Plasmon Bleaching Dynamics in Colloidal Gold-Iron Oxide Nanocrystal Heterodimers

被引:30
作者
Comin, Alberto [1 ]
Korobchevskaya, Kseniya
George, Chandramohan
Diaspro, Alberto
Manna, Liberato
机构
[1] Ist Italiano Tecnol, NanoPhys Unit, I-16163 Genoa, Italy
基金
欧洲研究理事会;
关键词
Nanocrystals; plasmon; carrier dynamics; gold/iron oxide hetero nanocrystals; CORE-SHELL NANOPARTICLES; METAL NANOPARTICLES; ULTRAFAST DYNAMICS; ELECTRON DYNAMICS; ENERGY RELAXATION; SIZE DEPENDENCE; HOT-ELECTRON; NANOSTRUCTURES;
D O I
10.1021/nl2039875
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Colloidal nanocrystal heterodimers composed of a plasmonic and a magnetic domain have been widely studied as potential materials for various applications in nanomedicine, biology, and photocatalysis. One of the most popular nanocrystal heteroclimers is represented by a structure made of a Au domain and a iron oxide domain joined together. Understanding the nature of the interface between the two domains in such type of dimer and how this influences the energy relaxation processes is a key issue. Here, we present the first broad-band transient absorption study on gold/iron oxide nanocrystal heterodimers that explains how the energy relaxation is affected by the presence of such interface. We found faster electron-electron and electron-phonon relaxation times for the gold "nested" in the iron oxide domain in the heterodimers with respect to gold "only" nanocrystals, that is, free-standing gold nanocrystals in solution. We relate this effect to the decreased electron screening caused by spill-out of the gold electron distribution at gold/iron oxide interface.
引用
收藏
页码:921 / 926
页数:6
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