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A One-Pot Synthesis of Monodispersed Iron Cobalt Oxide and Iron Manganese Oxide Nanoparticles from Bimetallic Pivalate Clusters

机译:从双金属新戊酸酯簇团一锅法合成单分散的氧化铁钴和氧化锰铁纳米颗粒

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摘要

Monodispersed iron cobalt oxide (Fe2CoO4) and iron manganese oxide (Mn_(0.43)Fe_(2.57)O4) nanoparticles have been synthesized using bimetallic pivalate clusters of [Fe2CoO-(O2C~tBu)6(HO2C~tBu)3] (1), Co4Fe2O2(O2C~tBu)_(10)(MeCN)2] (2), and [Fe2MnO(O2C~tBu)6(HO2C~tBu)3] (3) respectively as single source precursors. The precursors were thermolyzed in a mixture of oleylamine and oleic acid with either diphenyl ether or benzyl ether as solvent at their respective boiling points of 260 or 300 °C. The effect of reaction time, temperature and precursor concentration (0.25 or 0.50 mmol) on the stoichiometry, phases or morphology of the nanoparticles were studied. TEM showed that highly monodispersed spherical nanoparticles of Fe2CoO4 (3.6 ± 0.2 nm) and Mn_(0.43)Fe_(2.57)O4 (3.5 ± 0.2 nm) were obtained from 0.50 mmol of 1 or 3, respectively at 260 °C. The decomposition of the precursors at 0.25 mmol and 300 °C revealed that larger iron cobalt oxide or iron manganese oxide nanoparticles were obtained from 1 and 3, respectively, whereas the opposite was observed for iron cobalt oxide from 2 as smaller nanoparticles appeared. The reaction time was investigated for the three precursors at 0.25 mmol by withdrawing aliquots at 5 min, 15 min, 30 min, 1 h, and 2 h. The results obtained showed that aliquots withdrawn at reaction times of less than 1 h contain traces of iron oxide, whereas only pure, cubic iron cobalt oxide or iron manganese oxide was obtained after 1 h. Magnetic measurements revealed that all the nanoparticles are superparamagnetic at room temperature with high saturation magnetization values. XMCD confirmed that in iron cobalt oxide nanoparticles, most of the Co~(2+) cations are in the octahedral site. There is also evidence in the magnetic measurements for considerable hysteresis (>1T) observed at 5 K. EPMA analysis and ICP-OES measurements performed on iron cobalt oxide nanoparticles obtained from [Fe2CoO(O2C~tBu)6(HO2C~tBu)3] (1) revealed that stoichiometric Fe2CoO4 was obtained only for 0.50 mmol precursor concentration. All the nanoparticles were characterized by powder X-ray diffraction (p-XRD), transmission electron microscopy (TEM), inductively coupled plasma-optical emission spectroscopy (ICP-OES), electron probe microanalysis (EPMA), X-ray magnetic circular dichroism (XMCD), and superconducting quantum interference device (SQUID) magnetometry.
机译:使用[Fe2CoO-(O2C〜tBu)6(HO2C〜tBu)3]的双金属新戊酸酯簇合成了单分散的氧化铁钴(Fe2CoO4)和氧化锰铁(Mn_(0.43)Fe_(2.57)O4)纳米粒子(1) ,Co4Fe2O2(O2C〜tBu)_(10)(MeCN)2](2)和[Fe2MnO(O2C〜tBu)6(HO2C〜tBu)3](3)分别作为单一来源的前体。将前体在油胺和油酸的混合物中以二苯醚或苄基醚作为溶剂在各自的沸点260或300°C下加热。研究了反应时间,温度和前体浓度(0.25或0.50 mmol)对纳米粒子的化学计量,相或形态的影响。 TEM显示,在260℃下分别由0.50mmol的1或3获得高度单分散的Fe 2 CoO 4(3.6±0.2nm)和Mn_(0.43)Fe_(2.57)O4(3.5±0.2nm)的球形纳米颗粒。前体在0.25 mmol和300°C下的分解表明,从1和3分别获得了较大的氧化铁钴或氧化锰铁纳米颗粒,而从2观察到的氧化钴铁则相反,因为出现了较小的纳米颗粒。通过在5分钟,15分钟,30分钟,1小时和2小时取出等分试样,研究了0.25 mmol下三种前体的反应时间。获得的结果表明,在少于1小时的反应时间取出的等分试样中含有痕量的氧化铁,而1小时后仅获得纯的立方氧化铁钴或氧化锰铁。磁性测量表明,所有纳米粒子在室温下都是超顺磁性,具有高饱和磁化强度值。 XMCD证实,在氧化钴铁纳米颗粒中,大多数Co〜(2+)阳离子位于八面体位置。磁性测量中也有证据表明在5 K下观察到相当大的磁滞(> 1T)。对从[Fe2CoO(O2C〜tBu)6(HO2C〜tBu)3获得的氧化铁钴纳米粒子进行EPMA分析和ICP-OES测量。 (1)揭示仅在前驱体浓度为0.50 mmol时才能获得化学计量的Fe2CoO4。所有纳米颗粒的特征在于粉末X射线衍射(p-XRD),透射电子显微镜(TEM),电感耦合等离子体发射光谱(ICP-OES),电子探针显微分析(EPMA),X射线磁性圆二色性(XMCD)和超导量子干涉仪(SQUID)磁力计。

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