journal article·2017-04

In‐Plane 2H‐1T′ MoTe2 Homojunctions Synthesized by Flux‐Controlled Phase Engineering

Youngdong Yoo, Zachary P. DeGregorio, Yang Su, Steven J. Koester, James E. Johns

Advanced Materials· Volume 29· Issue 16
Publisher page

Abstract

The fabrication of in‐plane 2H‐1T′ MoTe2 homojunctions by the flux‐controlled, phase‐engineering of few‐layer MoTe2 from Mo nanoislands is reported. The phase of few‐layer MoTe2 is controlled by simply changing Te atomic flux controlled by the temperature of the reaction vessel. Few‐layer 2H MoTe2 is formed with high Te flux, while few‐layer 1T′ MoTe2 is obtained with low Te flux. With medium flux, few‐layer in‐plane 2H‐1T′ MoTe2 homojunctions are synthesized. As‐synthesized MoTe2 is characterized by Raman spectroscopy and X‐ray photoelectron spectroscopy. Kelvin probe force microscopy and Raman mapping confirm that in‐plane 2H‐1T′ MoTe2 homojunctions have abrupt interfaces between 2H and 1T′ MoTe2 domains, possessing a potential difference of about 100 mV. It is further shown that this method can be extended to create patterned metal–semiconductor junctions in MoTe2 in a two‐step lithographic synthesis. The flux‐controlled phase engineering method could be utilized for the large‐scale controlled fabrication of 2D metal–semiconductor junctions for next‐generation electronic and optoelectronic devices.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: 2D Materials and Applications · MXene and MAX Phase Materials · Perovskite Materials and Applications

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

Affiliations

Department of Chemistry University of Minnesota Minneapolis MN 55455 USA

Department of Electrical and Computer Engineering University of Minnesota Minneapolis MN 55455 USA

Funding

American Chemical Society Petroleum Research Fund · National Science Foundation

References (37)

Show source-provided references
1. 10.1038/nnano.2012.19310.1038/nnano.2012.193 ↗
2. 10.1038/nchem.158910.1038/nchem.1589 ↗
3. 10.1021/ar500284610.1021/ar5002846 ↗
4. 10.1021/nn400280c10.1021/nn400280c ↗
5. 10.1103/PhysRevLett.105.13680510.1103/PhysRevLett.105.136805 ↗
6. 10.1103/PhysRevLett.108.19680210.1103/PhysRevLett.108.196802 ↗
7. 10.1002/adma.20110479810.1002/adma.201104798 ↗
8. 10.1002/adma.20130438910.1002/adma.201304389 ↗
9. 10.1002/adma.20150477910.1002/adma.201504779 ↗
10. 10.1002/adma.20150394510.1002/adma.201503945 ↗
11. 10.1002/adma.20160027810.1002/adma.201600278 ↗
12. 10.1038/nmat408010.1038/nmat4080 ↗
13. 10.1038/ncomms521410.1038/ncomms5214 ↗
14. 10.1021/acs.chemmater.5b0098610.1021/acs.chemmater.5b00986 ↗
15. 10.1021/nl502557g10.1021/nl502557g ↗
16. 10.1021/acs.nanolett.6b0074810.1021/acs.nanolett.6b00748 ↗
17. 10.1021/nl504500710.1021/nl5045007 ↗
18. 10.1002/adma.20150258510.1002/adma.201502585 ↗
19. 10.1126/science.aab317510.1126/science.aab3175 ↗
20. 10.1021/acs.nanolett.5b0348110.1021/acs.nanolett.5b03481 ↗
21. 10.1038/nphys331410.1038/nphys3314 ↗
22. 10.1038/nmat468510.1038/nmat4685 ↗
23. 10.1038/nmat409110.1038/nmat4091 ↗
24. 10.1126/science.aab409710.1126/science.aab4097 ↗
25. 10.1002/adma.20150084610.1002/adma.201500846 ↗
26. 10.1021/jacs.5b0664310.1021/jacs.5b06643 ↗
27. 10.1002/adma.20150237510.1002/adma.201502375 ↗
28. 10.1021/acsnano.6b0287910.1021/acsnano.6b02879 ↗
29. 10.1038/nmat445210.1038/nmat4452 ↗
30. 10.1088/0957-4484/25/49/49560310.1088/0957-4484/25/49/495603 ↗
31. 10.1021/jacs.5b0745210.1021/jacs.5b07452 ↗
32. 10.1021/acs.nanolett.6b0134210.1021/acs.nanolett.6b01342 ↗
33. 10.1021/acs.nanolett.6b0266610.1021/acs.nanolett.6b02666 ↗
34. 10.1038/nmat446510.1038/nmat4465 ↗
35. 10.1002/adma.20160268710.1002/adma.201602687 ↗
36. 10.1021/ja01121a05910.1021/ja01121a059 ↗
37. 10.1103/PhysRevB.91.08542410.1103/PhysRevB.91.085424 ↗