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Phase stability of BSCF in low oxygen partial pressures

机译:BSCF在低氧分压下的相稳定性

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In situ X-ray diffraction has been used to investigate the phase stability of barium strontium cobalt iron oxide (BSCF) with the formula Ba0.5Sr0.5Fe1-xCoxO3-delta (X = 0, 0.2, 0.4, 0.6, 0.8, and 1). The thermal decomposition processes in both low partial pressures of oxygen (air-10(-5) atm pO(2)) and in reducing conditions have been detailed. BSCF manifests excellent stability down to 10(-5) atin pO(2); however, it decomposes through a complex series of oxides under reducing conditions. Increasing the cobalt content results in a decrease in the temperature range of stability of the material under 4% H-2 in N-2, with the initial decomposition taking place at 375, 425, 550, 600, 650 and 675 degrees C, for x = 1, 0.8, 0.6, 0.4, 0.2 and 0, respectively. Further, the thermal expansion is a strong function of the oxygen activity and Co content. The x = 0, 1 end member, BSC, undergoes a phase transition from rhombohedral to cubic symmetry at similar to 800 degrees C under 10(-5) atm pO(2), resulting in an ideal perovskite with a = 3.9892(3) angstrom at room temperature. (C) 2008 Elsevier Inc. All rights reserved.
机译:原位X射线衍射已用于研究钡BaSr0.5Fe1-xCoxO3-δ钡锶钴铁氧化物(BSCF)的相稳定性(X = 0、0.2、0.4、0.6、0.8和1 )。在氧气的低分压下(空气-10(-5)atm pO(2))和在还原条件下的热分解过程均已详细说明。 BSCF在pO(2)时低至10(-5)时表现出优异的稳定性;然而,它在还原条件下通过一系列复杂的氧化物分解。钴含量的增加会导致在N-2中4%H-2下材料的稳定性温度范围降低,初始分解发生在375、425、550、600、650和675摄氏度下。 x分别为1、0.8、0.6、0.4、0.2和0。此外,热膨胀是氧活度和Co含量的强函数。 x = 0,1个末端成员,BSC,在10(-5)atm pO(2)下,类似于800摄氏度,经历了从菱面体到立方对称的相变,从而得到a = 3.9892(3)的理想钙钛矿。室温下的埃。 (C)2008 Elsevier Inc.保留所有权利。

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