Single step hydrothermal approach for devising hierarchical Ag-ZnO heterostructures with significant enhancement in field emission performance

被引:29
作者
Warule, Sambhaji S. [1 ,2 ]
Chaudhari, Nilima S. [1 ]
Khare, Ruchita T. [2 ]
Ambekar, Jalinder D. [1 ]
Kale, Bharat B. [1 ]
More, Mahendra A. [2 ]
机构
[1] Govt India, C MET, Dept Informat Technol, Pune 411008, Maharashtra, India
[2] Univ Pune, Ctr Adv Studies Mat Sci & Condensed Matter Phys, Dept Phys, Pune 411007, Maharashtra, India
来源
CRYSTENGCOMM | 2013年 / 15卷 / 37期
关键词
ONE-POT SYNTHESIS; ELECTRON-EMISSION; NANOPARTICLES; NANORODS; NANOCRYSTALS; NANOWIRES; PHOTOLUMINESCENCE; FABRICATION; GROWTH; CARBON;
D O I
10.1039/c3ce40792f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hierarchical Ag-ZnO heterostructures have been synthesized via a template free single step hydrothermal method. Structural and morphological studies reveal the formation of heterostructures comprised of Ag nanoparticles (similar to 20 nm) organized on tapered ZnO nanorods under the prevailing experimental conditions. A plausible reaction and growth mechanism has been discussed. Furthermore, the hierarchical creation of ZnO with Ag as a relatively low work function material offers an effective approach to tailor its field emission properties. The field emission studies reveal a remarkable low turn-on field of similar to 1 V mu m(-1), corresponding to an emission current density of similar to 10 mu A cm(-2), and an emission current density of similar to 400 mu A cm(-2) has been drawn at an applied field of 2.24 V mu m(-1). In addition, the Ag-ZnO heterostructures exhibit a good emission current stability at the pre-set value of similar to 1 and 4 mu A over a duration of 3 h. The enhancement of the field emission characteristics resulting from Ag nanoparticles decorating the tapered ZnO nanorods is discussed on the basis of band structure modifications. The ease of the synthesis route and the remarkable field emission properties offer Ag-ZnO heterostructures as a promising electron source for high current density applications.
引用
收藏
页码:7475 / 7483
页数:9
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