Bonding environment and electronic structure of Gd metallofullerene and Gd nanowire filled single-wall carbon nanotubes

被引:17
|
作者
Pichler, T. [1 ]
Kramberger, C. [1 ,2 ]
Ayala, P. [3 ]
Shiozawa, H. [6 ]
Knupfer, M. [2 ]
Ruemmeli, M. H. [2 ]
Batchelor, D. [4 ]
Kitaura, R. [5 ]
Imazu, N. [5 ]
Kobayashi, K. [5 ]
Shinohara, H. [5 ]
机构
[1] Univ Vienna, Fac Phys, A-1190 Vienna, Austria
[2] IFW Dresden, D-01171 Dresden, Germany
[3] Helsinki Univ Technol, Dept Engn Phys, FIN-02150 Espoo, Finland
[4] BESSY, D-12489 Berlin, Germany
[5] Nagoya Univ, Dept Chem, Nagoya, Aichi 4648602, Japan
[6] Univ Surrey, Adv Technol Inst, Guildford GU2 7XH, Surrey, England
来源
PHYSICA STATUS SOLIDI B-BASIC SOLID STATE PHYSICS | 2008年 / 245卷 / 10期
关键词
D O I
10.1002/pssb.200879644
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
Being single-walled carbon nanotubes, archetypical 1D systems with peculiar anisotropic electronic properties, it is possible to infer modifications in a controlled manner by filling their inner hollow space. One successful approach was proposed for Gd, which regards filling with metallofullerenes and a successful transformation into different novel metal and a successful transformation into different novel metal nanowires by a versatile nanochemical reaction. In this contribution we report on a combined high resolution photoemission and X-ray absorption study on Gd@C82 peapods and Gd nanowires. From a detailed analysis of the Gd 4d reponse and the valence band in photoemission we are able to elucidate the changes in the bonding environment and charge transfer in these 1D systems. We observe a clear modification of the low energy electronic properties of the SWCNT by the filling with Gd nanowires. Our findings provide important input to understand the interplay between charge transfer and hyridisation in the nanochemical processes in these hybrid systems and to elucidate their electronic transport properties regarding their application potential in nanoelectronic devices. (C) 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
引用
收藏
页码:2038 / 2041
页数:4
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