journal article·2022-12-27

A “Click” Reaction to Engineer MoS2 Field-Effect Transistors with Low Contact Resistance

Jialei Miao, Linlu Wu, Zheng Bian, Qinghai Zhu, Tianjiao Zhang, Xin Pan, Jiayang Hu, Wei Xu, Yeliang Wang, Yang Xu, Bin Yu, Wei Ji, Xiaowei Zhang, Jingsi Qiao, Paolo Samorì, Yuda Zhao

ACS Nano· Volume 16· Issue 12
Publisher page

Abstract

Two-dimensional (2D) materials with the atomically thin thickness have attracted great interest in the post-Moore’s Law era because of their tremendous potential to continue transistor downscaling and offered advances in device performance at the atomic limit. However, the metal–semiconductor contact is the bottleneck in field-effect transistors (FETs) integrating 2D semiconductors as channel materials. A robust and tunable doping method at the source and drain region of 2D transistors to minimize the contact resistance is highly sought after. Here we report a stable carrier doping method via the mild covalent grafting of maleimides on the surface of 2D transition metal dichalcogenides. The chemisorbed interaction contributes to the efficient carrier doping without degrading the high-performance carrier transport. Density functional theory results further illustrate that the molecular functionalization leads to the mild hybridization and the negligible impact on the conduction bands of monolayer MoS2, avoiding the random scattering from the dopants. Differently from reported molecular treatments, our strategy displays high thermal stability (above 300 °C) and it is compatible with micro/nano processing technology. The contact resistance of MoS2 FETs can be greatly reduced by ∼12 times after molecular functionalization. The Schottky barrier of 44 meV is achieved on monolayer MoS2 FETs, demonstrating efficient charge injection between metal and 2D semiconductor. The mild covalent functionalization of molecules on 2D semiconductors represents a powerful strategy to perform the carrier doping and the device optimization.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: 2D Materials and Applications · MXene and MAX Phase Materials · Graphene research and applications

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

Affiliations

School of Micro-Nano Electronics, Hangzhou Global Scientific and Technological Innovation Centre, Zhejiang University, 38 Zheda Road, Hangzhou310027, China

Department of Electrical Engineering and Computer Science, Ningbo University, Ningbo315211, China

Beijing Key Laboratory of Optoelectronic Functional Materials & Micro-Nano Devices, Department of Physics, Renmin University of China, Beijing100872, China

Research Centre for Humanoid Sensing, Zhejiang Lab, Hangzhou311121, China

MIIT Key Laboratory for Low-Dimensional Quantum Structure and Devices, School of Integrated Circuits and Electronics, Beijing Institute of Technology, Beijing100081, China

University of Strasbourg, CNRS, ISIS UMR 7006, 8 allée Gaspard Monge, F-67000Strasbourg, France

Key Laboratory of Optoelectronic Chemical Materials and Devices of Ministry of Education, Jianghan University, Wuhan430056, China

Funding

China Association for Science and Technology · European Commission · Ministry of Science and Technology of the People's Republic of China · Renmin University of China · National Natural Science Foundation of China · Institut Universitaire de France · H2020 European Research Council · Key Laboratory of Optoelectronic Chemical Materials and Devices · Kun-Peng Program of Zhejiang Province

References (36)

Show source-provided references
1. 10.1038/nmat445210.1038/nmat4452 ↗
2. 10.1021/acsnano.6b0184210.1021/acsnano.6b01842 ↗
3. 10.1002/adfm.20160348410.1002/adfm.201603484 ↗
4. 10.1038/s41586-018-0129-810.1038/s41586-018-0129-8 ↗
5. 10.1038/nmat408010.1038/nmat4080 ↗
6. 10.1038/s41586-021-03472-910.1038/s41586-021-03472-9 ↗
7. 10.1002/adma.20170554010.1002/adma.201705540 ↗
8. 10.1021/ja503332710.1021/ja5033327 ↗
9. 10.1002/adfm.20180733810.1002/adfm.201807338 ↗
10. 10.1021/nl301702r10.1021/nl301702r ↗
11. 10.1021/acsaelm.1c0022510.1021/acsaelm.1c00225 ↗
12. 10.1021/jacs.8b1093010.1021/jacs.8b10930 ↗
13. 10.1002/pssb.20170018410.1002/pssb.201700184 ↗
14. 10.1021/nl403036h10.1021/nl403036h ↗
15. 10.1038/nmat350510.1038/nmat3505 ↗
16. 10.1021/acsnano.5b0134110.1021/acsnano.5b01341 ↗
17. 10.1021/acsami.0c1754410.1021/acsami.0c17544 ↗
18. 10.1021/acs.chemrev.1c0049710.1021/acs.chemrev.1c00497 ↗
19. 10.1103/PhysRevX.4.03100510.1103/PhysRevX.4.031005 ↗
20. 10.1021/acsnano.6b0715910.1021/acsnano.6b07159 ↗
21. 10.1038/nmat368710.1038/nmat3687 ↗
22. 10.1103/PhysRevB.85.11531710.1103/PhysRevB.85.115317 ↗
23. 10.1103/PhysRev.163.74310.1103/PhysRev.163.743 ↗
24. 10.1021/nl504957p10.1021/nl504957p ↗
25. 10.1021/acs.nanolett.5b0372710.1021/acs.nanolett.5b03727 ↗
26. 10.1021/nl303583v10.1021/nl303583v ↗
27. 10.1021/nl401015710.1021/nl4010157 ↗
28. 10.1021/acs.nanolett.7b0153610.1021/acs.nanolett.7b01536 ↗
29. 10.1002/adma.20160275710.1002/adma.201602757 ↗
30. 10.1103/PhysRevB.50.1795310.1103/PhysRevB.50.17953 ↗
31. 10.1103/PhysRevB.59.175810.1103/PhysRevB.59.1758 ↗
32. 10.1103/PhysRevLett.92.24640110.1103/PhysRevLett.92.246401 ↗
33. 10.1103/PhysRevB.82.08110110.1103/PhysRevB.82.081101 ↗
34. 10.1103/PhysRevB.83.19513110.1103/PhysRevB.83.195131 ↗
35. 10.1039/C5NR06293D10.1039/C5NR06293D ↗
36. 10.1002/adma.20150457210.1002/adma.201504572 ↗