On-Surface Single-Molecule Identification of Mass-Selected Cyclodextrin-Supported Polyoxovanadates for Multistate Resistive-Switching Memory Applications
Source abstract
Abstract
Polyoxovanadate anions immobilized on conducting substrates are promising candidates for molecule-based memory technologies. However, strong electronic interactions with the substrate and the formation of larger agglomerates remain bottlenecks on the way to their technical application. We demonstrate that ion soft-landing of mass selected cyclodextrin-functionalized hexavanadates enables deposition of these host–guest complexes as single memory units on surfaces without their quaternary ammonium countercations from solution. Cyclodextrin provides a stabilizing “shell” for the dianions. Multistate switching evidenced by the change in molecular resistance has been detected using scanning tunneling microscopy and spectroscopy and attributed to reduction of individual vanadium (+V) centers.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Memory and Neural Computing · Polyoxometalates: Synthesis and Applications · Electrochemical Analysis and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Leibniz Institute of Surface Engineering (IOM), Permoserstraße 15, 04318 Leipzig, Germany
Wilhelm-Ostwald-Institute for Physical and Theoretical Chemistry, University Leipzig, Linnéstraße 2, 04103 Leipzig, Germany
Physical Sciences Division, Pacific Northwest National Laboratory, Richland, Washington 999352, United States
Funding
Leibniz-Gemeinschaft · Basic Energy Sciences · Volkswagen Foundation
References (30)
Show source-provided references
1. 10.1016/j.cap.2011.01.02010.1016/j.cap.2011.01.020 ↗
2. 10.1038/s41565-020-0655-z10.1038/s41565-020-0655-z ↗
3. 10.1007/978-3-319-02630-5_810.1007/978-3-319-02630-5_8 ↗
4. 10.1142/9789814287005_001610.1142/9789814287005_0016 ↗
5. 10.1002/ange.20200217410.1002/ange.202002174 ↗
6. 10.1039/C8CS00614H10.1039/C8CS00614H ↗
7. 10.1038/s41598-017-08244-y10.1038/s41598-017-08244-y ↗
8. 10.1002/anie.20090248310.1002/anie.200902483 ↗
9. 10.1038/nature1395110.1038/nature13951 ↗
10. 10.1021/acs.accounts.1c0031110.1021/acs.accounts.1c00311 ↗
11. 10.1002/9781119951438.eibc261510.1002/9781119951438.eibc2615 ↗
12. 10.1021/jacs.8b0878010.1021/jacs.8b08780 ↗
13. 10.1002/admi.20220046110.1002/admi.202200461 ↗
14. 10.1002/anie.20190560010.1002/anie.201905600 ↗
15. 10.1039/C8NR08008A10.1039/C8NR08008A ↗
16. 10.1002/chem.20130163110.1002/chem.201301631 ↗
17. 10.1016/bs.adioch.2016.12.00910.1016/bs.adioch.2016.12.009 ↗
18. 10.1038/s41578-021-00302-210.1038/s41578-021-00302-2 ↗
19. 10.1021/ja511713c10.1021/ja511713c ↗
20. 10.1002/chem.20210268410.1002/chem.202102684 ↗
21. 10.1002/adma.20170395010.1002/adma.201703950 ↗
22. 10.1002/inf2.1207710.1002/inf2.12077 ↗
23. 10.1021/acs.analchem.9b0030910.1021/acs.analchem.9b00309 ↗
24. 10.1007/s13361-019-02266-810.1007/s13361-019-02266-8 ↗
25. 10.1021/ja00038a03310.1021/ja00038a033 ↗
26. 10.1002/anie.20210924910.1002/anie.202109249 ↗
27. 10.1002/jms.170910.1002/jms.1709 ↗
28. 10.1002/anie.20180459710.1002/anie.201804597 ↗
29. 10.1021/jacs.8b0752510.1021/jacs.8b07525 ↗
30. 10.1021/acs.inorgchem.2c0009510.1021/acs.inorgchem.2c00095 ↗