“…By choosing the correct type of precursor/monomer, polymer hydrogels can be designed to have the main structural, mechanical, and energy storage properties required for different wearable energy storage applications including high conductivity under strain (poly(3,4ethylenedioxythiophene)):poly(styrene sulfonate) hydrogels can present a high electrical conductivity of 50 000 S m −1 ), [8b] high stretchability (polyaniline/polyurethane hydrogels can have a strain of 1150%), [68] high specific capacitance (polypyrrole hydrogels have a capacitance of 400 F g −1 at 0.2 A g −1 ), [7b] high capacitance retention after mechanical deformations (lignin-based hydrogels have an energy density of 13.7 Wh kg −1 at the power density of 201.4 W kg −1 after 5000 charge/discharge cycles), [16n] mechanical properties similar to skin and organs for the design of wearable and implantable electronics (polyacrylamide hydrogels have Young's moduli of 80 kPa and an ultrasoft tissue-like structure), [69] etc. Acrylic acid, [70] vinyl-pyrrolidine, [71] aniline, [16a] acrylamides, [69] polypyrrole, [72] and polyvinyl alcohol (PVA), [73] are just some of the common monomers/polymeric precursors that can be used to fabricate conductive/highly stretchable electrode/electrolyte hydrogels for energy storage applications. In addition to conventional monomers/precursors, polymer hydrogels can be synthesized from cationic and anionic monomers called polyampholytes, to have randomly distributed cationic Figure 3.…”