oriented Attachment-Dominated Growth, High Environmental Sensitivity, and Real-Space Visualization of Multipolar Resonances [J].
Liang, Hongyan ;
Zhao, Haiguang ;
Rossouw, David ;
Wang, Wenzhong ;
Xu, Hongxing ;
Botton, Gianluigi A. ;
Ma, Dongling .
CHEMISTRY OF MATERIALS, 2012, 24 (12) :2339-2346