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Differentiating Grotthuss Proton Conduction Mechanisms by Nuclear Magnetic Resonance Spectroscopic Analysis of Frozen Samples

机译:冷冻样品的核磁共振波谱分析区分格罗斯质子传导机理

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Available methods to analyze proton conduction mechanisms cannot distinguish between two proton-conduction processes derived from the Grotthuss mechanism. The two mechanistic variations involve structural diffusion, for which water movement is indispensable, and the recently proposed "packed-acid mechanism," which involves the conduction of protons without the movement of water and is typically observed in materials consisting of highly concentrated (packed) acids. The latter mechanism could improve proton conductivity under low humidity conditions, which is desirable for polymer electrolyte fuel cells. We proposed a method with which to confirm quantitatively the packed-acid mechanism by combining ~2H and ~(17)O solid-state magic-angle-spinning nuclear magnetic resonance (MAS-NMR) measurement and ~1H pulsed-field gradient (PFG)-NMR analysis. In particular, the measurements were performed below the water-freezing temperature to prevent water movement, as confirmed by the ~(17)O-MAS-NMR spectra. Even without water movement, the high mobility of protons through short- and long-range proton conduction was observed by using ~2H-MAS-NMR and ~1H-PFG-NMR techniques, respectively, in the composite of zirconium sulfophenylphosphonate and sulfonated poly(arylene ether sulfone) (ZrSPP-SPES), which is a material composed of highly concentrated acids. Such behavior contrasts with that of a material conducting protons through structural diffusion or vehicle mechanisms (SPES), in which the peaks in both ~2H and ~(17)O NMR spectra diminished below water-freezing temperature. The activation energies of short-range proton movement are calculated to be 2.1 and 5.1 kJ/mol for ZrSPP-SPES and SPES, respectively, which indicate that proton conduction in ZrSPP-SPES is facilitated by the packed-acid mechanism. Furthermore, on the basis of the mean-square displacement using the diffusivity coefficient below water-freezing temperature, it was demonstrated that long-range proton movement, of the order of 1.3 μm, can take place in the packed-acid mechanism in ZrSPP-SPES.
机译:分析质子传导机制的可用方法无法区分源自格罗特斯机制的两个质子传导过程。这两种机制的变化涉及到结构扩散,而水的移动是必不可少的;最近提出的“堆积酸机理”涉及质子的传导而没有水的移动,通常在由高浓度(堆积)的材料中观察到酸。后一种机理可以改善低湿度条件下的质子传导性,这对于聚合物电解质燃料电池是合乎需要的。我们提出了一种方法,该方法通过结合〜2H和〜(17)O固态幻角自旋核磁共振(MAS-NMR)测量和〜1H脉冲场梯度(PFG)来定量确认填充酸机理NMR分析。尤其是,如〜(17)O-MAS-NMR光谱所证实,测量是在水冻结温度以下进行以防止水运动。即使没有水的移动,在磺基苯基膦酸锆和磺化聚()的复合物中,分别使用〜2H-MAS-NMR和〜1H-PFG-NMR技术,也观察到了质子通过短程和长程质子传导的高迁移率。亚芳基醚砜(ZrSPP-SPES),是一种由高浓度酸组成的材料。这种行为与通过结构扩散或载体机制(SPES)传导质子的材料的行为相反,在水冻结温度以下,〜2H和〜(17)O NMR谱中的峰均减小。对于ZrSPP-SPES和SPES,短程质子运动的活化能分别计算为2.1和5.1 kJ / mol,这表明ZrSPP-SPES中的质子传导是由填充酸机制促进的。此外,基于使用低于水冻结温度的扩散系数的均方位移,表明在ZrSPP-中的填充酸机理中可以发生1.3μm量级的远距离质子运动。 SPES。

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