journal article·2022-04Open access

Mechanofluorochromic Material toward a Recoverable Microscale Force Sensor

Jan Patrick Calupitan, Arnaud Brosseau, Pierre Josse, Clément Cabanetos, Jean Roncali, Rémi Métivier, Clémence Allain

Advanced Materials Interfaces· Volume 9· Issue 12

Abstract

Abstract Among the multiple classes of mechanofluorochromic (MFC) compounds reported in recent years, simple donor–acceptor molecules involving oligooxyethylene N‐substituted diphenylamine connected to a dicyanovinyl group by a thienyl spacer constitute a specific class of mechano‐stimulable smart materials with a unique combination of properties including turn‐on mechanofluorochromism with red‐light photoluminescence emission, turn‐off second harmonic generation, and self‐recovery in ambient conditions. While the dynamics of the MFC processes of thin films of these materials have already been investigated, the correlation of the behavior observed at the macroscale with elemental processes taking place at the micro‐ and nanoscopic scales remains largely unexplored. In this work, atomic force microscopy (AFM) coupled with wide‐field and confocal optical microscopies is used to investigate the turn‐on/recovery MFC behavior of microcrystals and nanostructures. It is shown that the red light photoluminescence of microcrystals and nano‐objects can be turned‐on by contact AFM and that the intensity of light emission is linearly correlated to the applied nominal force. Recovery is associated with a decrease in emission intensity, which can be reactivated again by subsequent contact scans. These results thus pave the way toward the development of micro‐/nanoscale recoverable force‐sensing technologies based on this particular class of smart molecular materials.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Luminescence and Fluorescent Materials · Polydiacetylene-based materials and applications · Molecular Sensors and Ion Detection

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

Affiliations

Université Paris‐Saclay, ENS Paris‐Saclay CNRS, PPSM Gif‐sur‐Yvette 91190 France

Moltech‐Anjou CNRS UMR 6200 University of Angers Angers 49045 France

Supramolecular Organic and Organometallic Chemistry Center Babes‐Bolyai University 11 Arany Janos str. Cluj‐Napoca 400028 Romania

Funding

European Research Council

References (55)

Show source-provided references
1. Urban M. U. · 2016
2. 10.1002/adma.20160611710.1002/adma.201606117 ↗
3. 10.1002/adma.20180017710.1002/adma.201800177 ↗
4. 10.1039/C7CS00240H10.1039/C7CS00240H ↗
5. 10.1016/S0010-8545(00)00246-010.1016/S0010-8545(00)00246-0 ↗
6. 10.1021/jacs.7b1240510.1021/jacs.7b12405 ↗
7. 10.1038/420759a10.1038/420759a ↗
8. 10.1038/s41565-019-0370-910.1038/s41565-019-0370-9 ↗
9. 10.1038/ncomms733010.1038/ncomms7330 ↗
10. 10.1021/cr500249p10.1021/cr500249p ↗
11. 10.1002/cplu.20180064010.1002/cplu.201800640 ↗
12. 10.1039/c3tc00818e10.1039/c3tc00818e ↗
13. 10.1002/adma.20150452510.1002/adma.201504525 ↗
14. 10.1002/adom.20180101310.1002/adom.201801013 ↗
15. 10.1002/tcr.20160006010.1002/tcr.201600060 ↗
16. 10.1021/jacs.9b0505410.1021/jacs.9b05054 ↗
17. 10.1002/anie.20180284210.1002/anie.201802842 ↗
18. 10.1021/cr300396p10.1021/cr300396p ↗
19. 10.1002/anie.20181154210.1002/anie.201811542 ↗
20. 10.1002/adma.20150258910.1002/adma.201502589 ↗
21. 10.1039/9781782623229-0000710.1039/9781782623229-00007 ↗
22. 10.1039/D0NJ00588F10.1039/D0NJ00588F ↗
23. 10.1002/adma.20150169710.1002/adma.201501697 ↗
24. 10.1002/adfm.20160126910.1002/adfm.201601269 ↗
25. 10.1039/C6TC00237D10.1039/C6TC00237D ↗
26. 10.1039/C9TC03646F10.1039/C9TC03646F ↗
27. 10.1039/C8TC04512G10.1039/C8TC04512G ↗
28. 10.1039/C9TC06297A10.1039/C9TC06297A ↗
29. 10.1038/nature0919810.1038/nature09198 ↗
30. 10.1039/C9CC05797H10.1039/C9CC05797H ↗
31. 10.1038/nnano.2013.30310.1038/nnano.2013.303 ↗
32. 10.1021/acs.jpclett.9b0192310.1021/acs.jpclett.9b01923 ↗
33. 10.1002/anie.20141024010.1002/anie.201410240 ↗
34. 10.1039/D1CP03458H10.1039/D1CP03458H ↗
35. 10.1021/acs.nanolett.0c0402710.1021/acs.nanolett.0c04027 ↗
36. 10.1021/acs.jpclett.1c0201510.1021/acs.jpclett.1c02015 ↗
37. 10.1002/chem.20200524510.1002/chem.202005245 ↗
38. 10.1039/C5TC01369K10.1039/C5TC01369K ↗
39. 10.1039/C7CC03898D10.1039/C7CC03898D ↗
40. 10.1039/C9PP00457B10.1039/C9PP00457B ↗
41. 10.1039/C6CC07093K10.1039/C6CC07093K ↗
42. 10.1039/c3tc00017f10.1039/c3tc00017f ↗
43. 10.1039/C4TC02161D10.1039/C4TC02161D ↗
44. 10.1039/C7RA08248G10.1039/C7RA08248G ↗
45. 10.1039/C7RA01006K10.1039/C7RA01006K ↗
46. 10.1016/j.matlet.2011.05.06810.1016/j.matlet.2011.05.068 ↗
47. 10.1021/acsami.5b0968810.1021/acsami.5b09688 ↗
48. Wu H. · Chem. Commun. · 2017 · 53 · 2651
49. 10.1002/cptc.20180026110.1002/cptc.201800261 ↗
50. 10.1002/adom.20200042010.1002/adom.202000420 ↗
51. 10.1021/acs.nanolett.6b0499510.1021/acs.nanolett.6b04995 ↗
52. 10.1039/C9DT02786F10.1039/C9DT02786F ↗
53. 10.1021/acs.jpcc.8b0358310.1021/acs.jpcc.8b03583 ↗
54. 10.1002/adfm.20060093110.1002/adfm.200600931 ↗
55. 10.1002/adma.1997009030810.1002/adma.19970090308 ↗