Proton exchange membrane water electrolyzers (PEMWEs) show potential for the clean production of renewable and high-purity hydrogen. [1] The widespread implementation of PEMWE usage faces performance and economic hurdles. In order to improve cell performance and durability, thus reducing capital cost, identifying and understanding the origins of performance losses is crucial. Overpotentials fall into three categories: ohmic, kinetic, and mass transport, which relate to various resistances within the cell during operation. Traditionally, electrochemical equivalent circuits (EEC) have been used to analyze electrochemical impedance spectroscopy (EIS) for polarizing processes, but this tool requires extensive background knowledge of both electrochemical processes and circuits. The use of distribution of relaxation times (DRT) as an EIS analysis tool allows for the objective distinguishing of individual and distinct electrochemical processes within the cell that contribute to these overpotentials [2,3,4]. DRT as an EIS analysis tool allows for more comprehensive understanding and comparison of overpotential processes, especially between cells of varying configurations. Understanding overpotential origins will provide a pathway for mitigating performance restricting processes and developing better performing, more durable, and more cost-effective build configurations. In this work, several configurations of a single cell 25 cm2 PEMWE were tested. Cell performance using titanium fiber porous transport layers (PTLs) is compared against the use of sintered titanium PTLs, in both unplated and plated configurations. Four PEMWE cells were built using Bekaert unplated and plated titanium fiber PTLs, and Mott 20 mil unplated and plated sintered titanium PTLs. Results show good cell performance. DRT analysis of diagnostic data allows for the objective identification, discussion, and comparison of overpotential contributions. References [1] Aricò, A. S., Siracusano, S., Briguglio, N., Baglio, V., Di Blasi, A., & Antonucci, V. (2012). Polymer electrolyte membrane water electrolysis: Status of technologies and potential applications in combination with renewable power sources. Journal of Applied Electrochemistry, 43(2), 107–118. https://doi.org/10.1007/s10800-012-0490-5 [2] Dierickx, S., Weber, A., & Ivers-Tiffée, E. (2020). How the distribution of relaxation times enhances complex equivalent circuit models for fuel cells. Electrochimica Acta, 355, 136764. https://doi.org/10.1016/j.electacta.2020.136764 [3] Ivers-Tiffée, E., Weber, A. (2017). Evaluation of electrochemical impedance spectra by the distribution of Relaxation Times. Journal of the Ceramic Society of Japan, 125(4), 193–201. https://doi.org/10.2109/jcersj2.16267 [4] Gado, A., Ouimet, R. J., Bonville, L., Bliznakov, S., & Maric, R. (2021). Analysis of electrochemical impedance spectroscopy using distribution of relaxation times for proton exchange membrane fuel cells and electrolyzers. ECS Meeting Abstracts, MA2021-02(41), 1261–1261. https://doi.org/10.1149/ma2021-02411261mtgabs
Proton exchange membrane water electrolyzers (PEMWEs) are a promising technology to produce zero-carbon emission, renewable, high-purity hydrogen. [1] There is a need to reduce capital cost while improving performance for the progression of widespread development. The crossover of hydrogen from the cathode into the anode not only restricts cell performance, but also poses a safety hazard, as the crossover reaches the lower explosive limit of hydrogen in oxygen. [2] Previous work has been conducted on the fabrication and testing of Pt recombination layers in PEMWEs. The addition of the Pt recombination layer has proven to be an effective mitigation strategy for hydrogen crossover while improving performance. [3, 4] Further investigation is needed to understand the mechanisms of the Pt recombination layer. In this work, reactive spray deposition technology (RSDT) was used to deposit two Pt recombination layers separated by a membrane. Testing of a single cell 25 cm2 PEMWE was conducted. Polarization analysis, electrochemical impedance spectroscopy, and distribution of relaxation times were used to investigate the cell performance. Results show good cell performance and hydrogen crossover reduction, as well as insight to the mechanisms of the chemical reactions that occur on the dual recombination layer. References [1] Aricò, A. S., Siracusano, S., Briguglio, N., Baglio, V., Di Blasi, A., & Antonucci, V. (2012). Polymer electrolyte membrane water electrolysis: Status of technologies and potential applications in combination with renewable power sources. Journal of Applied Electrochemistry, 43(2), 107–118. https://doi.org/10.1007/s10800-012-0490-5 [2] Schalenbach, M., Carmo, M., Fritz, D, L., Mergel, J., Stolten, D. Pressurized PEM water electrolysis: Efficiency and gas crossover, International Journal of Hydrogen Energy, 38(35), (2013), 14921-14933. [3] Klose, C., Trinke, P., Bohm, T., Bensmann, B., Vierrath, S., Hanke-Rauschenbach, R., Thiele, S. Membrane Interlayer with Pt Recombination Particles for Reduction of the Anodic Hydrogen Content in PEM Water Electrolysis, Journal of Electrochemical Society, 165(16), (2018), F1271-F1277. [4] Mirshekari, G., Ouimet, R., Zeng, Z., Yu, H., Bliznakov, S., Bonville, L., Niedzwiecki, A., Capuano, C., Ayers, K., Maric, R. High-performance and cost-effective membrane electrode assemblies for advanced proton exchange membrane water electrolyzers: Long-term durability assessment. International Journal of Hydrogen Energy, Volume 46, Issue 2, 2021, Pages 1526-1539, ISSN 0360-3199, https://doi.org/10.1016/j.ijhydene.2020.10.112.
