[[abstract]]Nanostructured materials are attracting great research interest due to their application as catalysts of organic reactions, as gas sensors and as advanced materials in future optic, electronic and magnetic devices.1–3 Recently, the fabrication of Fe-containing magnetic nanomaterials including iron,4 iron oxides5 and alloys such as FePt6 and FeCo7 became a very important issue in the potential application of their magnetic characteristics. Iron phosphide, FeP, a low-band gap semiconductor material with special magnetic properties, has traditionally been prepared by high-temperature reactions.8 Recently, Lukehart and Brock groups reported the preparation of Fe2P and FeP nanoparticles, respectively.9 Herein, we present the first example of synthesis of iron phosphide FeP nanowires by thermal decomposition of (4-cyclohexadiene)iron tricarbonyl, (4-C6H8)Fe(CO)3 in the presence of tri-n-octylphosphine oxide (TOPO) and tri-n-octylphosphine (TOP) as the stabilizing surfactants. In addition, magnetic properties of these products have been investigated in this study.The preparative procedure summarized in Scheme 1 is modified from the method for generation of Fe nanorods previously reported by Hyeon et al.4m Heating a mixture of 200 mg of (4-C6H8)Fe(CO)3 and 5.0 g of TOPO at 340 °C under a nitrogen atmosphere for 30 min afforded a black solution. To this black mixture in TOPO, was added a set amount of (4-C6H8)Fe(CO)3 (0 mg, sample A; 10 mg, sample B; 25 mg, sample C) in 5.0 ml of TOP and the solution was continuously heated at 360 °C for 30 min. This step was repeated once. After the resulting black mixture was cooled to room temperature, excess acetone was added to produce a black precipitate. The black powder product was collected by centrifugation and can be re-dispersed in pyridine or n-hexane to form a homogeneous solution.
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机译:[[摘要]]由于纳米结构材料作为有机反应的催化剂,气体传感器以及未来的光学,电子和磁性设备中的先进材料的应用,因此引起了极大的研究兴趣。1-3最近,含铁磁性材料的制造包括铁,4的氧化铁5和诸如FePt6和FeCo7的合金在内的纳米材料成为潜在应用其磁性特征的重要问题。磷化铁FeP是一种具有特殊磁性的低带隙半导体材料,传统上是通过高温反应制备的。8最近,Lukehart和Brock小组分别报道了Fe2P和FeP纳米颗粒的制备。9本文中,我们介绍了在三正辛基膦氧化物(TOPO)和三正辛基存在的情况下,通过(4-环己二烯)三羰基铁(4-C6H8)Fe(CO)3热分解合成磷化铁FeP纳米线的第一个例子辛基膦(TOP)作为稳定表面活性剂。此外,本研究还对这些产品的磁性能进行了研究。方案1中概述的制备方法是由Hyeon等人先前报道的制备Fe纳米棒的方法改进的。4m加热200 mg(4-将C6H8)Fe(CO)3和5.0 g TOPO在氮气气氛下于340°C放置30分钟,得到黑色溶液。向TOPO中的这种黑色混合物中加入5.0 ml TOP中的一定量的(4-C6H8)Fe(CO)3(0 mg,样品A; 10 mg,样品B; 25 mg,样品C)和溶液将其在360℃下连续加热30分钟。重复此步骤一次。将所得黑色混合物冷却至室温后,加入过量的丙酮以产生黑色沉淀物。通过离心收集黑色粉末产物,并且可以将其重新分散在吡啶或正己烷中以形成均匀溶液。
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