CAJ | 학술논문

以Fe(CO)_5和Ni(HCOO)_2为前驱物,十八烯为溶剂,在表面活性剂和分散剂油酸和油胺的协同作用下,通过前驱体的液相热分解和自合金化,制备铁镍合金纳米颗粒.通过XRD和TEM研究了产物的微观结构.并对产物的磁学性质进行了表征.结果表明,在反应温度为200℃,油胺与油酸及甲酸镍的物质的量比为4:2:1,反应时间为20 min时可得形貌可控、抗氧化性强的面心立方晶体结构的平面三角形纳米铁镍合金,晶粒尺寸为15～55 nm.磁性测量表明,300 K时三角形形貌铁镍合金的饱和磁化强度为15.5 emu·g~(-1),矫顽力趋近于零,呈现超顺磁性;在低温(4.2 K)时,铁镍合金的饱和磁化强度为17.5 emu·g~(-1),矫顽力增大明显.
이Fe(CO)_5화Ni(HCOO)_2위전구물,십팔희위용제,재표면활성제화분산제유산화유알적협동작용하,통과전구체적액상열분해화자합금화,제비철얼합금납미과립.통과XRD화TEM연구료산물적미관결구.병대산물적자학성질진행료표정.결과표명,재반응온도위200℃,유알여유산급갑산얼적물질적량비위4:2:1,반응시간위20 min시가득형모가공、항양화성강적면심립방정체결구적평면삼각형납미철얼합금,정립척촌위15～55 nm.자성측량표명,300 K시삼각형형모철얼합금적포화자화강도위15.5 emu·g~(-1),교완력추근우령,정현초순자성;재저온(4.2 K)시,철얼합금적포화자화강도위17.5 emu·g~(-1),교완력증대명현.
Fe-Ni alloy nanoparticles were synthesized by thermal decomposition of Ni(COOH)_2 and Fe(CO)_5 with 1-octadecene as the solvent and oleic acid (OA) and oleylamine(OLA) as surfactants. The produced Fe-Ni alloy nanoparticles were characterized by X-ray diffraction(XRD), transmission electron microscope(TEM) and vibrating sample magnetometer(VSM). The results showed that a shape controlled fcc phase Fe-Ni alloy nanoparticles of triangular shape was formed when the molar ratio, of OA, OLA and Ni(HCOO)_2 was 4:2:1 at 200 ℃ fo 20 min. Magnetic measurements revealed the alloy nanoparticles of triangular shape exhibit superparamagnetic behavior with a saturation magnetization of 15.5 emu·g~(-1) at 300 K; a saturation magnetization of 17.5 emu·g~(-1) and a coer-civity of 158 Oe at 4.2 K.