Selective Reduction Approach in Cocrystal Systems for Highly Conducting Organic Radical Crystals
Source abstract
Abstract
Many polycyclic aromatic hydrocarbon molecules are electrically inactive despite their high degree of π-conjugation. We solve this problem by forming molecular cocrystals with radical-generating molecules which upon post-treatment become highly conducting organic radical crystals. Fluoranthene (FA)–tetracyanoquinodimethane (TCNQ) cocrystals were prepared from a mechanochemically prepared FA–TCNQ mixture precursor by the physical vapor transport (PVT) process. While both FA crystals and as-prepared FA–TCNQ cocrystals show low electrical conductivity, FA–TCNQ cocrystals exposed to hydrazine show dramatically increased conductivity as hydrazine generates radicals in TCNQ which work as charge carriers in FA–TCNQ cocrystals. The systematic studies of electron paramagnetic resonance spectroscopy, Raman spectroscopy, and electrical device measurement support that the generation of radical species from TCNQ by the hydrazine reaction is responsible for the high conductivity.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic and Molecular Conductors Research · Crystallography and molecular interactions · Photochemistry and Electron Transfer Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Division of Advanced Materials Science, Pohang University of Science and Technology (POSTECH), 77 CheongamRo, Pohang37673, Korea
Department of Chemistry, Pohang University of Science and Technology (POSTECH), 77 CheongamRo, Pohang37673, Korea
Funding
Samsung · National Research Foundation of Korea
References (61)
Show source-provided references
1. 10.1039/D1TC04866J10.1039/D1TC04866J ↗
2. 10.1002/tcr.20200009810.1002/tcr.202000098 ↗
3. 10.1039/D0SC03521A10.1039/D0SC03521A ↗
4. 10.1016/j.chempr.2020.10.00110.1016/j.chempr.2020.10.001 ↗
5. 10.3389/fphy.2019.0005210.3389/fphy.2019.00052 ↗
6. 10.1080/0895795920824564510.1080/08957959208245645 ↗
7. 10.1016/j.orgel.2018.12.01010.1016/j.orgel.2018.12.010 ↗
8. 10.1038/s42004-018-0048-510.1038/s42004-018-0048-5 ↗
9. 10.1002/anie.20200626310.1002/anie.202006263 ↗
10. 10.1021/acs.jpclett.8b0307410.1021/acs.jpclett.8b03074 ↗
11. 10.1002/adma.20160150210.1002/adma.201601502 ↗
12. 10.1021/jp102562510.1021/jp1025625 ↗
13. 10.1021/acs.jpcc.0c1064410.1021/acs.jpcc.0c10644 ↗
14. 10.1021/jacs.7b0547110.1021/jacs.7b05471 ↗
15. 10.1021/acs.cgd.8b0168610.1021/acs.cgd.8b01686 ↗
16. 10.1126/science.107137210.1126/science.1071372 ↗
17. 10.1002/anie.20050230310.1002/anie.200502303 ↗
18. 10.1021/jacs.8b1330010.1021/jacs.8b13300 ↗
19. 10.1021/jacs.9b1067710.1021/jacs.9b10677 ↗
20. 10.1021/jacs.5b1235510.1021/jacs.5b12355 ↗
21. 10.1002/chem.20160412110.1002/chem.201604121 ↗
22. 10.1016/j.synthmet.2012.10.02610.1016/j.synthmet.2012.10.026 ↗
23. 10.1002/anie.20170208410.1002/anie.201702084 ↗
24. Boltalina O. V. · 2021
25. 10.3389/fchem.2021.76462810.3389/fchem.2021.764628 ↗
26. 10.1002/adma.20190232810.1002/adma.201902328 ↗
27. 10.1002/anie.20190050110.1002/anie.201900501 ↗
28. 10.1039/C7TC04982J10.1039/C7TC04982J ↗
29. 10.1002/anie.20160771210.1002/anie.201607712 ↗
30. 10.3390/cryst1011099310.3390/cryst10110993 ↗
31. 10.1039/C3CE41703D10.1039/C3CE41703D ↗
32. 10.1039/C9CE01507H10.1039/C9CE01507H ↗
33. 10.1039/C5NR02778K10.1039/C5NR02778K ↗
34. 10.1016/0371-1951(60)80139-710.1016/0371-1951(60)80139-7 ↗
35. 10.1016/j.physb.2016.05.02310.1016/j.physb.2016.05.023 ↗
36. 10.1021/jp075377710.1021/jp0753777 ↗
37. 10.1002/chem.20200121110.1002/chem.202001211 ↗
38. 10.1107/S160057751502163310.1107/S1600577515021633 ↗
39. 10.1016/S0076-6879(97)76066-X10.1016/S0076-6879(97)76066-X ↗
40. 10.1107/S010876730300548810.1107/S0108767303005488 ↗
41. 10.1107/S205322961402421810.1107/S2053229614024218 ↗
42. 10.1002/recl.1958077060510.1002/recl.19580770605 ↗
43. Sawyer D. T. · 1995
44. 10.1039/FT994900251710.1039/FT9949002517 ↗
45. 10.1016/j.joule.2017.07.00710.1016/j.joule.2017.07.007 ↗
46. 10.1021/ja963174i10.1021/ja963174i ↗
47. 10.1016/0379-6779(93)90353-X10.1016/0379-6779(93)90353-X ↗
48. 10.1063/1.43766210.1063/1.437662 ↗
49. 10.1002/aelm.20160020310.1002/aelm.201600203 ↗
50. 10.1021/jacs.8b0286710.1021/jacs.8b02867 ↗
51. 10.1002/anie.20210270810.1002/anie.202102708 ↗
52. 10.1021/ja900229810.1021/ja9002298 ↗
53. 10.1038/s41586-021-03942-010.1038/s41586-021-03942-0 ↗
54. 10.1038/s41467-020-16648-010.1038/s41467-020-16648-0 ↗
55. 10.1002/adma.20180183010.1002/adma.201801830 ↗
56. 10.1021/acsami.0c0438010.1021/acsami.0c04380 ↗
57. 10.1021/nn204566410.1021/nn2045664 ↗
58. 10.1021/acs.macromol.0c0046010.1021/acs.macromol.0c00460 ↗
59. 10.1016/j.matt.2019.12.01810.1016/j.matt.2019.12.018 ↗
60. 10.1246/bcsj.49.141710.1246/bcsj.49.1417 ↗
61. 10.1021/ac203051410.1021/ac2030514 ↗