Structural Evolution of Three-Component Nanoparticles in Polymer Nanoreactors

被引:55
作者
Chen, Peng-Cheng [1 ,2 ]
Du, Jingshan S. [1 ,2 ]
Meckes, Brian [2 ,3 ]
Huang, Liliang [1 ,2 ]
Xie, Zhuang [2 ,3 ]
Hedrick, James L. [2 ,4 ]
Dravid, Vinayak P. [1 ,2 ]
Mirkin, Chad A. [1 ,2 ,3 ,4 ]
机构
[1] Northwestern Univ, Dept Mat Sci & Engn, Evanston, IL 60208 USA
[2] Northwestern Univ, Int Inst Nanotechnol, Evanston, IL 60208 USA
[3] Northwestern Univ, Dept Chem, 2145 Sheridan Rd, Evanston, IL 60208 USA
[4] Northwestern Univ, Dept Chem & Biol Engn, Evanston, IL 60208 USA
基金
美国国家科学基金会;
关键词
LIQUID CELL; IN-SITU; HETEROSTRUCTURED NANOCRYSTALS; HETERODIMER NANOCRYSTALS; ELECTRON-MICROSCOPY; DIRECTED SYNTHESIS; GROWTH; NANOSTRUCTURES; SEMICONDUCTOR; NUCLEATION;
D O I
10.1021/jacs.7b03163
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Recent developments in scanning probe block copolymer lithography (SPBCL) enable the confinement of multiple metal precursors in a polymer nanoreactor and their subsequent transformation into a single multimetallic hetero-structured nanoparticle through Thermal annealing. However, the process by which multimetallic nanoparticles forth in SPBCL-patterned nanoreactors remains unclear. Here, we utilize the combination of PEO-b-P2VP and Au, Ag, and Cu salts as a model three-component system to investigate this process. The data suggest that the formation of single-component Au, Ag, or Cu nanoparticles within polymer nanoreactors consists of two stages: (I) nucleation, growth, and coarsening of the particles to yield a single particle in each reactor; (II) continued particle growth by depletion of the remaining precursor in the reactor until the particle reaches a stable size. Also, different aggregation rates are observed for single-component particle formation (Au > Ag > Cu). This behavior is also observed for two-component systems, where nucleation sites have greater Au content than the other metals. This information can be used to trap nanoparticles with kinetic structures. High-temperature treatment ultimately facilitates the structural evolution of the kinetic particle into a particle with a fixed structure. Therefore, with multicomponent systems, a third stage that involves elemental redistribution within the particle must be part of the description of the synthetic process. This work not only provides a glimpse at the mechanism underlying multicomponent nanoparticle formation in SPBCL-generated nanoreactors but also illustrates, for the first time, the utility of SPBCL as a platform for controlling the architectural evolution of multimetallic nanoparticles in general.
引用
收藏
页码:9876 / 9884
页数:9
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