Enhancement of field electron emission in topological insulator Bi2Se3 by Ni doping

被引:16
作者
Mazumder, Kushal [1 ]
Sharma, Alfa [2 ]
Kumar, Yogendra [2 ]
Bankar, Prashant [3 ,4 ]
More, Mahendra A. [4 ]
Devan, Rupesh [2 ]
Shirage, Parasharam M. [1 ,2 ]
机构
[1] Indian Inst Technol Indore, Discipline Phys, Simrol Campus,Khandwa Rd, Indore 453552, Madhya Pradesh, India
[2] Indian Inst Technol Indore, Discipline Met Engn & Mat Sci, Simrol Campus,Khandwa Rd, Indore 453552, Madhya Pradesh, India
[3] Natl Chem Lab, Phys & Mat Chem Div, CSIR, Dr Homi Bhabha Rd, Pune 411008, Maharashtra, India
[4] Savitribai Phule Pune Univ, Dept Phys, Pune 411007, Maharashtra, India
关键词
CARBON NANOTUBES; NANOSTRUCTURES; NANOSHEETS; SURFACE; NANORIBBONS; CONDUCTION; NANORODS; EMITTER; ARRAYS;
D O I
10.1039/c8cp01982g
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Nanostructures of bismuth selenide (Bi2Se3), a 3D topological insulator material, and nickel (Ni) doped Bi2Se3 samples were prepared by a hydrothermal method to explore the field emission properties. An enrichment in the field electron emission (FE) properties in terms of the threshold and turn-on field values of Bi2Se3 and Ni doped Bi2Se3 nanostructures was measured at a base pressure of similar to 1 x 10(-8) mbar. Using the background of the Fowler-Nordheim (FN) theory a field enhancement factor (beta) of 5.7 x 10(3) and a threshold field value of 2.5 V mu m(-1) for 7.5% Ni doped Bi2Se3 were determined by investigating the J-E plot of the FE data. The value of beta is three times higher than that of pure Bi2Se3 confirming the superior FE properties. The emission current was found to be very stable with the property of long standing durability as a negligible amount of variation was observed when measured at a constant value of 5 mA for 3 hours. The experimental results signify many opportunities for potential applications of Ni doped Bi2Se3 as a source of electrons in scanning as well as transmission electron microscopy, flat panel displays and as an X-ray generator, etc.
引用
收藏
页码:18429 / 18435
页数:7
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