Dual-Band Photomultiplication-Type Organic Photodetectors with Ultrahigh Signal-to-Noise Ratios
Source abstract
Abstract
A series of dual-band photomultiplication (PM)-type organic photodetectors (OPDs) were fabricated by employing a donor(s)/acceptor (100:1, wt/wt) mixed layer and an ultrathin Y6 layer as the active layers, as well as by using PNDIT-F3N as an interfacial layer near the indium tin oxide (ITO) electrode. The dual-band PM-type OPDs exhibit the response range of 330–650 nm under forward bias and the response range of 650–850 nm under reverse bias. The tunable spectral response range of dual-band PM-type OPDs under forward or reverse bias can be explained well from the trapped electron distribution near the electrodes. The dark current density ( J D ) of the dual-band PM-type OPDs can be efficiently suppressed by employing PNDIT-F3N as the anode interfacial layer and the special active layers with hole-only transport characteristics. The light current density ( J L ) of the dual-band PM-type OPDs can be slightly increased by incorporating wide-bandgap polymer P-TPDs with relatively large hole mobility (μ h ) in the active layers. The signal-to-noise ratios of the optimized dual-band PM-type OPDs reach 100,980 under −50 V bias and white light illumination with an intensity of 1.0 mW·cm –2, benefiting from the ultralow J D by employing wide-bandgap PNDIT-F3N as the anode interfacial buffer layer and the increased J L by incorporating appropriate P-TPD in the active layers.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Perovskite Materials and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Physical Science and Engineering, Beijing Jiaotong University, Beijing 100044, People’s Republic of China
College of Physics and Electronic Engineering, Taishan University, Taian 271000, Shandong Province, People’s Republic of China
Organic Optoelectronic Materials Laboratory, Department of Chemistry, College of Science, Korea University, Seoul 02841, Republic of Korea
Funding
Natural Science Foundation of Beijing Municipality · National Natural Science Foundation of China
References (54)
Show source-provided references
1. 10.1002/adma.20190204510.1002/adma.201902045 ↗
2. 10.1016/j.mattod.2021.08.00410.1016/j.mattod.2021.08.004 ↗
3. 10.1039/D1MH01215K10.1039/D1MH01215K ↗
4. 10.1063/1.514484010.1063/1.5144840 ↗
5. 10.1007/s40820-023-01114-510.1007/s40820-023-01114-5 ↗
6. 10.1002/lpor.20200026210.1002/lpor.202000262 ↗
7. 10.1002/aisy.20210016710.1002/aisy.202100167 ↗
8. 10.1063/5.016862610.1063/5.0168626 ↗
9. 10.1038/s41467-021-24500-210.1038/s41467-021-24500-2 ↗
10. 10.1126/sciadv.aaw806510.1126/sciadv.aaw8065 ↗
11. 10.3866/pku.Whxb20231102110.3866/pku.Whxb202311021 ↗
12. 10.1002/adom.20210226610.1002/adom.202102266 ↗
13. 10.1038/nnano.2012.18710.1038/nnano.2012.187 ↗
14. 10.1021/acsami.2c1215410.1021/acsami.2c12154 ↗
15. 10.1002/adfm.20210883910.1002/adfm.202108839 ↗
16. 10.1002/adma.20190368710.1002/adma.201903687 ↗
17. 10.1039/C9NR09926C10.1039/C9NR09926C ↗
18. 10.1002/adfm.20200644810.1002/adfm.202006448 ↗
19. 10.1002/adfm.20220360610.1002/adfm.202203606 ↗
20. 10.1021/acsnano.1c0490810.1021/acsnano.1c04908 ↗
21. 10.1039/D1TC00939G10.1039/D1TC00939G ↗
22. 10.1002/adfm.20230069510.1002/adfm.202300695 ↗
23. 10.1002/adfm.20230416910.1002/adfm.202304169 ↗
24. 10.1039/D2TC01297A10.1039/D2TC01297A ↗
25. 10.1039/D2TC03335F10.1039/D2TC03335F ↗
26. 10.1002/adma.20210468910.1002/adma.202104689 ↗
27. 10.1021/acsami.2c0792410.1021/acsami.2c07924 ↗
28. 10.1016/j.cej.2022.13497310.1016/j.cej.2022.134973 ↗
29. 10.1002/adma.20210296710.1002/adma.202102967 ↗
30. 10.1021/acsami.3c1300710.1021/acsami.3c13007 ↗
31. 10.1002/solr.20230092710.1002/solr.202300927 ↗
32. 10.1039/D3TA07228B10.1039/D3TA07228B ↗
33. 10.1002/advs.20210557510.1002/advs.202105575 ↗
34. 10.1002/adfm.20231375110.1002/adfm.202313751 ↗
35. 10.1063/1.499532010.1063/1.4995320 ↗
36. 10.1002/apxr.20220007510.1002/apxr.202200075 ↗
37. 10.1002/adma.20170205510.1002/adma.201702055 ↗
38. 10.1002/adfm.20170669010.1002/adfm.201706690 ↗
39. 10.1007/s11426-022-1296-210.1007/s11426-022-1296-2 ↗
40. 10.1002/adfm.20190420510.1002/adfm.201904205 ↗
41. 10.1021/acsami.0c1383310.1021/acsami.0c13833 ↗
42. 10.1002/adfm.20210802610.1002/adfm.202108026 ↗
43. 10.1002/adom.20230321610.1002/adom.202303216 ↗
44. 10.1002/adma.20160524210.1002/adma.201605242 ↗
45. 10.1002/adfm.20170236010.1002/adfm.201702360 ↗
46. 10.1016/j.nanoen.2023.10922610.1016/j.nanoen.2023.109226 ↗
47. 10.1021/acsami.2c2246110.1021/acsami.2c22461 ↗
48. 10.1002/adma.20220827910.1002/adma.202208279 ↗
49. 10.1038/s41377-020-0264-510.1038/s41377-020-0264-5 ↗
50. 10.1038/s41467-023-42742-010.1038/s41467-023-42742-0 ↗
51. 10.1002/adfm.20210632610.1002/adfm.202106326 ↗
52. 10.1002/adma.20200441610.1002/adma.202004416 ↗
53. 10.1039/D1MH00776A10.1039/D1MH00776A ↗
54. 10.1002/adom.20200158710.1002/adom.202001587 ↗