期刊文献+

复合阳极NiO-SDC+LSGM的性能研究 被引量:1

Study on performance of composite anode Ni-SDC+LSGM
下载PDF
导出
摘要 采用共压-共烧结法分别制备了以50%(质量分数)NiO-(50-x)%(质量分数)Ce0.8Sm0.2O1.9(SDC)+x%(质量分数)La0.9Sr0.1Ga0.8Mg0.2O3-a(LSGM)(x=0、10、20、30、40)为阳极支撑,LSGM为电解质、La0.9Sr0.1Co0.2Fe0.8O3-δ(LSCF)+Ce0.8Gd0.2O2-δ(GDC)为复合阴极的单电池片;用扫描电子显微镜(SEM)观察了电池片的微观结构;用X射线衍射(XRD)法分析了阳极材料于1250℃条件下烧结4h后的晶相结构;在350~600℃之间,以50℃为间隔,以干天然气为燃料气、氧气为氧化气测试了其电化学性能。结果表明:单电池阳极材料具有良好的孔道结构;在测试条件下,五种不同阳极组成的单电池中50%(质量分数)NiO-30%(质量分数)SDC+20%(质量分数)LSGM阳极支撑的单电池具有最佳的电化学性能,对天然气有更好的催化效果,在常压和600℃条件下其最大电流密度为229.32mA/cm2,最大比功率为45.86mW/cm2。 The 50%NiO-(50-x)%Ce0.8Sm0.2O1.9(SDC)+x%La0.9Sr0.1Ga0.6Mg0.2O3-α(LSGM) (x=0, 10, 20, 30, 40) anode supported cells were fabricated by dry-pressing process using LSGM as electrolyte and 85% LSCF+15% GDC as cathode. The crystal microstructure of cells was observed by scanning electron microscope (SEM). The crystal forms of the anode materials which had been sintered 4 h in 1 250 ℃ were analyzed by X-ray diffraction. The composite anode cells were tested and compared with un-composite anode cell from 350-600 ℃ every 50 ℃, using dry natural gas as fuel and oxygen as oxidant. The results of experiment show that the anode of the cells has good structure of hole. The 50% NiO-30% SDC+20% LSGM anode supported-cell has the best electrochemical performance among the five cells. The composite anode cell has better catalyze for natural gas than un-composite anode cell. The composite anode cell of maximum current density and power density at 600 ℃ are 229.32 mA/cm^2 and 45.86 mW/cm^2, respectively.
出处 《电源技术》 CAS CSCD 北大核心 2008年第1期43-46,共4页 Chinese Journal of Power Sources
基金 国家自然科学基金资助(50662005)
关键词 固体氧化物燃料电池 天然气 复合阳极 SOFC natural gas composite anode
  • 相关文献

参考文献9

  • 1CHOY, BI W, CHAROJROHKUL S, et al. The development of intermediate temperature solid oxide fuel cells for the next millennium [J], Journal of Power Source, 1998,71:361-369.
  • 2ISHIHARA T, MATSUDA H, TAKITA Y. Effects of rare earth cations doped for La site on the oxide ionic conductivity of LaGaO3-based perovskite type oxide [J].Solid State Ionics, 1995,79: 147-151.
  • 3HUANG K Q, FENG M, GOODENOUGH J B. Sol-gel synthesis of new oxide-ion conductor Sr-and Mg-doped LaGaO3 perovskit [J]. Am Cerarn So, 1996, 79:1100-1104.
  • 4GORTE R J, PARK S, VOHS J M, et al. Anodes for direct oxidation of dry hydrocarbon in a solid-oxides fuel cell [J].Advanced Material, 2000, 12: 1465-1469.
  • 5KIM H, PARK S, VOHS J M, et al. Direct oxidation of liquid fuels in a solid oxide fuel cell [J].J Electrochem Soc, 2001,148:A 693- A 695.
  • 6PARK S, GORTE R J, VOHS J M. Applications of heterogeneous catalysis in the direct oxidation of hydrocarbons in a solid-oxide fuel cell[J].Applied Catalysis A: General, 2000, 200: 55-61.
  • 7LU C, WORRELL W L, WANG C. Development of solid oxide fuel cells for the direct oxidation of hydrocarbon fuels [J]. Solid State Ionics, 2002, 152-153: 393-397.
  • 8ISHIHARA T, MATSUDA H, TAKITA Y. Doped LaGaO3 perovskite type oxide as a new oxide ionic conductor [J]. Am Chem Soc. 1994. 116:3801-3803.
  • 9郑文君,武丽艳,彭定坤,孟广耀.La_(0.9)Sr_(0.1)Ga_(0.8)Mg_(0.2)O_(3-α)的柠檬酸盐法制备和表征[J].无机材料学报,2001,16(2):358-362. 被引量:15

二级参考文献2

  • 1Ishihara T,第97次香山科学会议,1998年,67页
  • 2Huang K,J Am Ceram Soc,1996年,79卷,4期,1100页

共引文献14

同被引文献2

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部