Investigation of thin/well-tunable liquid/gas diffusion layers exhibiting superior multifunctional performance in low-temperature electrolytic water splitting

Zhenye Kang, Jingke Mo, Gaoqiang Yang, Scott T. Retterer, David A. Cullen, Todd J. Toops, Johney B. Green, Matthew M. Mench, Feng Yuan Zhang

Research output: Contribution to journalArticlepeer-review

192 Scopus citations

Abstract

Liquid/gas diffusion layers (LGDLs), which are located between the catalyst layer (CL) and bipolar plate (BP), play an important role in enhancing the performance of water splitting in proton exchange membrane electrolyzer cells (PEMECs). They are expected to transport electrons, heat, and reactants/products simultaneously with minimum voltage, current, thermal, interfacial, and fluidic losses. In this study, the thin titanium-based LGDLs with straight-through pores and well-defined pore morphologies are comprehensively investigated for the first time. The novel LGDL with a 400 μm pore size and 0.7 porosity achieved a best-ever performance of 1.66 V at 2 A cm-2 and 80°C, as compared to the published literature. The thin/well-tunable titanium based LGDLs remarkably reduce ohmic and activation losses, and it was found that porosity has a more significant impact on performance than pore size. In addition, an appropriate equivalent electrical circuit model has been established to quantify the effects of pore morphologies. The rapid electrochemical reaction phenomena at the center of the PEMEC are observed by coupling with high-speed and micro-scale visualization systems. The observed reactions contribute reasonable and pioneering data that elucidate the effects of porosity and pore size on the PEMEC performance. This study can be a new guide for future research and development towards high-efficiency and low-cost hydrogen energy.

Original languageEnglish
Pages (from-to)166-175
Number of pages10
JournalEnergy and Environmental Science
Volume10
Issue number1
DOIs
StatePublished - Jan 2017

Funding

The authors greatly appreciate the support from U.S. Department of Energy's National Energy Technology Laboratory under Award DE-FE0011585. This research was partially conducted at the Center for Nanophase Materials Sciences, which is a DOE Office of Science User Facility. The authors also wish to express their appreciation to Dr Bo Han, Dr Lee Leonard, Dr Jacqueline Anne Johnson, William Barnhill, Stuart Steen, Alexander Terekhov, Douglas Warnberg, Kate Lansford, and Andrew Mays for their help.

FundersFunder number
U.S. Department of Energy
Office of Science
National Energy Technology LaboratoryDE-FE0011585

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