journal article·2019-11-06

Rectification Behavior on Polyelectrolyte-Modified Flexible ITO Electrode via Ionic Charge-Selective Electron Transfer

Bingchen Li, Xuxian Zhao, Zhe Sun, Song Xue, Gangri Cai, Sung-Hwan Han

ACS Applied Materials & Interfaces· Volume 11· Issue 44
Publisher page

Abstract

New types of diodes, such as molecular and ionic diodes, have drawn considerable attention because of their advantages from the viewpoint of potential applications such as the downscaling of electronic devices, ionic circuits, and biological systems. Researchers are motivated to develop a simple, scalable, and promising system that can overcome the existing limitations because this can enable their application in various devices. This study proposes a system that not only integrates the advantages of ionic and single-molecule diodes but also avoids their disadvantages, denoting the rectification behavior due to ionic charge-selective electron transfer between two redox species, i.e., Fe(CN)63– and Ru(NH3)63+, on the polyelectrolyte multilayer (PEM)-modified flexible indium tin oxide (ITO) electrodes. Flexible current rectification devices were easily prepared by sandwiching an electrolytic solution of ionic redox species using bare and PEM-modified plastic ITO electrodes. An ionic bilayer was initially formed via Coulombic interactions on a PEM-modified charge-selective ITO surface. The ionic bilayer was analogous to a conventional single-molecule diode’s monolayer with consecutive molecular orbitals of two ionic redox species. Furthermore, the rectification ratio (RR) was increased from ∼6 to ∼10 using a conducting polymer to construct PEMs.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Molecular Junctions and Nanostructures · Conducting polymers and applications · Analytical Chemistry and Sensors

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

Affiliations

Tianjin Key Laboratory of Organic Solar Cells and Photochemical Conversion, Department of Applied Chemistry, Tianjin University of Technology, No. 391 Binshui Xidao, Xiqing District Tianjin 300384, P. R. China

Department of Chemistry, Hanyang University, 222, Wangsimni-ro, Seongdong-gu, Seoul 04763, Republic of Korea

Funding

National Research Foundation of Korea · National Natural Science Foundation of China

References (26)

Show source-provided references
1. 10.1016/0009-2614(74)85031-110.1016/0009-2614(74)85031-1 ↗
2. 10.1021/cr500459d10.1021/cr500459d ↗
3. 10.1021/acsami.9b0231510.1021/acsami.9b02315 ↗
4. 10.1021/jacs.6b0749910.1021/jacs.6b07499 ↗
5. 10.1038/379833a010.1038/379833a0 ↗
6. 10.1039/c001349h10.1039/c001349h ↗
7. 10.1038/ncomms151410.1038/ncomms1514 ↗
8. 10.1021/jacs.7b0505810.1021/jacs.7b05058 ↗
9. 10.1021/acs.jpclett.6b0197110.1021/acs.jpclett.6b01971 ↗
10. 10.1039/C4CS00143E10.1039/C4CS00143E ↗
11. 10.1063/1.12376510.1063/1.123765 ↗
12. 10.1063/1.12435410.1063/1.124354 ↗
13. 10.1063/1.11987110.1063/1.119871 ↗
14. 10.1103/PhysRevLett.74.210210.1103/PhysRevLett.74.2102 ↗
15. 10.1038/ncomms312110.1038/ncomms3121 ↗
16. 10.1021/am400349w10.1021/am400349w ↗
17. 10.1002/anie.20120500710.1002/anie.201205007 ↗
18. 10.1021/ja106149g10.1021/ja106149g ↗
19. 10.1021/acs.jpcc.5b1131410.1021/acs.jpcc.5b11314 ↗
20. 10.1002/adfm.20180107910.1002/adfm.201801079 ↗
21. 10.1021/ja901120f10.1021/ja901120f ↗
22. 10.1021/acs.langmuir.8b0022210.1021/acs.langmuir.8b00222 ↗
23. 10.1021/ja205773a10.1021/ja205773a ↗
24. 10.1016/j.cap.2008.08.04510.1016/j.cap.2008.08.045 ↗
25. 10.1166/jnn.2009.162610.1166/jnn.2009.1626 ↗
26. 10.1016/j.elecom.2006.10.02010.1016/j.elecom.2006.10.020 ↗