journal article·2020-01-02Open access

Elastic flexibility of ferroelectric supramolecular co-crystals

Qianqian Luo, Chunli Jiang, Hechun Lin, Chunhua Luo, Ruijuan Qi, Hui Peng

Soft Materials· Volume 18· Issue 1

Abstract

In recent years, great efforts are paying to design and understand the origins of elastic flexibility of molecular crystals. In this work, we investigate the elastic flexibility of two ferroelectric supramolecular co-crystals, phenazine-chloranilic acid (Phz-H2ca) and phenazine-bromanilic acid (Phz-H2ba) for the first time. Both of them show good elastic flexibility while the flexibility of the Phz-H2ca co-crystal is better. The measurements of mechanical properties show that the Phz-H2ca co-crystal has larger elastic modulus and smaller hardness value than the Phz-H2ba co-crystal. The bent co-crystal still keeps the ferroelectric properties. The Raman spectra reveal that the weak hydrogen-bond, halogen-bond and π···π stacking interactions contribute to the observed elastic flexibility of the co-crystals.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Acoustic Wave Resonator Technologies · Crystallography and molecular interactions · Solid-state spectroscopy and crystallography

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

Affiliations

Key Laboratory of Polar Materials and Devices (MOE), Department of Optoelectronics, East China Normal University, Shanghai, China

National Laboratory for Infrared Physics, Shanghai Institute of Technical Physics, Chinese Academy of Sciences, Shanghai, China

Collaborative Innovation Center of Extreme Optics, Shanxi University, Taiyuan, Shanxi, China

References (32)

Show source-provided references
1. 10.1038/natrevmats.2016.8710.1038/natrevmats.2016.87 ↗
2. 10.1021/acs.chemrev.5b0049510.1021/acs.chemrev.5b00495 ↗
3. 10.1021/nn506723210.1021/nn5067232 ↗
4. 10.1016/j.memsci.2014.03.05510.1016/j.memsci.2014.03.055 ↗
5. 10.1038/nature1139510.1038/nature11395 ↗
6. 10.1038/ncomms232210.1038/ncomms2322 ↗
7. 10.1126/science.aas933010.1126/science.aas9330 ↗
8. 10.1126/science.122967510.1126/science.1229675 ↗
9. 10.1039/c5cs00308c10.1039/c5cs00308c ↗
10. 10.1002/anie.20120460410.1002/anie.201204604 ↗
11. 10.1002/anie.20141073010.1002/anie.201410730 ↗
12. 10.1002/ange.20150931910.1002/ange.201509319 ↗
13. 10.1038/ncomms1310810.1038/ncomms13108 ↗
14. 10.1002/anie.20180643110.1002/anie.201806431 ↗
15. 10.1002/anie.20180013710.1002/anie.201800137 ↗
16. 10.1038/nchem.284810.1038/nchem.2848 ↗
17. 10.1002/anie.20131101410.1002/anie.201311014 ↗
18. 10.1038/nmat129810.1038/nmat1298 ↗
19. 10.1038/nchem.220610.1038/nchem.2206 ↗
20. 10.1002/adma.20110035910.1002/adma.201100359 ↗
21. 10.1007/s10870-014-0527-110.1007/s10870-014-0527-1 ↗
22. 10.1107/S205252061500408410.1107/S2052520615004084 ↗
23. 10.1107/S010876730704393010.1107/S0108767307043930 ↗
24. 10.1107/S002188980804272610.1107/S0021889808042726 ↗
25. 10.1021/cg400735f10.1021/cg400735f ↗
26. 10.1021/ja00275a01210.1021/ja00275a012 ↗
27. Desiraju Gautam, R.; Ho, P. S.; Kloo, L.; Legon Anthony, C.; Marquardt, R.; Metrangolo, P.; Politzer, P.; Resnati, G.; Rissanen, K. Definition of the Halogen Bond (IUPAC Recommendations 2013). Pure Appl. Chem. 2013, 85(8), 1711–1713.
28. 10.1016/S0009-2614(00)00852-610.1016/S0009-2614(00)00852-6 ↗
29. 10.1016/j.molstruc.2008.05.03810.1016/j.molstruc.2008.05.038 ↗
30. 10.1002/poc.63310.1002/poc.633 ↗
31. 10.1021/acs.jpcb.5b0327910.1021/acs.jpcb.5b03279 ↗
32. 10.1038/nchem.212310.1038/nchem.2123 ↗