Tuning Catalyst Activation and Utilization Via Controlled Electrode Patterning for Low-Loading and High-Efficiency Water Electrolyzers.
Shule YuKui LiWeitian WangZhiqiang XieLei DingZhenye KangJacob WrubelZhiwen MaGuido BenderHaoran YuJefferey BaxterDavid A CullenAlex KeaneKathy AyersChristopher B CapuanoFeng-Yuan ZhangPublished in: Small (Weinheim an der Bergstrasse, Germany) (2022)
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 mg Ir 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.
Keyphrases
- room temperature
- ionic liquid
- reduced graphene oxide
- highly efficient
- metal organic framework
- carbon dioxide
- visible light
- single cell
- gold nanoparticles
- carbon nanotubes
- cell therapy
- high efficiency
- solid state
- electron transfer
- induced apoptosis
- stem cells
- quantum dots
- endoplasmic reticulum stress
- risk assessment
- cell cycle arrest