journal article·2022-01-25Open access

Exciton Delocalization in a DNA-Templated Organic Semiconductor Dimer Assembly

Xiao Wang, Ruojie Sha, William B. Knowlton, Nadrian C. Seeman, James W. Canary, Bernard Yurke

ACS Nano· Volume 16· Issue 1

Abstract

A chiral dimer of an organic semiconductor was assembled from octaniline (octamer of polyaniline) conjugated to DNA. Facile reconfiguration between the monomer and dimer of octaniline-DNA was achieved. The geometry of the dimer and the exciton coupling between octaniline molecules in the assembly was studied both experimentally and theoretically. The octaniline dimer was readily switched between different electronic states by protonic doping and exhibited a Davydov splitting comparable to those previously reported for DNA-dye systems employing dyes with strong transition dipoles. This approach provides a possible platform for studying the fundamental properties of organic semiconductors with DNA-templated assemblies, which serve as candidates for artificial light-harvesting systems and excitonic devices.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Conducting polymers and applications · Advanced biosensing and bioanalysis techniques · Perovskite Materials and Applications

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

Affiliations

Department of Chemistry, New York University, New York, New York 10003, United States

Micron School for Materials Science and Engineering and Department of Electrical & Computer Engineering, Boise State University, Boise, Idaho 83725, United States

Funding

Division of Computing and Communication Foundations · Division of Chemistry · Office of Naval Research · Division of Electrical, Communications and Cyber Systems · U.S. Department of Energy · Human Frontiers Science Program

References (40)

Show source-provided references
1. 10.1016/S0969-2126(96)00063-910.1016/S0969-2126(96)00063-9 ↗
2. 10.1023/A:102240670311010.1023/A:1022406703110 ↗
3. 10.1038/nature0567810.1038/nature05678 ↗
4. 10.1146/annurev-physchem-040214-12171310.1146/annurev-physchem-040214-121713 ↗
5. 10.1021/ja111513810.1021/ja1115138 ↗
6. 10.1021/ja509018g10.1021/ja509018g ↗
7. 10.1103/PhysRevA.81.03381410.1103/PhysRevA.81.033814 ↗
8. 10.1038/nature0140610.1038/nature01406 ↗
9. 10.1038/3502052410.1038/35020524 ↗
10. 10.1021/ja021153k10.1021/ja021153k ↗
11. 10.1002/chem.20090036910.1002/chem.200900369 ↗
12. 10.1039/c3cc42103a10.1039/c3cc42103a ↗
13. 10.1021/acs.jpcb.8b0213410.1021/acs.jpcb.8b02134 ↗
14. 10.1063/1.502008410.1063/1.5020084 ↗
15. 10.1021/acs.jpcb.0c0673210.1021/acs.jpcb.0c06732 ↗
16. 10.1021/acs.jpclett.0c0102010.1021/acs.jpclett.0c01020 ↗
17. 10.1039/C3CC47490A10.1039/C3CC47490A ↗
18. 10.1039/C1OB06400B10.1039/C1OB06400B ↗
19. 10.1016/0022-5193(82)90002-910.1016/0022-5193(82)90002-9 ↗
20. 10.1038/305829a010.1038/305829a0 ↗
21. 10.1021/acs.jpca.7b0434410.1021/acs.jpca.7b04344 ↗
22. 10.1021/acs.jpca.7b1266810.1021/acs.jpca.7b12668 ↗
23. 10.1021/acs.jpclett.9b0040410.1021/acs.jpclett.9b00404 ↗
24. 10.1021/acs.jpca.7b1266810.1021/acs.jpca.7b12668 ↗
25. 10.1038/s42004-021-00456-810.1038/s42004-021-00456-8 ↗
26. 10.1016/j.chempr.2020.12.02010.1016/j.chempr.2020.12.020 ↗
27. 10.1038/nnano.2015.19010.1038/nnano.2015.190 ↗
28. 10.1021/acs.nanolett.8b0033210.1021/acs.nanolett.8b00332 ↗
29. 10.1002/anie.20170046210.1002/anie.201700462 ↗
30. 10.1021/cm501445u10.1021/cm501445u ↗
31. 10.1021/acs.nanolett.7b0262310.1021/acs.nanolett.7b02623 ↗
32. 10.1021/acs.jpcb.0c0648010.1021/acs.jpcb.0c06480 ↗
33. 10.3390/s1903046910.3390/s19030469 ↗
34. 10.1038/s41467-018-06239-510.1038/s41467-018-06239-5 ↗
35. 10.1039/c2cc38575a10.1039/c2cc38575a ↗
36. 10.1021/nn305424e10.1021/nn305424e ↗
37. Sutherland J. C. · 2012 · 1 · 3510.1002/9781118120187.ch2 ↗
38. 10.1126/science.288.5470.140410.1126/science.288.5470.1404 ↗
39. 10.1039/b515476f10.1039/b515476f ↗
40. 10.1021/ja00286a05710.1021/ja00286a057 ↗