journal article·2022-01

Ultra‐High Alignment of Polymer Semiconductor Blends Enabling Photodetectors with Exceptional Polarization Sensitivity

Harry M. Schrickx, Pratik Sen, Ronald E. Booth, Ali Altaqui, Jacob Burleson, Jeromy J. Rech, Jin‐Woo Lee, Melike Biliroglu, Kenan Gundogdu, Bumjoon J. Kim, Wei You, Michael W. Kudenov, Brendan T. O'Connor

Advanced Functional Materials· Volume 32· Issue 2
Publisher page

Abstract

Abstract Photodetectors that can sense not only light intensity but also light's polarization state add valuable information that is beneficial in a wide array of applications. Polymer semiconductors are an attractive material system to achieve intrinsic polarization sensitivity due to their anisotropic optoelectronic properties. In this report, the thermomechanical properties of the polymer semiconductors PBnDT‐FTAZ and P(NDI2OD‐T2) are leveraged to realize bulk heterojunction (BHJ) films with record in‐plane alignment. Two polymer blends with distinct weight average molar masses (Mw) are considered and either a strain‐ or rub‐alignment process is applied to align the polymer blend films. Optimized processing yields films with dichroic ratios (DR) of over 11 for the high Mw system and nearly 17 for the low Mw system. Incorporating the aligned films into photodetectors results in a polarized photocurrent ratio of 15.25 with corresponding anisotropy ratio of 0.88 at a wavelength of 530 nm, representing the highest reported photocurrent ratio for photodiodes that can operate in a self‐powered regime. The demonstrated performance showcases the ability of polymer semiconductors to achieve BHJ films with exceptional in‐plane polymer alignment, enabling high performance polarization sensitive photodetectors for incorporation into novel device architectures.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Perovskite Materials and Applications · Nanowire Synthesis and Applications

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

Affiliations

Department of Mechanical and Aerospace Engineering and Organic and Carbon Electronics Laboratories (ORaCEL) North Carolina State University Raleigh NC 27695 USA

Department of Electrical and Computer Engineering North Carolina State University Raleigh NC 27695 USA

Department of Chemistry University of North Carolina Chapel Hill NC 27599 USA

Department of Chemical and Biomolecular Engineering Korea Advanced Institute of Science and Technology Daejeon 34141 Republic of Korea

Department of Physics and Organic and Carbon Electronics Laboratories (ORaCEL) North Carolina State University Raleigh NC 27695 USA

Funding

National Science Foundation · National Research Foundation · Changchun Institute of Applied Chemistry · Chinese Academy of Sciences

References (64)

