A Quasielastic Neutron Scattering Study of Water Diffusion in Model Anion Exchange Membranes over Localized and Extended Volume Increments

被引:18
|
作者
Melchior, Jan-Patrick [1 ]
Jalarvo, Niina H. [1 ,2 ]
机构
[1] Oak Ridge Natl Lab, Neutron Scattering Div, Oak Ridge, TN 37831 USA
[2] Forschungszentrum Julich, JCNS 1, D-52425 Julich, Germany
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2019年 / 123卷 / 23期
关键词
FUEL-CELL; PERFLUORINATED SURFACTANTS; TRANSPORT MECHANISM; PROTON TRANSPORT; DYNAMICS; HYDROXIDE; MOBILITY; SOLVATION; SYSTEM; IONS;
D O I
10.1021/acs.jpcc.9b01873
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Anion exchange membranes provide the basis for potentially more cost-effective fuel cells, electrochemical energy conversion, and energy storage. The membranes consist of a polymer domain with tethered cationic side groups and a pervading aqueous domain that conducts water and anions. Water diffusion is investigated through temperature-dependent quasielastic neutron scattering (QENS) at application relevant water contents, employing the BASIS spectrometer at ORNL. The spectrometer resolves two distinct quasielastic components corresponding to localized water diffusion (on length scales lower than the water domain thickness) and to extended water diffusion (on length scales approaching the water domain thickness). Water diffusion coefficients in membranes are time and length scale dependent and water exchanges between diffusion on a localized and extended volume increment. An exchange model for QENS is developed to describe the exchange of water between the two volume increments. The populations and lifetimes of water in each volume are discussed in terms of their connection to long-range water transport and membrane nanomorphology.
引用
收藏
页码:14195 / 14206
页数:12
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