Atomic Layer Deposition (ALD) has emerged as a promising technique for fabricating thin films that enhance the performance of solid oxide fuel cells and solid oxide electrolysis cells. ALD allows for precise control over film thickness and composition at the atomic level, resulting in uniform and dense thin films. These characteristics enable the deposition of thin, homogeneous layers of various materials onto the porous electrode surfaces of solid oxide cells, thereby increasing electrochemical activity and reducing activation losses. Additionally, thin-film electrolytes produced through ALD can achieve high ionic conductivity and low ohmic losses, facilitating a reduction in the operating temperature of solid oxide cells. This review summarizes recent research trends in applying ALD technology to the fuel electrode, air electrode, and electrolyte of solid oxide cells and discusses design strategies aimed at improving efficiency and long-term stability.
In this study, we introduce a novel flash light sintering (FLS) method to address the issue of secondary phase formation in conventional high-temperature thermal sintering processes. The microstructure and cross section of the Lanthanum strontium cobalt (LSC) air electrode were analyzed using field emission scanning electron microscopy (FE-SEM). The presence of secondary phases was evaluated using X-ray diffraction (XRD) and energy-dispersive spectroscopy (EDS) in SEM. Electrochemical performance was assessed using NiO-YSZ anode-supported LSC cathode cells at 750oC. The maximum power density of the thermally sintered LSC cathode at 900oC was 272.4 mW/cm², while the flash light sintered LSC cathode by 18.5 J/cm² achieved 2,222 mW/cm². These results demonstrate that the flash light sintering process can effectively prevent secondary phase formation and successfully sinter the electrode, thereby enhancing the performance and reliability of SOFCs.
In this study, polymer electrolyte membrane fuel cells (PEMFCs) were humidified with NaCl solutions. NaCl solutions were provided to the cathode side of fuel cells by bubbling. De-Ionized water, 3.5 wt% NaCl solution, and 20 wt% NaCl solution were used to evaluate the effects of NaCl. Current density-voltage curves and electrochemical impedance spectroscopies (EIS) of fuel cells were measured. Additionally, the constant-voltage mode long-term stability of PEMFCs humidified with NaCl solution were investigated. Constant-voltage measurements and EIS results imply that the degradation of fuel cells is clearly related with the concentration of NaCl solutions.
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Effects of NaCl Solution on Proton Exchange Membrane Fuel Cell with Serpentine Flow Channel of Different Depths Dong Kun Song, Ho Jun Yoo, Jung Soo Kim, Ki Won Hong, Do Young Jung, George Ilhwan Park, Gu Young Cho Journal of the Korean Society for Precision Engineering.2025; 42(5): 399. CrossRef
Analysis of Electrochemical Behavior of PEMFC Humidified with NaCl Solution Mist Using an Ultrasonic Vibrator Ho Jun Yoo, Gye Eun Jang, Young Jo Lee, Dong Kun Song, Heeyun Lee, Gu Young Cho Journal of the Korean Society for Precision Engineering.2022; 39(12): 939. CrossRef
To study the geometrical scale dependency of thin film solid oxide fuel cells (SOFCs), we fabricated three thin films SOFCs with the same cross-sectional structure but with different electrode areas of 1, 4 and 9 ㎟. Since the activation and ohmic losses of SOFCs depend on their active region, we examined the variations of the power density of the cells with a Pt (anode)/sputtered YSZ/Pt (cathode) structure. We found that a cathode electrode with a low aspect ratio may suffer from high ohmic and activation losses because of the geometrical scale dependency.