Hiroyuki Shimada*, Konosuke Watanabe, Masaya Fujioka, Katsuhiro Nomura, Aman Sharma, Yuki Yamaguchi, Hirofumi Sumi and Yasunobu Mizutani,
{"title":"掺镱锆酸钡高性能质子陶瓷燃料电池:通过改善电解质表面条件降低阴极极化。","authors":"Hiroyuki Shimada*, Konosuke Watanabe, Masaya Fujioka, Katsuhiro Nomura, Aman Sharma, Yuki Yamaguchi, Hirofumi Sumi and Yasunobu Mizutani, ","doi":"10.1021/acsami.5c04806","DOIUrl":null,"url":null,"abstract":"<p >Protonic ceramic fuel cells (PCFCs) have great potential to realize ultrahigh energy-conversion efficiency, but higher power density is required for future commercialization. The present work reports the effect of the electrolyte surface condition related to chemical composition such as stoichiometry and element distribution on cathode performance as a key for high-performance PCFCs. In our PCFCs, Ce-free Yb-doped BaZrO<sub>3</sub> (BZYb20) electrolytes are prepared using two BZYb20 raw powder materials with different A/B ratios, i.e., Ba<sub>0.97</sub>Zr<sub>0.8</sub>Yb<sub>0.2</sub>O<sub>3−δ</sub> (Cell-97) and Ba<sub>0.99</sub>Zr<sub>0.8</sub>Yb<sub>0.2</sub>O<sub>3−δ</sub> (Cell-99). These PCFCs exhibit different element distributions on their BZYb20 electrolyte surfaces, namely, a heterogeneous element distribution with segregation of Yb<sub>2</sub>O<sub>3</sub> for Cell-97 and a homogeneous distribution for Cell-99. The maximum power density of Cell-99 is higher than that of Cell-97 and reaches exceptionally high values, e.g., ∼1.3 W cm<sup>–2</sup> at 600 °C and ∼0.7 W cm<sup>–2</sup> at 500 °C, which are the highest attained for PCFCs with Ce-free BaZrO<sub>3</sub>-based electrolytes. The distribution of relaxation times and fitting analysis reveals that the cathode polarization resistance of Cell-99 is much lower than that of Cell-97 even when using the same cathode material. In conclusion, an optimal electrolyte surface condition significantly reduces cathode polarization resistance, leading to the achievement of high-performance PCFCs.</p>","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":"17 28","pages":"40639–40649"},"PeriodicalIF":8.2000,"publicationDate":"2025-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/pdf/10.1021/acsami.5c04806","citationCount":"0","resultStr":"{\"title\":\"High-Performance Protonic Ceramic Fuel Cell with Ytterbium-Doped Barium Zirconate: Reducing Cathode Polarization by Improving Electrolyte Surface Condition\",\"authors\":\"Hiroyuki Shimada*, Konosuke Watanabe, Masaya Fujioka, Katsuhiro Nomura, Aman Sharma, Yuki Yamaguchi, Hirofumi Sumi and Yasunobu Mizutani, \",\"doi\":\"10.1021/acsami.5c04806\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Protonic ceramic fuel cells (PCFCs) have great potential to realize ultrahigh energy-conversion efficiency, but higher power density is required for future commercialization. The present work reports the effect of the electrolyte surface condition related to chemical composition such as stoichiometry and element distribution on cathode performance as a key for high-performance PCFCs. In our PCFCs, Ce-free Yb-doped BaZrO<sub>3</sub> (BZYb20) electrolytes are prepared using two BZYb20 raw powder materials with different A/B ratios, i.e., Ba<sub>0.97</sub>Zr<sub>0.8</sub>Yb<sub>0.2</sub>O<sub>3−δ</sub> (Cell-97) and Ba<sub>0.99</sub>Zr<sub>0.8</sub>Yb<sub>0.2</sub>O<sub>3−δ</sub> (Cell-99). These PCFCs exhibit different element distributions on their BZYb20 electrolyte surfaces, namely, a heterogeneous element distribution with