TY - JOUR
T1 - Facile and Eco-Friendly Approach to Multifunctional Supramolecular Poly(ionic liquid) Nanoporous Membranes Containing Hydrophilic Anions (Br-, MBry-, M = Sn, Pb, Sb, Bi)
AU - Wang, Binmin
AU - Wang, Yong Lei
AU - Zhao, Peng
AU - Wu, Tom
AU - Wang, Hong
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/5/28
Y1 - 2024/5/28
N2 - Polyelectrolyte porous membranes (PPMs) have numerous applications in modern science and technology. Here, we describe a new platform for creating multifunctional supramolecular PPMs (SPPMs) by cross-linking of single-component homopoly(ionic liquid)s (PILs) containing hydrophilic anions (Br-, MBry-, M = Sn, Pb, Sb, Bi) with H2O molecules. With a range of experimental evidence and support from theoretical calculations, we show that the porous architecture is formed by H2O molecules-induced phase separation of the polycationic moieties of the homo-PILs between their polar and apolar domains, which are cross-linked together by multiple hydrogen (H)-bonding interactions. Furthermore, we discover these SPPMs show reversible, dynamic, wide-range color tuning, depending on the excitation wavelength, as well as ultrasensitive color change toward humidity and temperature stimuli, endowing them with great promise in color-on-demand applications. These findings, together with the scalable and green synthetic approach, bode well for advanced membrane materials and color-on-demand applications based upon such SPPM systems.
AB - Polyelectrolyte porous membranes (PPMs) have numerous applications in modern science and technology. Here, we describe a new platform for creating multifunctional supramolecular PPMs (SPPMs) by cross-linking of single-component homopoly(ionic liquid)s (PILs) containing hydrophilic anions (Br-, MBry-, M = Sn, Pb, Sb, Bi) with H2O molecules. With a range of experimental evidence and support from theoretical calculations, we show that the porous architecture is formed by H2O molecules-induced phase separation of the polycationic moieties of the homo-PILs between their polar and apolar domains, which are cross-linked together by multiple hydrogen (H)-bonding interactions. Furthermore, we discover these SPPMs show reversible, dynamic, wide-range color tuning, depending on the excitation wavelength, as well as ultrasensitive color change toward humidity and temperature stimuli, endowing them with great promise in color-on-demand applications. These findings, together with the scalable and green synthetic approach, bode well for advanced membrane materials and color-on-demand applications based upon such SPPM systems.
UR - http://www.scopus.com/inward/record.url?scp=85193463499&partnerID=8YFLogxK
U2 - 10.1021/acs.macromol.4c00285
DO - 10.1021/acs.macromol.4c00285
M3 - Journal article
AN - SCOPUS:85193463499
SN - 0024-9297
VL - 57
SP - 5073
EP - 5080
JO - Macromolecules
JF - Macromolecules
IS - 10
ER -