Spacing-dependent dipolar interactions in dendronized magnetic iron oxide nanoparticle 2D arrays and powders

被引:51
作者
Fleutot, Solenne [1 ]
Nealon, Gareth L. [1 ]
Pauly, Matthias [1 ]
Pichon, Benoit P. [1 ]
Leuvrey, Cedric [1 ]
Drillon, Marc [1 ]
Gallani, Jean-Louis [1 ]
Guillon, Daniel [1 ]
Donnio, Bertrand [1 ]
Begin-Colin, Sylvie [1 ]
机构
[1] Inst Phys & Chim Mat Strasbourg, UMR CNRS UdS 7504, F-67034 Strasbourg 2, France
关键词
GLASS COLLECTIVE STATE; NANOCRYSTALS; DYNAMICS; ORGANIZATION; TEMPERATURE; RELAXATION; ASSEMBLIES; MONOLAYER; PARTICLES;
D O I
10.1039/c2nr32117c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Self-assembly of nanoparticles (NPs) into tailored structures is a promising strategy for the production and design of materials with new functions. In this work, 2D arrays of iron oxide NPs with interparticle distances tuned by grafting fatty acids and dendritic molecules at the NPs surface have been obtained over large areas with high density using the Langmuir-Blodgett technique. The anchoring agent of molecules and the Janus structure of NPs are shown to be key parameters driving the deposition. Finally the influence of interparticle distance on the collective magnetic properties in powders and in monolayers is clearly demonstrated by DC and AC SQUID measurements. The blocking temperature T-B increases as the interparticle distance decreases, which is consistent with the fact that dipolar interactions are responsible for this increase. Dipolar interactions are found to be stronger for particles assembled in thin films compared to powdered samples and may be described by using the Vogel Fulcher model.
引用
收藏
页码:1507 / 1516
页数:10
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