期刊
MATERIALS CHEMISTRY AND PHYSICS
卷 119, 期 1-2, 页码 153-157出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.matchemphys.2009.08.044
关键词
Gold nanoparticle; Nanochain; Nanowire; Interfacial self-assembly
资金
- National Natural Science Foundation [20703016]
- Ministry of Education of China
- U.S. Department of Energy
By utilizing the strong capillary attraction between interfacial nanoparticles, large-scale one-dimensional Au nanochain networks were fabricated at the n-butanol/water interface, and could be conveniently transferred onto hydrophilic substrates. Furthermore, the length of the nanochains could be adjusted simply by controlling the density of Au nanoparticles (AuNPs) at the n-butanol/water interface. Surprisingly, the resultant Au nanochains could further transform into smooth nanowires by increasing the aging time, forming a nanowire network. Combined characterization by HRTEM and UV-vis spectroscopy indicates that the formation of Au nanochains stemmed from a stochastic assembly of interfacial AuNPs due to strong capillary attraction, and the evolution of nanochains to nanowires follows an Ostwald ripening mechanism rather than an oriented attachment. This method could be utilized to fabricate large-area nanochain or nanowire networks more uniformly on solid substrates than that of evaporating a solution of nanochain colloid, since it eliminates the three-dimensional aggregation behavior. (C) 2009 Elsevier B.V. All rights reserved.
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