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 language | English |
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Article number | 2107745 |
Journal | Small |
Volume | 18 |
Issue number | 14 |
DOIs | |
State | Published - 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.
Funders | Funder number |
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U.S. Department of Energy | |
Office of Science | |
Office of Energy Efficiency and Renewable Energy | |
Hydrogen and Fuel Cell Technologies Office | DE‐EE0008426, DE‐EE0008423 |
Keywords
- catalyst utilization
- hydrogen production
- in situ visualization
- integrated thin/tunable electrodes
- proton exchange membrane water electrolyzers