Hydrogen-Bond-Directed Chirality Transfer in Helical Polyacetylene–Perovskite–PDMS Elastomeric Films for Stretching-Tunable Multicolor Circularly Polarized Luminescence
Source abstract
Abstract
Circularly polarized luminescence (CPL) has emerged as a critical technology for anticounterfeiting and optical display applications due to its unique chiroptical properties. We report a multicolor CPL-emitting elastomeric film (P37/PSK@SiO 2 -PDMS) that synergistically combines chiral helical polyacetylene (P37) and a surface-engineered perovskite (PSK@SiO 2 ) through hydrogen-bond-directed assembly. Confinement within the PDMS matrix drives P37 to self-assemble into a chiral supramolecular structure through hydrogen bonding, inducing a chiroptical inversion. Simultaneously, surface modification of PSK@SiO 2 enhances its compatibility with PDMS while enabling efficient chirality and energy transfer from P37 via interfacial hydrogen bonds. The resulting material exhibits exceptional CPL performance, achieving a maximum dissymmetry factor of 4.3 × 10 –2 and a high photoluminescence quantum yield up to 67%. The PDMS matrix not only stabilizes the PSK components but also enables reversible, strain-tunable CPL modulation through its elastomeric properties. This work establishes a hydrogen-bonding paradigm for designing high-performance chiral PSK materials, while demonstrating their potential for dynamic photonic applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Synthesis and Properties of Aromatic Compounds · Polydiacetylene-based materials and applications · Perovskite Materials and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Organic−Inorganic Composites and College of Materials Science and Engineering
State Key Laboratory of Chemical Resource Engineering
College of Materials Science and Engineering
Beijing University of Chemical Technology
Funding
Fundamental Research Funds for the Central Universities · National Natural Science Foundation of China
References (51)
Show source-provided references
1. 10.1038/s41377-023-01334-910.1038/s41377-023-01334-9 ↗
2. 10.1002/anie.20240738510.1002/anie.202407385 ↗
3. 10.1002/anie.20242029010.1002/anie.202420290 ↗
4. 10.1038/s41377-020-00435-z10.1038/s41377-020-00435-z ↗
5. 10.1002/adfm.20241730810.1002/adfm.202417308 ↗
6. 10.1038/s41467-023-43650-z10.1038/s41467-023-43650-z ↗
7. 10.1016/j.carbpol.2023.12085610.1016/j.carbpol.2023.120856 ↗
8. 10.1038/s41467-022-34464-610.1038/s41467-022-34464-6 ↗
9. 10.1126/sciadv.adi994410.1126/sciadv.adi9944 ↗
10. 10.1002/advs.20241425910.1002/advs.202414259 ↗
11. 10.3390/molecules2312337610.3390/molecules23123376 ↗
12. 10.1038/s41467-023-44643-810.1038/s41467-023-44643-8 ↗
13. 10.1002/anie.20240951410.1002/anie.202409514 ↗
14. 10.1021/jacs.1c1276710.1021/jacs.1c12767 ↗
15. 10.1021/jz402016210.1021/jz4020162 ↗
16. 10.1038/s41586-018-0575-310.1038/s41586-018-0575-3 ↗
17. 10.1038/nphoton.2016.10810.1038/nphoton.2016.108 ↗
18. 10.1038/s41928-022-00745-710.1038/s41928-022-00745-7 ↗
19. 10.1002/adma.20200878510.1002/adma.202008785 ↗
20. 10.1007/s12274-021-3594-610.1007/s12274-021-3594-6 ↗
21. 10.1016/j.chempr.2022.01.01410.1016/j.chempr.2022.01.014 ↗
22. 10.1039/D4NR00644E10.1039/D4NR00644E ↗
23. 10.1002/adom.20230016110.1002/adom.202300161 ↗
24. 10.1002/adfm.20221209510.1002/adfm.202212095 ↗
25. 10.1002/anie.20191591210.1002/anie.201915912 ↗
26. 10.1016/j.cej.2023.14830610.1016/j.cej.2023.148306 ↗
27. 10.1021/acsnano.9b0030210.1021/acsnano.9b00302 ↗
28. 10.1021/acsnano.0c0362810.1021/acsnano.0c03628 ↗
29. 10.1002/anie.20210723910.1002/anie.202107239 ↗
30. 10.1021/acsnano.0c0341810.1021/acsnano.0c03418 ↗
31. 10.1021/acsnano.0c0390910.1021/acsnano.0c03909 ↗
32. 10.1016/j.matt.2022.05.01210.1016/j.matt.2022.05.012 ↗
33. 10.1002/adma.20220726510.1002/adma.202207265 ↗
34. 10.1021/acsami.2c2071610.1021/acsami.2c20716 ↗
35. 10.1021/jacs.2c1252710.1021/jacs.2c12527 ↗
36. 10.1002/anie.20240076910.1002/anie.202400769 ↗
37. 10.1021/acs.macromol.1c0056310.1021/acs.macromol.1c00563 ↗
38. 10.1021/cr900162q10.1021/cr900162q ↗
39. 10.1016/j.matt.2023.02.00310.1016/j.matt.2023.02.003 ↗
40. 10.1002/anie.20240420210.1002/anie.202404202 ↗
41. 10.1002/anie.20250017310.1002/anie.202500173 ↗
42. 10.1016/j.compscitech.2022.10984010.1016/j.compscitech.2022.109840 ↗
43. 10.1016/j.compscitech.2024.11062510.1016/j.compscitech.2024.110625 ↗
44. 10.1021/acs.macromol.8b0230510.1021/acs.macromol.8b02305 ↗
45. 10.1021/acs.chemmater.2c0332210.1021/acs.chemmater.2c03322 ↗
46. 10.1021/ma049807s10.1021/ma049807s ↗
47. 10.1002/adom.20230303910.1002/adom.202303039 ↗
48. 10.1021/acsnano.3c0071310.1021/acsnano.3c00713 ↗
49. 10.1002/anie.20210905410.1002/anie.202109054 ↗
50. 10.1002/marc.20130034210.1002/marc.201300342 ↗
51. 10.1039/C5PY01945A10.1039/C5PY01945A ↗