The role of nanoparticle size and ligand coverage in size focusing of colloidal metal nanoparticles

被引:63
|
作者
Mozaffari, Saeed [1 ]
Li, Wenhui [1 ]
Dixit, Mudit [2 ]
Seifert, Soenke [3 ]
Lee, Byeongdu [4 ]
Kovarik, Libor [5 ]
Mpourmpakis, Giannis [2 ]
Karim, Ayman M. [1 ]
机构
[1] Virginia Polytech Inst & State Univ, Dept Chem Engn, Blacksburg, VA 24060 USA
[2] Univ Pittsburgh, Dept Chem Engn, Pittsburgh, PA 15261 USA
[3] Argonne Natl Lab, Adv Photon Source, Argonne, IL 60439 USA
[4] Argonne Natl Lab, Xray Sci Div, Argonne, IL 60439 USA
[5] Pacific Northwest Natl Lab, Environm Mol Sci Lab, Richland, WA 99352 USA
来源
NANOSCALE ADVANCES | 2019年 / 1卷 / 10期
基金
美国国家科学基金会;
关键词
KINETICALLY EFFECTIVE NUCLEUS; IN-SITU; PALLADIUM NANOPARTICLES; GOLD NANOPARTICLES; QUANTITATIVE-ANALYSIS; ADSORPTION ENERGY; NUCLEATION; GROWTH; NANOCRYSTALS; MECHANISM;
D O I
10.1039/c9na00348g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Controlling the size distribution of nanoparticles is important for many applications and typically involves the use of ligands during synthesis. In this study, we show that the mechanism of size focusing involves a dependence of the growth rate on the size of the nanoparticles and the ligand coverage on the surface of the nanoparticles. To demonstrate these effects, we used in situ small angle X-ray scattering (SAXS) and population balance kinetic modeling (PBM) to investigate the evolution of size distribution during the synthesis of colloidal Pd metal nanoparticles. Despite temporal overlap of nucleation and growth, our in situ SAXS show size focusing of the distribution under different synthetic conditions (different concentrations of metal and ligand as well as solvent type). To understand the mechanism of size focusing using PBM, we systematically studied how the evolution of the nanoparticle size distribution is affected by nucleation rate, and dependence of the growth rate constant on ligand surface coverage, and size of the nanoparticles. We show that continuous nucleation contributes to size defocusing. However, continuous nucleation results in different reaction times for the nanoparticle population leading to time and size-dependent ligand surface coverage. Using density functional theory (DFT) calculations and BrOnsted-Evans-Polanyi relations, we show that as the population grows, larger nanoparticles grow more slowly than smaller ones due to lower intrinsic activity and higher ligand coverage on the surface. Therefore, despite continuous nucleation, the faster growth of smaller nanoparticles in the population leads to size focusing. The size focusing behaviour (due to faster growth of smaller nanoparticles) was found to be model independent and similar results were demonstrated under different nucleation and growth pathways (e.g. growth via ion reduction on the surface and/or monomer addition). Our results provide a microscopic connection between kinetics and thermodynamics of nanoparticle growth and metal-ligand binding, and their effect on the size distribution of colloidal nanoparticles.
引用
收藏
页码:4052 / 4066
页数:15
相关论文
共 50 条
  • [41] Role of proteins in controlling selenium nanoparticle size
    Dobias, J.
    Suvorova, E. I.
    Bernier-Latmani, R.
    NANOTECHNOLOGY, 2011, 22 (19)
  • [42] Metal and metal oxide nanoparticles in aqueous environments: Impacts of nanoparticle aging, surface coatings and size on aggregation and dissolution
    Grassian, Vicki H.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2012, 243
  • [43] Polymer/Nanoparticle Hybrid Materials of Precise Dimensions by Size-Exclusive Fishing of Metal Nanoparticles
    Fan, Ziyin
    Serrano, Melissa Koehn
    Schaper, Andreas
    Agarwal, Seema
    Greiner, Andreas
    ADVANCED MATERIALS, 2015, 27 (26) : 3888 - +
  • [44] Determination of particles size and crystalline phases in colloidal silicon nanoparticle suspensions
    Scholz, S.M.
    Hofmann, H.
    Journal of Materials Science and Technology, 1999, 15 (06): : 548 - 550
  • [45] Size and size distribution balance the dispersion of colloidal CeO2 nanoparticles in organic solvents
    Arita, Toshihiko
    Yoo, Jungwoo
    Ueda, Yu
    Adschiri, Tadafumi
    NANOSCALE, 2010, 2 (05) : 689 - 693
  • [46] The influence of metal nanoparticle size distribution in photoelectron spectroscopy
    Minati, L.
    Speranza, G.
    Calliari, L.
    Micheli, V.
    Baranov, A.
    Fanchenko, S.
    JOURNAL OF PHYSICAL CHEMISTRY A, 2008, 112 (34): : 7856 - 7861
  • [47] Modelling transition metal nanoparticles:: the role of size reduction in electronic structure and catalysis
    Guczi, L
    Pászti, Z
    Petö, G
    NANOTECHNOLOGY IN CATALYSIS, VOLS 1 AND 2, 2004, : 467 - 496
  • [48] Impact of Size Dispersity, Ligand Coverage, and Ligand Length on the Structure of PbS Nanocrystal Superlattices
    Weidman, Mark C.
    Quan Nguyen
    Smilgies, Detlef-M.
    Tisdale, William A.
    CHEMISTRY OF MATERIALS, 2018, 30 (03) : 807 - 816
  • [49] Intermethod comparison of the particle size distributions of colloidal silica nanoparticles
    Tuoriniemi, Jani
    Johnsson, Ann-Cathrin J. H.
    Holmberg, Jenny Perez
    Gustafsson, Stefan
    Gallego-Urrea, Julian A.
    Olsson, Eva
    Pettersson, Jan B. C.
    Hassellov, Martin
    SCIENCE AND TECHNOLOGY OF ADVANCED MATERIALS, 2014, 15 (03)
  • [50] Influence of precursor on the particle size and stability of colloidal gold nanoparticles
    Alshammari, A.
    Koeckritz, A.
    Kalevaru, V. N.
    Martin, A.
    SCIENTIFIC BASES FOR THE PREPARATION OF HETEROGENEOUS CATALYSTS: PROCEEDINGS OF THE 10TH INTERNATIONAL SYMPOSIUM, 2010, 175 : 409 - 412