The processing improvement and performance analysis of the La0.85Sr0.15Ga0.8Mg0.2O2.825 electrolyte-supported fuel cell

碩士 === 國立臺北科技大學 === 材料科學與工程研究所 === 104 === It is known that the La1−xSrxGa1−yMgyO3−δ electrolyte material has the highest conductivity among solid electrolytes. The La0.85Sr0.15Ga0.8Mg0.2O2.825(LSGM1520), La0.6Sr0.4Co0.2Fe0.8O3−δ (LSCF6428), La0.4Ce0.6O1.8 (LDC46) and Ce0.8Sm0.2O1.9 (SDC20) powders...

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Main Authors: Wei-Han Huang, 黃洧瀚
Other Authors: Yu-Chuan Wu
Format: Others
Online Access:http://ndltd.ncl.edu.tw/handle/4p4gp5
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spelling ndltd-TW-104TIT051590352019-05-15T23:00:43Z http://ndltd.ncl.edu.tw/handle/4p4gp5 The processing improvement and performance analysis of the La0.85Sr0.15Ga0.8Mg0.2O2.825 electrolyte-supported fuel cell La0.85Sr0.15Ga0.8Mg0.2O2.825電解質支撐型固態氧化物燃料電池的製程改良與性能之研究 Wei-Han Huang 黃洧瀚 碩士 國立臺北科技大學 材料科學與工程研究所 104 It is known that the La1−xSrxGa1−yMgyO3−δ electrolyte material has the highest conductivity among solid electrolytes. The La0.85Sr0.15Ga0.8Mg0.2O2.825(LSGM1520), La0.6Sr0.4Co0.2Fe0.8O3−δ (LSCF6428), La0.4Ce0.6O1.8 (LDC46) and Ce0.8Sm0.2O1.9 (SDC20) powders were synthesized by the solid-state reaction. The LSCF/LSGM/SDC+Ni (Cell A), LSCF/LSGM/porous LSGM/SDC+Ni (Cell B), and LSCF/LSGM/LDC/SDC+Ni (Cell C) cells were prepared in the study. The LDC and porous LSGM layers were used as a buffer layer and an anode functional layer, respecti vely. The two interlayers were effective to reduce the electrode polarization resistance and further to improve the adhesion between electrolyte and anode so as to enhance the power performance.The performances and properties of electrolyte-supported cells were analyzed by XRD, SEM, electrochemical instrument and AC impedance spectroscopy. Finally, the performances and properties of degradation in these cells were also further carried out for the long-term durability testing. Yu-Chuan Wu 吳玉娟 學位論文 ; thesis 0
collection NDLTD
format Others
sources NDLTD
description 碩士 === 國立臺北科技大學 === 材料科學與工程研究所 === 104 === It is known that the La1−xSrxGa1−yMgyO3−δ electrolyte material has the highest conductivity among solid electrolytes. The La0.85Sr0.15Ga0.8Mg0.2O2.825(LSGM1520), La0.6Sr0.4Co0.2Fe0.8O3−δ (LSCF6428), La0.4Ce0.6O1.8 (LDC46) and Ce0.8Sm0.2O1.9 (SDC20) powders were synthesized by the solid-state reaction. The LSCF/LSGM/SDC+Ni (Cell A), LSCF/LSGM/porous LSGM/SDC+Ni (Cell B), and LSCF/LSGM/LDC/SDC+Ni (Cell C) cells were prepared in the study. The LDC and porous LSGM layers were used as a buffer layer and an anode functional layer, respecti vely. The two interlayers were effective to reduce the electrode polarization resistance and further to improve the adhesion between electrolyte and anode so as to enhance the power performance.The performances and properties of electrolyte-supported cells were analyzed by XRD, SEM, electrochemical instrument and AC impedance spectroscopy. Finally, the performances and properties of degradation in these cells were also further carried out for the long-term durability testing.
author2 Yu-Chuan Wu
author_facet Yu-Chuan Wu
Wei-Han Huang
黃洧瀚
author Wei-Han Huang
黃洧瀚
spellingShingle Wei-Han Huang
黃洧瀚
The processing improvement and performance analysis of the La0.85Sr0.15Ga0.8Mg0.2O2.825 electrolyte-supported fuel cell
author_sort Wei-Han Huang
title The processing improvement and performance analysis of the La0.85Sr0.15Ga0.8Mg0.2O2.825 electrolyte-supported fuel cell
title_short The processing improvement and performance analysis of the La0.85Sr0.15Ga0.8Mg0.2O2.825 electrolyte-supported fuel cell
title_full The processing improvement and performance analysis of the La0.85Sr0.15Ga0.8Mg0.2O2.825 electrolyte-supported fuel cell
title_fullStr The processing improvement and performance analysis of the La0.85Sr0.15Ga0.8Mg0.2O2.825 electrolyte-supported fuel cell
title_full_unstemmed The processing improvement and performance analysis of the La0.85Sr0.15Ga0.8Mg0.2O2.825 electrolyte-supported fuel cell
title_sort processing improvement and performance analysis of the la0.85sr0.15ga0.8mg0.2o2.825 electrolyte-supported fuel cell
url http://ndltd.ncl.edu.tw/handle/4p4gp5
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