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Sulfophenylated centimeter-sized graphene membrane in a direct methanol fuel cell
Weizhe Zhang1, Max Makurat2, Xue Liu2,3
1Leiden Institute of Chemistry, Faculty of Science, Leiden University, Leiden, The Netherlands. w.zhang@lic.leidenuniv.nl.
Nature Communications
|November 27, 2025
Summary
Functionalized graphene membranes show enhanced proton conductivity and fuel impermeability for fuel cells. This breakthrough offers a promising alternative to conventional polymer membranes in electrochemical energy devices.
Area of Science:
- Materials Science
- Electrochemistry
- Nanotechnology
Background:
- Proton exchange membranes (PEMs) are crucial for fuel cells, balancing proton conductivity and fuel impermeability.
- Conventional polymer membranes face challenges with the antagonistic relationship between conductivity and selectivity.
- Methanol crossover in methanol fuel cells significantly degrades catalyst activity and reduces efficiency.
Purpose of the Study:
- To investigate the potential of chemically functionalized monolayer graphene as a proton exchange membrane.
- To enhance proton transport properties of graphene through sulfophenyl group functionalization.
- To evaluate functionalized graphene as an alternative to traditional polymer membranes in electrochemical energy devices.
Main Methods:
- Chemical functionalization of monolayer graphene with sulfophenyl groups.
- Measurement of proton transport properties, including conductance and energy barrier.
- Characterization of graphene's impermeability to fuels.
Main Results:
- Chemical functionalization significantly enhanced proton transport properties of graphene.
- Conductance increased from 6.9 ± 1.1 to 30.9 ± 2.3 S·cm⁻².
- The energy barrier for proton transport was reduced to 6.9 kJ·mol⁻¹.
Conclusions:
- Functionalized graphene exhibits superior proton conductivity and fuel impermeability compared to conventional membranes.
- Sulfophenyl group functionalization is an effective strategy to improve graphene's proton transport.
- Functionalized graphene presents a viable alternative for next-generation electrochemical energy devices.

