journal article·2019-10-30Open access

Charge Separation in Epitaxial SnS/MoS2 Vertical Heterojunctions Grown by Low-Temperature Pulsed MOCVD

Jack N. Olding, Alex Henning, Jason T. Dong, Qunfei Zhou, Michael J. Moody, Paul J. M. Smeets, Pierre Darancet, Emily A. Weiss, Lincoln J. Lauhon

ACS Applied Materials & Interfaces· Volume 11· Issue 43

Abstract

The weak van der Waals bonding between monolayers in layered materials enables fabrication of heterostructures without the constraints of conventional heteroepitaxy. Although many novel heterostructures have been created by mechanical exfoliation and stacking, the direct growth of 2D chalcogenide heterostructures creates new opportunities for large-scale integration. This paper describes the epitaxial growth of layered, p-type tin sulfide (SnS) on n-type molybdenum disulfide (MoS2) by pulsed metal-organic chemical vapor deposition at 180 °C. The influence of precursor pulse and purge times on film morphology establishes growth conditions that favor layer-by-layer growth of SnS, which is critical for materials with layer-dependent electronic properties. Kelvin probe force microscopy measurements determine a built-in potential as high as 0.95 eV, and under illumination a surface photovoltage is generated, consistent with the expected Type-II band alignment for a multilayer SnS/MoS2 heterostructure. The bottom-up growth of a nonisostructural heterojunction comprising 2D semiconductors expands the combinations of materials available for scalable production of ultrathin devices with field-tunable responses.
Source: europepmc · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: 2D Materials and Applications · Perovskite Materials and Applications · Chalcogenide Semiconductor Thin Films

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

Affiliations

Applied Physics Graduate Program, Northwestern University, Evanston, Illinois 60208, United States

Department of Materials Science and Engineering, Northwestern University, Evanston, Illinois 60208, United States

Materials Research Science and Engineering Center, Northwestern University, Evanston, Illinois 60208, United States

Center for Nanoscale Materials, Argonne National Laboratory, 9700 South Cass Avenue, Lemont, Illinois 60439, United States

NUANCE Center, Northwestern University, Evanston, Illinois 60208, United States

Department of Chemistry, Northwestern University, Evanston, Illinois 60208-3113, United States

Funding

Deutsche Forschungsgemeinschaft · Northwestern University Materials Science and Engineering Center · Northwestern University International Institute for Nanotechnology

References (53)

Show source-provided references
1. 10.1038/nmat351810.1038/nmat3518 ↗
2. 10.1039/C7CS00880E10.1039/C7CS00880E ↗
3. 10.1021/nn502738810.1021/nn5027388 ↗
4. 10.1073/pnas.131722611010.1073/pnas.1317226110 ↗
5. 10.1038/nnano.2014.15010.1038/nnano.2014.150 ↗
6. 10.1088/1361-6528/aabd9010.1088/1361-6528/aabd90 ↗
7. 10.1038/nnano.2014.22210.1038/nnano.2014.222 ↗
8. 10.1038/nmat409110.1038/nmat4091 ↗
9. 10.1038/nmat406410.1038/nmat4064 ↗
10. 10.1021/acs.chemmater.7b0136710.1021/acs.chemmater.7b01367 ↗
11. 10.1021/acs.nanolett.7b0231110.1021/acs.nanolett.7b02311 ↗
12. 10.1038/nature1441710.1038/nature14417 ↗
13. 10.1021/nn507328610.1021/nn5073286 ↗
14. 10.1109/JPROC.2012.219016810.1109/JPROC.2012.2190168 ↗
15. 10.1007/s11671-010-9689-810.1007/s11671-010-9689-8 ↗
16. 10.1021/acsnano.5b0639810.1021/acsnano.5b06398 ↗
17. 10.1021/acs.nanolett.5b0131110.1021/acs.nanolett.5b01311 ↗
18. 10.1021/nl501000k10.1021/nl501000k ↗
19. 10.1038/s41467-017-02093-z10.1038/s41467-017-02093-z ↗
20. 10.1021/acs.nanolett.5b0242310.1021/acs.nanolett.5b02423 ↗
21. 10.1038/ncomms831110.1038/ncomms8311 ↗
22. 10.1021/acsnano.5b0612610.1021/acsnano.5b06126 ↗
23. 10.1021/acs.chemmater.6b0532310.1021/acs.chemmater.6b05323 ↗
24. 10.1021/acs.chemmater.5b0322010.1021/acs.chemmater.5b03220 ↗
25. 10.1021/am401127s10.1021/am401127s ↗
26. 10.1021/cm403901y10.1021/cm403901y ↗
27. 10.1149/05810.0087ecst10.1149/05810.0087ecst ↗
28. 10.1021/jp912024410.1021/jp9120244 ↗
29. 10.1002/aenm.20110033010.1002/aenm.201100330 ↗
30. 10.1021/acs.nanolett.9b0141910.1021/acs.nanolett.9b01419 ↗
31. 10.1524/zkri.1935.92.1.16110.1524/zkri.1935.92.1.161 ↗
32. 10.1021/acsnano.5b0194310.1021/acsnano.5b01943 ↗
33. Murthy, A. A.; Stanev, T. K.; dos Reis, R.; Hao, S.; Wolverton, C.; Stern, N. P.; Dravid, V. P. Direct Vizualization of Electric Field induced Structural Dynamics in Monolayer Transition Metal Dichalcogenides. 2019, arXiv: 1910.02879; https://arxiv.org/abs/1910.02879 (accessed Oct 7, 2019).
34. 10.1016/j.apsusc.2017.11.09810.1016/j.apsusc.2017.11.098 ↗
35. 10.1016/0040-6090(92)90872-910.1016/0040-6090(92)90872-9 ↗
36. 10.1021/acsnano.8b0923010.1021/acsnano.8b09230 ↗
37. 10.1021/ja312509610.1021/ja3125096 ↗
38. 10.1021/nn500385810.1021/nn5003858 ↗
39. 10.1021/nn500532f10.1021/nn500532f ↗
40. 10.1016/j.cplett.2013.10.03410.1016/j.cplett.2013.10.034 ↗
41. 10.1021/jp051822r10.1021/jp051822r ↗
42. 10.1063/1.493963510.1063/1.4939635 ↗
43. 10.1063/1.481752010.1063/1.4817520 ↗
44. 10.1021/acs.cgd.5b0026910.1021/acs.cgd.5b00269 ↗
45. 10.1116/1.283508710.1116/1.2835087 ↗
46. 10.1021/acs.jpcc.7b1257910.1021/acs.jpcc.7b12579 ↗
47. 10.1021/acsami.7b1461610.1021/acsami.7b14616 ↗
48. 10.1103/PhysRevB.64.23530510.1103/PhysRevB.64.235305 ↗
49. 10.1063/1.480131310.1063/1.4801313 ↗
50. 10.1063/1.36959010.1063/1.369590 ↗
51. 10.1002/adma.20160169410.1002/adma.201601694 ↗
52. 10.1002/aenm.20150082910.1002/aenm.201500829 ↗
53. 10.1038/s41699-018-0049-310.1038/s41699-018-0049-3 ↗