journal article·2016-09-27

Circular Dichroism of Electric-Field-Oriented CdSe/CdS Quantum Dots-in-Rods

Maria V. Mukhina, Anvar S. Baimuratov, Ivan D. Rukhlenko, Vladimir G. Maslov, Finn Purcell Milton, Yurii K. Gun’ko, Alexander V. Baranov, Anatoly V. Fedorov

ACS Nano· Volume 10· Issue 9
Publisher page

Abstract

Here we report anisotropy of intrinsic chiroptical response in CdSe/CdS quantum dot-in-rod systems. These nanostructures being oriented in an external electric field demonstrate dependence of circular dichroism signal on the orientation of the nanocrystals. The type of circular polarization in these nanostructures correlates with preferential direction of linear polarization, and the degree of circular polarization is the maximal for the first circular dichroism band corresponding to the absorption band edge. We also support our experimental data with a theoretical model. Using this model, we show a direct connection between theoretically derived morphological parameters of twisting in nanocrystals lattices and calculated from experimental data parameters of circular dichroism anisotropy.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Quantum Dots Synthesis And Properties · Metamaterials and Metasurfaces Applications · Advanced biosensing and bioanalysis techniques

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

Affiliations

Department of Optical Physics and Modern Natural Science, ITMO University, Saint Petersburg 197101, Russia

Monash University, Clayton Campus, Victoria 3800, Australia

School of Chemistry and CRANN Institute, Trinity College, Dublin, Dublin 2, Ireland

Funding

Science Foundation Ireland · Ministry of Education and Science of the Russian Federation · Seventh Framework Programme · Government of the Russian Federation

References (38)

Show source-provided references
1. 10.1039/C2CS35332F10.1039/C2CS35332F ↗
2. 10.1021/nl801453g10.1021/nl801453g ↗
3. 10.1021/nn404832f10.1021/nn404832f ↗
4. 10.1038/nprot.2015.02810.1038/nprot.2015.028 ↗
5. Govan, J.; Gun’ko, Y. K.Nanoscience;RSC:Cambridge, 2016; Vol.3; pp1–30.10.1039/9781782623717-00001 ↗
6. 10.1039/C5NH00072F10.1039/C5NH00072F ↗
7. 10.1021/acsnano.6b0056710.1021/acsnano.6b00567 ↗
8. 10.1038/srep2332110.1038/srep23321 ↗
9. 10.1002/ange.20120748910.1002/ange.201207489 ↗
10. 10.1364/OL.41.00243810.1364/OL.41.002438 ↗
11. 10.1021/nl504369x10.1021/nl504369x ↗
12. 10.1021/nl504439w10.1021/nl504439w ↗
13. 10.1021/cr00082a00410.1021/cr00082a004 ↗
14. 10.1002/bip.36030031810.1002/bip.360300318 ↗
15. 10.1103/PhysRevLett.90.09740210.1103/PhysRevLett.90.097402 ↗
16. 10.1557/opl.2015.65210.1557/opl.2015.652 ↗
17. 10.1021/nl200519b10.1021/nl200519b ↗
18. 10.1103/PhysRevB.85.03512610.1103/PhysRevB.85.035126 ↗
19. 10.1038/srep2417710.1038/srep24177 ↗
20. 10.1364/OL.38.00342610.1364/OL.38.003426 ↗
21. Jennings, B. R.InNato Science Series B;Krause, S., Ed.Springer:New York, 1981; Vol.64; pp27–60.
22. 10.1016/S0006-3495(90)82599-610.1016/S0006-3495(90)82599-6 ↗
23. 10.1364/AO.11.00052710.1364/AO.11.000527 ↗
24. 10.1021/ja00781a00110.1021/ja00781a001 ↗
25. 10.1021/j150546a00510.1021/j150546a005 ↗
26. 10.1063/1.169691410.1063/1.1696914 ↗
27. 10.1143/JPSJ.23.8810.1143/JPSJ.23.88 ↗
28. 10.1016/0301-0104(76)80105-X10.1016/0301-0104(76)80105-X ↗
29. 10.1016/j.cplett.2003.12.01710.1016/j.cplett.2003.12.017 ↗
30. 10.1103/PhysRevB.72.12532510.1103/PhysRevB.72.125325 ↗
31. 10.1021/jz302116710.1021/jz3021167 ↗
32. 10.1021/jp013204q10.1021/jp013204q ↗
33. 10.1021/nl020231z10.1021/nl020231z ↗
34. 10.1126/science.106081010.1126/science.1060810 ↗
35. 10.1021/jp409559t10.1021/jp409559t ↗
36. 10.1039/j1971000198810.1039/j19710001988 ↗
37. 10.1016/0009-2614(95)01036-910.1016/0009-2614(95)01036-9 ↗
38. 10.1039/c3cs60139k10.1039/c3cs60139k ↗