Influence of Asymmetric Contact Form on Contact Resistance and Schottky Barrier, and Corresponding Applications of Diode
Source abstract
Abstract
We have fabricated carbon nanotube and MoS 2 field-effect transistors with asymmetric contact forms of source–drain electrodes, from which we found the current directionality of the devices and different contact resistances under the two current directions. By designing various structures, we can conclude that the asymmetric electrical performance was caused by the difference in the effective Schottky barrier height (Φ SB ) caused by the different contact forms. A detailed temperature-dependent study was used to extract and compare the Φ SB for both contact forms of CNT and MoS 2 devices; we found that the Φ SB for the metal-on-semiconductor form was much lower than that of the semiconductor-on-metal form and is suitable for all p-type, n-type, or ambipolar semiconductors. This conclusion is meaningful with respect to the design and application of nanomaterial electronic devices. Additionally, using the difference in barrier height caused by the contact forms, we have also proposed and fabricated Schottky barrier diodes with a current ratio up to 10 4; rectifying circuits consisting of these diodes were able to work in a wide frequency range. This design avoided the use of complex chemical doping or heterojunction methods to achieve fundamental diodes that are relatively simple and use only a single material; these may be suitable for future application in nanoelectronic radio frequency or integrated circuits.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: 2D Materials and Applications · Semiconductor materials and interfaces · Adhesion, Friction, and Surface Interactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Low-Dimensional Quantum Physics, Department of Physics and Tsinghua-Foxconn Nanotechnology Research Center, Tsinghua University, Beijing 100084, China
Collaborative Innovation Center of Quantum Matter, Beijing 100084, China
Funding
Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China
References (66)
Show source-provided references
1. 10.1021/cr900296210.1021/cr9002962 ↗
2. 10.1021/acsnano.5b0672610.1021/acsnano.5b06726 ↗
3. 10.1002/adma.20130226510.1002/adma.201302265 ↗
4. 10.1021/nn302617210.1021/nn3026172 ↗
5. 10.1038/nnano.2011.110.1038/nnano.2011.1 ↗
6. 10.1021/nn505941910.1021/nn5059419 ↗
7. 10.1103/PhysRevLett.84.294110.1103/PhysRevLett.84.2941 ↗
8. 10.1021/nl025577o10.1021/nl025577o ↗
9. 10.1021/nl303583v10.1021/nl303583v ↗
10. 10.1002/adma.20140139510.1002/adma.201401395 ↗
11. 10.1038/nnano.2010.27910.1038/nnano.2010.279 ↗
12. 10.1103/PhysRevB.67.03340710.1103/PhysRevB.67.033407 ↗
13. 10.1021/nl301335q10.1021/nl301335q ↗
14. 10.1126/science.aac800610.1126/science.aac8006 ↗
15. 10.1021/nl203701g10.1021/nl203701g ↗
16. 10.1039/C6NR00876C10.1039/C6NR00876C ↗
17. 10.1021/nl303583v10.1021/nl303583v ↗
18. 10.1021/nl035185x10.1021/nl035185x ↗
19. 10.1088/0957-4484/19/11/11520310.1088/0957-4484/19/11/115203 ↗
20. 10.1103/PhysRevLett.84.469310.1103/PhysRevLett.84.4693 ↗
21. 10.1002/pssa.20072352810.1002/pssa.200723528 ↗
22. 10.1038/nmat445210.1038/nmat4452 ↗
23. 10.1038/nnano.2011.610.1038/nnano.2011.6 ↗
24. 10.1021/nl503897h10.1021/nl503897h ↗
25. 10.1021/nl502075n10.1021/nl502075n ↗
26. 10.1021/acsnano.6b0184210.1021/acsnano.6b01842 ↗
27. 10.1021/nl503748410.1021/nl5037484 ↗
28. 10.1021/nl050829h10.1021/nl050829h ↗
29. 10.1063/1.219070710.1063/1.2190707 ↗
30. 10.1063/1.293909510.1063/1.2939095 ↗
31. 10.1021/nl071905e10.1021/nl071905e ↗
32. 10.1063/1.482360210.1063/1.4823602 ↗
33. 10.1038/srep1044010.1038/srep10440 ↗
34. 10.1002/adma.20070321010.1002/adma.200703210 ↗
35. 10.1016/j.carbon.2009.12.00310.1016/j.carbon.2009.12.003 ↗
36. 10.1038/srep2220310.1038/srep22203 ↗
37. 10.1002/adma.20150371510.1002/adma.201503715 ↗
38. 10.1038/nnano.2010.22010.1038/nnano.2010.220 ↗
39. 10.1021/nn302185d10.1021/nn302185d ↗
40. 10.1021/nn305277d10.1021/nn305277d ↗
41. 10.1021/nn504873410.1021/nn5048734 ↗
42. 10.1021/nl401015710.1021/nl4010157 ↗
43. 10.1002/adma.20160275710.1002/adma.201602757 ↗
44. 10.1103/PhysRevLett.92.04830110.1103/PhysRevLett.92.048301 ↗
45. 10.1002/smll.20160039810.1002/smll.201600398 ↗
46. 10.1021/nl049745j10.1021/nl049745j ↗
47. 10.1088/0957-4484/16/8/07410.1088/0957-4484/16/8/074 ↗
48. 10.1021/nn301302n10.1021/nn301302n ↗
49. 10.1021/nl034700o10.1021/nl034700o ↗
50. 10.1088/0957-4484/20/19/19520210.1088/0957-4484/20/19/195202 ↗
51. 10.1103/PhysRevLett.89.10680110.1103/PhysRevLett.89.106801 ↗
52. Sze S. M. · 200610.1002/0470068329 ↗
53. 10.1038/srep0692810.1038/srep06928 ↗
54. 10.1016/j.carbon.2016.07.03310.1016/j.carbon.2016.07.033 ↗
55. 10.1021/nl403465v10.1021/nl403465v ↗
56. 10.1103/PhysRevX.4.03100510.1103/PhysRevX.4.031005 ↗
57. 10.1021/acsami.6b1669210.1021/acsami.6b16692 ↗
58. 10.1039/C6CP02132H10.1039/C6CP02132H ↗
59. 10.1088/1361-6463/aa61d910.1088/1361-6463/aa61d9 ↗
60. 10.1021/acsnano.6b0212610.1021/acsnano.6b02126 ↗
61. 10.1021/acs.nanolett.6b0204610.1021/acs.nanolett.6b02046 ↗
62. 10.1126/science.aaj162810.1126/science.aaj1628 ↗
63. 10.1038/ncomms168210.1038/ncomms1682 ↗
64. 10.1021/nn901251610.1021/nn9012516 ↗
65. 10.1021/acsnano.5b0423310.1021/acsnano.5b04233 ↗
66. 10.1002/aelm.20160048310.1002/aelm.201600483 ↗