Correlated interfacial water transport and proton conductivity in perfluorosulfonic acid membranes

被引:38
|
作者
Ling, Xiao [1 ]
Bonn, Mischa [1 ]
Domke, Katrin F. [1 ]
Parekh, Sapun H. [1 ,2 ]
机构
[1] Max Planck Inst Polymer Res, Dept Mol Spect, D-55128 Mainz, Germany
[2] Univ Texas Austin, Dept Biomed Engn, Austin, TX 78712 USA
基金
欧盟第七框架计划;
关键词
proton-exchange membranes; water transport; confined water; nanoscale chemistry; proton transport; MOLECULAR-DYNAMICS; LIQUID WATER; EXCHANGE MEMBRANES; SELF-DIFFUSION; HEAVY-WATER; NAFION; MORPHOLOGY; SOLVATION; SIMULATIONS; SORPTION;
D O I
10.1073/pnas.1817470116
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Water must be effectively transported and is also essential for maximizing proton conductivity within fuel-cell proton-exchange membranes (PEMs). Therefore, identifying relationships between PEM properties, water transport, and proton conductivity is essential for designing optimal PEMs. Here, we use coherent Raman spectroscopy to quantify real-time, in situ diffusivities of water subspecies, bulk-like and nonbulk-like (interfacial) water, in five different perfluorosulfonic acid (PFSA) PEMs. Although the PEMs were chemically diverse, water transport within them followed the same rule: Total water diffusivity could be represented by a linear combination of the bulk-like and interfacial water diffusivities. Moreover, the diffusivity of interfacial water was consistently larger than that of bulk-like water. These measurements of microscopic transport were combined with through-plane proton conductivity measurements to reveal the correlation between interfacial water transport and proton conductivity. Our results demonstrate the importance of maximizing the diffusivity and fractional contribution of interfacial water to maximize the proton conductivity in PFSA PEMs.
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页码:8715 / 8720
页数:6
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