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Updated: Oct 15, 2026

Measuring Proton Conductivity in MOF-Based Mixed Matrix Membranes by Electrochemical Impedance Spectroscopy
Published on: June 16, 2026
Molecularly Anchored n-Type Quinone/Graphene Heterostructures Enabling High-Capacity and Ultra-stable Proton Storage
Shimeng Guo1, Shaopei Yang1, Baiting Li1
1State Key Laboratory of Applied Organic Chemistry, Institute of Polymer Science and Engineering, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou730000, China.
Abstract:
Quinone-based organic electrodes are attractive for aqueous proton batteries owing to their fast and reversible proton-coupled redox chemistry. However, their practical application is largely restricted by severe dissolution in acidic electrolytes, poor structural stability, and low electronic conductivity. Herein, we report a molecularly anchored n-type quinone/graphene heterostructure constructed by integrating tetraaminobenzoquinone (TABq) with reduced graphene oxide (rGO) through a facile solvothermal strategy. Strong π-π stacking, hydrogen-bonding interactions, and covalent linkages effectively immobilize TABq molecules on the conductive rGO framework, thereby suppressing active-material dissolution, enhancing electrode integrity, and constructing efficient electron/proton transport pathways. The open heterointerface and abundant redox-active sites further promote rapid proton uptake/release and accelerate charge-transfer kinetics. Benefiting from this rational heterostructure design, the optimized TABq/rGO electrode delivers a high specific capacity of 349.78 mAh g-1 at 1 A g-1, remarkable rate capability of 131.12 mAh g-1 even at 100 A g-1, and excellent cycling durability. When coupled with a 3,4,9,10-perylenetetracarboxylic dianhydride anode, the full cell achieves a reversible capacity of 129.03 mAh g-1 at 0.75 A g-1 and maintains 75.43% of its capacity after 1000 cycles. Moreover, TABq/rGO-based symmetric proton battery exhibits outstanding long-term stability, retaining 74.17% of its capacity after 10,000 cycles. Experimental characterizations combined with density functional theory calculations reveal that the TABq/rGO heterointerface regulates charge distribution, stabilizes the quinone redox centers, and lowers the kinetic barrier for proton storage. This work highlights an effective molecular anchoring strategy for developing high-capacity, high-rate, and durable organic electrodes for advanced aqueous proton batteries.

