聚氯乙烯
膜
质子
材料科学
电导率
化学工程
质子交换膜燃料电池
纳米纤维
热传导
磷酸
高分子化学
化学
复合材料
物理化学
生物化学
物理
量子力学
工程类
冶金
作者
Ke Liu,Xiaoqing Wei,Shu Hu,Qingquan Li,Weimin Gao,Dan Wu,Quantong Che
标识
DOI:10.1016/j.seppur.2023.124679
摘要
Carbon dots (CDs) as the easy-to-get and cheap carbon nanomaterials exhibited the great potential in various high-performance electrolytes. In this research, we constructed high temperature proton exchange membranes with multilayered microstructures through a couple of polyvinyl chloride (PVC) nanofibers layers wrapping a thin CDs layer. In the prepared (PVC/CDs/PVC)es membrane, the CDs provided a mount of sites to anchor phosphoric acid (PA) molecules with the formation of the (PVC/CDs/PVC)es/PA membrane. The proton conduction was accelerated by the continuous proton conduction channels consisting of the CDs layer and PA molecular chains. Notably, the proton conduction behavior was guided by the PVC nanofibers in the (PVC/CDs/PVC)es/PA membrane. Furthermore, a large number of hydrophilic oxygenated functional groups surrounding CDs facilitated the proton conduction process owing to the reduced proton conduction resistance in the hydrophilic membrane. For the PVC/ImCDs/PA membrane, the imidazolium groups could enhance proton conductivity. From our perspective, the imidazolium groups grafted CDs (ImCDs) participated into the proton conduction process through providing imidazolium groups for ameliorating proton conduction network. The enhanced proton conduction was achieved through constructing multilayered structure. Specifically, the (PVC/CDs/PVC)es/PA membrane exhibited the proton conductivity of 5.61 × 10-3 S/cm at 150 °C, which was higher than 7.73 × 10-4 S/cm of the PVC/CDs/PA membrane. Notably, the PA doped membrane could retain the mechanical strength without microstructure expansion.
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