Fabrication and Investigation of Anode-supported Intermediate Temperature Solid Oxide Fuel Cells with Composite Ceria-based Electrolyte Films

博士 === 國立臺灣大學 === 化學研究所 === 96 === Ce0.8Gd0.2O2-δ (CGO) powder samples were synthesized using citrate sol-gel combustion method, and then the composite electrolyte materials were prepared by a small amount of 1mol% Bi2O3, GeO2, Nb2O5 to CGO. The results show that the densification and conductivity o...

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Main Authors: Cheng-Hung Chung, 鍾振泓
Other Authors: 鄭淑芬
Format: Others
Language:zh-TW
Published: 2008
Online Access:http://ndltd.ncl.edu.tw/handle/02103700146146232649
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spelling ndltd-TW-096NTU050650312016-05-11T04:16:50Z http://ndltd.ncl.edu.tw/handle/02103700146146232649 Fabrication and Investigation of Anode-supported Intermediate Temperature Solid Oxide Fuel Cells with Composite Ceria-based Electrolyte Films 陽極負載複合氧化鈰電解質中溫固體氧化物燃料電池之製備與性能研究 Cheng-Hung Chung 鍾振泓 博士 國立臺灣大學 化學研究所 96 Ce0.8Gd0.2O2-δ (CGO) powder samples were synthesized using citrate sol-gel combustion method, and then the composite electrolyte materials were prepared by a small amount of 1mol% Bi2O3, GeO2, Nb2O5 to CGO. The results show that the densification and conductivity of composite electrolyte were improved. In addition, undergoing 10% H2/N2 for ~ 85h, the conductivity at 700°C in air of the samples could be retained nearly at their starting conductivity. The fabrication of anode-supported intermediate temperature solid oxide fuel cell (IT-SOFC) was carry out by using sandwiched dry-pressed technique with flour layers, because of humid environment in Taiwan, ultrafine CGO powder as electrolyte material. The single cell showed that electrolyte was 16 ± 2 μm in most thin thickness, anode (60wt%-NiO/CGO) and cathode (La0.8Sr0.2Co0.8Fe0.2O3-δ) were 493 ± 7 and 152 ± 4 μm in thickness, respectively. At our best knowledge to build the electrochemical testing device, and the performances of single cell were ~ 450 mW/cm2 (PPD) and ~ 0.79V (OCV), while 100%H2 and air with optimum flow rate of 50 and 150 mL/min at 700°C. On the other hand, under 100%H2 and 100%O2 with optimum flow rate of 50 and 90 mL/min, the the performances were ~ 504 mW/cm2 and ~ 0.82V. The rate-determining step (RDS) was depended on operation temperature: Under 550°C, RDS was oxygen reduction reaction. Above 600°C, RDS was ohmic loss. To exchange of electrolyte material, the addition of 1mol% GeO2 to CGO film was made, under the optimum flow rate through air and 100%O2 in turn, the PPD of single cell were ~ 462 and ~ 521 mW/cm2, respectively, which were improving ~ 12 and ~ 17 mW/cm2, respectively. To exchange of cathode material, the addition of 5.02wt% Pt to LSCF cathode was made, under the optimum flow rate through air and 100%O2 in turn, the PPD of single cell were ~ 526 and ~ 582 mW/cm2, respectively, which were improving ~ 76 and ~ 78 mA/cm2, respectively. To exchange of anode material, the addition of 2.5wt% Mn to Ni/CGO anode was made, under flow rate of 5mL/min through 100%H2 and 100%CH4 at 700°C in turn, the sample displayed about one-third and three-fifth times of the performances of pure Ni/CGO anode, in addition, the performance decreased with long-time. The primary reasons were suggested following: the addition of 1mol% GeO2 to CGO was improving oxide-ion conductivity of electrolyte, thus the influence improved the performance of single cell. However, a small amount of 1mol% Bi2O3 or Nb2O5 to CGO was deteriorating short-circuit short-circuit of electrolyte. For composite Pt/LSCF cathode, the adequate amount of Pt to LSCF was selected due to low oxide-ion conductivity and optimum microstructure surface of self. For composite Mn-Ni/CGO anode, the dense microstructure on surface was observed by the addition of Mn to Ni/CGO , thus the performance of single cell was deteriorating for the direct electrochemical oxidation of methane. 鄭淑芬 2008 學位論文 ; thesis 172 zh-TW
