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首页> 外文期刊>Journal of Applied Physics >Enhancement of Curie temperature in electrochemically prepared crystalline thin films of Prussian blue analogs K_jFe_k~Ⅱ[Cr~Ⅲ(CN)_6]_l·mH_2O
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Enhancement of Curie temperature in electrochemically prepared crystalline thin films of Prussian blue analogs K_jFe_k~Ⅱ[Cr~Ⅲ(CN)_6]_l·mH_2O

机译:电化学制备的普鲁士蓝类似物K_jFe_k〜Ⅱ[Cr〜Ⅲ(CN)_6] _l·mH_2O的晶体薄膜中居里温度的提高

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摘要

Structural and magnetic properties of electrochemically prepared crystalline films of Prussian blue analogs (PBAs) K_jFe_k~Ⅱ[Cr~Ⅲ(CN)_6]_l·mH_2O, with varying deposition time and electrode voltage, which result into change in film thickness and stoichiometry, respectively, have been investigated by using x-ray diffraction (XRD), infrared (IR) spectroscopy, and dc magnetization measurement techniques. An atomic force microscopy (AFM) and XRD study reveal uniform and crystalline nature of all films. As the film thickness increases from 1 μm to 5 μm, the Curie temperature (T_C), coercive field, and maximum magnetization increase from 11 K to 21 K, 20 Oe to 160 Oe, and 5.7 μB to 6.5μB, respectively. For the films prepared with variation in electrode voltage, it has been found that the alkali metal ions are introduced into the films just by using suitable electrode voltage, contrary to usual method where alkali metal ions are intentionally introduced into the lattice by using additional compounds of alkali metals as starting materials. In addition, an enhancement in T_C with an increasing electrode voltage has been observed. The film deposited with a lower electrode voltage of -0.6 V shows a T_C of ~21 K, close to the previously reported value of T_C. Whereas, for films prepared with an electrode voltage of -0.9 V, an increase in T_C(~65 K) is observed. The rise in T_C is attributed to the decrease in Fe~Ⅱ/Cr~Ⅲ ratio with an increasing electrode voltage. The ability of tuning T_C just by changing the electrode voltage could be useful in designing thin films of new molecule based magnets.
机译:电化学制备的普鲁士蓝类似物(PBA)K_jFe_k〜Ⅱ[Cr〜Ⅲ(CN)_6] _l·mH_2O的晶体膜的结构和磁性能,随沉积时间和电极电压的变化而变化,导致膜厚度和化学计量的变化,分别通过使用X射线衍射(XRD),红外(IR)光谱和dc磁化测量技术进行了研究。原子力显微镜(AFM)和XRD研究揭示了所有薄膜的均匀和结晶性质。随着膜厚度从1μm增加到5μm,居里温度(T_C),矫顽场和最大磁化强度分别从11 K增加到21 K,从20 Oe增加到160 Oe,从5.7μB增加到6.5μB。对于在电极电压变化的情况下制备的薄膜,发现仅通过使用合适的电极电压就可以将碱金属离子引入薄膜中,这与通常的方法不同,在常规方法中,碱金属离子是通过使用以下化合物额外引入的:以碱金属为原料。另外,已经观察到随着电极电压的增加,T_C提高。以-0.6 V的较低电极电压沉积的薄膜显示的T_C为〜21 K,接近先前报道的T_C值。而对于电极电压为-0.9 V的薄膜,观察到T_C(〜65 K)升高。 T_C的升高归因于F​​e〜Ⅱ/ Cr〜Ⅲ比随电极电压的升高而降低。仅通过改变电极电压来调节T_C的能力可能对设计基于新分子的磁体的薄膜有用。

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  • 来源
    《Journal of Applied Physics 》 |2010年第2期| P.023916.1-023916.6| 共6页
  • 作者单位

    Solid State Physics Division, Bhabha Atomic Research Centre, Mumbai 400085, India;

    Solid State Physics Division, Bhabha Atomic Research Centre, Mumbai 400085, India;

    Solid State Physics Division, Bhabha Atomic Research Centre, Mumbai 400085, India;

    Physics Group, Bhabha Atomic Research Centre, Mumbai 400085, India;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
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  • 正文语种 eng
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