segregation of Yb<sub>2</sub>O<sub>3</sub> for Cell-97 and a homogeneous distribution for Cell-99. The maximum power density of Cell-99 is higher than that of Cell-97 and reaches exceptionally high values, e.g., ∼1.3 W cm<sup>–2</sup> at 600 °C and ∼0.7 W cm<sup>–2</sup> at 500 °C, which are the highest attained for PCFCs with Ce-free BaZrO<sub>3</sub>-based electrolytes. The distribution of relaxation times and fitting analysis reveals that the cathode polarization resistance of Cell-99 is much lower than that of Cell-97 even when using the same cathode material. In conclusion, an optimal electrolyte surface condition significantly reduces cathode polarization resistance, leading to the achievement of high-performance PCFCs.</p>\",\"PeriodicalId\":5,\"journal\":{\"name\":\"ACS Applied Materials & Interfaces\",\"volume\":\"17 28\",\"pages\":\"40639–40649\"},\"PeriodicalIF\":8.2000,\"publicationDate\":\"2025-07-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.acs.org/doi/pdf/10.1021/acsami.5c04806\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Materials & Interfaces\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acsami.5c04806\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Materials & Interfaces","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsami.5c04806","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
质子陶瓷燃料电池(pcfc)具有实现超高能量转换效率的巨大潜力,但未来商业化需要更高的功率密度。本文报道了电解质表面状况对阴极性能的影响,如化学计量和元素分布,是高性能pcfc的关键。在pcfc中,采用Ba0.97Zr0.8Yb0.2O3-δ (Cell-97)和Ba0.99Zr0.8Yb0.2O3-δ (Cell-99)两种不同A/B比的BZYb20原料粉末制备了无ce掺杂BaZrO3 (BZYb20)电解质。这些pcfc在其BZYb20电解质表面表现出不同的元素分布,即Cell-97为Yb2O3偏析的非均相元素分布,而Cell-99为均匀分布。Cell-99的最大功率密度高于Cell-97,并且达到非常高的值,例如,在600°C时为~ 1.3 W cm-2,在500°C时为~ 0.7 W cm-2,这是使用无ce bazro3基电解质的pcfc所能达到的最高功率密度。弛豫时间分布和拟合分析表明,即使使用相同的阴极材料,Cell-99的阴极极化电阻也远低于Cell-97。综上所述,最佳的电解质表面条件可以显著降低阴极极化电阻,从而实现高性能pcfc。
High-Performance Protonic Ceramic Fuel Cell with Ytterbium-Doped Barium Zirconate: Reducing Cathode Polarization by Improving Electrolyte Surface Condition
Protonic ceramic fuel cells (PCFCs) have great potential to realize ultrahigh energy-conversion efficiency, but higher power density is required for future commercialization. The present work reports the effect of the electrolyte surface condition related to chemical composition such as stoichiometry and element distribution on cathode performance as a key for high-performance PCFCs. In our PCFCs, Ce-free Yb-doped BaZrO3 (BZYb20) electrolytes are prepared using two BZYb20 raw powder materials with different A/B ratios, i.e., Ba0.97Zr0.8Yb0.2O3−δ (Cell-97) and Ba0.99Zr0.8Yb0.2O3−δ (Cell-99). These PCFCs exhibit different element distributions on their BZYb20 electrolyte surfaces, namely, a heterogeneous element distribution with segregation of Yb2O3 for Cell-97 and a homogeneous distribution for Cell-99. The maximum power density of Cell-99 is higher than that of Cell-97 and reaches exceptionally high values, e.g., ∼1.3 W cm–2 at 600 °C and ∼0.7 W cm–2 at 500 °C, which are the highest attained for PCFCs with Ce-free BaZrO3-based electrolytes. The distribution of relaxation times and fitting analysis reveals that the cathode polarization resistance of Cell-99 is much lower than that of Cell-97 even when using the same cathode material. In conclusion, an optimal electrolyte surface condition significantly reduces cathode polarization resistance, leading to the achievement of high-performance PCFCs.
期刊介绍:
ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.