Liu Jun, Yu Bowen, Zhang Qiankun, Hou Lizhen, Huang Qiulai, Song Chunrui, Wang Shiliang, Wu Yueqin, He Yuehui, Zou Jin, Huang Han
School of Physics and Electronics, State Key Laboratory of Powder Metallurgy, Central South University, Changsha, 410083, People's Republic of China.
Nanotechnology. 2015 Feb 27;26(8):085601. doi: 10.1088/0957-4484/26/8/085601. Epub 2015 Feb 3.
Fe3C-C core-shell nanoparticles were fabricated on a large scale by metal-organic chemical vapor deposition at 700 °C with ferric acetylacetonate as the precursor. Analysis results of x-ray diffraction, transmission electron microscope and Raman spectroscope showed that the Fe3C cores with an average diameter of ∼35 nm were capsulated by the graphite-like C layers with the thickness of 2-5 nm. The comparative experiments revealed that considerable Fe3O4-Fe3C core-shell nanoparticles and C nanotubes were generated simultaneously at 600 and 800 °C, respectively. A formation mechanism was proposed for the as-synthesized core-shell nanostructures, based on the temperature-dependent catalytic activity of Fe3C nanoclusters and the coalescence process of Fe3C-C nanoclusters. The Fe3C-C core-shell nanoparticles exhibited a saturation magnetization of 23.6 emu g(-1) and a coercivity of 550 Oe at room temperature.
以乙酰丙酮铁为前驱体,通过金属有机化学气相沉积法在700℃大规模制备了Fe3C-C核壳纳米颗粒。X射线衍射、透射电子显微镜和拉曼光谱的分析结果表明,平均直径约为35nm的Fe3C核被厚度为2-5nm的类石墨C层包裹。对比实验表明,分别在600℃和800℃时会同时生成大量的Fe3O4-Fe3C核壳纳米颗粒和C纳米管。基于Fe3C纳米团簇的温度依赖性催化活性以及Fe3C-C纳米团簇的聚结过程,提出了所合成核壳纳米结构的形成机制。Fe3C-C核壳纳米颗粒在室温下表现出23.6 emu g(-1)的饱和磁化强度和550 Oe的矫顽力。