We report a supramolecular strategy to prepare conductive hydrogels with outstanding mechanical and electrochemical properties, which are utilized for flexible solid‐state supercapacitors (SCs) with high performance. The supramolecular assembly of polyaniline and polyvinyl alcohol through dynamic boronate bond yields the polyaniline–polyvinyl alcohol hydrogel (PPH), which shows remarkable tensile strength (5.3 MPa) and electrochemical capacitance (928 F g−1). The flexible solid‐state supercapacitor based on PPH provides a large capacitance (306 mF cm−2 and 153 F g−1) and a high energy density of 13.6 Wh kg−1, superior to other flexible supercapacitors. The robustness of the PPH‐based supercapacitor is demonstrated by the 100 % capacitance retention after 1000 mechanical folding cycles, and the 90 % capacitance retention after 1000 galvanostatic charge–discharge cycles. The high activity and robustness enable the PPH‐based supercapacitor as a promising power device for flexible electronics.
Ring-opening polymerization is used to prepare polyesters with precisely controlled molecular weights, molecular weight distributions, and tacticities. Herein, we report a newly developed Co/Zn catalytic system that can be activated by an electrical current to mediate efficient ring-opening polymerization of enantiopure O-carboxyanhydrides, allowing for the synthesis of isotactic functionalized polyesters with high molecular weights (>140 kDa) and narrow molecular weight distributions (M w /M n < 1.1). We also demonstrate that these catalysts can be used for stereoselective ring-opening polymerization of racemic O-carboxyanhydrides to synthesize syndiotactic or stereoblock copolymers with different glass transition temperatures compared with their atactic counterparts. File list (2) download file view on ChemRxiv Co-Zn-OCA-electro-040520.pdf (567.43 KiB) download file view on ChemRxiv SI-draft.pdf (3.25 MiB)
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