journal article·2020-12-07

Design and Synthesis of Solution-Processable Donor–Acceptor Dithienophosphole Oxide Derivatives for Multilevel Organic Resistive Memories

Yat-Hin Cheng, Hok-Lai Wong, Eugene Yau-Hin Hong, Ming-Yi Leung, Shiu-Lun Lai, Vivian Wing-Wah Yam

ACS Materials Letters· Volume 2· Issue 12
Publisher page

Abstract

A class of solution-processable, donor–acceptor-decorated dithienophosphole oxide derivatives has been successfully synthesized and employed to fabricate solution-processed resistive memory devices with a simple indium–tin oxide/active layer/aluminum structure. The intramolecular charge transfer (ICT) characters of the donor–acceptor dithienophosphole oxide derivatives were established from photophysical, solvatochromic, and computational studies. The number of conductance states in the organic memory devices was found to be altered by slight changes in molecular structures. The mechanism for the tristable memory property of the devices was proposed based on the correlation of the extent of ICT characters and the computed structural parameters of the compounds, current–voltage characteristics of the devices and the fitting to theoretical conduction models. These findings offer important insights for the realization of multilevel resistive memory devices through the modification of the ICT character of the active compounds.
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Research context

OpenAlex topics: Advanced Memory and Neural Computing · Perovskite Materials and Applications · Conducting polymers and applications

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

Affiliations

Institute of Molecular Functional Materials and Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, People’s Republic of China

Funding

Research Grants Council, University Grants Committee · University of Hong Kong

References (49)

Show source-provided references
1. 10.1021/cr050159010.1021/cr0501590 ↗
2. 10.1002/aenm.20160224210.1002/aenm.201602242 ↗
3. 10.1021/jacs.7b1323910.1021/jacs.7b13239 ↗
4. 10.1021/jacs.8b0920510.1021/jacs.8b09205 ↗
5. Tang M.-C. · 2017 · 6710.1007/978-3-319-59304-3_3 ↗
6. 10.1021/jacs.7b0047910.1021/jacs.7b00479 ↗
7. 10.1002/adma.20130632710.1002/adma.201306327 ↗
8. 10.1038/nature2401010.1038/nature24010 ↗
9. 10.1002/adma.20130434610.1002/adma.201304346 ↗
10. 10.1021/cm102006v10.1021/cm102006v ↗
11. 10.1021/ja305354y10.1021/ja305354y ↗
12. 10.1002/adma.20150227410.1002/adma.201502274 ↗
13. 10.1038/srep1068310.1038/srep10683 ↗
14. 10.1002/anie.20150499710.1002/anie.201504997 ↗
15. 10.1002/anie.20151094610.1002/anie.201510946 ↗
16. 10.1002/adfm.20150349310.1002/adfm.201503493 ↗
17. 10.1021/jacs.7b0089510.1021/jacs.7b00895 ↗
18. 10.1002/chem.20160222810.1002/chem.201602228 ↗
19. 10.1016/j.mser.2014.06.00210.1016/j.mser.2014.06.002 ↗
20. 10.1109/JPROC.2012.219017010.1109/JPROC.2012.2190170 ↗
21. 10.1021/jacs.6b0262910.1021/jacs.6b02629 ↗
22. 10.1002/anie.20150022910.1002/anie.201500229 ↗
23. 10.1002/anie.20130482710.1002/anie.201304827 ↗
24. 10.1002/chem.20140569110.1002/chem.201405691 ↗
25. 10.1039/C6SC02928K10.1039/C6SC02928K ↗
26. 10.1021/jacs.7b0833310.1021/jacs.7b08333 ↗
27. 10.1002/anie.20180627210.1002/anie.201806272 ↗
28. 10.1021/acsami.9b1390010.1021/acsami.9b13900 ↗
29. 10.1039/C4CC05247A10.1039/C4CC05247A ↗
30. 10.1002/adfm.20130229410.1002/adfm.201302294 ↗
31. 10.1002/chem.20170411010.1002/chem.201704110 ↗
32. 10.1039/C6CS00257A10.1039/C6CS00257A ↗
33. 10.1039/C8SC02265H10.1039/C8SC02265H ↗
34. 10.1038/s41570-020-0199-710.1038/s41570-020-0199-7 ↗
35. 10.1002/chem.20050015210.1002/chem.200500152 ↗
36. 10.1002/chem.20070039910.1002/chem.200700399 ↗
37. 10.1002/chem.20080248210.1002/chem.200802482 ↗
38. 10.1002/adfm.20150093410.1002/adfm.201500934 ↗
39. 10.1021/om500937810.1021/om5009378 ↗
40. 10.1021/jacs.7b0089510.1021/jacs.7b00895 ↗
41. 10.1021/acsami.6b1240410.1021/acsami.6b12404 ↗
42. 10.1002/cnma.20160036510.1002/cnma.201600365 ↗
43. 10.1021/jacs.7b0495210.1021/jacs.7b04952 ↗
44. 10.1021/jacs.7b0763810.1021/jacs.7b07638 ↗
45. 10.1002/adma.20110112910.1002/adma.201101129 ↗
46. 10.1016/0040-6090(75)90136-410.1016/0040-6090(75)90136-4 ↗
47. 10.1063/1.34143310.1063/1.341433 ↗
48. 10.1002/ange.20050436510.1002/ange.200504365 ↗
49. 10.1002/adma.20050022510.1002/adma.200500225 ↗