In2Se3 Nanocubes as High Current Density Cold Cathode Materials
Source abstract
Abstract
In the present study, we report a simple method to prepare indium(III) selenide (In2Se3) nanocubes synthesized by laser ablation in aqueous medium. The morphological characterization carried out using field-emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM) reveal that the nanocubes have an average size of 70 nm. X-ray diffraction and Raman analysis clearly imply formation of pure and crystalline In2Se3 phases only, without any impurity phases, despite laser ablation being carried out in aqueous medium. In addition, the field emission and charge carrier behavior of In2Se3 nanocubes have been investigated. The laser-ablated sample shows a cubical morphology having a 70 nm average particle size. The ultrafast transient absorption spectroscopy (UTAS) suggests the slow decay behavior of charge carriers and an increase in the trap state levels after laser ablation, in contrast to the untreated bulk sample. Surprisingly, the In2Se3 nanocubes on a carbon tape emitter exhibits superior FE properties characterized by lower values of turn-on and threshold fields as compared to In2Se3 nanowire emitters and the ability to deliver very large current density ∼2656 μA/cm2 by applying a field of 9.7 V/μm. Furthermore, the In2Se3 nanocube emitter showed very good emission stability at the pre-set value 10 μA over a duration of 5 h. The superior FE characteristics of the In2Se3 nanocube emitter is attributed to unique morphology characterized by nanometric cubes and improved electrical properties, as revealed by UTAS analysis. The observed results imply the potential of In2Se3 nanocube emitters for practical applications in vacuum nano-microelectronic devices.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Quantum Dots Synthesis And Properties · Chalcogenide Semiconductor Thin Films · Laser-Ablation Synthesis of Nanoparticles
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Optical Nanomaterial Laboratory, Department of Optical Science, Tokushima University, 2-1 Minamijosanjima Cho, Tokushima 7708506, Japan
Centre for Advanced Studies in Materials Science and Condensed Matter Physics, Department of Physics, Savitribai Phule Pune University, Pune 411007, India
Funding
Government of India
References (56)
Show source-provided references
1. 10.1016/j.apsusc.2018.05.20910.1016/j.apsusc.2018.05.209 ↗
2. 10.1021/acsami.8b1019410.1021/acsami.8b10194 ↗
3. 10.1016/j.physe.2017.11.01110.1016/j.physe.2017.11.011 ↗
4. 10.1021/acs.jpcc.5b0017610.1021/acs.jpcc.5b00176 ↗
5. 10.1039/c7tc02488f10.1039/c7tc02488f ↗
6. 10.1021/nn406647310.1021/nn4066473 ↗
7. 10.1103/physrevlett.105.13680510.1103/physrevlett.105.136805 ↗
8. 10.1038/s41699-018-0074-210.1038/s41699-018-0074-2 ↗
9. 10.1021/acsami.6b1337910.1021/acsami.6b13379 ↗
10. 10.1021/acsphotonics.5b0021410.1021/acsphotonics.5b00214 ↗
11. 10.1021/acsami.7b0607110.1021/acsami.7b06071 ↗
12. 10.1038/nphoton.2015.28210.1038/nphoton.2015.282 ↗
13. 10.1063/1.479231310.1063/1.4792313 ↗
14. 10.1016/j.vacuum.2013.06.00710.1016/j.vacuum.2013.06.007 ↗
15. 10.1016/j.jallcom.2015.05.19310.1016/j.jallcom.2015.05.193 ↗
16. 10.1016/j.jallcom.2014.03.12910.1016/j.jallcom.2014.03.129 ↗
17. 10.1016/j.sse.2012.10.00710.1016/j.sse.2012.10.007 ↗
18. 10.1364/ome.9.00044910.1364/ome.9.000449 ↗
19. 10.1016/j.apcatb.2015.03.04810.1016/j.apcatb.2015.03.048 ↗
20. 10.1016/j.apsusc.2015.01.08210.1016/j.apsusc.2015.01.082 ↗
21. 10.1002/adfm.20150420210.1002/adfm.201504202 ↗
22. 10.1016/s1010-6030(01)00583-410.1016/s1010-6030(01)00583-4 ↗
23. 10.1039/b305434a10.1039/b305434a ↗
24. 10.1021/acs.nanolett.7b0528310.1021/acs.nanolett.7b05283 ↗
25. 10.1016/j.susc.2015.08.01110.1016/j.susc.2015.08.011 ↗
26. 10.1063/1.482855810.1063/1.4828558 ↗
27. 10.1016/j.omx.2019.10002610.1016/j.omx.2019.100026 ↗
28. 10.1142/9789814503464_008710.1142/9789814503464_0087 ↗
29. 10.1021/am404461810.1021/am4044618 ↗
30. 10.1063/1.496326010.1063/1.4963260 ↗
31. 10.3390/nano905071710.3390/nano9050717 ↗
32. 10.1002/smll.20130000210.1002/smll.201300002 ↗
33. 10.1002/adfm.20170611310.1002/adfm.201706113 ↗
34. 10.1016/j.materresbull.2019.04.01510.1016/j.materresbull.2019.04.015 ↗
35. 10.1002/smll.20130334010.1002/smll.201303340 ↗
36. 10.1038/s41598-019-39605-410.1038/s41598-019-39605-4 ↗
37. 10.1039/C8NR09068H10.1039/C8NR09068H ↗
38. 10.1002/aelm.20190012810.1002/aelm.201900128 ↗
39. 10.1039/c4tc00025k10.1039/c4tc00025k ↗
40. 10.1039/d0ce00347f10.1039/d0ce00347f ↗
41. 10.1002/ejic.20140244810.1002/ejic.201402448 ↗
42. 10.1016/j.ultramic.2014.10.00410.1016/j.ultramic.2014.10.004 ↗
43. 10.1063/1.491781710.1063/1.4917817 ↗
44. 10.1139/cjc-2016-056910.1139/cjc-2016-0569 ↗
45. 10.1021/acs.inorgchem.8b0077810.1021/acs.inorgchem.8b00778 ↗
46. 10.1021/jp047134+10.1021/jp047134+ ↗
47. 10.1002/chem.20040092710.1002/chem.200400927 ↗
48. 10.1021/jacs.5b0464110.1021/jacs.5b04641 ↗
49. 10.1016/j.jallcom.2018.09.33510.1016/j.jallcom.2018.09.335 ↗
50. 10.1039/c2dt32589f10.1039/c2dt32589f ↗
51. 10.1021/am400128e10.1021/am400128e ↗
52. 10.1039/c7nr05149b10.1039/c7nr05149b ↗
53. 10.1039/c5ra10160c10.1039/c5ra10160c ↗
54. 10.1021/am200099c10.1021/am200099c ↗
55. 10.1016/j.matlet.2008.01.02210.1016/j.matlet.2008.01.022 ↗
56. 10.1007/s12648-018-1276-310.1007/s12648-018-1276-3 ↗