成核
抗坏血酸
材料科学
化学工程
纳米结构
动力学
微晶
纳米颗粒
合金
纳米技术
化学
沉积(地质)
冶金
有机化学
古生物学
物理
食品科学
量子力学
沉积物
工程类
生物
作者
Yun Yang,Shuhua Han,Guangju Zhou,Lijie Zhang,Xingliang Li,Chao Zou,Shaoming Huang
出处
期刊:Nanoscale
[Royal Society of Chemistry]
日期:2013-01-01
卷期号:5 (23): 11808-11808
被引量:55
摘要
We present a general route for synthesizing M@ZnO nanoparticles (NPs) by using ascorbic acid (AA) to induce deposition of ZnO on various shaped and structured cationic-surfactant-capped NP surfaces (noble, magnetic, semiconductor, rod-like, spherical, cubic, dendrite, alloy, core@shell). The results show that the complexing (AA and Zn2+) and cooperative effects (AA and CTAB) play important roles in the formation of polycrystalline ZnO shells. Besides, the growth kinetics of M@ZnO was systematically studied. It was found that the slow growth rate favors the successful formation of uniform core@ZnO NPs with relatively loose shells. An appropriate growth rate allows achieving high quality M@ZnO NPs with dense shells. However, very fast growth causes significant additional nucleation and the formation of pure ZnO NPs. This general method is suitable for preparing M@ZnO using seed NPs prepared in both water and organic phases. It might be an alternative route for functionalizing NPs for bioapplications (ZnO is biocompatible), modulating material properties as designed, or synthesizing template materials for building other nanostructures.
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