journal article·2021-06-17

Light-Induced Quantitative and Electrical-Field-Induced Barrierless Switching of Spiropyran Derivative on Graphite Surface

Himani Malik, Thomas Halbritter, Alexander Heckel, Thiruvancheril G. Gopakumar

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Abstract

A new class of pyridine-based spiropyran (SP) shows photoinduced reversible switching between the closed SP and ring-opened merocyanine (MC). We show that a condensed crystalline monolayer of SP on graphite can be quantitatively converted to MC upon UV irradiation. In solution only ∼10% of SP can be transformed to MC because of the establishment of a photostationary state. Using an electrical field applied by a scanning tunneling microscopy (STM) tip, single molecules are reversibly switched between SP and MC forms in their condensed phases without any threshold voltage at ambient conditions. The microscopic structure of submonolayer films of SP and MC are investigated using atomic force microscopy (AFM) and STM.
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Research context

OpenAlex topics: Photochromic and Fluorescence Chemistry · Photoreceptor and optogenetics research · Metamaterials and Metasurfaces Applications

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

Affiliations

Department of Chemistry, Indian Institute of Technology Kanpur, Kanpur, UP 208016, India

Institute for Organic Chemistry and Chemical Biology, Goethe-University Frankfurt, 60438 Frankfurt, Germany

Funding

Ministry of Electronics and Information technology · Science and Engineering Research Board

References (37)

Show source-provided references
1. 10.1021/cr980071510.1021/cr9800715 ↗
2. 10.1038/425145a10.1038/425145a ↗
3. 10.1021/acsami.6b0785310.1021/acsami.6b07853 ↗
4. 10.1016/j.mtadv.2020.10005810.1016/j.mtadv.2020.100058 ↗
5. 10.1021/jp902681710.1021/jp9026817 ↗
6. 10.1039/c0jm01903h10.1039/c0jm01903h ↗
7. 10.15406/ijbsbe.2017.03.0007810.15406/ijbsbe.2017.03.00078 ↗
8. 10.1021/jp711134p10.1021/jp711134p ↗
9. 10.1088/0953-8984/23/48/48400510.1088/0953-8984/23/48/484005 ↗
10. 10.1039/C4CP04353G10.1039/C4CP04353G ↗
11. 10.1088/1361-648X/aa78be10.1088/1361-648X/aa78be ↗
12. 10.1103/PhysRevLett.99.03830110.1103/PhysRevLett.99.038301 ↗
13. 10.1088/0953-8984/24/39/39400110.1088/0953-8984/24/39/394001 ↗
14. 10.1021/acs.jpclett.8b0287510.1021/acs.jpclett.8b02875 ↗
15. 10.1002/anie.20050222910.1002/anie.200502229 ↗
16. 10.1021/jp074186110.1021/jp0741861 ↗
17. 10.1038/nnano.2008.26910.1038/nnano.2008.269 ↗
18. 10.1021/ja065449s10.1021/ja065449s ↗
19. 10.1021/jacs.0c0019210.1021/jacs.0c00192 ↗
20. 10.1021/ja01591a07510.1021/ja01591a075 ↗
21. 10.1021/la400192c10.1021/la400192c ↗
22. 10.1021/cr60221a00510.1021/cr60221a005 ↗
23. 10.1016/j.dyepig.2016.08.03910.1016/j.dyepig.2016.08.039 ↗
24. 10.1021/acs.jpcc.8b0259410.1021/acs.jpcc.8b02594 ↗
25. 10.1103/PhysRevLett.109.02610210.1103/PhysRevLett.109.026102 ↗
26. 10.1021/ja901238p10.1021/ja901238p ↗
27. 10.3390/molecules2212223610.3390/molecules22122236 ↗
28. 10.1021/acsami.0c1498710.1021/acsami.0c14987 ↗
29. 10.1002/1438-5171(200204)3:1<25::AID-SIMO25>3.0.CO;2-K10.1002/1438-5171(200204)3:1<25::AID-SIMO25>3.0.CO;2-K ↗
30. 10.1021/ja907397u10.1021/ja907397u ↗
31. 10.1021/acs.jpcc.6b0077410.1021/acs.jpcc.6b00774 ↗
32. 10.1038/srep3851910.1038/srep38519 ↗
33. 10.1002/slct.20170086810.1002/slct.201700868 ↗
34. 10.1088/1361-651X/aa8ff010.1088/1361-651X/aa8ff0 ↗
35. 10.1103/PhysRevLett.96.15610610.1103/PhysRevLett.96.156106 ↗
36. 10.1134/S199079310902004310.1134/S1990793109020043 ↗
37. 10.1155/2015/16124810.1155/2015/161248 ↗