Ge Wanyin, Sato Ryota, Wu Hsin-Lun, Teranishi Toshiharu
Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, 611-0011, Japan.
Chemphyschem. 2015 Oct 26;16(15):3200-5. doi: 10.1002/cphc.201500605. Epub 2015 Aug 26.
The shape and size of monodisperse Fe3 O4 nanoparticles (NPs) are controlled using a chemical solution synthesis in the presence of the surfactant cetylpyridinium chloride (CPC). Cubic Fe3 O4 NPs surrounded by six {100} planes are obtained in the absence of CPC. Increasing the CPC content during synthesis causes the shape of the resulting Fe3 O4 NPs to change from cubic to truncated cubic, cuboctahedral, truncated octahedral, and finally octahedral. During this evolution, the predominantly exposed planes of the Fe3 O4 NPs vary from {100} to {111}. The shape control results from the synergistic effect of the pyridinium cations, chloride anions, and long-chain alkyl groups of CPC, which is confirmed by comparison with NPs synthesized in the presence of various related cationic surfactants. The size of the cubic Fe3 O4 NPs can be tuned from 50 to 200 nm, by changing the concentration of oleic acid in the reaction solution. The Fe3 O4 NPs exhibit shape-dependent saturation magnetization, remanent magnetization, and coercivity.
在表面活性剂十六烷基吡啶氯化物(CPC)存在的情况下,通过化学溶液合成法控制单分散Fe₃O₄纳米颗粒(NPs)的形状和大小。在没有CPC的情况下可获得由六个{100}面围绕的立方Fe₃O₄ NPs。在合成过程中增加CPC的含量会导致所得Fe₃O₄ NPs的形状从立方变为截角立方、立方八面体、截角八面体,最终变为八面体。在这个演变过程中,Fe₃O₄ NPs主要暴露的面从{100}变为{111}。形状控制源于CPC的吡啶鎓阳离子、氯离子阴离子和长链烷基的协同作用,这通过与在各种相关阳离子表面活性剂存在下合成的NPs进行比较得到证实。通过改变反应溶液中油酸的浓度,立方Fe₃O₄ NPs的尺寸可在50至200 nm之间调节。Fe₃O₄ NPs表现出形状依赖的饱和磁化强度、剩余磁化强度和矫顽力。