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請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/58593
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dc.contributor.advisor鄭淑芬
dc.contributor.authorYu-Chieh Chengen
dc.contributor.author鄭妤潔zh_TW
dc.date.accessioned2021-06-16T08:21:19Z-
dc.date.available2014-03-08
dc.date.copyright2014-03-08
dc.date.issued2013
dc.date.submitted2014-01-27
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dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/58593-
dc.description.abstract本研究以Pechini法製備鐠、釓共摻雜的氧化鈰粉末,其化學式為Ce0.8Gd0.2-XPrXO2-δ(X=0.01-0.05) 作為中溫固態氧化物燃料電池(ITSOFC)的電解質。對所得粉末進行一系列性質探討,由粉末繞射儀結果說明,經煆燒700℃共摻镨、釓的氧化鈰有純相螢石結構和較釓摻雜氧化鈰(Ce0.8Gd0.2O2-δ)大的晶格常數。由Scherrer公式計算出的粒徑與從穿透式電子顯微鏡圖量測的粒徑大小一致。由掃描式電子顯微鏡圖和電解質相對密度計算可以說明镨摻雜有提高電解質密度的效果。镨、釓共摻雜的電解質材料的氧離子導電性與電解質相對密度和X射線光電子能譜O 1s譜圖中氧空位/晶格氧的的面積比率趨勢大致一致。其中Ce0.8Gd0.18Pr0.02O2-δ在700℃下有最高的氧離子導電性6.15 S/m 。以厚度20 μm的Ce0.8Gd0.18Pr0.02O2-δ作為電解質,La0.6Sr0.4Co0.2Fe0.8作為陰極,60%NiO - 40%Ce0.8Gd0.2O2-δ為陽極,利用共壓法製成陽極支撐的電池在700℃以160 mL/min的氫氣作為燃料和160 mL/min的氧氣作為氧化劑時,開路電壓為0.82 V,能量密度為0.739 W/cm2,其表現較以Ce0.8Gd0.2O2-δ為電解質的能量密度高 。zh_TW
dc.description.abstractThe Pr, Gd co-doped CeO2 powders with the chemical formula Ce0.8Gd0.2-XPrXO2 (X=0.01-0.05) were prepared by Pechini method and used as electrolyte material for intermediate temperature solid oxide fuel cell (ITSOFC). The XRD results showed that Pr, Gd co-doped CeO2 calcined at 700℃ had pure fluorite structure and slightly larger lattice parameters than Gd-doped CeO2 (Ce0.8Gd0.2O2-δ). The particle sizes calculated by Scherrer equation were in good agreement with those obtained from TEM images. The oxide ion conductivities of the co-doped materials were found to be directly proportional to the ratios of oxygen vacancies/lattice oxygen determined by the area ratios of O 1s XPS spectra. Among these co-doped materials, Ce0.8Gd0.18Pr0.02O2 gave the highest oxide ion conductivity (6.15 S/m at 700℃). The anode-supported single cell, fabricated by a simple co-pressing method using Ce0.8Gd0.18Pr0.02O2 of thickness of 20 μm as the electrolyte, La0.6Sr0.4Co0.2Fe0.8 as cathode, and 60%NiO-40%Ce0.8Gd0.2O2-δ as anode, gave a high power density of 0.739 W/cm2 and OCV of 0.82 V at 700℃ using 160 mL/min hydrogen as the fuel and 160 mL/min oxygen as the oxidant, and the single cell gave higher power density than that withCe0.8Gd0.2O2-δ as the electrolyte.en
dc.description.provenanceMade available in DSpace on 2021-06-16T08:21:19Z (GMT). No. of bitstreams: 1
ntu-102-R00223138-1.pdf: 6387514 bytes, checksum: 388669b482c3c80a3fdbc24d25525831 (MD5)
Previous issue date: 2013
en
dc.description.tableofcontents謝誌 2
中文摘要 I
Abstract II
目錄 III
表目錄 V
圖目錄 VI
第一章 緒論 1
1-1燃料電池 1
1-2固態氧化物燃料電池 3
1–2–1 發電原理 3
1–2–2 SOFC電解質材料 4
1–2–3 SOFC陰極材料 10
1–2–4 電紡絲法(Electrocspinning)製備SOFC陰極 14
1–2–5 SOFC陽極材料 19
1–3 研究目標 20
第二章 實驗部分 22
2–1 化學藥品 22
2–2 實驗步驟 23
2–2–1 Citric Acid-PEG (C.P.)溶液配製 23
2–2–2 電解質粉體製備 23
2–2–3 單電池製備 23
2–2–4 電紡絲法製備陰極 24
2–3 電池材料的鑑定 25
第三章 Pr, Gd共摻雜CeO2 做為SOFC電解質材料 28
3-1 Powder X-ray diffraction analysis 28
3-2 TEM & SEM images 31
3-3 Laser Scattering Particle Size Distribution Analyzer 39
3-4 Conductivity 41
3-5 XPS study 44
3-5 X-ray absorption near-edge structure analysis 48
3-6 Effect of Electrolyte thickness of Ce0.8Gd0.18Pr0.02O2-δ on single cell performance 53
3-6 Single cell performance with Ce0.8Gd0.18Pr0.02O2-δ electrolytes 58
3-7 Single cell performance of Ce0.8Gd0.18Pr0.02O2-δ electrolytes compared with CGO electrolytes 62
第四章 電紡絲法製備LSCF固態氧化物燃料電池陰極 69
第五章 結論 78
第六章 參考文獻 80
dc.language.isozh-TW
dc.subject釓zh_TW
dc.subject鐠zh_TW
dc.subject氧化鈰zh_TW
dc.subject電解質zh_TW
dc.subject固態氧化物燃料電池zh_TW
dc.subject導電度zh_TW
dc.subjectconductivityen
dc.subjectelectrolyteen
dc.subjectceriaen
dc.subjectPren
dc.subjectGden
dc.subjectSOFCen
dc.title鐠、釓共摻雜之氧化鈰電解質於中溫固態氧化物燃料電池之研究zh_TW
dc.titlePr, Gd Co-doped Ceria Based Materials in IT-SOFCen
dc.typeThesis
dc.date.schoolyear102-1
dc.description.degree碩士
dc.contributor.oralexamcommittee王錫福,劉如熹
dc.subject.keyword固態氧化物燃料電池,電解質,氧化鈰,鐠,釓,導電度,zh_TW
dc.subject.keywordSOFC,electrolyte,ceria,Pr,Gd,conductivity,en
dc.relation.page81
dc.rights.note有償授權
dc.date.accepted2014-01-28
dc.contributor.author-college理學院zh_TW
dc.contributor.author-dept化學研究所zh_TW
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