Modulation of thermodynamic and kinetic inverted phase behavior of block copolymers by inorganic polyoxometalates

Tan, JY (Tan, Junyan)^{[ 1 ]} ; Liu, ZY (Liu, Zhiyao)^{[ 2 ]} ; Wang, R (Wang, Rong)^{[ 1 ]} ; Zhou, Y (Zhou, Yue)^{[ 1 ]} ; Xie, SY (Xie, Siyu)^{[ 1 ]} ; Li, BH (Li, Baohui)^{[ 2 ]} ; Wan, XH (Wan, Xinhua)^{[ 1 ]} ; Zhang, J (Zhang, Jie)^{[ 1 ]}

SOFT MATTER, 2019, 15(35):  6988-6993

DOI: 10.1039/c9sm01041f

摘要

The Keggin polyoxometalates (POM) H3PW12O40 (PW) electrostatically complexed with poly(styrene-block-2-vinyl pyridine) (PS-b-P2VP) in DMF, and ordered microphase separation occurred through solvent evaporation. The phase behaviors of PS-b-P2VP/PW in bulk were systematically investigated by using SAXS and TEM to discover the effect of POM content and molecular weight of the block copolymers. Computational simulation was also performed to reveal the same phase transition sequence as the experimental results. As the POM content increases, the PS-b-P2VP/PW complex with a low molecular weight changed from lamellar phase (LAM) to hexagonal cylindrical phase (HEX), and finally transited into spherical phase (SPH). Unexpectedly, PS-b-P2VP/PW complexes with a high molecular weight were inclined to form a kinetic-trapped intermediate phase (inverted HEX). The mechanism of formation of inverted phases was proposed based on simulation that asymmetric swelling in the concentrated DMF solution would result in the ultimate kinetic-trapped nanostructure in the bulk.