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Self‐Assembled Platinum Nanochain Networks Driven by Induced Magnetic Dipoles
Author(s) -
Gao MinRui,
Zhang ShiRan,
Xu YunFei,
Zheng YaRong,
Jiang Jun,
Yu ShuHong
Publication year - 2014
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.201302262
Subject(s) - materials science , nucleation , platinum , nanoscopic scale , nanotechnology , ferromagnetism , dipole , paramagnetism , nanoparticle , platinum nanoparticles , polyvinylpyrrolidone , self assembly , chemical physics , condensed matter physics , biochemistry , chemistry , physics , organic chemistry , polymer chemistry , catalysis
Developing a reliable technique to organize nanoscale building blocks into ordered one‐dimensional assemblies is of particular interest in a range of practical applications. Here, for the first time, it is reported that platinum (Pt) nanoparticle chain networks can be assembled spontaneously in solution on a large scale. The in‐situ induced magnetic dipoles are believed to be the driving force for producing such elegant assembled nanochains. The alterant electronic structure of Pt modified by a very thin layer of polyvinylpyrrolidone (PVP) molecules leads to the ferromagnetism of Pt (a traditional paramagnetic metal), which has been verified by a series of analysis techniques and theoretical modeling. The temperature‐ and time‐dependent nucleation, growth, and organization processes of Pt chain networks are carefully investigated. These findings not only present the uncommon ferromagnetism of Pt, but also raise a possibility for expanding this strategy towards other assemblies of nonmagnetic nanoscale building blocks.
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