{"title":"掺杂 Sc 的 CaTiO3 氧化物中的 A 位缺陷对质子-氧化物离子混合传导特性的影响","authors":"Shin-ichi Hashimoto , Hiroaki Kato , Mei Nakane , Tomoaki Namioka , Katsuhiro Nomura","doi":"10.1016/j.ssi.2024.116570","DOIUrl":null,"url":null,"abstract":"<div><p>In this study, A-site defective Ca<sub><em>y</em></sub>Ti<sub>0.93</sub>Sc<sub>0.07</sub>O<sub>3-α</sub> oxides were prepared to examine their ionic conduction properties. The electrical conductivities of two typical compositions were measured as functions of oxygen partial pressure <em>P</em><sub>O2</sub>, temperature, and humidity. Additionally, phase transition, chemical expansion, and CO<sub>2</sub> tolerance were examined in Ca<sub>0.985</sub>Ti<sub>0.93</sub>Sc<sub>0.07</sub>O<sub>3-α</sub> using an atmosphere-controlled high-temperature X-ray diffraction. In Ca<sub>0.947</sub>Ti<sub>0.93</sub>Sc<sub>0.07</sub>O<sub>3-α</sub>, the ionic conduction domain over a wide range of <em>P</em><sub>O2</sub> was observed at 500–800 °C, even though the humidity dependence of conductivities was confirmed only at 500 °C. Conversely, in Ca<sub>0.985</sub>Ti<sub>0.93</sub>Sc<sub>0.07</sub>O<sub>3-α</sub>, the conductivities were enhanced in humidified atmospheres at 500–800 °C, while the ionic conductivities in dry atmospheres were higher than those of 8YSZ. As protonic and oxide ionic conductivities are comparable, the proton-oxide ion mixed conduction can be considered to occur in Ca<sub>0.985</sub>Ti<sub>0.93</sub>Sc<sub>0.07</sub>O<sub>3-α</sub>. Therefore, a small percentage of Ca defect in Ca<sub><em>y</em></sub>Ti<sub>0.93</sub>Sc<sub>0.07</sub>O<sub>3-α</sub> affects not only conductivity but also conductive ionic species. Furthermore, Ca<sub>0.985</sub>Ti<sub>0.93</sub>Sc<sub>0.07</sub>O<sub>3-α</sub> did not show any phase transition and chemical expansion with hydration up to 900 °C. The crystal phase of Ca<sub>0.985</sub>Ti<sub>0.93</sub>Sc<sub>0.07</sub>O<sub>3-α</sub> during the CO<sub>2</sub> tolerance test was observed to be stable. Therefore, the material properties of Ca<sub><em>y</em></sub>Ti<sub>0.93</sub>Sc<sub>0.07</sub>O<sub>3-α</sub> suggest its high potential as electrolytes in high temperature electrochemical devices.</p></div>","PeriodicalId":431,"journal":{"name":"Solid State Ionics","volume":"413 ","pages":"Article 116570"},"PeriodicalIF":3.0000,"publicationDate":"2024-06-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effect of A-site defects in Sc-doped CaTiO3 oxides on proton-oxide ion mixed conduction properties\",\"authors\":\"Shin-ichi Hashimoto , Hiroaki Kato , Mei Nakane , Tomoaki Namioka , Katsuhiro Nomura\",\"doi\":\"10.1016/j.ssi.2024.116570\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>In this study, A-site defective Ca<sub><em>y</em></sub>Ti<sub>0.93</sub>Sc<sub>0.07</sub>O<sub>3-α</sub> oxides were prepared to examine their ionic conduction properties. The electrical conductivities of two typical compositions were measured as functions of oxygen partial pressure <em>P</em><sub>O2</sub>, temperature, and humidity. Additionally, phase transition, chemical expansion, and CO<sub>2</sub> tolerance were examined in Ca<sub>0.985</sub>Ti<sub>0.93</sub>Sc<sub>0.07</sub>O<sub>3-α</sub> using an atmosphere-controlled high-temperature X-ray diffraction. In Ca<sub>0.947</sub>Ti<sub>0.93</sub>Sc<sub>0.07</sub>O<sub>3-α</sub>, the ionic conduction domain over a wide range of <em>P</em><sub>O2</sub> was observed at 500–800 °C, even though the humidity dependence of conductivities was confirmed only at 500 °C. Conversely, in Ca<sub>0.985</sub>Ti<sub>0.93</sub>Sc<sub>0.07</sub>O<sub>3-α</sub>, the conductivities were enhanced in humidified atmospheres at 500–800 °C, while the ionic conductivities in dry atmospheres were higher than those of 8YSZ. As protonic and oxide ionic conductivities are comparable, the proton-oxide ion mixed conduction can be considered to occur in