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首页> 外文期刊>RSC Advances >Combined effects of hole doping and off-stoichiometry on the structures, transport, and magnetic properties of Sr(2?y)NayFe(1?x)Mo(1+x)O6 (x = 0/5x = y; y = 0, 0.05, 0.1, 0.15, 0.2, and 0.3)
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Combined effects of hole doping and off-stoichiometry on the structures, transport, and magnetic properties of Sr(2?y)NayFe(1?x)Mo(1+x)O6 (x = 0/5x = y; y = 0, 0.05, 0.1, 0.15, 0.2, and 0.3)

机译:空穴掺杂和化学计量比对Sr (2? y Na y Fe (1? x Mo (1+ x The 6 x = 0/5 x = y ; y = 0,0.05,0.1, 0.15、0.2和0.3)

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A series of double perovskite, Sr(2?y)NayFeMoO6 (y = 0, 0.05, 0.1, 0.15, 0.2, and 0.3) and Sr(2?y)NayFe(1?x)Mo(1+x)O6 (5x = y; y = 0.05, 0.1, 0.15, 0.2, and 0.3), ceramics were synthesized via a solid-state reaction. The influences of the doped Na (y) and off-stoichiometry (excess Mo: x) content on the structure, magnetization, chemical states, resistivity, magnetoresistance (MR), and the Curie temperature (TC) were systematically and comparatively investigated. The X-ray diffraction results indicated that the Fe/Mo ordering degree in Sr(2?y)NayFeMoO6 and Sr(2?y)NayFe(1?x)Mo(1+x)O6 exhibited a slight suppression for y = 0–0.15, whereas a significant decrease was observed for y = 0.2 and 0.3. X-ray photoelectron spectroscopy results confirmed that the chemical states of Fe and Mo cations in all the samples had +3 and +5 valences. With the decreasing y values, it was observed that the saturated magnetization Ms demonstrated a gradual decrease, in good agreement with the suppression of the Fe/Mo ordering degree. This close correlation between the magnetic properties and the Fe/Mo ordering degree indicates that the magnetic behaviors are predominantly controlled by the ordering degree of Fe/Mo in all the ceramics. The MR behavior in the samples is mainly determined by the grain boundary conditions. Upon comparing Sr(2?y)NayFeMoO6 with Sr(2?y)NayFe(1?x)Mo(1+x)O6 (5x = y) for the same y value, Sr(2?y)NayFe(1?x)Mo(1+x)O6 (5x = y) showed a decreased grain boundary strength (the resistivity); thus, a diminished MR performance was observed, indicating that introducing excess Mo into the hole-doped Sr2FeMoO6 system was disadvantageous for practical applications. Interestingly, the TC of both Sr(2?y)NayFeMoO6 and Sr(2?y)NayFe(1?x)Mo(1+x)O6 (5x = y) gradually decreased until y = 0.15, but improved on further increasing the y value. This composition-dependent tendency of TC cannot be explained only on the basis of the itinerant electron density, which is responsible for the optimized TC in the electron-doped Sr2FeMoO6 systems.
机译:一系列双重钙钛矿Sr (2? y Na y FeMoO 6 y = 0、0.05、0.1、0.15、0.2和0.3)和Sr (2? y Na y Fe (1? x Mo (1+ x O 6 (5 x = y ; y = 0.05,0.1,0.15 ,0.2和0.3),通过固相反应 合成了陶瓷。掺杂的Na( y )和非化学计量比(过量的Mo: x )对结构,磁化强度,化学状态,电阻率,磁阻(MR)的影响,对居里温度( T C )进行了系统的比较研究。 X射线衍射结果表明,Sr (2? y Na < em> y FeMoO 6 和Sr (2? y Na y Fe (1? x Mo (1+ x O 6 y = 0-0.15表现出轻微的抑制作用,而对 y = 0.2和0.3则有明显的抑制作用。 X射线光电子能谱结果证实,所有样品中的Fe和Mo阳离子的化学态均具有+3和+5价。随着 y 值的减小,观察到饱和磁化强度 M s 呈逐渐减小的趋势,同意抑制Fe / Mo有序度。磁性和Fe / Mo有序度之间的这种紧密相关性表明,在所有陶瓷中,磁性行为主要受Fe / Mo有序度控制。样品中的MR行为主要取决于晶界条件。比较Sr (2? y Na y FeMoO 6 ,带有Sr (2? y Na y Fe (1? x Mo (1+ x O 6 (5 x = y )表示相同的 y 值,即Sr (2? y Na y Fe (1? x Mo (1+ x O 6 (5 x = y )显示出降低的晶界强度(电阻率);因此,观察到MR性能下降,这表明将过量的Mo引入到掺杂了空穴的Sr 2 FesmallO 6 系统对实际应用不利。有趣的是,两个Sr (2? y T C > Na y FeMoO 6 和Sr < sub>(2? y Na y Fe < sub>(1? x Mo (1+ x O 6 (5 x = y )逐渐减小,直到 y = 0.15,但是在进一步增加 y 值方面进行了改进。 T C 的这种与组分有关的趋势不能仅基于流动电子密度来解释,该电子密度负责优化 T 掺电子的Sr 2 FeMoO 6中的> T C 系统。

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