1530 nm Electroluminescence from Metal–Semiconductor–Metal Structured Devices Based on Oxygen–Erbium Co-doped MoS2
Source abstract
Abstract
The 1530 nm emission of the Er intra-4f transition ( 4 I 13/2 → 4 I 15/2 ) is essential for telecom communication because it corresponds to the minimum-loss window of silica optical fibers. Herein, we develop a metal–semiconductor–metal structured light source based on O–Er co-doped MoS 2 . The electroluminescence device exhibits the 1530 nm emission at low drive voltages (<5 V), which is beneficial from the impact excitation with the space–charge-limited conduction mechanism. The characteristic of symmetric structure allows the devices to exhibit consistent electrical and electroluminescence performance at positive and negative voltages. The O doping contributes to such high-current electrical behavior, and the Er doping leads to increased trap-filled-limited voltage due to increased trap density. This work lays the foundation for developing near-infrared light sources constructed with two-dimensional materials.
Source: openalex_inverted_index · Quality: baseline
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
School of Materials Science and Engineering, South China University of Technology, Guangzhou 510641, China
Henan Key Laboratory of Nanocomposites and Applications, Institute of Nanostructured Functional Materials, Huanghe Science and Technology College, Zhengzhou 450006, China
References (38)
Show source-provided references
1. 10.1063/1.512017310.1063/1.5120173 ↗
2. 10.1063/5.006422110.1063/5.0064221 ↗
3. 10.1063/1.489658810.1063/1.4896588 ↗
4. 10.1063/1.499785810.1063/1.4997858 ↗
5. 10.1063/1.480462610.1063/1.4804626 ↗
6. 10.1063/1.491722410.1063/1.4917224 ↗
7. 10.1002/adma.20150409010.1002/adma.201504090 ↗
8. 10.1038/nnano.2010.27910.1038/nnano.2010.279 ↗
9. 10.1063/1.487595910.1063/1.4875959 ↗
10. 10.1002/adma.20160183310.1002/adma.201601833 ↗
11. 10.1088/1361-6463/aa6a7510.1088/1361-6463/aa6a75 ↗
12. 10.1016/j.jlumin.2020.11718910.1016/j.jlumin.2020.117189 ↗
13. 10.1021/acs.jpcc.2c0711310.1021/acs.jpcc.2c07113 ↗
14. 10.1002/adfm.20220360210.1002/adfm.202203602 ↗
15. 10.1021/acs.nanolett.5b0388510.1021/acs.nanolett.5b03885 ↗
16. 10.1186/s40580-021-00262-x10.1186/s40580-021-00262-x ↗
17. 10.1002/smll.20170380810.1002/smll.201703808 ↗
18. 10.1021/nn500385810.1021/nn5003858 ↗
19. 10.1002/smll.20200427610.1002/smll.202004276 ↗
20. 10.1016/j.jhazmat.2023.13189410.1016/j.jhazmat.2023.131894 ↗
21. 10.1021/acsnano.3c0603410.1021/acsnano.3c06034 ↗
22. 10.1088/0957-4484/27/44/44570510.1088/0957-4484/27/44/445705 ↗
23. 10.1021/jp200618310.1021/jp2006183 ↗
24. 10.1016/j.mseb.2003.08.02110.1016/j.mseb.2003.08.021 ↗
25. 10.1111/jace.1649010.1111/jace.16490 ↗
26. 10.1021/jp510239d10.1021/jp510239d ↗
27. 10.1063/1.348495610.1063/1.3484956 ↗
28. 10.1063/1.362214510.1063/1.3622145 ↗
29. 10.1063/1.346746110.1063/1.3467461 ↗
30. 10.1103/PhysRevB.73.24542710.1103/PhysRevB.73.245427 ↗
31. 10.1021/acsenergylett.9b0272010.1021/acsenergylett.9b02720 ↗
32. 10.1021/acsenergylett.0c0259910.1021/acsenergylett.0c02599 ↗
33. 10.1002/smtd.20210009110.1002/smtd.202100091 ↗
34. 10.1016/j.colsurfa.2020.12495010.1016/j.colsurfa.2020.124950 ↗
35. 10.1088/0022-3727/49/29/29530510.1088/0022-3727/49/29/295305 ↗
36. 10.1002/smll.20160403410.1002/smll.201604034 ↗
37. 10.1063/1.496622410.1063/1.4966224 ↗
38. 10.1063/1.478867910.1063/1.4788679 ↗