Enhanced Performance of MIL-100(Cr)-COOH Incorporated Sulfonated Polystyrene@Polyethylene Membranes for Direct Methanol Fuel Cells
نویسندگان
1 Department of Applied Chemistry, University of Gonabad, Gonabad, Iran
2 Department of Chemistry, Yasouj University, Yasouj, Iran
3 Department of Chemistry, Yasouj University, Yasouj, Iran
4 Department of Applied Chemistry, University of Gonabad, Gonabad, Iran
doi
10.48309/jaoc.2026.560971.1363چکیده
The increasing demand for clean, efficient, and economically viable energy technologies has intensified research on high-performance proton exchange membranes for fuel cell systems. In this study, advanced SPS@PE composite membranes were fabricated by incorporating MIL-100(Cr)-COOH nanofillers at varying concentrations (5, 10, and 15 wt%). Unlike previously reported fillers such as MIL-53(Fe)-(COOH)₂, MIL-100(Cr)-COOH provides a significantly higher BET surface area, larger mesoporous cages, and a greater density of accessible –COOH groups, enabling improved water retention and the formation of extended hydrogen-bonding networks within the polymer matrix. These structural advantages contribute to enhanced proton transport efficiency and a more favorable conductivity–permeability balance. Comprehensive characterization using FTIR, SEM, and BET confirmed strong interfacial interactions between the MOF particles and the SPS@PE matrix, resulting in improved mechanical integrity, thermal stability, and controlled membrane swelling. Electrochemical measurements revealed that the membrane containing 10 wt% filler (MM-10) offered the best overall performance, achieving a proton conductivity of 0.0963 S·cm⁻¹ at 80 °C and 60% relative humidity—values surpassing those reported for many previously published SPS- and MOF-based membranes. Moreover, single-cell DMFC tests demonstrated a maximum power density of 87 mW·cm⁻², confirming the excellent catalytic and transport properties of the optimized composite. These findings demonstrate that MIL-100(Cr)-COOH is a highly effective functional filler that significantly enhances the durability, proton selectivity, and operational performance of SPS-based membranes, making them strong candidates for next-generation direct methanol fuel cell applications.