Circularly Polarized Emission from Organic–Inorganic Hybrid Perovskites via Chiral Fano Resonances
Source abstract
Abstract
Organic-inorganic hybrid perovskites hold great potential for various optoelectronic devices with exceptional properties. Although the direct generation of circularly polarized emission from perovskites would enable various compact devices, achieving a large degree of circular polarization (DCP) at room temperature still remains challenging. Herein, we demonstrate that DCP can be strongly enhanced at the narrow mode position of chiral Fano resonances. In our design, a perovskite film is spin-coated on a symmetry-broken structure with a relatively large feature size. A large DCP of more than 0.5 is achieved at room temperature without the direct patterning of the perovskite layer. Reciprocity calculation reveals that chiral field enhancement enables the emission of opposite helicity to couple into counter-propagating slab modes and leads to a large DCP. Our design is very general and scalable. Our work may lead to circularly polarized light sources based on various perovskite materials.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Perovskite Materials and Applications · Metamaterials and Metasurfaces Applications · Organic Light-Emitting Diodes Research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science and Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919, Republic of Korea
School of Energy and Chemical Engineering, UNIST, Ulsan 44919, Republic of Korea
Department of Physics, Korea University, Seoul 02841, Republic of Korea
Department of Physics, University of California, Berkeley, California 94720, United States
Funding
Ulsan National Institute of Science and Technology · National Research Foundation of Korea
References (68)
Show source-provided references
1. 10.1038/natrevmats.2015.710.1038/natrevmats.2015.7 ↗
2. 10.1038/natrevmats.2016.9910.1038/natrevmats.2016.99 ↗
3. Park N.-G. · 201610.1007/978-3-319-35114-8 ↗
4. 10.1126/science.abc441710.1126/science.abc4417 ↗
5. 10.1021/acs.nanolett.7b0322510.1021/acs.nanolett.7b03225 ↗
6. 10.1021/acsnano.0c0496810.1021/acsnano.0c04968 ↗
7. 10.1002/adma.20200233310.1002/adma.202002333 ↗
8. 10.1021/acsnano.1c0067310.1021/acsnano.1c00673 ↗
9. 10.1038/nphoton.2016.6210.1038/nphoton.2016.62 ↗
10. 10.1002/adma.20160066910.1002/adma.201600669 ↗
11. 10.1039/C7MH00197E10.1039/C7MH00197E ↗
12. 10.1038/s41566-018-0220-610.1038/s41566-018-0220-6 ↗
13. 10.1021/acsnano.9b0030210.1021/acsnano.9b00302 ↗
14. 10.1038/s41578-020-0181-510.1038/s41578-020-0181-5 ↗
15. Kim D.-Y. · J. Korean Phys. Soc. · 2006 · 49 · S505
16. 10.1063/1.358291710.1063/1.3582917 ↗
17. 10.1364/OE.27.01166110.1364/OE.27.011661 ↗
18. Tuchin V. V. · 200610.1007/978-3-540-45321-5 ↗
19. 10.1016/j.jqsrt.2009.02.02810.1016/j.jqsrt.2009.02.028 ↗
20. 10.1002/adom.20190035010.1002/adom.201900350 ↗
21. 10.1021/acs.jpclett.0c0000410.1021/acs.jpclett.0c00004 ↗
22. 10.1002/adom.20170018210.1002/adom.201700182 ↗
23. 10.1002/adom.20170004010.1002/adom.201700040 ↗
24. 10.1103/PhysRevLett.106.05740210.1103/PhysRevLett.106.057402 ↗
25. 10.1103/PhysRevB.88.04140710.1103/PhysRevB.88.041407 ↗
26. 10.1021/ph500288u10.1021/ph500288u ↗
27. 10.1103/PhysRevB.89.04531610.1103/PhysRevB.89.045316 ↗
28. 10.1021/acsnano.5b0723110.1021/acsnano.5b07231 ↗
29. 10.1002/lpor.20180027610.1002/lpor.201800276 ↗
30. 10.1038/s41565-020-0758-610.1038/s41565-020-0758-6 ↗
31. 10.1002/adom.20190123310.1002/adom.201901233 ↗
32. 10.1021/jz502471h10.1021/jz502471h ↗
33. 10.1088/1464-4258/11/7/07400910.1088/1464-4258/11/7/074009 ↗
34. 10.1021/nl300316f10.1021/nl300316f ↗
35. 10.1515/nanoph-2019-032110.1515/nanoph-2019-0321 ↗
36. 10.1515/nanoph-2020-013010.1515/nanoph-2020-0130 ↗
37. 10.1038/nmat281010.1038/nmat2810 ↗
38. 10.1515/nanoph-2013-000910.1515/nanoph-2013-0009 ↗
39. 10.1038/nphoton.2017.14210.1038/nphoton.2017.142 ↗
40. 10.1021/acsnano.7b0481010.1021/acsnano.7b04810 ↗
41. 10.1021/acs.nanolett.8b0280810.1021/acs.nanolett.8b02808 ↗
42. 10.1038/ncomms489210.1038/ncomms4892 ↗
43. 10.1002/lpor.20150022210.1002/lpor.201500222 ↗
44. 10.1103/PhysRevB.93.19541810.1103/PhysRevB.93.195418 ↗
45. 10.1021/acsphotonics.8b0100710.1021/acsphotonics.8b01007 ↗
46. Piao X. · 2018
47. 10.1002/adma.20190707710.1002/adma.201907077 ↗
48. 10.1103/PhysRevB.66.04510210.1103/PhysRevB.66.045102 ↗
49. 10.1002/adma.20160426810.1002/adma.201604268 ↗
50. 10.1126/science.aba459710.1126/science.aba4597 ↗
51. Lide D. R. · 2009
52. 10.1016/j.synthmet.2015.03.03510.1016/j.synthmet.2015.03.035 ↗
53. 10.1515/nanoph-2019-011010.1515/nanoph-2019-0110 ↗
54. 10.1038/nnano.2015.15910.1038/nnano.2015.159 ↗
55. 10.1126/science.aan801010.1126/science.aan8010 ↗
56. 10.1126/science.123489210.1126/science.1234892 ↗
57. 10.1038/s42254-020-00276-010.1038/s42254-020-00276-0 ↗
58. 10.1063/1.45173510.1063/1.451735 ↗
59. 10.1021/nl503931410.1021/nl5039314 ↗
60. 10.1038/4550910.1038/45509 ↗
61. 10.1038/4550210.1038/45502 ↗
62. 10.1126/science.abf529110.1126/science.abf5291 ↗
63. 10.1021/acsnano.0c0890310.1021/acsnano.0c08903 ↗
64. 10.1002/adom.20180053810.1002/adom.201800538 ↗
65. 10.1039/C9CS00680J10.1039/C9CS00680J ↗
66. 10.1021/acs.nanolett.8b0191210.1021/acs.nanolett.8b01912 ↗
67. 10.1063/1.510744910.1063/1.5107449 ↗
68. 10.1515/nanoph-2020-034310.1515/nanoph-2020-0343 ↗