离聚物
Nafion公司
材料科学
电导率
高分子化学
聚苯乙烯
离子电导率
膜
基质(水族馆)
千分尺
化学工程
复合材料
电化学
共聚物
化学
物理化学
聚合物
电极
物理
工程类
生物化学
海洋学
光学
电解质
地质学
作者
Shyambo Chatterjee,Oghenetega Allen Obewhere,Ehsan Zamani,Rajesh Keloth,Seefat Farzin,Martha Morton,Anandakumar Sarella,Shudipto Konika Dishari
标识
DOI:10.1016/j.xcrp.2023.101282
摘要
Sub-micrometer-thick ion-conducting polymer (ionomer) layers often suffer from poor ionic conductivity at the substrate/catalyst interface. The weak proton conductivity makes the electrochemical reaction at the cathode of proton-exchange-membrane fuel cells sluggish. To address this, here we report on a class of polystyrene-based ionomers having sub-nanometer-sized, sulfonated macrocyclic calix[4]arene-based pendants (PS-calix). In films with thickness comparable to that of ionomer-based binder layers, the conductivity of PS-calix film (∼41 mS/cm) is ∼13 times higher than that of the current state-of-the-art ionomer, Nafion. We observe a similar improvement in proton conductivity when PS-calix interfaces with Pt nanoparticles, demonstrating the potential of PS-calix in catalyst ink. Leveraging a favorable interfacial chemical composition, PS-calix enhances proton conduction at the film-substrate interface, a shortcoming of Nafion. Moreover, the water in PS-calix films diffuses faster than bulk water and the water confined in Nafion films, suggesting an important role played by sub-nanometer-sized calix[4]arene cavities in creating unique water/ion transport pathways.
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