A Nonaqueous Approach to the Preparation of Iron Phosphide Nanowires
© The Author(s) 2010
Received: 7 January 2010
Accepted: 30 January 2010
Published: 16 February 2010
Previous preparation of iron phosphide nanowires usually employed toxic and unstable iron carbonyl compounds as precursor. In this study, we demonstrate that iron phosphide nanowires can be synthesized via a facile nonaqueous chemical route that utilizes a commonly available iron precursor, iron (III) acetylacetonate. In the synthesis, trioctylphosphine (TOP) and trioctylphosphine oxide (TOPO) have been used as surfactants, and oleylamine has been used as solvent. The crystalline structure and morphology of the as-synthesized products were characterized by powder X-ray diffraction (XRD) and transmission electron microscopy (TEM). The obtained iron phosphide nanowires have a typical width of ~16 nm and a length of several hundred nanometers. Structural and compositional characterization reveals a hexagonal Fe2P crystalline phase. The morphology of as-synthesized products is greatly influenced by the ratio of TOP/TOPO. The presence of TOPO has been found to be essential for the growth of high-quality iron phosphide nanowires. Magnetic measurements reveal ferromagnetic characteristics, and hysteresis behaviors below the blocking temperature have been observed.
KeywordsIron phosphides Nanowire Synthesis Magnetic properties
Nanoscale building blocks have attracted much interest due to their potential applications in replacement of traditional materials in the coming next few decades. However, most of the work in the synthesis of nanocrystals using solution-phase chemical method is focused on VI-II semiconductor systems and noble metals . Transition metal phosphides exhibit unique catalytic, optical, electronic, and magnetic properties depending on their phases . For example, Fe3P is ferromagnet that has a high transition temperature (Tc = 716 K) , while FeP2 is a small-bandgap semiconductor with a Tc of 15 K. Some preparation methods have been developed for the interest of studying the size-property relations of nanoscale iron phosphides. For example, Gu et al.  prepared 200 nm orthorhombic FeP via solvothermal synthesis employing FeCl3 and Na3P at 180°C. Luo et al.  synthesized nanocrystalline Fe2P in a similar way at 180°C. Hu et al.  obtained a mixture of iron oxide nanoshells and hollow iron phosphide nanoparticles using sonichemistry method. Brock et al.  prepared FeP nanoparticles via a de-silylation route using a highly reactive phosphine source, P(SiMe3)3. Later, Brock  found that trioctylphosphine (TOP), which is a less-reactive reagent compared with P(SiMe3)3, can be used as phosphine source as well as surfactant and solvent in the preparation of MnP and FeP using metal carbonyls as metal source. Liu et al.  synthesized FeP nanorods by injecting Fe(CO)5/TOP into hot solution of TOP and trioctylphosphine oxide (TOPO). Hyeon et al.  studied the relation between the injection rate and length of Fe2P nanorods synthesized using a syringe pump. Fe2P nanorods can also be prepared without using a syringe pump as shown in the work of Whitmire et al.  who developed a single-source organometallic method to control morphology by varying the ratio of tri-n-octylamine (TOA) to oleic acid (OA) in a one-pot reaction.
We recently reported the synthesis of Ni2P nanowires in the system of TOA/OA via an injection approach . In this work, we present a primary result on the synthesis of iron phosphide nanowires using a solution-phase chemical approach. Instead of using toxic and unstable iron carbonyl compounds that were usually employed in most of previous work on the synthesis of iron phosphide nanowires, we developed a approach that uses a metal precursor of iron (III) acetylacetonate (Fe(acac)3),which is low toxicity, inexpensive and rather stable at ambient condition. The structure and magnetic properties of as-synthesized nanowires are also presented in this work.