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description 博士 === 國立臺灣大學 === 化學研究所 === 96 === Ce0.8Gd0.2O2-δ (CGO) powder samples were synthesized using citrate sol-gel combustion method, and then the composite electrolyte materials were prepared by a small amount of 1mol% Bi2O3, GeO2, Nb2O5 to CGO. The results show that the densification and conductivity of composite electrolyte were improved. In addition, undergoing 10% H2/N2 for ~ 85h, the conductivity at 700°C in air of the samples could be retained nearly at their starting conductivity. The fabrication of anode-supported intermediate temperature solid oxide fuel cell (IT-SOFC) was carry out by using sandwiched dry-pressed technique with flour layers, because of humid environment in Taiwan, ultrafine CGO powder as electrolyte material. The single cell showed that electrolyte was 16 ± 2 μm in most thin thickness, anode (60wt%-NiO/CGO) and cathode (La0.8Sr0.2Co0.8Fe0.2O3-δ) were 493 ± 7 and 152 ± 4 μm in thickness, respectively. At our best knowledge to build the electrochemical testing device, and the performances of single cell were ~ 450 mW/cm2 (PPD) and ~ 0.79V (OCV), while 100%H2 and air with optimum flow rate of 50 and 150 mL/min at 700°C. On the other hand, under 100%H2 and 100%O2 with optimum flow rate of 50 and 90 mL/min, the the performances were ~ 504 mW/cm2 and ~ 0.82V. The rate-determining step (RDS) was depended on operation temperature: Under 550°C, RDS was oxygen reduction reaction. Above 600°C, RDS was ohmic loss. To exchange of electrolyte material, the addition of 1mol% GeO2 to CGO film was made, under the optimum flow rate through air and 100%O2 in turn, the PPD of single cell were ~ 462 and ~ 521 mW/cm2, respectively, which were improving ~ 12 and ~ 17 mW/cm2, respectively. To exchange of cathode material, the addition of 5.02wt% Pt to LSCF cathode was made, under the optimum flow rate through air and 100%O2 in turn, the PPD of single cell were ~ 526 and ~ 582 mW/cm2, respectively, which were improving ~ 76 and ~ 78 mA/cm2, respectively. To exchange of anode material, the addition of 2.5wt% Mn to Ni/CGO anode was made, under flow rate of 5mL/min through 100%H2 and 100%CH4 at 700°C in turn, the sample displayed about one-third and three-fifth times of the performances of pure Ni/CGO anode, in addition, the performance decreased with long-time. The primary reasons were suggested following: the addition of 1mol% GeO2 to CGO was improving oxide-ion conductivity of electrolyte, thus the influence improved the performance of single cell. However, a small amount of 1mol% Bi2O3 or Nb2O5 to CGO was deteriorating short-circuit short-circuit of electrolyte. For composite Pt/LSCF cathode, the adequate amount of Pt to LSCF was selected due to low oxide-ion conductivity and optimum microstructure surface of self. For composite Mn-Ni/CGO anode, the dense microstructure on surface was observed by the addition of Mn to Ni/CGO , thus the performance of single cell was deteriorating for the direct electrochemical oxidation of methane.
author2 鄭淑芬
author_facet 鄭淑芬
Cheng-Hung Chung
鍾振泓
author Cheng-Hung Chung
鍾振泓
spellingShingle Cheng-Hung Chung
鍾振泓
Fabrication and Investigation of Anode-supported Intermediate Temperature Solid Oxide Fuel Cells with Composite Ceria-based Electrolyte Films
author_sort Cheng-Hung Chung
title Fabrication and Investigation of Anode-supported Intermediate Temperature Solid Oxide Fuel Cells with Composite Ceria-based Electrolyte Films
title_short Fabrication and Investigation of Anode-supported Intermediate Temperature Solid Oxide Fuel Cells with Composite Ceria-based Electrolyte Films
title_full Fabrication and Investigation of Anode-supported Intermediate Temperature Solid Oxide Fuel Cells with Composite Ceria-based Electrolyte Films
title_fullStr Fabrication and Investigation of Anode-supported Intermediate Temperature Solid Oxide Fuel Cells with Composite Ceria-based Electrolyte Films
title_full_unstemmed Fabrication and Investigation of Anode-supported Intermediate Temperature Solid Oxide Fuel Cells with Composite Ceria-based Electrolyte Films
title_sort fabrication and investigation of anode-supported intermediate temperature solid oxide fuel cells with composite ceria-based electrolyte films
publishDate 2008
url http://ndltd.ncl.edu.tw/handle/02103700146146232649
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