Lele Wang, Sanser Celenk, Qian Wang, Qingfeng Li, Jingshuai Yang
{"title":"Long-Durability Poly(dibenzofuran-co-terphenyl N-methylimidazole) Copolymer Membranes for High-Temperature Polymer Electrolyte Membrane Fuel Cells","authors":"Lele Wang, Sanser Celenk, Qian Wang, Qingfeng Li, Jingshuai Yang","doi":"10.1021/acs.macromol.5c00024","DOIUrl":null,"url":null,"abstract":"Phosphoric acid (PA)-doped polybenzimidazoles (PBIs) are a state-of-the-art membrane for high-temperature polymer electrolyte membrane fuel cells (HT-PEMFCs). Herein, we develop a new series of imidazole-containing copolymers with π-conjugated structures and multiple hydrogen bonding sites via straightforward polymerization of dibenzofuran, <i>p</i>-terphenyl, and 1-methyl-2-imidazolecarboxaldehyde. The high reactivity of the dibenzofuran monomer provides P(BF<sub><i>x</i>%</sub>-TP<sub><i>y</i>%</sub>-Im) copolymers with high viscosity, while the π-conjugated and hydrophilic furan units also serve as additional PA-binding sites that facilitate the acid doping and proton conduction. The resulting P(BF<sub>20%</sub>-TP<sub>80%</sub>-Im)/202%PA membrane demonstrates exceptional performance in H<sub>2</sub>–O<sub>2</sub> and H<sub>2</sub>–air fuel cells, achieving peak power densities of 1085 and 539 mW cm<sup>–2</sup> at 180 °C, respectively, under ambient pressure and humidification. Notably, the H<sub>2</sub>–air cell equipped with this membrane shows remarkable stability, maintaining the high performance at 400 mA cm<sup>–2</sup> and 180 °C, with a voltage decay rate as low as 4.3 μV h<sup>–1</sup> over 720 h, likely the best durability result under these highly stressed conditions.","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":"7 1","pages":""},"PeriodicalIF":5.1000,"publicationDate":"2025-05-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecules","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.macromol.5c00024","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
Phosphoric acid (PA)-doped polybenzimidazoles (PBIs) are a state-of-the-art membrane for high-temperature polymer electrolyte membrane fuel cells (HT-PEMFCs). Herein, we develop a new series of imidazole-containing copolymers with π-conjugated structures and multiple hydrogen bonding sites via straightforward polymerization of dibenzofuran, p-terphenyl, and 1-methyl-2-imidazolecarboxaldehyde. The high reactivity of the dibenzofuran monomer provides P(BFx%-TPy%-Im) copolymers with high viscosity, while the π-conjugated and hydrophilic furan units also serve as additional PA-binding sites that facilitate the acid doping and proton conduction. The resulting P(BF20%-TP80%-Im)/202%PA membrane demonstrates exceptional performance in H2–O2 and H2–air fuel cells, achieving peak power densities of 1085 and 539 mW cm–2 at 180 °C, respectively, under ambient pressure and humidification. Notably, the H2–air cell equipped with this membrane shows remarkable stability, maintaining the high performance at 400 mA cm–2 and 180 °C, with a voltage decay rate as low as 4.3 μV h–1 over 720 h, likely the best durability result under these highly stressed conditions.
期刊介绍:
Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.