Synthesis of recyclable, chemically cross-linked, high toughness, high conductivity ion gels by sequential triblock copolymer self-assembly and disulfide bond cross-linking

In this article, we report the synthesis of a disulfide bonded reversibly chemically cross-linked ion gel with high toughness and conductivity by sequential triblock copolymer self-assembly and the subsequent oxidation of thiol groups. Through reversible thiol-disulfide exchange, the ion gels had both high toughness of chemicals and recyclability of physical cross-linked ion gels. The triblock copolymer (SOS-SH) was prepared as follows: first, the RAFT copolymerization of styrene and 4-vinylbenzyl chloride (VBC) using CTA-PEO-CTA as a bi-functional macroRAFT agent was performed to obtain a triblock copolymer (SOS-Cl); then, the chloride group of SOS-Cl was replaced by an azido group to obtain SOS-N 3 ; and finally, the click reaction of SOS-N 3 with O -ethyl- S -prop-2-ynyl carbonodithioate and subsequent aminolysis were conducted to obtain SOS-SH. The disulfide bonded reversibly chemically cross-linked ion gel could be re-dissolved when mixed with a little amount of mild reducing agent ( e.g. , DTT) in CH 2 Cl 2 with vigorous stirring, which reformed again after the removal of solvent and oxidation of thiol groups. The ion gels could undergo the reduction-oxidation cycle at least twice with a little loss of ionic conductivity and toughness (less than 25%), exhibiting good recyclability. Raman measurements were performed to confirm the existence and the key role of disulfide bond on the recyclability. We reported the synthesis of a high toughness, high conductivity ion gels by a sequential triblock copolymer self-assembly and disulfide bond cross-linking, combining the high toughness of chemical with recyclability of physical cross-linking ones.