...
首页> 外文期刊>Journal of the European Ceramic Society >Formation and properties of high entropy oxides in Co-Cr-Fe-Mg-Mn-Ni-O system: Novel (Cr,Fe,Mg,Mn,Ni)(3)O-4 and (Co,Cr,Fe,Mg,Mn)(3)O-4 high entropy spinels
【24h】

Formation and properties of high entropy oxides in Co-Cr-Fe-Mg-Mn-Ni-O system: Novel (Cr,Fe,Mg,Mn,Ni)(3)O-4 and (Co,Cr,Fe,Mg,Mn)(3)O-4 high entropy spinels

机译:Co-Cr-Fe-Mg-Mn-Ni-O系统中高熵氧化物的形成与性能:新型(Cr,Fe,Mg,Mn,Ni)(3)O-4和(CO,Cr,Fe,Mg ,Mn)(3)O-4高熵尖晶石

获取原文
获取原文并翻译 | 示例
           

摘要

Possibility of formation of quinary and senary equimolar high entropy oxides from the Co-Cr-Fe-Mg-Mn-Ni-O system is presented. Different proposed compositions are synthesized using the solid-state reaction route at high temperatures (900 - 1100 degrees C) and quenched to room temperature. Phase composition of the samples is studied, showing tendency toward formation of two main phases: rock salt-structured Fm-3 m and spinel-structured Fd-3 m. It is documented that the annealing temperature has a profound effect on stability of both structures, and at 1100 degrees C usually the highest content of Fm-3 m phase is usually observed. Three different oxides, namely, (Co,Cr,Fe,Mn,Ni)(3)O-4, (Co,Cr,Fe,Mg,Mn)(3)O-4 and (Cr,Fe,Mg,Mn,Ni)(3)O-4 are obtained as single-phase materials, which structure can be described as the high entropy Fd-3 m spinel one. The latter two compounds have not been previously reported in the literature. Activated character of the electrical conductivity dependence on temperature is observed, with relatively high total conductivity at high temperatures and corresponding high absolute values of Seebeck coefficient.
机译:提出了来自CO-CR-Fe-Mg-MN-Ni-O系统的Quary和老年等摩尔高熵氧化物的形成的可能性。使用高温(900-1100℃)的固态反应途径合成不同的提出的组合物并将其淬灭至室温。研究了样品的相组成,显示出形成两个主要阶段的趋势:岩盐结构FM-3M和尖晶石结构FD-3M。记录的是,退火温度对两个结构的稳定性产生深远的影响,并且在1100℃下通常观察到最高含量的FM-3M相。三种不同的氧化物,即(CO,Cr,Fe,Mn,Ni)(3)O-4,(CO,Cr,Fe,Mg,Mn)(3)O-4和(Cr,Fe,Mg,Mn ,Ni)(3)O-4作为单相材料获得,该结构可以描述为高熵FD-3M尖晶石。后两种化合物以前尚未在文献中报道。观察到对温度的电导率依赖性的激活特征,在高温下具有相对高的总电导率和塞贝克系数的相应高绝对值。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号