Polariton Dynamics in Two-Dimensional Ruddlesden–Popper Perovskites Strongly Coupled with Plasmonic Lattices
Source abstract
Abstract
Strong coupling between light and matter can produce hybrid eigenstates known as exciton-polaritons. Although polariton dynamics are important photophysical properties, the relaxation pathways of polaritons in different coupling regimes have seen limited attention. This paper reports the dynamics of hybridized states from 2D Ruddlesden-Popper perovskites coupled to plasmonic nanoparticle lattices. The open cavity architecture of Al lattices enables the coupling strength to be modulated by varying either the lead halide perovskite film thickness or the superstrate refractive index. Both experiments and finite-difference time-domain simulations of the optical dispersion diagrams showed avoided crossings that are a signature of strong coupling. Our analytical model also elucidated the correlation between the exciton/plasmon mixing ratio and polariton coupling strength. Using fs-transient absorption spectroscopy, we found that both the upper and lower polaritons have shorter lifetimes than the excitons and that polaritons can show faster excited-state dynamics when they have access to additional energy transfer channels.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Strong Light-Matter Interactions · Thermal Radiation and Cooling Technologies · Spectroscopy and Quantum Chemical Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Northwestern University, Evanston, Illinois 60208, United States
Department of Materials Science and Engineering, Northwestern University, Evanston, Illinois 60208, United States
Funding
Office of Naval Research · U.S. Department of Defense · U.S. Department of Energy · Northwestern University · Division of Materials Research · International Institute for Nanotechnology, Northwestern University
References (64)
Show source-provided references
1. 10.1039/C9SC90225B10.1039/C9SC90225B ↗
2. 10.1038/s42254-020-0224-210.1038/s42254-020-0224-2 ↗
3. 10.1515/nanoph-2018-006710.1515/nanoph-2018-0067 ↗
4. 10.1021/acs.nanolett.7b0195610.1021/acs.nanolett.7b01956 ↗
5. 10.1038/s41563-021-01035-x10.1038/s41563-021-01035-x ↗
6. 10.1002/adfm.20180176110.1002/adfm.201801761 ↗
7. 10.1021/nn101973p10.1021/nn101973p ↗
8. 10.1002/adfm.20187034210.1002/adfm.201870342 ↗
9. 10.1126/sciadv.aat961810.1126/sciadv.aat9618 ↗
10. 10.1103/PhysRevB.56.755410.1103/PhysRevB.56.7554 ↗
11. 10.1103/PhysRevB.62.R228310.1103/PhysRevB.62.R2283 ↗
12. 10.1002/adfm.20160145210.1002/adfm.201601452 ↗
13. 10.1039/C6NR01588C10.1039/C6NR01588C ↗
14. 10.1021/acs.jpclett.9b0156810.1021/acs.jpclett.9b01568 ↗
15. 10.1088/1674-4926/40/4/04190110.1088/1674-4926/40/4/041901 ↗
16. 10.1038/s41467-018-04659-x10.1038/s41467-018-04659-x ↗
17. 10.1021/jacs.8b1085110.1021/jacs.8b10851 ↗
18. 10.1088/1367-2630/10/6/06500710.1088/1367-2630/10/6/065007 ↗
19. 10.1021/acsphotonics.8b0098410.1021/acsphotonics.8b00984 ↗
20. 10.1021/acsnano.8b0373710.1021/acsnano.8b03737 ↗
21. 10.1021/acsami.9b1996810.1021/acsami.9b19968 ↗
22. 10.1126/sciadv.aav996710.1126/sciadv.aav9967 ↗
23. 10.1364/OE.21.02741110.1364/OE.21.027411 ↗
24. 10.1021/nl403521910.1021/nl4035219 ↗
25. 10.1021/acsphotonics.7b0066110.1021/acsphotonics.7b00661 ↗
26. 10.1038/s41467-020-16906-110.1038/s41467-020-16906-1 ↗
27. 10.1021/acs.nanolett.0c0123610.1021/acs.nanolett.0c01236 ↗
28. 10.1021/acsnano.0c0278510.1021/acsnano.0c02785 ↗
29. 10.1021/acs.nanolett.5b0458810.1021/acs.nanolett.5b04588 ↗
30. 10.1021/acs.nanolett.7b0224510.1021/acs.nanolett.7b02245 ↗
31. 10.1021/acsphotonics.8b0145910.1021/acsphotonics.8b01459 ↗
32. 10.1364/JOSAB.36.000E8810.1364/JOSAB.36.000E88 ↗
33. 10.1016/j.mattod.2017.09.00210.1016/j.mattod.2017.09.002 ↗
34. 10.1073/pnas.200881811710.1073/pnas.2008818117 ↗
35. 10.1021/acs.jpclett.9b0107610.1021/acs.jpclett.9b01076 ↗
36. 10.1073/pnas.181890211610.1073/pnas.1818902116 ↗
37. 10.1021/acs.nanolett.1c0274010.1021/acs.nanolett.1c02740 ↗
38. 10.1021/acsnano.9b0946610.1021/acsnano.9b09466 ↗
39. 10.1021/acs.nanolett.9b0534210.1021/acs.nanolett.9b05342 ↗
40. 10.1021/acs.nanolett.9b0266110.1021/acs.nanolett.9b02661 ↗
41. 10.1021/acsnano.9b0114210.1021/acsnano.9b01142 ↗
42. 10.1021/acs.nanolett.8b0177410.1021/acs.nanolett.8b01774 ↗
43. 10.1021/nn502502r10.1021/nn502502r ↗
44. 10.1038/ncomms793910.1038/ncomms7939 ↗
45. 10.1103/PhysRevLett.112.15300210.1103/PhysRevLett.112.153002 ↗
46. 10.1103/PhysRevLett.121.24390410.1103/PhysRevLett.121.243904 ↗
47. 10.1002/adfm.20190131710.1002/adfm.201901317 ↗
48. 10.1021/jacs.9b0132710.1021/jacs.9b01327 ↗
49. 10.1021/nl102206x10.1021/nl102206x ↗
50. 10.1021/nl050614810.1021/nl0506148 ↗
51. 10.1021/nl061670r10.1021/nl061670r ↗
52. 10.1073/pnas.161528111310.1073/pnas.1615281113 ↗
53. 10.1103/PhysRevB.95.15542310.1103/PhysRevB.95.155423 ↗
54. 10.1021/acsphotonics.7b0067410.1021/acsphotonics.7b00674 ↗
55. 10.1038/nnano.2016.11010.1038/nnano.2016.110 ↗
56. 10.1063/1.500966310.1063/1.5009663 ↗
57. 10.1021/acs.jpclett.0c0024710.1021/acs.jpclett.0c00247 ↗
58. 10.1021/acs.jpcc.6b0407210.1021/acs.jpcc.6b04072 ↗
59. 10.1021/acsnano.8b0502910.1021/acsnano.8b05029 ↗
60. 10.1117/1.AP.2.5.05400110.1117/1.AP.2.5.054001 ↗
61. 10.1126/science.aaa533310.1126/science.aaa5333 ↗
62. 10.1021/acs.jpclett.0c0077210.1021/acs.jpclett.0c00772 ↗
63. 10.1021/acs.jpclett.9b0344710.1021/acs.jpclett.9b03447 ↗
64. 10.1073/pnas.200881811710.1073/pnas.2008818117 ↗