Ca<sub>0.985</sub>Ti<sub>0.93</sub>Sc<sub>0.07</sub>O<sub>3-α</sub>. Therefore, a small percentage of Ca defect in Ca<sub><em>y</em></sub>Ti<sub>0.93</sub>Sc<sub>0.07</sub>O<sub>3-α</sub> affects not only conductivity but also conductive ionic species. Furthermore, Ca<sub>0.985</sub>Ti<sub>0.93</sub>Sc<sub>0.07</sub>O<sub>3-α</sub> did not show any phase transition and chemical expansion with hydration up to 900 °C. The crystal phase of Ca<sub>0.985</sub>Ti<sub>0.93</sub>Sc<sub>0.07</sub>O<sub>3-α</sub> during the CO<sub>2</sub> tolerance test was observed to be stable. Therefore, the material properties of Ca<sub><em>y</em></sub>Ti<sub>0.93</sub>Sc<sub>0.07</sub>O<sub>3-α</sub> suggest its high potential as electrolytes in high temperature electrochemical devices.</p></div>\",\"PeriodicalId\":431,\"journal\":{\"name\":\"Solid State Ionics\",\"volume\":\"413 \",\"pages\":\"Article 116570\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2024-06-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Solid State Ionics\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0167273824001188\",\"RegionNum\":4,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Solid State Ionics","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0167273824001188","RegionNum":4,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
摘要
本研究制备了有 A 位缺陷的 CayTi0.93Sc0.07O3-α 氧化物,以检验其离子传导特性。测量了两种典型成分的电导率与氧分压 PO2、温度和湿度的函数关系。此外,还使用大气控制高温 X 射线衍射法研究了 Ca0.985Ti0.93Sc0.07O3-α 的相变、化学膨胀和二氧化碳耐受性。在 Ca0.947Ti0.93Sc0.07O3-α中,尽管导电率的湿度依赖性仅在 500 ℃时得到证实,但在 500-800 ℃时,在很宽的 PO2 范围内都观察到了离子传导域。相反,对于 Ca0.985Ti0.93Sc0.07O3-α,在 500-800 °C的潮湿气氛中,其电导率有所提高,而在干燥气氛中的离子电导率则高于 8YSZ。由于质子和氧化物离子导电率相当,可以认为 Ca0.985Ti0.93Sc0.07O3-α 中发生了质子-氧化物离子混合传导。因此,CayTi0.93Sc0.07O3-α 中少量的 Ca 缺陷不仅会影响导电性,还会影响导电离子种类。此外,Ca0.985Ti0.93Sc0.07O3-α 在高达 900 °C 的水化过程中没有出现任何相变和化学膨胀。在二氧化碳耐受性测试中观察到,Ca0.985Ti0.93Sc0.07O3-α 的晶体相是稳定的。因此,CayTi0.93Sc0.07O3-α 的材料特性表明,它很有可能成为高温电化学设备中的电解质。
Effect of A-site defects in Sc-doped CaTiO3 oxides on proton-oxide ion mixed conduction properties
In this study, A-site defective CayTi0.93Sc0.07O3-α oxides were prepared to examine their ionic conduction properties. The electrical conductivities of two typical compositions were measured as functions of oxygen partial pressure PO2, temperature, and humidity. Additionally, phase transition, chemical expansion, and CO2 tolerance were examined in Ca0.985Ti0.93Sc0.07O3-α using an atmosphere-controlled high-temperature X-ray diffraction. In Ca0.947Ti0.93Sc0.07O3-α, the ionic conduction domain over a wide range of PO2 was observed at 500–800 °C, even though the humidity dependence of conductivities was confirmed only at 500 °C. Conversely, in Ca0.985Ti0.93Sc0.07O3-α, the conductivities were enhanced in humidified atmospheres at 500–800 °C, while the ionic conductivities in dry atmospheres were higher than those of 8YSZ. As protonic and oxide ionic conductivities are comparable, the proton-oxide ion mixed conduction can be considered to occur in Ca0.985Ti0.93Sc0.07O3-α. Therefore, a small percentage of Ca defect in CayTi0.93Sc0.07O3-α affects not only conductivity but also conductive ionic species. Furthermore, Ca0.985Ti0.93Sc0.07O3-α did not show any phase transition and chemical expansion with hydration up to 900 °C. The crystal phase of Ca0.985Ti0.93Sc0.07O3-α during the CO2 tolerance test was observed to be stable. Therefore, the material properties of CayTi0.93Sc0.07O3-α suggest its high potential as electrolytes in high temperature electrochemical devices.
期刊介绍:
This interdisciplinary journal is devoted to the physics, chemistry and materials science of diffusion, mass transport, and reactivity of solids. The major part of each issue is devoted to articles on:
(i) physics and chemistry of defects in solids;
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(iii) ion transport measurements, mechanisms and theory;
(iv) solid state electrochemistry;
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