Proton exchange membrane water electrolyzers (PEMWEs) are a leading industry solution to large scale production of green hydrogen, and as a form of energy storage [5]. The PEMWEs have the advantages of having greater energy efficiency, higher product purity, and are environmentally friendly. Within the construction of a PEMWE stack, there are many catalysts coated membranes (CCMs) sandwiched between anode porous transport layers (PTLs) and cathode Gas Diffusion Layers. The PTL is constructed of sintered titanium powder or fibers. The Ti-PTL is on the anode side of a PEMWE cell where the water diffuses towards the CCM. The anode half-cell reaction or oxygen evolution reaction (OER) occurs on this side of the cell. This is important as the PTL is in contact with the bipolar plate (BPP) and the anode catalyst layer [9]. A key aspect plaguing the PEMWEs is the highly oxidative and corrosive environment that is typically observed on the anode side. This significantly affects the interfacial contact resistance (ICR) of the components as the corrosion can cause the ohmic resistance of the PTL to increase. In order to combat the corrosion in the PTLs, in this work we use two thin film deposition methods, Physical Vapor Deposition (PVD) and Vacuum Sputtering, to deposit protective metal layers on top of the state-of-the-art Ti PTLs [2]. The explored metal coatings of interest are Platinum (Pt) and Gold (Au) [9]. For the purposes of these experiments, Au and Pt coatings with various thicknesses are deposited on Ti-PTLs by using either PVD or vacuum spattering method. As deposited thin films are characterized by scanning electron microscopy (SEM), digital optical microscopy, and inductively coupled plasma (ICP) analysis. Also, the in-plane conductivity and the ICR of all samples of interest are measured before and after the electrochemical tests by using the 4-probe method and in-house build setup for ICR measurements. The optimal deposition parameters for fabrication of thin, continuous and smooth Pt and Au protective coatings that result in minimum ICR and improved in-plane conductivity of the PTLs of interest are identified, and the results will be reported at the ECS 241 meeting. References: [1] Mo, Jingke, Steen, Stuart, Kang, Zhenye, Yang, Gaoqiang, Taylor, Derrick A., Li, Yifan, Toops, Todd J., Brady, Michael P., Retterer, Scott T., Cullen, David A., Green, Johney B., and Zhang, Feng-Yuan. Study on corrosion migrations within catalyst-coated membranes of proton exchange membrane electrolyzer cells. United States: N. p., 2017. Web. [2] Rojas, Nuria & Sevilla, Gema & Sánchez-Molina, Margarita & Amores, Ernesto & Bueno, Rebeca & Almandoz, Eluxka & Cruz, Marlon & Colominas, Carles. (2018). Materials selection for bipolar plates in PEMWE. [3] Oluwatosin Ijaodola, Emmanuel Ogungbemi, Fawwad Nisar. Khatib,Tabbi Wilberforce, Mohamad Ramadan, Zaki El Hassan, James Thompson andAbdul Ghani Olab. Evaluating the effect of metal bipolar plate coating on the performance of proton exchange membrane fuel cells. Energies, MDPI AG, 5 Oct. 2021 [4] Sigrid Lædre, Ole Edvard Kongstein, Anders Oedegaard, Frode Seland, and Håvard Karoliussen. Measuring In Situ Interfacial Contact Resistance in a Proton Exchange Membrane Fuel Cell. Journal of the Electrochemical Society, 166 (13) F853-F859 (2019) [5] Peter Holzapfela, Melanie Bühler, ChuyenVan Phamc, Friedemann Hegge, Thomas Böhm, David McLaughlin, Matthias Breitwieser, Simon Thielead. Directly coated membrane electrode assemblies for proton exchange membrane water electrolysis. Electrochemical Communications, volume 110, January 2020, 106640. [6] S. Stiber, N. Sata, T. Morawietz, S. A. Ansar, T. Jahnke, J. K. Lee, A. Bazylak, A. Fallisch, A. S. Gago and K. A. Friedrich. A high-performance, durable and low-cost proton exchange membrane electrolyser with stainless steel components. Journal, Energy & Environmental Science [7] Chang Liu, Marcelo Carmo, Guido Bender, Andreas Everwand, Thomas Lickert, James L. Young, Tom Smolinka, Detlef Stolten, Werner Lehnert, Performance enhancement of PEM electrolyzers through iridium-coated titanium porous transport layers, Electrochemistry Communications, Volume 97, 2018, Pages 96-99, ISSN 1388-2481, [8] Gago, Aldo & Ansar, Asif & Gazdzicki, Pawel & Wagner, Norbert & Arnold, Johannes. (2014). Low Cost Bipolar Plates for Large Scale PEM Electrolyzers. ECS Transactions. 64. 10.1149/06403.1039ecst. [9] Novel components in Proton Exchange Membrane (PEM) Water Electrolyzers (PEMWE): Status, challenges and future needs. A mini review, Electrochemistry Communications, Volume 114, 2020, 106704
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