TY - JOUR
T1 - Enhanced Electric Polarization and Polar Switching of Dipolar Aromatic Liquids Confined in Supramolecular Gel Networks
AU - Yamamoto, Ryosuke
AU - Minami, Yusuke
AU - Hui, Joseph K.H.
AU - Morikawa, Masa Aki
AU - Kimizuka, Nobuo
N1 - Funding Information:
This work is financially supported by JSPS KAKENHI Grants JP25220805, JP16H06513 (Coordination Asymmetry), and The Ogasawara Foundation for the Promotion of Science & Engineering (2018–2019). The authors are grateful for Professors S. Ogo and T. Matsumoto for the use of GC/MS.
Publisher Copyright:
© 2019 American Chemical Society.
PY - 2020/1/22
Y1 - 2020/1/22
N2 - Dipolar aromatic liquids confined in the interstitial domains of chiral organogels show significantly enhanced electric polarization, as compared with those of pure liquids alone or organogels formed with nonpolar liquids. Intriguingly, nitrobenzene gels showed a supramolecular polar switching phenomenon; i.e., hysteresis in the polarization (P)-electric field (E) curves was observed for the gel above the melting point of the solvent. This indicates that the nitrobenzene molecules confined in the chiral nanofibrous gel networks exert macroscopic polarization whose direction is inversed depending on the direction of the external electric field. The anomalously enhanced electric polarization and polar switching phenomenon of supramolecular gels in varied solvents are scrutinized by the positive-up-negative-down (PUND) measurements, and the interactions between the gel nanofibers and the polar solvent molecules play crucial roles for the emergence of the polar switching phenomenon. This work presents for the first time that dipolar liquid molecules filling the interstitial space of supramolecular gels exhibit a significant confinement effect. It provides a new perspective to design electric-field-responsive soft materials based on the functional liquid domains confined in their porous networks.
AB - Dipolar aromatic liquids confined in the interstitial domains of chiral organogels show significantly enhanced electric polarization, as compared with those of pure liquids alone or organogels formed with nonpolar liquids. Intriguingly, nitrobenzene gels showed a supramolecular polar switching phenomenon; i.e., hysteresis in the polarization (P)-electric field (E) curves was observed for the gel above the melting point of the solvent. This indicates that the nitrobenzene molecules confined in the chiral nanofibrous gel networks exert macroscopic polarization whose direction is inversed depending on the direction of the external electric field. The anomalously enhanced electric polarization and polar switching phenomenon of supramolecular gels in varied solvents are scrutinized by the positive-up-negative-down (PUND) measurements, and the interactions between the gel nanofibers and the polar solvent molecules play crucial roles for the emergence of the polar switching phenomenon. This work presents for the first time that dipolar liquid molecules filling the interstitial space of supramolecular gels exhibit a significant confinement effect. It provides a new perspective to design electric-field-responsive soft materials based on the functional liquid domains confined in their porous networks.
UR - http://www.scopus.com/inward/record.url?scp=85078341673&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85078341673&partnerID=8YFLogxK
U2 - 10.1021/jacs.9b11276
DO - 10.1021/jacs.9b11276
M3 - Article
C2 - 31880931
AN - SCOPUS:85078341673
SN - 0002-7863
VL - 142
SP - 1424
EP - 1432
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 3
ER -