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Updated: Aug 30, 2026

Preparation of DNA-crosslinked Polyacrylamide Hydrogels
Published on: August 27, 2014
Effects of Cu2+/Zn2+ on the electrochemical performance of polyacrylamide hydrogels as advanced flexible electrode
Syed Faizan1, Luqman Ali Shah1, Bakhtawara1
1Polymer Laboratory, National Centre of Excellence in Physical Chemistry, University of Peshawar Peshawar 25120 Pakistan luqman_alisha@uop.edu.pk luqman_alisha@yahoo.com +92919216671 +92919216766.
Abstract:
Previously, solid-state electrode materials have been utilized for the fabrication of energy storage devices; however, their application is impeded by their brittle nature and ion mobility problems. To address issues faced in such a modern era where energy saving and utility is of prior importance, a novel approach has been applied for the preparation of electrode materials based on polyacrylamide hydrogels embedded with reduced graphene oxide and transition metals, namely, Cu2+ and Zn2+. The fabricated hydrogel exhibits high electrical properties and flexibility that make it a favorable candidate to be used in energy storage devices, where both elastic and electrical properties are desired. For the first time, a multi-cross-linked polyacrylamide hydrogel was constructed and compared in the presence of other electro-active materials such as reduced graphene oxide and transition metals. Polyacrylamide hydrogels embedded with reduced graphene oxide demonstrate excellent electrical properties such as specific capacitance, least impedance, low phase angle shift and AC conductivity of 22.92 F g-1, 2115 Ω, 2.88° and 0.67 μδ m-1 respectively as compared to Cu2+- and Zn2+-loaded hydrogels, which block all available active sites causing an increase in impedance with a parallel decrease in capacitance. The capacitance retention and coulombic efficiency calculated were 88.22% and 77.23% respectively, indicating high stability up to 150 cycles at 0.1 A g-1. Storage moduli obtained were 10.52 kPa, which infers the more elastic nature of the hydrogel loaded with graphene oxide than that of other synthesized hydrogels.

