Tuning Catalyst Activation and Utilization Via Controlled Electrode Patterning for Low-Loading and High-Efficiency Water Electrolyzers

Shule Yu, Kui Li, Weitian Wang, Zhiqiang Xie, Lei Ding, Zhenye Kang, Jacob Wrubel, Zhiwen Ma, Guido Bender, Haoran Yu, Jefferey Baxter, David A. Cullen, Alex Keane, Kathy Ayers, Christopher B. Capuano, Feng Yuan Zhang

Research output: Contribution to journalArticlepeer-review

54 Scopus citations

Abstract

An anode electrode concept of thin catalyst-coated liquid/gas diffusion layers (CCLGDLs), by integrating Ir catalysts with Ti thin tunable LGDLs with facile electroplating in proton exchange membrane electrolyzer cells (PEMECs), is proposed. The CCLGDL design with only 0.08 mgIr cm−2 can achieve comparative cell performances to the conventional commercial electrode design, saving ≈97% Ir catalyst and augmenting a catalyst utilization to ≈24 times. CCLGDLs with regulated patterns enable insight into how pattern morphology impacts reaction kinetics and catalyst utilization in PEMECs. A specially designed two-sided transparent reaction-visible cell assists the in situ visualization of the PEM/electrode reaction interface for the first time. Oxygen gas is observed accumulating at the reaction interface, limiting the active area and increasing the cell impedances. It is demonstrated that mass transport in PEMECs can be modified by tuning CCLGDL patterns, thus improving the catalyst activation and utilization. The CCLGDL concept promises a future electrode design strategy with a simplified fabrication process and enhanced catalyst utilization. Furthermore, the CCLGDL concept also shows great potential in being a powerful tool for in situ reaction interface research in PEMECs and other energy conversion devices with solid polymer electrolytes.

Original languageEnglish
Article number2107745
JournalSmall
Volume18
Issue number14
DOIs
StatePublished - Apr 7 2022

Funding

The authors greatly appreciate the support from U.S. Department of Energy's Office of Energy Efficiency and Renewable Energy (EERE) under the Fuel Cell Technologies Office Award Nos. DE‐EE0008426 and DE‐EE0008423. A portion of the research was performed and 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. Gaoqiang Yang, Dr. Yifan Li, Alexander Terekhov, Douglas Warnberg, and Dr. Brian Canfield for their help. The authors greatly appreciate the support from U.S. Department of Energy's Office of Energy Efficiency and Renewable Energy (EERE) under the Fuel Cell Technologies Office Award Nos. DE-EE0008426 and DE-EE0008423. A portion of the research was performed and 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. Gaoqiang Yang, Dr. Yifan Li, Alexander Terekhov, Douglas Warnberg, and Dr. Brian Canfield for their help.

FundersFunder number
U.S. Department of Energy
Office of Science
Office of Energy Efficiency and Renewable Energy
Hydrogen and Fuel Cell Technologies OfficeDE‐EE0008426, DE‐EE0008423

    Keywords

    • catalyst utilization
    • hydrogen production
    • in situ visualization
    • integrated thin/tunable electrodes
    • proton exchange membrane water electrolyzers

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