High-Performance All-Polymer Photodetectors Enabled by New Random Terpolymer Acceptor with Fine-Tuned Molecular Weight
Source abstract
Abstract
Reducing the dark current density and enhancing the overall performance of the device is the focal point in research for organic photodetectors. Two novel random terpolymers (P3 and P4) with different molecular weights are synthesized and evaluated as acceptors in bulk heterojunction (BHJ) polymer photodetectors. Compared with known acceptor materials, such as N2200 (P1) and F-N2200 (P2), polymer P4 has a lower lowest unoccupied molecular orbital (LUMO) energy level, favorable morphology, and good miscibility with a donor material J71, which leads to proper phase separation of the blend film and better dissociation of excitons and transport of carriers. Therefore, a considerably low dark current density (Jd) of 1.9 × 10–10 A/cm2 and a high specific detectivity (D*) of 1.8 × 1013 cm Hz1/2/W (also “Jones”) at 580 nm under a −0.1 V bias are realized for the P4-based photodetector. More importantly, the device also exhibits a fast response speed (τr/τf = 1.24/1.87 μs) and a wide linear dynamic range (LDR) of 109.2 dB. This work demonstrates that high-performance all-polymer photodetectors with ideal morphology can be realized by random polymer acceptors with a fine-tuned molecular weight.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Organic Light-Emitting Diodes Research · Nanowire Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Fine Chemicals, Department of Polymer Science & Materials, School of Chemical Engineering, Dalian University of Technology, Dalian 116024, P. R. China
Department of Materials Science and Engineering and Department of Chemistry, Johns Hopkins University, Baltimore, Maryland 21218, United States
Funding
National Natural Science Foundation of China
References (66)
Show source-provided references
1. 10.1021/acsami.0c1383310.1021/acsami.0c13833 ↗
2. 10.1002/adfm.20210632610.1002/adfm.202106326 ↗
3. 10.1021/jacs.0c1281810.1021/jacs.0c12818 ↗
4. 10.1002/lpor.20200026210.1002/lpor.202000262 ↗
5. 10.1002/adfm.20180894810.1002/adfm.201808948 ↗
6. 10.1021/acsami.0c1826010.1021/acsami.0c18260 ↗
7. 10.1038/s41467-021-25638-910.1038/s41467-021-25638-9 ↗
8. 10.1021/acsmaterialslett.2c0019110.1021/acsmaterialslett.2c00191 ↗
9. 10.1088/1674-4926/42/10/10020210.1088/1674-4926/42/10/100202 ↗
10. 10.1002/adfm.20210600910.1002/adfm.202106009 ↗
11. 10.1021/acsami.0c2280810.1021/acsami.0c22808 ↗
12. 10.1002/adma.20210058210.1002/adma.202100582 ↗
13. 10.1002/solr.20200013910.1002/solr.202000139 ↗
14. 10.1039/C7TA10391C10.1039/C7TA10391C ↗
15. 10.1016/j.progpolymsci.2019.10117510.1016/j.progpolymsci.2019.101175 ↗
16. 10.1002/adma.20180727510.1002/adma.201807275 ↗
17. 10.1021/acsami.9b1281410.1021/acsami.9b12814 ↗
18. 10.1021/jacs.8b0214410.1021/jacs.8b02144 ↗
19. 10.1016/j.scib.2020.05.02310.1016/j.scib.2020.05.023 ↗
20. 10.1021/jacs.0c1252710.1021/jacs.0c12527 ↗
21. 10.1002/inf2.1227110.1002/inf2.12271 ↗
22. 10.1039/D1TA06041D10.1039/D1TA06041D ↗
23. 10.1016/j.joule.2021.04.00710.1016/j.joule.2021.04.007 ↗
24. 10.1021/acsmacrolett.8b0000910.1021/acsmacrolett.8b00009 ↗
25. 10.1021/acsami.9b0209210.1021/acsami.9b02092 ↗
26. 10.1021/jacs.9b1093510.1021/jacs.9b10935 ↗
27. 10.1002/anie.20200535710.1002/anie.202005357 ↗
28. 10.1039/C9TC03142A10.1039/C9TC03142A ↗
29. 10.1021/acs.chemmater.0c0472110.1021/acs.chemmater.0c04721 ↗
30. 10.1039/C6PY01828A10.1039/C6PY01828A ↗
31. 10.1002/adfm.20180557010.1002/adfm.201805570 ↗
32. 10.1021/acs.chemmater.9b0446410.1021/acs.chemmater.9b04464 ↗
33. 10.1016/j.nanoen.2019.10393110.1016/j.nanoen.2019.103931 ↗
34. 10.1002/tcr.20160001310.1002/tcr.201600013 ↗
35. 10.1016/j.nanoen.2020.10471810.1016/j.nanoen.2020.104718 ↗
36. 10.1002/adom.20180003810.1002/adom.201800038 ↗
37. 10.1021/acsenergylett.0c0101010.1021/acsenergylett.0c01010 ↗
38. 10.1002/adma.20190516110.1002/adma.201905161 ↗
39. 10.1039/C9TA10040G10.1039/C9TA10040G ↗
40. 10.1021/acs.chemmater.9b0063910.1021/acs.chemmater.9b00639 ↗
41. 10.1002/adma.20190825810.1002/adma.201908258 ↗
42. 10.1016/j.orgel.2018.01.03310.1016/j.orgel.2018.01.033 ↗
43. 10.1002/solr.20180024610.1002/solr.201800246 ↗
44. 10.1002/adma.20190428310.1002/adma.201904283 ↗
45. 10.1007/s10118-021-2548-510.1007/s10118-021-2548-5 ↗
46. 10.1002/adfm.20140194810.1002/adfm.201401948 ↗
47. 10.1021/acs.macromol.5b0085910.1021/acs.macromol.5b00859 ↗
48. 10.1126/science.117670610.1126/science.1176706 ↗
49. 10.1039/D0MH01445A10.1039/D0MH01445A ↗
50. 10.1021/acsnano.0c0942610.1021/acsnano.0c09426 ↗
51. 10.1002/adma.20190602710.1002/adma.201906027 ↗
52. 10.1021/acsami.9b1946710.1021/acsami.9b19467 ↗
53. 10.1002/adfm.20170395310.1002/adfm.201703953 ↗
54. 10.1002/adom.20200138810.1002/adom.202001388 ↗
55. 10.1002/adma.20180722010.1002/adma.201807220 ↗
56. 10.1039/C9EE04020J10.1039/C9EE04020J ↗
57. 10.1021/acs.chemmater.9b0491110.1021/acs.chemmater.9b04911 ↗
58. 10.1002/adfm.20160162510.1002/adfm.201601625 ↗
59. 10.1039/C7TA11339K10.1039/C7TA11339K ↗
60. 10.1002/adfm.20190397010.1002/adfm.201903970 ↗
61. 10.1021/acsenergylett.8b0010010.1021/acsenergylett.8b00100 ↗
62. 10.1021/acs.chemmater.9b0235510.1021/acs.chemmater.9b02355 ↗
63. 10.1002/adfm.20170651710.1002/adfm.201706517 ↗
64. 10.1039/C7EE00844A10.1039/C7EE00844A ↗
65. 10.1039/C8TA11004B10.1039/C8TA11004B ↗
66. 10.1002/adfm.20190680910.1002/adfm.201906809 ↗