Solution Processable Iridescent Self-Assembled Nanoplatelets with Finely Tunable Interlayer Distances Using Charge- and Sterically Stabilizing Oligomeric Polyoxyalkyleneamine Surfactants
Source abstract
Abstract
Photonic structures that are processable in organic solvents are critical to large-scale fabrication of device components. To provide a viable alternative to traditional lithographic methods, solution processable photonic structures are required to demonstrate fine control over critical device dimensions in the fabrication process. Photonic structures typically require long-range electrostatic forces that are effective only in aqueous solutions. Here we report a novel strategy of using oligomeric polyoxyalkyleneamine surfactants to prepare charge- and sterically stabilized nanoplatelets that can self-assemble into lamellar phases in nonaqueous solutions with finely tunable large interlamellar distances that can exceed 100 nm. Brilliant iridescence in the visible spectrum with tunable colors is demonstrated. The nanoplatelets are shown to circumvent the typical phase transition behavior from isotropic to nematic to columnar phase and transitioned into smectic phase at concentrations of ϕ < 0.01.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Photonic Crystals and Applications · Luminescence and Fluorescent Materials · Liquid Crystal Research Advancements
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute for Materials Chemistry and Engineering, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka 819-0395, Japan
Erato Takahara Soft Interfaces Project, Japan Science and Technology Agency (JST), 744 Motooka, Nishi-ku, Fukuoka 819-0385, Japan
References (49)
Show source-provided references
1. Bonaccorso F. · Nat. Photon. · 2010 · 4 · 61110.1038/nphoton.2010.186 ↗
2. Blake P. · Nano Lett. · 2008 · 8 · 170410.1021/nl080649i ↗
3. Li S.-S. · ACS Nano · 2010 · 4 · 316910.1021/nn100551j ↗
4. Reina A. · J. Phys. Chem. C · 2008 · 112 · 1774110.1021/jp807380s ↗
5. Rugge A. · Langmuir · 2002 · 18 · 705710.1021/la025710s ↗
6. Leunissen M. E. · Nature · 2005 · 437 · 23510.1038/nature03946 ↗
7. Roberts G. S. · Langmuir · 2008 · 24 · 653010.1021/la703908n ↗
8. Ge J. · J. Am. Chem. Soc. · 2009 · 131 · 348410.1021/ja809772v ↗
9. Yang H. · Langmuir · 2010 · 26 · 1317310.1021/la101721v ↗
10. Jethmalani J. M. · Chem. Mater. · 1996 · 8 · 213810.1021/cm960065u ↗
11. Maeda Y. · Colloids Surf. · 1983 · 6 · 110.1016/0166-6622(83)80001-8 ↗
12. Mourad M. C. D. · J. Mater. Chem. · 2008 · 18 · 300410.1039/b803564b ↗
13. Mourad M. C. D. · Langmuir · 2010 · 26 · 1418210.1021/la100797x ↗
14. Platz G. · Prog. Colloid Polym. Sci. · 1990 · 83 · 16710.1007/BFb0116256 ↗
15. Hoffmann H. · Adv. Mater. · 1994 · 6 · 11610.1002/adma.19940060204 ↗
16. Satoh N. · J. Phys. Chem. · 1987 · 91 · 662910.1021/j100311a015 ↗
17. Gabriel J.-C. P. · Nature · 2001 · 413 · 50410.1038/35097046 ↗
18. Geim A. · Nat. Mater. · 2007 · 6 · 18310.1038/nmat1849 ↗
19. Li P. · ACS Photonics · 2014 · 1 · 7910.1021/ph400093c ↗
20. Coleman J. · Science · 2011 · 331 · 56810.1126/science.1194975 ↗
21. Osada M. · J. Mater. Chem. · 2009 · 19 · 250310.1039/b820160a ↗
22. Thunig, C.; Hoffmann, H.; Platz, G.InTrends in Colloid and Interface Science III;Bothorel, P.; Dufourc, E., Eds.Springer:Berlin/Heidelberg, 1989; pp297–307.
23. Haque M. A. · Soft Matter · 2012 · 8 · 800810.1039/c2sm25670c ↗
24. Hsu M. F. · Langmuir · 2005 · 21 · 488110.1021/la046751m ↗
25. Kleshchanok D. · J. Am. Chem. Soc. · 2012 · 134 · 598510.1021/ja300527w ↗
26. van der Kooij F. M. · Nature · 2000 · 406 · 86810.1038/35022535 ↗
27. Veerman J. A. C. · Phys. Rev. A · 1992 · 45 · 563210.1103/PhysRevA.45.5632 ↗
28. van der Beek D. · Langmuir · 2004 · 20 · 858210.1021/la049455i ↗
29. Okubo T. · Acc. Chem. Res. · 1988 · 21 · 28110.1021/ar00151a005 ↗
30. Sun L. · New J. Chem. · 2007 · 31 · 3910.1039/B604054C ↗
31. Novoselov K. S. · Science · 2004 · 306 · 66610.1126/science.1102896 ↗
32. Mas-Balleste R. · Nanoscale · 2011 · 3 · 2010.1039/C0NR00323A ↗
33. Neto A. H. C. · Mater. Express · 2011 · 1 · 1010.1166/mex.2011.1002 ↗
34. Sun L. · Chem. Mater. · 2005 · 17 · 560610.1021/cm051160i ↗
35. Alberti G. · J. Mol. Catal. · 1984 · 27 · 23510.1016/0304-5102(84)85083-X ↗
36. Koizumi N. · Bull. Inst. Chem. Res., Kyoto Univ. · 1964 · 42 · 115
37. Nallet F. · J. Phys. II · 1993 · 3 · 487
38. Meyer J. C. · Nature · 2007 · 446 · 6010.1038/nature05545 ↗
39. Castellanos-Gomez A. · Adv. Mater. · 2012 · 24 · 77210.1002/adma.201103965 ↗
40. Shibayama M. · Macromolecules · 1986 · 19 · 74010.1021/ma00157a043 ↗
41. Kim H.-N. · Chem. Mater. · 1997 · 9 · 141410.1021/cm970027q ↗
42. Sun D. Z. · Phys. Rev. E · 2009 · 80 · 04170410.1103/PhysRevE.80.041704 ↗
43. Clearfield A. · Inorg. Chem. · 1969 · 8 · 43110.1021/ic50073a005 ↗
44. Xu Z. · Nat. Commun. · 2011 · 2 · 57110.1038/ncomms1583 ↗
45. Barton A. F. M. · 1991
46. Barton A. F. M. · 1990
47. Mieczkowski R. · Eur. Polym. J. · 1991 · 27 · 37710.1016/0014-3057(91)90191-P ↗
48. Lide D. R. · 1999
49. Masunaga H. · Polym. J. · 2011 · 43 · 47110.1038/pj.2011.18 ↗