The dual-phase proton ceramic electrolyte produced by the low-temperature synthesis process exhibits enhanced sintering characteristics, enabling a reduction in the sintering temperature of conventional processes. As a result, the intrinsic properties of the electrolyte can be realized in the device, improving cell performance.
(A) Single-phase electrolyte powder material exhibits grain growth according to its inherent sintering properties as the temperature increases. (B) The dual-phase electrolyte powder, composed of two phases with high and low sintering properties, accelerates the initial sintering properties as one phase determines the initial sintering, while the remaining refractory phase undergoes grain growth via the Ostwald ripening phenomenon, ultimately forming a single-phase.
The new process, which does not use sintering aids or special sintering methods, achieved the lowest sintering temperature for electrolyte membranes.
Newswise — Dr. Ho-Il Ji from the Hydrogen Energy Materials Research Center at the Korea Institute of Science and Technology (KIST, President Sang-Rok Oh), along with Professor Sihyuk Choi's team from Kumoh National Institute of Technology, announced that they have developed a new synthesis method that can significantly reduce the sintering temperature required for the densification process of the electrolyte in next-generation high-efficiency protonic ceramic cells.
Existing solid oxide cells (SOC) can produce electricity in fuel cell operation and hydrogen in electrolysis operation. Notably, they operate at high temperatures above 600°C, offering higher power conversion efficiency compared to other fuel cells. However, the downside is the high production cost due to the need for materials that can withstand high temperatures, as well as performance degradation over time due to thermal deterioration.
Recently, protonic ceramic cells (PCCs), which utilize proton (hydrogen ion) transport instead of oxygen ions, have emerged as a next-generation energy conversion devices such as fuel cells and electrolyzers. Unlike conventional oxygen ion-conducting electrolytes, PCCs transport the smaller hydrogen ions, enabling higher ionic conductivity. However, to produce the electrolyte for PCCs, sintering at temperatures above 1,500°C is required. During this process, component evaporation or precipitation occurs, degrading the electrolyte’s ion-conducting properties, which has been a major obstacle to the commercialization of PCCs.
To lower the sintering temperature, the research team developed a new process for synthesizing electrolyte materials. Typically, the electrolyte for proton ceramic cells is produced by sintering a powder composed of a single compound. However, when additives are used to lower the sintering temperature, residual additives can remain in the electrolyte, reducing the cell's power density. The research team discovered that, by synthesizing a powder containing two different compounds through low-temperature synthesis, a single compound with excellent sintering properties forms during the sintering process accompanying the reaction to single phase. This allows the sintering temperature to drop to 1,400°C without the need for additives.
The proton ceramic electrolyte synthesized through this new process forms a dense membrane even at lower temperatures, enhancing the electrochemical properties of the cell. When applied to actual proton ceramic cells, this electrolyte demonstrated superior proton conductance, achieving a power density of 950mW/cm² at 600°C—approximately double that of existing cells. This is expected to reduce process time and simultaneously improve thermal stability and the performance of ceramic electrolytes. The research team plans to apply this new process, which utilizes the accelerated sintering between the two compounds, to the production of large-area cells for the commercialization of proton ceramic cells.
Dr. Ji of KIST stated, "This research has resolved the chronic sintering issues in the production of proton ceramic cells. If large-area technology is successfully developed, it will enable efficient energy management through green hydrogen production via electrolysis and pink hydrogen production by utilizing waste heat from nuclear power plants."
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KIST was established in 1966 as the first government-funded research institute in Korea. KIST now strives to solve national and social challenges and secure growth engines through leading and innovative research. For more information, please visit KIST’s website at https://eng.kist.re.kr/
This research was supported by the Ministry of Science and ICT (Minister Sang Im Yoo) through KIST's major project and the Future Hydrogen Fundamental Technology Development Project , as well as by the Ministry of Trade, Industry, and Energy (Minister Duk-Geun Ahn) through the Core Technology Development Project for New and Renewable Energy. The research results were published in the international journal Advanced Energy Materials (IF 24.4, JCR 2.6%).
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Credit: Korea Institute of Science and Technology
Caption: The dual-phase proton ceramic electrolyte produced by the low-temperature synthesis process exhibits enhanced sintering characteristics, enabling a reduction in the sintering temperature of conventional processes. As a result, the intrinsic properties of the electrolyte can be realized in the device, improving cell performance.
Credit: Korea Institute of Science and Technology
Caption: (A) Single-phase electrolyte powder material exhibits grain growth according to its inherent sintering properties as the temperature increases. (B) The dual-phase electrolyte powder, composed of two phases with high and low sintering properties, accelerates the initial sintering properties as one phase determines the initial sintering, while the remaining refractory phase undergoes grain growth via the Ostwald ripening phenomenon, ultimately forming a single-phase.
Credit: Korea Institute of Science and Technology
Caption: The new process, which does not use sintering aids or special sintering methods, achieved the lowest sintering temperature for electrolyte membranes.
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