Observing proton motion on the nanoscale in polymeric electrolyte membranes with quasielastic neutron scattering

被引:11
作者
Holderer, O. [1 ]
Ivanova, O. [1 ]
Hopfenmueller, B. [1 ]
Zamponi, M. [1 ]
Maier, W. [2 ]
Majerus, A. [2 ]
Lehnert, W. [2 ,3 ]
Monkenbusch, M. [4 ,5 ]
Zorn, R. [4 ,5 ]
机构
[1] Forschungszentrum Julich, Heinz Maier Leibnitz Zentrum MLZ, JCNS, D-85747 Garching, Germany
[2] Forschungszentrum Julich, Inst Energy & Climate Res IEK 3, D-52425 Julich, Germany
[3] Rhein Westfal TH Aachen, Fac Mech Engn, D-52062 Aachen, Germany
[4] Forschungszentrum Julich, JCNS, D-52425 Julich, Germany
[5] Forschungszentrum Julich, Inst Complex Syst, D-52425 Julich, Germany
关键词
Fuel cells; Neutron scattering; Backscattering; Neutron spin echo; HT-PEFC; PHOSPHORIC-ACID; FUEL-CELLS; MOLECULAR-DYNAMICS; POLYBENZIMIDAZOLE; CONDUCTIVITY; SPECTROSCOPY; TRANSPORT; SYSTEM; NMR;
D O I
10.1016/j.ijhydene.2014.09.018
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
The mechanism of proton conductivity in high temperature polymer electrolyte fuel cells (HT-PEFCs) has been investigated with macroscopic conductivity measurements and on a microscopic scale with quasielastic neutron scattering techniques. Polybenzimidazole membranes, which are used in HT-PEFCs, are doped with phosphoric acid (PA) to achieve the desired proton conductivity. Neutron spin echo experiments showed that the polymer matrix is very rigid incoherent scattering experiments, but incoherent scattering revealed rather fast diffusion processes, compatible with macroscopic conductivity measurements. The measured diffusion is faster than anticipated from the conductivity of a phosphoric acid doped FBI membrane, but slower than that expected for pure phosphoric acid. Over larger distances the fractal polymer membrane network slows down the locally fast diffusion to the macroscopic values. With elastic fixed window scans on a backscattering spectrometer an activation energy of 7.6 kJ/mol is obtained at typical conditions in an HTPEFC. Copyright (C) 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:21657 / 21662
页数:6
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