Electron field emitters based on multiwalled carbon nanotubes decorated with nanoscale metal clusters

被引:29
|
作者
Rakhi, R. B.
Reddy, A. Leela Mohana
Shaijumon, M. M.
Sethupathi, K.
Ramaprabhu, S. [1 ]
机构
[1] Indian Inst Technol, Alternat Energy Technol Lab, Dept Phys, Madras 600036, Tamil Nadu, India
[2] Indian Inst Technol, Low Temp Lab, Dept Phys, Madras 600036, Tamil Nadu, India
关键词
carbon nanotubes; chemical vapour deposition; alloy hydride; DyNi2 alloy hydride; flexible graphitized carbon cloth; CNT field emitter; Fowler-Nordheim theory; nanocrystalline metal cluster;
D O I
10.1007/s11051-007-9240-8
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The present work describes the field emission characteristics of nanocrystalline metal clusters decorated multi walled carbon nanotubes (MWNT) field emitters fabricated over flexible graphitized carbon cloth. MWNT have been synthesized by catalytic chemical vapour decomposition (CCVD) of acetylene over Rare Earth (RE) based AB(2) (DyNi2) alloy hydride catalyst. Fine powders of RE based AB(2) alloy hydride catalysts have been prepared by hydrogen decrepitation technique. The as-grown carbon nanotubes (CNTs) are purified by acid and heat treatments and characterized using XRD, SEM and TEM. Purified MWNT have been decorated with nanocrystalline Pd, Pt and Pt-Ru metal clusters using a simple chemical reduction method. The characterization of metal decorated CNTs were done by using XRD, SEM, TEM, HRTEM and EDX. Nanocrystalline Pd, Pt and Pt-Ru metal clusters decorated MWNT field emitters have been fabricated over graphitized carbon fabric using spin coating method. The field emission characteristics have been studied using an indigenously fabricated set up and the results are discussed. The samples show excellent emission properties with a fairly stable emission current over a period of 4 h. As the presence of the graphitic layer provides strong adhesion between the nanotubes and carbon cloth, the use of graphitized carbon cloth as substrate opens new possibilities for CNT field emitters.
引用
收藏
页码:179 / 189
页数:11
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