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On the origin of enhanced thermoelectricity in Fe doped Ca3Co4O9

机译:铁掺杂Ca3Co4O9中增强热电的起源

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Resistivity and Seebeck coefficient measurements on Ca3Co_(4-x)Fe_xO9 (x = 0, 0.05, 0.1, 0.2 and 0.25) reveal enhanced thermoelectric performance with an optimalx value of 0.2. X-ray diffraction measurements show continuous Fe doping into the host lattice, while X-ray absorption experiments reveal that Fe substitutes for Co in the Ca2CoO3 (rock salt) block. The Fe substitution for Co produces electron doping. The local structure around Fe in the Ca2CoO3 block becomes disordered, while the structure in the conducting CoO2 layer becomes more ordered. The structural change in the CoO2 layer plays the key role to enhance the electron transport. The highest ordered structure is achieved at x = 0.2 with the lowest resistivity. Soft X-ray absorption measurements find no Co site spin-state change with Fe doping. Thermoelectric property enhancement associated with doping induced structural change points to a new approach for creating materials with improved ZT in complex oxide systems.
机译:在Ca3Co_(4-x)Fe_xO9(x = 0、0.05、0.1、0.2和0.25)上的电阻率和塞贝克系数测量显示出最佳的x值为0.2时增强了热电性能。 X射线衍射测量表明,Fe连续掺杂到主体晶格中,而X射线吸收实验表明,Fe替代了Ca2CoO3(岩盐)块中的Co。 Fe替代Co会产生电子掺杂。 Ca2CoO3嵌段中Fe周围的局部结构变得无序,而导电CoO2层中的结构变得更有序。 CoO2层中的结构变化起着增强电子传输的关键作用。在x = 0.2时,电阻率最低,可获得最高的有序结构。软X射线吸收测量发现,Fe掺杂不会使Co位置自旋态发生变化。与掺杂引起的结构变化相关的热电性能增强,为在复杂氧化物系统中创建具有改进ZT的材料的新方法提供了一种新方法。

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