High-Performance and Stable Sb2S3 Thin-Film Photodetectors for Potential Application in Visible Light Communication
Source abstract
Abstract
Photodetectors (PDs) are critical parts of visible light communication (VLC) systems for achieving efficient photoelectronic conversion and high-fidelity transmission of signals. Antimony sulfide (Sb 2 S 3 ) as a nontoxic, high optical absorption coefficient, and low-cost semiconductor becomes a promising candidate for applications in VLC systems. Particularly, Sb 2 S 3 PDs were verified to have significantly weak light detection ability in the visible region. However, the response speed of Sb 2 S 3 PDs with existing device structures is still relatively slow. Herein, through optimizing the device structure for the p–i–n type PDs, a p-type Sb 2 Se 3 hole transport layer (HTL) is designed to enhance the built-in electric field and to accelerate the migration of photogenerated carriers for the high responsivity and fast response speed. The optimal thickness of the structure is obtained through the simulation of SCAPS-1D software, and the optimized devices show high-performance parameters, including a responsivity of 0.34 A W –1, a specific detectivity ( D * ) of 2.20 × 10 12 Jones, the −3 dB bandwidth of 440 kHz, high stability, and the value of the Sb 2 S 3 PDs can reach 60% in the range of 360–600 nm, which indicates that the device is very suitable for working in the visible light band. In addition, the resulting Sb 2 S 3 PD is successfully integrated into VLC systems by designing a matched light detection circuit. The results suggest that the Sb 2 S 3 PDs are expected to provide an alternative to future VLC system applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Chalcogenide Semiconductor Thin Films · Quantum Dots Synthesis And Properties · Perovskite Materials and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Information Engineering, Nanchang University, Nanchang 330031, Jiangxi, China
School of Physics and Materials Science, Nanchang University, Nanchang 330031, Jiangxi, China
Institute of Space Science and Technology, Nanchang University, Nanchang 330031, Jiangxi, China
College of Physics and Information Engineering, Institute of Micro-Nano Devices and Solar Cells, Fuzhou University, Fuzhou 350108, Fujian, China
Funding
National Natural Science Foundation of China · Natural Science Foundation of Jiangxi Province
References (51)
Show source-provided references
1. 10.1016/j.dcan.2016.07.00410.1016/j.dcan.2016.07.004 ↗
2. 10.1109/MCOM.2013.668575410.1109/MCOM.2013.6685754 ↗
3. 10.1109/JPHOT.2015.250514510.1109/JPHOT.2015.2505145 ↗
4. 10.1063/1.487487810.1063/1.4874878 ↗
5. 10.1038/nnano.2013.10010.1038/nnano.2013.100 ↗
6. 10.1364/AO.54.00806210.1364/AO.54.008062 ↗
7. 10.1002/adom.20190173510.1002/adom.201901735 ↗
8. 10.1002/adma.20180342210.1002/adma.201803422 ↗
9. 10.1002/smll.20190359910.1002/smll.201903599 ↗
10. 10.1021/acsami.0c1216110.1021/acsami.0c12161 ↗
11. 10.1002/smll.20160399610.1002/smll.201603996 ↗
12. 10.1002/admi.20210150410.1002/admi.202101504 ↗
13. 10.1016/j.mtener.2017.02.00110.1016/j.mtener.2017.02.001 ↗
14. 10.1016/j.joule.2018.04.00310.1016/j.joule.2018.04.003 ↗
15. 10.1002/solr.20190002610.1002/solr.201900026 ↗
16. 10.1002/adfm.20210026510.1002/adfm.202100265 ↗
17. 10.1002/adfm.20221262710.1002/adfm.202212627 ↗
18. 10.1021/acsami.1c2525610.1021/acsami.1c25256 ↗
19. 10.1016/j.solmat.2018.06.01710.1016/j.solmat.2018.06.017 ↗
20. 10.1016/j.jmst.2020.10.00510.1016/j.jmst.2020.10.005 ↗
21. 10.1039/C7NR03574H10.1039/C7NR03574H ↗
22. 10.1002/adfm.20200660110.1002/adfm.202006601 ↗
23. 10.1021/acsnano.2c0728810.1021/acsnano.2c07288 ↗
24. 10.1002/inf2.1240010.1002/inf2.12400 ↗
25. 10.1002/adma.20210907810.1002/adma.202109078 ↗
26. 10.1016/j.cej.2021.13335910.1016/j.cej.2021.133359 ↗
27. 10.1002/solr.20210101710.1002/solr.202101017 ↗
28. 10.1002/adfm.20150029610.1002/adfm.201500296 ↗
29. 10.1016/j.jpowsour.2021.22973710.1016/j.jpowsour.2021.229737 ↗
30. 10.1002/pip.298010.1002/pip.2980 ↗
31. 10.1016/S1005-8885(11)60422-610.1016/S1005-8885(11)60422-6 ↗
32. 10.3390/s1809304510.3390/s18093045 ↗
33. 10.1109/JSAC.2015.243255110.1109/JSAC.2015.2432551 ↗
34. 10.1007/s11082-017-1280-410.1007/s11082-017-1280-4 ↗
35. 10.1109/41.72032810.1109/41.720328 ↗
36. 10.1109/TPWRD.2004.83864110.1109/TPWRD.2004.838641 ↗
37. 10.1021/acsenergylett.0c0266010.1021/acsenergylett.0c02660 ↗
38. 10.1016/j.solener.2019.02.01710.1016/j.solener.2019.02.017 ↗
39. 10.1021/acsphotonics.9b0160910.1021/acsphotonics.9b01609 ↗
40. 10.1002/adom.20180069710.1002/adom.201800697 ↗
41. 10.1109/JLT.2020.298155410.1109/JLT.2020.2981554 ↗
42. 10.1002/adma.20170320910.1002/adma.201703209 ↗
43. 10.1126/science.117670610.1126/science.1176706 ↗
44. 10.1002/adma.20160524210.1002/adma.201605242 ↗
45. 10.1002/lpor.20220100610.1002/lpor.202201006 ↗
46. 10.1109/LED.2022.319217810.1109/LED.2022.3192178 ↗
47. 10.1021/acsami.6b0994310.1021/acsami.6b09943 ↗
48. Liu Y. · J. Mater. Chem. · 2019 · 7 · 917
49. 10.1002/smll.20190213510.1002/smll.201902135 ↗
50. 10.1021/acsnano.6b0856710.1021/acsnano.6b08567 ↗
51. Tan C.-T. · J. Audio Eng. Soc. · 2003 · 51 · 1012