journal article·2021-03Open access

Contact‐Barrier Free, High Mobility, Dual‐Gated Junctionless Transistor Using Tellurium Nanowire

Pushkar Dasika, Debadarshini Samantaray, Krishna Murali, Nithin Abraham, Kenji Watanbe, Takashi Taniguchi, N Ravishankar, Kausik Majumdar

Advanced Functional Materials· Volume 31· Issue 13

Abstract

Abstract The gate‐all‐around nanowire transistor, due to its extremely tight electrostatic control and vertical integration capability, is a highly promising candidate for sub‐5 nm technology nodes. In particular, the junctionless nanowire transistors are highly scalable with reduced variability due to avoidance of steep source/drain junction formation by ion implantation. Here a dual‐gated junctionless nanowire p‐type field effect transistor is demonstrated using tellurium nanowire as the channel. The dangling‐bond‐free surface due to the unique helical crystal structure of the nanowire, coupled with an integration of dangling‐bond‐free, high quality hBN gate dielectric, allows for a phonon‐limited field effect hole mobility of 570 cm2 V−1 s−1 at 270 K, which is well above state‐of‐the‐art strained Si hole mobility. By lowering the temperature, the mobility increases to 1390 cm2 V−1 s−1 and becomes primarily limited by Coulomb scattering. The combination of an electron affinity of ≈4 eV and a small bandgap of tellurium provides zero Schottky barrier height for hole injection at the metal‐contact interface, which is remarkable for reduction of contact resistance in a highly scaled transistor. Exploiting these properties, coupled with the dual‐gated operation, we achieve a high drive current of 216 μA μm−1 while maintaining an on‐off ratio in excess of 2 × 104. The findings have intriguing prospects for alternate channel material based next‐generation electronics.
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Research context

OpenAlex topics: Advancements in Semiconductor Devices and Circuit Design · Nanowire Synthesis and Applications · Semiconductor materials and devices

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Electrical Communication Engineering Indian Institute of Science Bangalore 560012 India

Materials Research Center Indian Institute of Science Bangalore 560012 India

Research Center for Functional Materials National Institute for Materials Science 1‐1 Namiki Tsukuba 305‐044 Japan

International Center for Materials Nanoarchitectonics National Institute for Materials Science 1‐1 Namiki Tsukuba 305‐044 Japan

Funding

Indian Space Research Organisation · Ministry of Human Resource Development · Science and Engineering Research Board · Ministry of Electronics and Information technology · Ministry of Education, Culture, Sports, Science and Technology · Japan Society for the Promotion of Science

References (52)

Show source-provided references
1. 10.1021/nl025875l10.1021/nl025875l ↗
2. 10.1109/LED.2006.87338110.1109/LED.2006.873381 ↗
3. 10.1109/TED.2008.200801110.1109/TED.2008.2008011 ↗
4. 10.1109/TED.2012.219312910.1109/TED.2012.2193129 ↗
5. 10.1109/MM.2017.424134710.1109/MM.2017.4241347 ↗
6. L.Armasu2019 https://www.tomshardware.com/news/samsung‐3nm‐gaafet‐production‐2021 38426.html(accessed: June 2020).
7. 10.1021/acs.nanolett.5b0492610.1021/acs.nanolett.5b04926 ↗
8. 10.1109/VLSIT.2012.624251310.1109/VLSIT.2012.6242513 ↗
9. 10.1109/LED.2007.89126810.1109/LED.2007.891268 ↗
10. 10.1063/1.161164410.1063/1.1611644 ↗
11. 10.1063/1.307941110.1063/1.3079411 ↗
12. 10.1109/LED.2011.216230910.1109/LED.2011.2162309 ↗
13. 10.1063/1.280258610.1063/1.2802586 ↗
14. 10.1063/1.297775810.1063/1.2977758 ↗
15. 10.1109/TED.2010.205217110.1109/TED.2010.2052171 ↗
16. 10.1016/j.matchemphys.2008.07.10110.1016/j.matchemphys.2008.07.101 ↗
17. 10.1038/s41928-020-0365-410.1038/s41928-020-0365-4 ↗
18. 10.1021/acsnano.7b0222510.1021/acsnano.7b02225 ↗
19. 10.1038/s41565-019-0585-910.1038/s41565-019-0585-9 ↗
20. 10.1103/PhysRevLett.119.10610110.1103/PhysRevLett.119.106101 ↗
21. 10.1021/acsami.6b1206410.1021/acsami.6b12064 ↗
22. 10.1002/adma.20130065710.1002/adma.201300657 ↗
23. 10.1039/C7NR01860F10.1039/C7NR01860F ↗
24. 10.1021/acs.nanolett.8b0514410.1021/acs.nanolett.8b05144 ↗
25. Lin S. · Nature Commun. · 2016 · 7 · 1
26. 10.1103/PhysRevB.4.35610.1103/PhysRevB.4.356 ↗
27. 10.1021/acs.nanolett.7b0171710.1021/acs.nanolett.7b01717 ↗
28. 10.1021/la100772n10.1021/la100772n ↗
29. 10.1021/cg701125k10.1021/cg701125k ↗
30. 10.1088/2053-1583/1/1/01100210.1088/2053-1583/1/1/011002 ↗
31. 10.1021/la06327210.1021/la063272 ↗
32. 10.1021/acsnano.7b0353110.1021/acsnano.7b03531 ↗
33. 10.1007/s00460005008510.1007/s004600050085 ↗
34. 10.1038/s41928-018-0058-410.1038/s41928-018-0058-4 ↗
35. 10.1021/nl051855i10.1021/nl051855i ↗
36. 10.1021/nn900284b10.1021/nn900284b ↗
37. Pierret R. F. · 1996
38. 10.1016/j.mejo.2007.07.05010.1016/j.mejo.2007.07.050 ↗
39. 10.1002/047006832910.1002/0470068329 ↗
40. 10.1021/nl071330l10.1021/nl071330l ↗
41. 10.1063/1.233785310.1063/1.2337853 ↗
42. 10.1038/nnano.2013.3010.1038/nnano.2013.30 ↗
43. 10.1515/jnum-2012-001310.1515/jnum-2012-0013 ↗
44. 10.1021/nl304182j10.1021/nl304182j ↗
45. 10.1063/1.492110910.1063/1.4921109 ↗
46. 10.1109/TED.2012.218570110.1109/TED.2012.2185701 ↗
47. 10.1109/16.33744910.1109/16.337449 ↗
48. 10.1103/PhysRevB.88.16531610.1103/PhysRevB.88.165316 ↗
49. 10.1038/nmat368710.1038/nmat3687 ↗
50. 10.1021/acsnano.8b0342410.1021/acsnano.8b03424 ↗
51. 10.1002/adma.20180310910.1002/adma.201803109 ↗
52. 10.1038/s41467-020-16125-810.1038/s41467-020-16125-8 ↗