journal article·2020-06-10

Self-Terminated Surface Monolayer Oxidation Induced Robust Degenerate Doping in MoTe2 for Low Contact Resistance

Xiaochi Liu, Deshun Qu, Yahua Yuan, Jian Sun, Won Jong Yoo

ACS Applied Materials & Interfaces· Volume 12· Issue 23
Publisher page

Abstract

We introduce an effective method to degenerately dope MoTe2 by oxidizing its surface into the p-dopant MoOx in oxygen plasma. As a self-terminated process, the oxidation is restricted only in the very top layer, therefore offering us an easy and efficient control. The degenerate p-doping with the hole concentration of 2.5 × 1013 cm–2 can be obtained by applying a ∼300 s O2 plasma treatment. Using the degenerately doped MoTe2, we demonstrate a record low contact resistance of 0.6 kΩ μm for MoTe2. Our measurement highlights an excellent stability for the plasma-doped MoTe2. The doped characteristics are robust with no significant degradation even after a one-year exposure to the air. The oxygen plasma doping technique is compatible with the conventional semiconductor processes, which can be utilized to realize high-performance MoTe2 field-effect transistors (FETs) or tunnel FETs in the future.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: 2D Materials and Applications · Molecular Junctions and Nanostructures · Graphene research and applications

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

Affiliations

School of Physics and Electronics, Central South University, 932 South Lushan Road, Changsha 410083, China

SKKU Advanced Institute of Nano-Technology (SAINT), Sungkyunkwan University, 2066 Seobu-ro, Jangan-gu, Suwon, Gyeonggi-do 16419, Republic of Korea

Funding

Hunan Provincial Science and Technology Department · National Research Foundation of Korea · National Natural Science Foundation of China

References (31)

Show source-provided references
1. 10.1016/j.mattod.2016.10.00210.1016/j.mattod.2016.10.002 ↗
2. 10.1038/natrevmats.2016.5210.1038/natrevmats.2016.52 ↗
3. 10.1021/acsnano.5b0073610.1021/acsnano.5b00736 ↗
4. 10.1063/1.490152710.1063/1.4901527 ↗
5. 10.1021/acsnano.7b0130610.1021/acsnano.7b01306 ↗
6. 10.1038/nmat445210.1038/nmat4452 ↗
7. 10.1063/1.496329010.1063/1.4963290 ↗
8. 10.1039/c5nr01044f10.1039/c5nr01044f ↗
9. 10.1021/nl303583v10.1021/nl303583v ↗
10. 10.1038/nmat408010.1038/nmat4080 ↗
11. 10.1021/acs.nanolett.7b0153610.1021/acs.nanolett.7b01536 ↗
12. 10.1038/s41586-018-0129-810.1038/s41586-018-0129-8 ↗
13. 10.1126/science.aab317510.1126/science.aab3175 ↗
14. 10.1021/acs.nanolett.5b0506610.1021/acs.nanolett.5b05066 ↗
15. 10.1021/nl504975310.1021/nl5049753 ↗
16. 10.1021/acs.nanolett.6b0039010.1021/acs.nanolett.6b00390 ↗
17. 10.1021/acsami.8b1100310.1021/acsami.8b11003 ↗
18. 10.3390/nano905075610.3390/nano9050756 ↗
19. 10.1073/pnas.161718611410.1073/pnas.1617186114 ↗
20. 10.1016/s0039-6028(01)00714-210.1016/s0039-6028(01)00714-2 ↗
21. 10.1016/s0169-4332(03)00697-410.1016/s0169-4332(03)00697-4 ↗
22. 10.1021/acsnano.5b0652910.1021/acsnano.5b06529 ↗
23. 10.1002/adma.20160643310.1002/adma.201606433 ↗
24. 10.1088/1361-6528/aaebc510.1088/1361-6528/aaebc5 ↗
25. 10.1021/acs.nanolett.9b0061310.1021/acs.nanolett.9b00613 ↗
26. 10.1088/2053-1583/3/2/02501010.1088/2053-1583/3/2/025010 ↗
27. 10.1039/c8nr05699d10.1039/c8nr05699d ↗
28. 10.1021/ja503332710.1021/ja5033327 ↗
29. 10.1016/j.ssc.2014.09.02710.1016/j.ssc.2014.09.027 ↗
30. 10.1021/nl503251h10.1021/nl503251h ↗
31. 10.1002/pssr.20190020810.1002/pssr.201900208 ↗