journal article·2019-12-24

Enhanced p-Type Work Function Tunability Induced by Electrostatic Molecular Alignment and Surface Coverage in Conjugated Small-Molecule Electrolyte

Jong-Hoon Lee, Sooncheol Kwon, Song Yi Jeong, Byoungwook Park, Soonil Hong, Jehan Kim, Soo-Young Jang, Kwanghee Lee

ACS Applied Electronic Materials· Volume 1· Issue 12
Publisher page

Abstract

We report that a chemically p-doped conjugated small-molecule electrolyte (CSE) can be used as a strong and uniform dipole array for highly efficient optoelectronic devices via electrostatically induced molecular alignment and surface coverage on metal electrodes. On the basis of the structural and electrical characterization as well as evaluation of the surface potential, we confirm a close structure–property relationship in the p-doped CSE; the CSE molecules can interact electrostatically with each other and with the metal surface, leading to an out-of-plane orientation and full surface coverage, respectively, providing a superior WF tunability compared to that of its polymeric counterpart. Our results clearly indicate that the overall strength of the electric dipoles in the thin-film interfacial layer can be controlled by the degree of molecular alignment and coverage, making this material broadly applicable in highly efficient optoelectronics.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Organic Electronics and Photovoltaics · Perovskite Materials and Applications · Conducting polymers and applications

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

Affiliations

Pohang Accelerator Laboratory, Pohang University of Science and Technology, Pohang 790-784, Republic of Korea

Funding

National Research Foundation of Korea · Ministry of Trade, Industry and Energy · Korea Institute of Energy Technology Evaluation and Planning · Gwangju Institute of Science and Technology

References (34)

Show source-provided references
1. 10.1088/2058-7058/12/3/2710.1088/2058-7058/12/3/27 ↗
2. 10.1002/pola.1040510.1002/pola.10405 ↗
3. 10.1146/annurev.matsci.36.022805.09475710.1146/annurev.matsci.36.022805.094757 ↗
4. 10.1038/nmat191510.1038/nmat1915 ↗
5. 10.1002/pssa.20082442810.1002/pssa.200824428 ↗
6. 10.1038/nature1231410.1038/nature12314 ↗
7. 10.1038/nature1147610.1038/nature11476 ↗
8. 10.1002/adfm.20090223610.1002/adfm.200902236 ↗
9. 10.1038/3500661010.1038/35006610 ↗
10. 10.1016/S1369-7021(07)70019-610.1016/S1369-7021(07)70019-6 ↗
11. 10.1039/C4EE03824J10.1039/C4EE03824J ↗
12. 10.1002/adma.20080053310.1002/adma.200800533 ↗
13. 10.1002/adma.20130339110.1002/adma.201303391 ↗
14. 10.1021/acsami.9b0421110.1021/acsami.9b04211 ↗
15. 10.1002/admi.20140018910.1002/admi.201400189 ↗
16. 10.1002/admi.20180089710.1002/admi.201800897 ↗
17. 10.1021/ja801451e10.1021/ja801451e ↗
18. 10.1002/adfm.20170507910.1002/adfm.201705079 ↗
19. 10.1039/C8EE00162F10.1039/C8EE00162F ↗
20. 10.1021/cm502864s10.1021/cm502864s ↗
21. 10.1002/adfm.20130181010.1002/adfm.201301810 ↗
22. 10.1039/C5TA04695E10.1039/C5TA04695E ↗
23. 10.1002/aenm.20140165310.1002/aenm.201401653 ↗
24. 10.1002/aenm.20150129210.1002/aenm.201501292 ↗
25. 10.1021/acs.chemmater.7b0498210.1021/acs.chemmater.7b04982 ↗
26. 10.1002/adfm.20150516110.1002/adfm.201505161 ↗
27. 10.1002/aenm.20140076810.1002/aenm.201400768 ↗
28. 10.1038/ncomms668810.1038/ncomms6688 ↗
29. 10.1021/ja711068d10.1021/ja711068d ↗
30. 10.1002/anie.20120995910.1002/anie.201209959 ↗
31. 10.1038/nphoton.2015.12610.1038/nphoton.2015.126 ↗
32. 10.1039/C4CP04295F10.1039/C4CP04295F ↗
33. 10.1002/aenm.20140129810.1002/aenm.201401298 ↗
34. 10.1002/adma.20150298010.1002/adma.201502980 ↗