Evaluation of La0.8Sr0.2MnO3 perovskite prepared by fast solution combustion

被引:6
|
作者
Rendon, Ramon Cobo [1 ]
Udayabhaskar, R. [2 ]
Salvo, Christopher [3 ]
Sepulveda, Erwin [1 ]
Rodriguez, Jose Jimenez [4 ]
Camurri, Carlos P. [1 ]
Viswanathan, Mangalaraja Ramalinga [1 ,5 ]
机构
[1] Univ Concepcion, Fac Engn, Dept Mat Engn, Adv Ceram & Nanotechnol Lab, Concepcion, Chile
[2] Univ Atacama, Inst Invest Cient & Tecnol IDICTEC, Copayapu 485, Copiapo, Chile
[3] Univ Bio Bio, Fac Ingn, Dept Ingn Mecan, Concepcion 4030000, Chile
[4] CSIC, CENIM, Natl Ctr Met Res, Super Council Sci Invest,Xray Lab, Madrid, Spain
[5] Univ Adolfo Ibanez, Fac Engn & Sci, Diagonal Torres 2640, Santiago, Chile
关键词
LSM; Fast solution combustion synthesis; Microstructure; ReSOFC; HYDROTHERMAL SYNTHESIS; FUEL; TEMPERATURE; TRANSPORT; BEHAVIOR; PBTIO3; POWDER; DELTA; LSM; SR;
D O I
10.1016/j.ceramint.2022.08.105
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
La0.8Sr0.2MnO3 (LSM) perovskite as oxygen electrode material for the reversible solid oxide fuel cells (ReSOFC) was synthesized by the fast solution combustion method and assessed for subsequent calcination influence. The microstructural, morphological, compositional and optical properties of the obtained material were analyzed with X-ray diffraction (XRD), high-resolution transmission electron microscopy (HR-TEM), scanning electron microscopy (SEM) coupled with an energy-dispersive X-ray spectroscopy detector (EDS) and UV-visible spectroscopy techniques. The XRD results showed the coexistence of rhombohedral R-3c and Pm-3m polymorphs for the perovskite phase, with a decreased fraction of the cubic phase as the temperature and/or time used for the calcination were increased. The HR-TEM images confirmed the existence of the R-3c and Pm-3m polymorphs for the sample subjected to calcination at 1300 degrees C, showing that the rapid combustion method did not allow the pure formation of the La0.8Sr0.2MnO3 phase for the calcination temperatures below 1400 degrees C, due to the swiftness of the combustion synthesis 500 degrees C for 5 min. The average grain size was found to be increased with the calcination time. The EDS analysis depicted a better agreement in stoichiometry with the theoretical composition. The apparent porosity was decreased with the increase in the temperature and calcination time due to the coalescence of the sintering pores. The sample obtained after the calcination at 1400 degrees C for 8 h exhibited 1.6% of porosity. The hardness was improved with the higher calcination time and temperature and reached a maximum value of 5.7 GPa that merely matched the bulk density. A similar trend was observed in the temperature dependence resistivity studies and all the samples presented a low resistivity of similar to 1.2 Omega cm in the temperature range of 600-700 degrees C. The optical characterization exhibited a broad absorption in 560-660 nm.
引用
收藏
页码:35100 / 35107
页数:8
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