首页> 外文期刊>Journal of the European Ceramic Society >Phase evolution during reactive flash sintering of Li6.25Al0.25La3Zr2O12 starting from a chemically prepared powder
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Phase evolution during reactive flash sintering of Li6.25Al0.25La3Zr2O12 starting from a chemically prepared powder

机译:Li6.25Al0.25LA3ZR2O12从化学制备的粉末开始的反应性闪蒸过程中的相位演化

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摘要

Reactive flash sintering (RFS) of a chemically prepared multiphase precursor powder was performed to fabricate Li6.25Al0.25La3Zr2O12 (Al-LLZO) ceramics. This approach allowed for obtaining single-phase dense samples in a remarkably short processing time of 30 s, at a furnace temperature of 600 ?C, with an electric field of 50 V cm-1 and a current limit of 150 mA mm-2. The ceramics display high bulk conductivity of 0.18 mS cm-1 at room temperature. Furthermore, phase evolution is studied by in-situ X-ray diffraction during: i) conventional heating and ii) RFS under current rate mode. As expected, the intermediate phases progressively dissolved into the AlLLZO matrix by conventional heating. On the other hand, RFS promoted the growth of the intermediate La2Zr2O7, an effect that was overcome by the thermally driven formation of Al-LLZO at higher temperatures. The observed different reaction pathway suggests that RFS can be used for stabilizing phases that are not thermodynamically favored upon conventional heating.
机译:对化学制备的多相前驱体粉末进行反应闪速烧结(RFS)以制备Li6。25Al0。25La3Zr2O12(Al-LLZO)陶瓷。这种方法允许在炉膛温度为600°C的情况下,在30 s的短处理时间内获得单相致密样品?C、 电场为50 V cm-1,电流限制为150 mA mm-2。在室温下,陶瓷的体电导率高达0.18ms-cm-1。此外,通过原位X射线衍射研究了:i)常规加热和ii)电流速率模式下的RFS过程中的相演变。正如预期的那样,中间相通过常规加热逐渐溶解到AlLLZO基质中。另一方面,RFS促进了中间产物La2Zr2O7的生长,这一效应通过在更高温度下热驱动形成Al LLZO而被克服。观察到的不同反应途径表明,RFS可用于稳定在热力学上不利于常规加热的相。

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