Laser‐Like Emission from a Sandwiched MoTe2 Heterostructure on a Silicon Single‐Mode Resonator
Source abstract
Abstract
Abstract Molybdenum ditelluride (MoTe2) has recently shown promise as a gain material for silicon photonics. Reliable single‐mode operation and material stability remain two of the major issues that need to be addressed to advance this exciting technology, however. Here, laser‐like emission from a sandwiched MoTe2 heterostructure on a silicon single‐mode resonator is reported. The heterostructure consists of a layer of MoTe2 sandwiched between thin films of hexagonal boron nitride. It is known that tellurium compounds are sensitive to oxygen exposure, which leads to rapid degradation of the exposed layers in air. By encapsulating the MoTe2 gain material, much improved environmental stability is observed. Using a recently introduced single‐mode resonator design, better control over the mode spectrum of the cavity is exercised and single‐mode operation with a wide free spectral range is demonstrated. At room temperature, a Q‐factor of 4500 and a threshold of 4.2 kW cm−2 at 1319 nm wavelength are achieved. These results lend further support to the paradigm of 2D material‐based integrated light sources on the silicon platform.
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Research context
OpenAlex topics: Photonic and Optical Devices · Advanced Fiber Laser Technologies · Mechanical and Optical Resonators
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Optoelectronic Materials and Technologies School of Physics Sun Yat‐Sen University Guangzhou 510275 China
Department of Physics University of York York YO10 5DD UK
Funding
National Basic Research Program of China · National Natural Science Foundation of China · Natural Science Foundation of Guangdong Province · Sun Yat-sen University · Engineering and Physical Sciences Research Council
References (33)
Show source-provided references
1. 10.1002/lpor.20170006310.1002/lpor.201700063 ↗
2. 10.1038/nphoton.2010.16710.1038/nphoton.2010.167 ↗
3. 10.1038/lsa.2015.13110.1038/lsa.2015.131 ↗
4. 10.1515/nanoph-2016-015510.1515/nanoph-2016-0155 ↗
5. 10.1021/jacs.5b0745210.1021/jacs.5b07452 ↗
6. 10.1103/PhysRevB.88.04531810.1103/PhysRevB.88.045318 ↗
7. 10.1103/PhysRevLett.113.07680210.1103/PhysRevLett.113.076802 ↗
8. 10.1021/nl503799t10.1021/nl503799t ↗
9. 10.1038/nnano.2014.20710.1038/nnano.2014.207 ↗
10. 10.1038/nnano.2017.20910.1038/nnano.2017.209 ↗
11. 10.1021/acsami.8b1407610.1021/acsami.8b14076 ↗
12. 10.1002/smtd.20180001910.1002/smtd.201800019 ↗
13. 10.1063/1.498459710.1063/1.4984597 ↗
14. 10.1021/acsnano.5b0098510.1021/acsnano.5b00985 ↗
15. 10.1002/adom.20180027210.1002/adom.201800272 ↗
16. 10.1021/acs.nanolett.8b0074910.1021/acs.nanolett.8b00749 ↗
17. 10.1038/s42005-018-0083-710.1038/s42005-018-0083-7 ↗
18. 10.1209/0295-5075/109/5800410.1209/0295-5075/109/58004 ↗
19. 10.1038/ncomms463110.1038/ncomms4631 ↗
20. 10.1039/C5TA00252D10.1039/C5TA00252D ↗
21. 10.1126/science.124435810.1126/science.1244358 ↗
22. 10.1063/1.488609610.1063/1.4886096 ↗
23. 10.1021/acsnano.5b0134110.1021/acsnano.5b01341 ↗
24. 10.1103/PhysRevX.7.02102610.1103/PhysRevX.7.021026 ↗
25. Han B. · Phys. Rev. X · 2018 · 8 · 031073
26. 10.1038/s41598-017-09739-410.1038/s41598-017-09739-4 ↗
27. 10.1038/nature1429010.1038/nature14290 ↗
28. 10.1038/nphoton.2015.19710.1038/nphoton.2015.197 ↗
29. 10.1021/acs.nanolett.5b0166510.1021/acs.nanolett.5b01665 ↗
30. 10.1038/s41467-017-00743-w10.1038/s41467-017-00743-w ↗
31. 10.1002/lpor.20180001510.1002/lpor.201800015 ↗
32. 10.1038/nnano.2017.12810.1038/nnano.2017.128 ↗
33. Z.Wang H.Sun Q.Zhang J.Feng J.Zhang Y.Li C.Ning arXiv:1812.04296 2018.