In a typical synthesis, 0.5 mmol of Fe(acac)3(96%, Acros) was added in 10 mL of oleylamine (OM, 80–90%, Acros) and heated to 130°C. The resulting solution was continuously injected into a stock solution of 5 ml of OM, 5 mmol of TOP (97%, Acros), and 2.5 mmol of TOPO (90%, Acros) at 340°C using a syringe pump. The whole injection time varied from 3 to 6 h. A one-pot reaction was also attempted by reacting a mixture of 0.5 mmol of Fe(acac)3, 4 mmol of TOP, 2 mmol of TOPO, and 6 mL of OM directly at 350°C for 1 h. The obtained product precipitates were washed by hexane and acetone, and separated from solution by centrifugation.
Powder X-ray diffraction (XRD) data were collected on a Panalytical X’pert PRO X-ray diffractometer using Cu Kα radiation. Transmission electron microscopy (TEM) was performed on a TECNAI F-30 transmission electron microscope. Samples for TEM analyses were prepared by sonicating the as-synthesized powders in hexane and dropping a small volume onto a carbon-coated copper TEM grid followed by solvent evaporation. Magnetic analysis was performed using a superconducting quantum interference device (SQUID) magnetometer (MPMS-5).
Results and Discussion
It can be inferred from the above results that the anisotropic shape of nanowires comes mainly from the intrinsically anisotropic nature of hexagonal crystalline structure. The monomer concentration of the injection route is relatively low, which favors the growth of existing seeds formed in the early stage of continuous delivery. Another important prerequisite for the formation of anisotropic nanostructures is related to the surfactants used. Usually, a multi-surfactant system favors the formation of an anisotropic nanostructure. In our case, the employed TOP and TOPO both can act as surfactants to cover different crystallographic surfaces of newly formed nanocrystal seeds, and eventually lead to the anisotropic growth toward c axis, forming a one-dimensional nanostructure.
The formation process of Fe2P nanowires may be as follows. At first, the complex of Fe(acac)3-OM decomposes to iron clusters once added to hot solvent of OM. Then, these iron clusters will be attached to TOP molecules, and the P–C bonds located at the particle surface may break and cause phosphorus to react with iron, forming iron phosphide. Once Fe2P seeds with an anisotropic structure forms, the growth along  direction will be favored due to the cooperation of anisotropic nature and the side-protection effect of surfactant molecules. This eventually leads to the formation of a one-dimensional nanostructure.
We also explored one-pot reaction for the synthesis of iron phosphide nanowires. As shown in Fig. 2b, the obtained products via one-pot reaction consist of nanowires plus nanosheets or nanoblocks. The shape singularity of the products from the one-pot reaction is not superior to the continuous-injection approach. Considering the robustness of the reaction, this difference should not come from the small difference in TOP amount. It is certain that continuous-injection route is crucial to keep the singularity of the products. A possible reason is that one-pot synthesis incurs a high concentration of nuclei, some of which are unable to develop into nanowires due to insufficient protections of surfactant molecules, whereas for the injection approach, the nuclei concentration at the beginning stage is restricted by the delivering rate, and the relatively low concentration of nuclei plus the continuous delivery of source materials will allow nuclei to fully grow into nanowires.
Iron phosphide nanowires have been synthesized through a nonaqueous approach that utilizes Fe(acac)3 as an iron source, TOP as a phosphorus source and oleylamine as solvent. The as-prepared nanowires have a hexagonal Fe2P structure and grow along c axis. The dimension of nanowires can be tuned via reaction parameters such as injection rate, reaction temperature, and TOP/TOPO ratio. Both injection method and one-pot reaction can produce iron phosphide nanowires, although the former can generate products with much better uniformity and yield. The magnetic tests reveal ferromagnetic characteristics below the blocking temperature, and a large coercive force of ~5,000 Oe has been observed. The reported synthetic approach does not use commonly used toxic iron carbonyl compounds as iron precursor, which provides a convenient access to further studies of their special physical and chemical properties.
This work was partially supported by the National Natural Science Foundation of China (Grant nos. 50701036 and 50671087) and the National Outstanding Youth Science Foundation of China (Grant no. 50825101).
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