Formation of InN nanoparticle and nanorod structures by nitrogen plasma annealing method
Source abstract
Abstract
In the present study, a novel method involving nitrogen plasma annealing has been reported for preparing InN nanoparticle/nanorod structures and for improving the properties of InN nanoparticle layers. Plasma annealed structures have been characterized by X-ray diffraction, atomic force microscopy and photoluminescence spectroscopy techniques. InN nanoparticle layers have been prepared using activated reactive evaporation set up. It has been observed that there is a remarkable improvement in the conductivity and crystallinity of InN nanoparticle layers on annealing in nitrogen plasma. This has been attributed to the increase in the nitrogen content of the samples. Experiments involving plasma annealing of In nanorods deposited oxide template has also been carried out. It was found that on plasma treatment In nanorods get converted to mixed phase InN nanorods with hexagonal and cubic fractions.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: GaN-based semiconductor devices and materials · ZnO doping and properties · Semiconductor Quantum Structures and Devices
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (17)
Show source-provided references
1. Bhuiyan A G, Hashimoto A and Yamamoto A 2003 J. Appl. Phys. 94 277910.1063/1.1595135 ↗
2. Butcher K S A and Tansley T L 2005 Superlattices and Microstructures 38 110.1016/j.spmi.2005.03.004 ↗
3. Chai X M, Cheung K Y Djurišić and Xie M H 2007 Mater. Lett. 61 156310.1016/j.matlet.2006.07.079 ↗
4. Davydov Y Yu et al 2002 Phys. Status Solidi (b) 229 R110.1002/1521-3951(200202)229:3<R1::AID-PSSB99991>3.0.CO;2-O ↗
5. Fu S P and Chen Y F 2004 Appl. Phys. Lett. 85 152310.1063/1.1787615 ↗
6. Guha P, Kar S and Chaudhuri S 2004 Appl. Phys. Lett. 85 385110.1063/1.1808886 ↗
7. Inushima T, Mamutin V V, Vekshin V A, Ivanov S V, Sakon T, Motokawa M and Ohoya S 2001 J. Cryst. Growth 227–228 48110.1016/S0022-0248(01)00747-3 ↗
8. Koukitu A, Takahashi N and Seki H 1997 Jpn J. Appl. Phys. 36 L113610.1143/JJAP.36.L1136 ↗
9. Mahboob I, Veal T D, McConville C F, Lu H and Schaff W J 2004 Phys. Rev. Lett. 92 03680410.1103/PhysRevLett.92.036804 ↗
10. Mann A K, Varandani D, Mehta B R, Malhotra L K and Shivaprasad S M 2005 J. Nanosci. Nanotechnol. 5 185810.1166/jnn.2005.424 ↗
11. Mann A K, Varandani D, Mehta B R and Malhotra L K 2007 J. Appl. Phys. 101 08430410.1063/1.2718289 ↗
12. Nakamura T, Tokumoto Y, Katayama R, Yamamoto T and Onabe K 2007 J. Crystal Growth 301–302 50810.1016/j.jcrysgro.2006.11.046 ↗
13. Tansley T L and Foley C P 1986 J. Appl. Phys. 59 324110.1063/1.336906 ↗
14. Wu J et al 2002 Appl. Phys. Lett. 80 396710.1063/1.1482786 ↗
15. Wu J et al 2004 Appl. Phys. Lett. 84 280510.1063/1.1704853 ↗
16. Xiao J, Xie Y, Tang R and Luo W 2003 Inorg. Chem. 42 10710.1021/ic0258330 ↗
17. Yodo T, Yona H, Ando H, Nosei D and Harada Y 2002 Appl. Phys. Lett. 80 96810.1063/1.1450255 ↗