Show source-provided references
1. Zhao Y. · 2013
2. 10.1364/OL.22.00093410.1364/OL.22.000934 ↗
3. 10.1364/OL.39216710.1364/OL.392167 ↗
4. 10.1002/adma.20200385210.1002/adma.202003852 ↗
5. 10.1002/adfm.20150454610.1002/adfm.201504546 ↗
6. 10.1039/C7NR03040A10.1039/C7NR03040A ↗
7. 10.1038/nnano.2015.11210.1038/nnano.2015.112 ↗
8. 10.1039/C4NR02164A10.1039/C4NR02164A ↗
9. 10.1021/acsnano.6b0416510.1021/acsnano.6b04165 ↗
10. 10.1126/science.106234010.1126/science.1062340 ↗
11. 10.1021/nl034313e10.1021/nl034313e ↗
12. 10.1016/j.nanoen.2017.05.00410.1016/j.nanoen.2017.05.004 ↗
13. 10.3847/1538-4357/ab2a0310.3847/1538-4357/ab2a03 ↗
14. 10.1002/advs.20200005810.1002/advs.202000058 ↗
15. 10.1016/S0379-6779(99)00342-210.1016/S0379-6779(99)00342-2 ↗
16. 10.1063/1.12652510.1063/1.126525 ↗
17. 10.1021/ma500762x10.1021/ma500762x ↗
18. 10.1038/nmat464510.1038/nmat4645 ↗
19. 10.1063/1.486804110.1063/1.4868041 ↗
20. 10.1364/OE.24.01473710.1364/OE.24.014737 ↗
21. 10.1002/adom.20180134610.1002/adom.201801346 ↗
22. 10.1002/adom.20170027610.1002/adom.201700276 ↗
23. 10.1002/adma.1995007010810.1002/adma.19950070108 ↗
24. Sariciftci N. S. · C. Pac, Appl. Phys. Lett. · 1999 · 11 · 1449
25. 10.1063/1.214208210.1063/1.2142082 ↗
26. 10.1002/adfm.20110090410.1002/adfm.201100904 ↗
27. 10.1002/adfm.20130335110.1002/adfm.201303351 ↗
28. 10.1002/aenm.20130165910.1002/aenm.201301659 ↗
29. 10.1002/aelm.20170048010.1002/aelm.201700480 ↗
30. 10.1002/adma.20050183810.1002/adma.200501838 ↗
31. 10.1021/acsami.6b0185210.1021/acsami.6b01852 ↗
32. 10.1021/acsami.5b0871010.1021/acsami.5b08710 ↗
33. 10.1002/adma.20170546310.1002/adma.201705463 ↗
34. 10.1016/0079-6700(90)90025-V10.1016/0079-6700(90)90025-V ↗
35. 10.1039/C9ME00042A10.1039/C9ME00042A ↗
36. 10.1002/adfm.20060067310.1002/adfm.200600673 ↗
37. 10.1002/adma.20140117910.1002/adma.201401179 ↗
38. 10.1002/adma.20150243710.1002/adma.201502437 ↗
39. 10.1002/aelm.20160038810.1002/aelm.201600388 ↗
40. 10.1002/adfm.20140337710.1002/adfm.201403377 ↗
41. 10.1364/AO.56.00176810.1364/AO.56.001768 ↗
42. 10.1364/AO.59.00015610.1364/AO.59.000156 ↗
43. 10.1002/aenm.20120059510.1002/aenm.201200595 ↗
44. 10.1021/acs.chemmater.9b0333310.1021/acs.chemmater.9b03333 ↗
45. 10.1021/acs.chemmater.9b0101110.1021/acs.chemmater.9b01011 ↗
46. 10.1021/ma400516d10.1021/ma400516d ↗
47. 10.1002/adfm.20170017310.1002/adfm.201700173 ↗
48. 10.1021/acsapm.9b0022010.1021/acsapm.9b00220 ↗
49. 10.1021/jz300710a10.1021/jz300710a ↗
50. 10.1021/nn800574f10.1021/nn800574f ↗
51. 10.1038/s41563-020-00872-610.1038/s41563-020-00872-6 ↗
52. 10.1002/adma.20110151410.1002/adma.201101514 ↗
53. 10.1126/sciadv.abe319610.1126/sciadv.abe3196 ↗
54. 10.1364/OE.24.0A132110.1364/OE.24.0A1321 ↗
55. 10.1002/adma.20060016310.1002/adma.200600163 ↗
56. 10.1002/admi.20180096010.1002/admi.201800960 ↗
57. 10.1002/advs.20190113410.1002/advs.201901134 ↗
58. 10.1038/s41566-018-0239-810.1038/s41566-018-0239-8 ↗
59. 10.1039/C5NR03400K10.1039/C5NR03400K ↗
60. 10.1002/adom.20180035110.1002/adom.201800351 ↗
61. 10.1021/acsnano.9b0399410.1021/acsnano.9b03994 ↗
62. 10.1021/ja111259510.1021/ja1112595 ↗
63. 10.1021/acs.chemmater.8b0511410.1021/acs.chemmater.8b05114 ↗
64. 10.1021/acsami.8b0996810.1021/acsami.8b09968 ↗