Molecular-Level Modification of Sulfonated Poly(arylene ether ketone sulfone) with Polyoxovanadate–Ionic Liquid for High-Performance Proton Exchange Membranes

In this work, a proton-conductive inorganic filler based on polyoxovanadate (NH<sub>4</sub>)<sub>7</sub>[MnV<sub>13</sub>O<sub>38</sub>] (AMV) and 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl) imide (EMIM TFSI) was synthesized for hybridization with sulfonated poly(aryl ether ketone sulfone) (SPAEKS) to address the "trade-off" between high proton conductivity and mechanical strength. The novel inorganic filler AMV-EMIM TFSI (AI) was uniformly dispersed and stable within the polymer matrix due to the enhanced ionic interaction. AI provided additional proton transport sites, leading to an elevated ion exchange capacity (IEC) and improved proton conductivity, even at low swelling ratios. The optimized SPAEKS-50/AI-5 (50 for degree of sulfonation of SPAEKS and 5 for weight percentage of AI filler) membrane exhibited the highest proton conductivity of 0.188 S·cm<sup>-1</sup> at 80 °C with an IEC of 2.38 mmol·g<sup>-1</sup>. The enhancement of intermolecular forces improved the mechanical strength from 35 to 55 MPa and improved the elongation at break from 17 to 45%, indicating excellent mechanical properties. The hybrid membrane also demonstrated reinforced methanol resistance due to the hydrogen bonding network and blocking effect, making it suitable for direct methanol fuel cell (DMFC) applications, which exhibited a power density of 15.1 mW·cm<sup>-2</sup> at 80 °C. The possibility of further functionalizing these hybrid membranes to tailor their properties for specific applications presents exciting new avenues for research and development. By modification of the type and distribution of fillers or incorporation of additional functional groups, the membranes could be customized to meet the unique demands of various energy storage and conversion systems, enhancing their performance and broadening their application scope. This work provides new insights into the design of polymer electrolyte membranes through inorganic filler hybridization.

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Publication Details

Journal
ACS Applied Materials & Interfaces
Published
2024-08-16
DOI
https://doi.org/10.1021/acsami.4c09126
Citations
11
Primary Topic
Fuel Cells and Related Materials
Type
article
Field-Weighted Citation Impact
2.30

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article

Molecular-Level Modification of Sulfonated Poly(arylene ether ketone sulfone) with Polyoxovanadate–Ionic Liquid for High-Performance Proton Exchange Membranes

Yuanlong Wu, Zhe Wang, Yishan Li, Jiahao Lu et al.
11 citations
ACS Applied Materials & Interfaces
Fuel Cells and Related Materials
2.30
article

Molecular-Level Modification of Sulfonated Poly(arylene ether ketone sulfone) with Polyoxovanadate–Ionic Liquid for High-Performance Proton Exchange Membranes

Yuanlong Wu, Zhe Wang, Yishan Li, Jiahao Lu, Yanchao Zhang, Jinsheng Li, Jiaran Song, Wenjing Li
article en
11 citations

Abstract

In this work, a proton-conductive inorganic filler based on polyoxovanadate (NH<sub>4</sub>)<sub>7</sub>[MnV<sub>13</sub>O<sub>38</sub>] (AMV) and 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl) imide (EMIM TFSI) was synthesized for hybridization with sulfonated poly(aryl ether ketone sulfone) (SPAEKS) to address the "trade-off" between high proton conductivity and mechanical strength. The novel inorganic filler AMV-EMIM TFSI (AI) was uniformly dispersed and stable within the polymer matrix due to the enhanced ionic interaction. AI provided additional proton transport sites, leading to an elevated ion exchange capacity (IEC) and improved proton conductivity, even at low swelling ratios. The optimized SPAEKS-50/AI-5 (50 for degree of sulfonation of SPAEKS and 5 for weight percentage of AI filler) membrane exhibited the highest proton conductivity of 0.188 S·cm<sup>-1</sup> at 80 °C with an IEC of 2.38 mmol·g<sup>-1</sup>. The enhancement of intermolecular forces improved the mechanical strength from 35 to 55 MPa and improved the elongation at break from 17 to 45%, indicating excellent mechanical properties. The hybrid membrane also demonstrated reinforced methanol resistance due to the hydrogen bonding network and blocking effect, making it suitable for direct methanol fuel cell (DMFC) applications, which exhibited a power density of 15.1 mW·cm<sup>-2</sup> at 80 °C. The possibility of further functionalizing these hybrid membranes to tailor their properties for specific applications presents exciting new avenues for research and development. By modification of the type and distribution of fillers or incorporation of additional functional groups, the membranes could be customized to meet the unique demands of various energy storage and conversion systems, enhancing their performance and broadening their application scope. This work provides new insights into the design of polymer electrolyte membranes through inorganic filler hybridization.

ACS Applied Materials & InterfacesVol. 16(34)
Chinese Academy of Sciences (CN), Changchun Institute of Applied Chemistry (CN), Changchun University of Technology (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 11%
Fuel Cells and Related Materials
2.30
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