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作 者:邵寒梅[1,2] 王一龙[1,3] 章桥新[1] 官建国[1]
机构地区:[1]武汉理工大学材料复合新技术国家重点实验室,湖北武汉430070 [2]武汉理工大学化学工程学院,湖北武汉430070 [3]武汉理工大学理学院应用化学系,湖北武汉430070
出 处:《功能材料》2007年第A06期2177-2181,共5页Journal of Functional Materials
基 金:基金项目:国家高技术研究发展计划(863计划)资助项目(2006AA03ZA61);国防预研基金资助项目(51447020105QT6903)
摘 要:首次引入活性SiO2微球作为核基,采用自组装液相还原技术,定向的在核基上沉积纳米银颗粒得到SiO2/Ag核壳复合粒子;并用红外、x射线衍射、场发射扫描电镜、能谱等分析表征该核壳复合粒子的形貌与结构。结果表明:利用活性SiO2作为核基,pH值为12.4,有表面活性剂参与的条件下,通过改变银前驱体浓度,可实现表面包覆致密、银壳厚度可控的核壳复合粒子化学制备技术。Silver coated silica microspheres core-shell composite particles could be prepared by first introducing activated silica microspheres as a nuclear, with the self-assembled liquid-reduction technology, because the silver nanoparticals would easily deposit on this nuclear directly. The morphology and structure of these nanocomposite particles were characterized by an Infrared Spectrogram, X-ray diffraction, Scanning electron microscope and X-ray energy dispersive spectrum. The results show that the technology of preparing silica core-silver shell particles which coated dense silver shell have been realized with activated silica as nuclear, the pH of 12.4, a surfactant in the conditions, and the thickness of silver shell is controllable by changing the silver precursor concentration.
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