Transparent and Highly Responsive Phototransistors Based on a Solution-Processed, Nanometers-Thick Active Layer, Embedding a High-Mobility Electron-Transporting Polymer and a Hole-Trapping Molecule
Source abstract
Abstract
Organic materials are suitable for light sensing devices showing unique features such as low cost, large area, and flexibility. Moreover, transparent photodetectors are interesting for smart interfaces, windows, and display-integrated electronics. The ease of depositing ultrathin organic films with simple techniques enables low light absorbing active layers, resulting in the realization of transparent devices. Here, we demonstrate a strategy to obtain high efficiency organic photodetectors and phototransistors based on transparent active layers with a visible transmittance higher than 90%. The photoactive layer is composed of two phases, each a few nanometers thick. First, an acceptor polymer, which is a good electron-transporting material, on top of which a small molecule donor material is deposited, forming noncontinuous domains. The small molecule phase acts as a trap for holes, thus inducing a high photoconductive gain, resulting in a high photoresponsivity. The organic transparent detectors proposed here can reach very high external quantum efficiency and responsivity values, which in the case of the phototransistors can be as high as ∼74000% and 340 A W –1 at 570 nm respectively, despite an absorber total thickness below 10 nm. Moreover, frequency dependent 2D photocurrent mapping allows discrimination between the contribution of a fast but inefficient and highly spatially localized photoinduced injection mechanism at the electrodes, and the onset of a slower and spatially extended photoconductive process, leading to high responsivity.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Molecular Junctions and Nanostructures · Nanowire Synthesis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Center for Nano Science and Technology @PoliMi, Istituto Italiano di Tecnologia, Via Pascoli 70/3, 20133 Milano, Italy
Dipartimento di Fisica, Politecnico di Milano, Piazza L. da Vinci 32, 20133 Milano, Italy
Dipartimento di Scienza dei Materiali e INSTM, Università di Milano-Bicocca, Via Roberto Cozzi 55, 20125 Milano, Italy
Funding
FP7 People: Marie-Curie Actions
References (61)
Show source-provided references
1. Wager J. F. · 2008
2. 10.1002/adma.20140494510.1002/adma.201404945 ↗
3. 10.1002/adma.20100258910.1002/adma.201002589 ↗
4. 10.1002/adma.20100293910.1002/adma.201002939 ↗
5. 10.1039/C0NR00588F10.1039/C0NR00588F ↗
6. 10.1038/ncomms640410.1038/ncomms6404 ↗
7. 10.1002/adma.20140511610.1002/adma.201405116 ↗
8. 10.1002/adfm.20140202010.1002/adfm.201402020 ↗
9. 10.1002/anie.20130758110.1002/anie.201307581 ↗
10. 10.1002/adfm.20120178610.1002/adfm.201201786 ↗
11. 10.1002/adma.20120497910.1002/adma.201204979 ↗
12. 10.1063/1.272365310.1063/1.2723653 ↗
13. 10.1038/ncomms734310.1038/ncomms7343 ↗
14. 10.1063/1.481650210.1063/1.4816502 ↗
15. 10.1002/adma.20130347310.1002/adma.201303473 ↗
16. 10.1002/adma.20130128510.1002/adma.201301285 ↗
17. 10.1002/adma.20140291810.1002/adma.201402918 ↗
18. 10.1021/acs.nanolett.5b0038010.1021/acs.nanolett.5b00380 ↗
19. 10.1038/srep0943910.1038/srep09439 ↗
20. 10.1063/1.346496710.1063/1.3464967 ↗
21. 10.1002/adma.20060016310.1002/adma.200600163 ↗
22. 10.1109/TNS.2012.220195410.1109/TNS.2012.2201954 ↗
23. 10.1016/j.orgel.2009.07.01110.1016/j.orgel.2009.07.011 ↗
24. 10.1038/srep0504110.1038/srep05041 ↗
25. 10.1038/srep0533110.1038/srep05331 ↗
26. 10.1038/srep0918110.1038/srep09181 ↗
27. 10.1063/1.11152710.1063/1.111527 ↗
28. 10.1002/adfm.20090166210.1002/adfm.200901662 ↗
29. 10.1016/j.orgel.2014.06.00710.1016/j.orgel.2014.06.007 ↗
30. 10.1002/adfm.20120184810.1002/adfm.201201848 ↗
31. 10.1016/j.orgel.2014.02.02010.1016/j.orgel.2014.02.020 ↗
32. 10.1039/C4TC02462A10.1039/C4TC02462A ↗
33. 10.1039/c3nr03989g10.1039/c3nr03989g ↗
34. 10.1002/adma.20160040010.1002/adma.201600400 ↗
35. 10.1002/aelm.20150007110.1002/aelm.201500071 ↗
36. 10.1002/adfm.20150052510.1002/adfm.201500525 ↗
37. 10.1002/adma.20140069710.1002/adma.201400697 ↗
38. 10.1088/0957-4484/26/6/06520110.1088/0957-4484/26/6/065201 ↗
39. 10.1016/j.orgel.2015.02.00710.1016/j.orgel.2015.02.007 ↗
40. 10.1088/1468-6996/15/2/02420210.1088/1468-6996/15/2/024202 ↗
41. 10.1039/C5PY01373A10.1039/C5PY01373A ↗
42. 10.1002/adma.20150299610.1002/adma.201502996 ↗
43. 10.1038/srep0342510.1038/srep03425 ↗
44. 10.1038/ncomms939410.1038/ncomms9394 ↗
45. 10.1016/j.orgel.2015.03.03110.1016/j.orgel.2015.03.031 ↗
46. 10.1063/1.475023910.1063/1.4750239 ↗
47. 10.1039/c2ta00673a10.1039/c2ta00673a ↗
48. 10.1002/adma.20120146410.1002/adma.201201464 ↗
49. 10.1021/ja306844f10.1021/ja306844f ↗
50. Rose A. · 1963
51. 10.1103/PhysRevB.68.12520810.1103/PhysRevB.68.125208 ↗
52. 10.1002/(SICI)1521-4095(199803)10:5<365::AID-ADMA365>3.0.CO;2-U10.1002/(SICI)1521-4095(199803)10:5<365::AID-ADMA365>3.0.CO;2-U ↗
53. 10.1109/22.55646710.1109/22.556467 ↗
54. 10.1109/22.5492610.1109/22.54926 ↗
55. 10.1063/1.173927810.1063/1.1739278 ↗
56. 10.1063/1.206189210.1063/1.2061892 ↗
57. 10.1016/j.tsf.2014.07.05510.1016/j.tsf.2014.07.055 ↗
58. 10.1021/jp806120q10.1021/jp806120q ↗
59. 10.1063/1.327333210.1063/1.3273332 ↗
60. 10.1063/1.273842910.1063/1.2738429 ↗
61. 10.1002/adma.20130095810.1002/adma.201300958 ↗