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Nanoindentation of porous bulk and thin films of La_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3-δ)

机译:La_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3-δ)多孔体薄膜的纳米压痕

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摘要

In this paper we show how reliable measurements on porous ceramic films can be made by appropriate nanoindentation experiments and analysis. Room-temperature mechanical properties of the mixed-conducting perovskite material La_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3-δ) (LSCF6428) were investigated by nanoindentation of porous bulk samples and porous films sintered at temperatures from 900 to 1200℃. A spherical indenter was used so that the contact area was much greater than the scale of the porous microstructure. The elastic modulus of the bulk samples was found to increase from 33.8 to 174.3 GPa and hardness from 0.64 to 5.32 GPa as the porosity decreased from 45 to 5 after sintering at 900-1200℃. Densification under the indenter was found to have little influence on the measured elas?tic modulus. The residual porosity in the "dense" sample was found to account for the discrepancy between the elastic moduli measured by indentation and by impulse excitation. Crack-free LSCF6428 films of acceptable surface roughness for indentation were also prepared by sintering at 900-1200℃. Reliable measurements of the true properties of the films were obtained by data extrapolation provided that the ratio of indentation depth to film thickness was in the range 0.1-0.2. The elastic moduli of the films and bulk materials were approximately equal for a given porosity. The 3-D microstructures of films before and after indentation were characterized using focused ion beam/scanning electron microscopy tomography. Finite-element modelling of the elastic deformation of the actual microstructures showed excellent agreement with the nanoindentation results.
机译:在本文中,我们展示了如何通过适当的纳米压痕实验和分析对多孔陶瓷薄膜进行可靠的测量。通过对900-1200°C温度下烧结的多孔块状样品和多孔薄膜进行纳米压痕,研究了混合导电钙钛矿材料La_(0.6)Sr_(0.4)Co_(0.2)Fe_(0.8)O_(3-δ)(LSCF6428)的室温力学性能.使用球形压头,使接触面积远大于多孔微观结构的尺度。在900-1200°C烧结后,随着孔隙率从45%下降到5%,块状样品的弹性模量从33.8 GPa增加到174.3 GPa,硬度从0.64 GPa增加到5.32 GPa。发现压头下的致密化对测得的弹性模量影响不大。发现“致密”样品中的残余孔隙率解释了通过压痕和脉冲激励测量的弹性模量之间的差异。通过在900-1200°C下烧结,还制备了表面粗糙度可接受的无裂纹LSCF6428膜。如果压痕深度与薄膜厚度的比值在0.1-0.2范围内,则通过数据外推获得了薄膜真实性能的可靠测量。对于给定的孔隙率,薄膜和块状材料的弹性模量大致相等。采用聚焦离子束/扫描电子显微镜断层扫描技术对压痕前后薄膜的三维微观结构进行了表征。对实际微观结构弹性变形的有限元建模与纳米压痕结果非常吻合。

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