Abstract

Ionomer membranes are crucial components of many electrochemical devices. In this work, confocal Raman microscopy is employed to characterize Nafion ionomers quantitatively in pristine status and after usage as a proton exchange membrane in a fuel cell. Confocal Raman microscopy allows non-destructive thickness and equivalent weight measurements of Nafion with a 95% confidence interval of ±13 g mol−1 at an equivalent weight of 1000 g mol−1, which is significantly more accurate than previously reported methods. Characterization can be performed at a spatial resolution better than 2 μm, providing insights into local membrane degradation after fuel cell operation. Membrane thinning to less than 40% of the initial thickness of Nafion NR-211 occurs after a 100 h open circuit voltage hold, accompanied by an anisotropic increase of the equivalent weight from 1035 g mol−1 to an average of 1200 g mol−1. Most pronounced increases are found close to the anode. Further, the characterization of a Nafion XL membrane shows that its microporous reinforcement is represented as increased equivalent weight with local heterogeneities within the membrane. These results show that confocal Raman microscopy is a valuable tool to investigate ionomers that are used as ion exchange membranes in electrochemical devices.

Highlights

  • The ionomer membrane is crucial for the performance and safety of electrochemical devices such as proton exchange membrane fuel cells (PEMFC)

  • In this work we investigated the capabilities of confocal Raman microscopy for the analysis of ionomers that are used as proton exchange membranes in fuel cells

  • Confocal Raman microscopy offers the power of a depthresolved analysis of multi-layered and aged ionomer membranes

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Summary

Introduction

The ionomer membrane is crucial for the performance and safety of electrochemical devices such as proton exchange membrane fuel cells (PEMFC). Besides a basic characterization of the ionomer itself,[26] Raman and IR spectroscopy have been used to investigate water in Nafion,[27,28] even within an operating fuel cell.[29] a qualitative analysis of the sidechainloss of Nafion upon membrane degradation using Raman spectroscopy has been reported.[30] the EW of Nafion has been quantified by IR spectroscopy.[31] This method is highly related to Raman spectroscopy since they both are based on the detection of molecular vibrations, but they produce different spectra of a sample due to different sensitivities of Raman and IR spectroscopy toward different vibrational modes of molecules.

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