journal article·2020-10-28

Nonfullerene-Based Organic Photodetectors for Ultrahigh Sensitivity Visible Light Detection

Helen Bristow, Polina Jacoutot, Alberto D. Scaccabarozzi, Maxime Babics, Maximilian Moser, Andrew Wadsworth, Thomas D. Anthopoulos, Artem Bakulin, Iain McCulloch, Nicola Gasparini

ACS Applied Materials & Interfaces· Volume 12· Issue 43
Publisher page

Abstract

It is well established that for organic photodetectors (OPDs) to compete with their inorganic counterparts, low dark currents at reverse bias must be achieved. Here, two rhodanine-terminated nonfullerene acceptors O-FBR and O-IDTBR are shown to deliver low dark currents at −2 V of 0.17 and 0.84 nA cm–2, respectively, when combined with the synthetically scalable polymer PTQ10 in OPD. These low dark currents contribute to the excellent sensitivity to low light of the detectors, reaching values of 0.57 μW cm−2 for PTQ10:O-FBR-based OPD and 2.12 μW cm−2 for PTQ10:O-IDTBR-based OPD. In both cases, this sensitivity exceeds that of a commercially available silicon photodiode. The responsivity of the PTQ10:O-FBR-based OPD of 0.34 AW–1 under a reverse bias of −2 V also exceeds that of a silicon photodiode. Meanwhile, the responsivity of the PTQ10:O-IDTBR of 0.03 AW–1 is limited by the energetic offset of the blend. The OPDs deliver high specific detectivities of 9.6 × 1012 Jones and 3.3 × 1011 Jones for O-FBR- and O-IDTBR-based blends, respectively. Both active layers are blade-coated in air, making them suitable for high-throughput methods. Finally, all three of the materials can be synthesized at low cost and on a large scale, making these blends good candidates for commercial OPD applications.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Conducting polymers and applications · Transition Metal Oxide Nanomaterials

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry and Centre for Processable Electronics, Imperial College London, London SW72AZ, U.K.

King Abdullah University of Science and Technology (KAUST), KAUST Solar Center (KSC), Thuwal 23955, Saudi Arabia

Department of Chemistry, Chemistry Research Laboratory, University of Oxford, Oxford OX1 3TA, U.K.

Funding

Engineering and Physical Sciences Research Council · H2020 LEIT Information and Communication Technologies · FP7 Ideas: European Research Council · Global Collaborative Research, King Abdullah University of Science and Technology

References (38)

Show source-provided references
1. 10.1038/nature2100410.1038/nature21004 ↗
2. 10.1002/adma.20150511810.1002/adma.201505118 ↗
3. 10.1126/sciadv.150185610.1126/sciadv.1501856 ↗
4. 10.1038/s41560-017-0001-310.1038/s41560-017-0001-3 ↗
5. 10.1002/adfm.20190420510.1002/adfm.201904205 ↗
6. 10.1002/adma.20150540510.1002/adma.201505405 ↗
7. 10.1002/lpor.20140008110.1002/lpor.201400081 ↗
8. 10.1038/ncomms734310.1038/ncomms7343 ↗
9. 10.1038/nphoton.2017.1510.1038/nphoton.2017.15 ↗
10. 10.1002/adma.20200176310.1002/adma.202001763 ↗
11. 10.1126/science.270.5243.178910.1126/science.270.5243.1789 ↗
12. 10.1088/0034-4885/73/9/09640110.1088/0034-4885/73/9/096401 ↗
13. 10.1038/s41566-018-0288-z10.1038/s41566-018-0288-z ↗
14. 10.1002/adfm.20190948710.1002/adfm.201909487 ↗
15. 10.1002/adom.20190156810.1002/adom.201901568 ↗
16. 10.1039/C7CS00892A10.1039/C7CS00892A ↗
17. 10.1088/2058-8585/ab56dd10.1088/2058-8585/ab56dd ↗
18. 10.1002/adma.20190602710.1002/adma.201906027 ↗
19. 10.1002/admt.20190112210.1002/admt.201901122 ↗
20. 10.1002/admt.20170033310.1002/admt.201700333 ↗
21. 10.1002/adma.20190825810.1002/adma.201908258 ↗
22. 10.1002/admt.20180010410.1002/admt.201800104 ↗
23. 10.1039/C8EE01150H10.1039/C8EE01150H ↗
24. 10.1038/s41467-018-03207-x10.1038/s41467-018-03207-x ↗
25. 10.1002/aenm.20170077010.1002/aenm.201700770 ↗
26. 10.1021/ja511060210.1021/ja5110602 ↗
27. 10.1021/acsaelm.9b0013610.1021/acsaelm.9b00136 ↗
28. 10.1002/adom.20190172210.1002/adom.201901722 ↗
29. 10.1002/adma.20190725710.1002/adma.201907257 ↗
30. 10.1038/nphoton.2009.7210.1038/nphoton.2009.72 ↗
31. 10.1038/srep3920110.1038/srep39201 ↗
32. 10.1002/adfm.20090173410.1002/adfm.200901734 ↗
33. 10.1039/C6EE02598F10.1039/C6EE02598F ↗
34. 10.1021/acsami.0c0019110.1021/acsami.0c00191 ↗
35. 10.1021/acsami.8b1601810.1021/acsami.8b16018 ↗
36. 10.1038/ncomms1158510.1038/ncomms11585 ↗
37. 10.1021/acs.chemmater.0c0034710.1021/acs.chemmater.0c00347 ↗
38. 10.1038/nmat479710.1038/nmat4797 ↗