TY - JOUR
T1 - Tuning Catalyst Activation and Utilization Via Controlled Electrode Patterning for Low-Loading and High-Efficiency Water Electrolyzers
AU - Yu, Shule
AU - Li, Kui
AU - Wang, Weitian
AU - Xie, Zhiqiang
AU - Ding, Lei
AU - Kang, Zhenye
AU - Wrubel, Jacob
AU - Ma, Zhiwen
AU - Bender, Guido
AU - Yu, Haoran
AU - Baxter, Jefferey
AU - Cullen, David
AU - Keane, Alex
AU - Ayers, Kathy
AU - Capuano, Christopher
AU - Zhang, Feng-Yuan
N1 - Publisher Copyright:
© 2022 Wiley-VCH GmbH.
PY - 2022
Y1 - 2022
N2 - 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.
AB - 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.
KW - catalyst utilization
KW - hydrogen production
KW - in situ visualization
KW - integrated thin/tunable electrodes
KW - proton exchange membrane water electrolyzers
UR - http://www.scopus.com/inward/record.url?scp=85124733317&partnerID=8YFLogxK
U2 - 10.1002/smll.202107745
DO - 10.1002/smll.202107745
M3 - Article
C2 - 35174962
AN - SCOPUS:85124733317
SN - 1613-6810
VL - 18
JO - Small
JF - Small
IS - 14
M1 - 2107745
ER -