Iwahori K, Yamashita I
CREST, Japan Science and Technology Agency, 4-1-8 Honcho, Kawaguchi, Saitama 332-0012, Japan. Graduate School of Materials Science, Nara Institute of Science and Technology, 8916-5, Takayama, Ikoma, Nara 630-0101, Japan.
Nanotechnology. 2008 Dec 10;19(49):495601. doi: 10.1088/0957-4484/19/49/495601. Epub 2008 Nov 19.
A simple size-controlled synthesis of cadmium sulfide (CdS) nanoparticle (NP) cores in the cavity of apoferritin from horse spleen (HsAFr) was performed by a slow chemical reaction synthesis and a two-step synthesis protocol. We found that the CdS NP core synthesis was slow and that premature CdS NP cores were formed in the apoferritin cavity when the concentration of ammonia water was low. It was proven that the control of the ammonia water concentration can govern the CdS NP core synthesis and successfully produce size-controlled CdS NP cores with diameters from 4.7 to 7.1 nm with narrow size dispersion. X-ray powder diffraction (XRD), energy dispersive spectroscopy (EDS) analysis and high-resolution transmission electron microscopy (HR-TEM) observation characterized the CdS NP cores obtained as cubic polycrystalline NPs, which showed photoluminescence with red shifts depending on their diameters. From the research of CdS NP core synthesis in the recombinant apoferritins, the zeta potential of apoferritin is important for the biomineralization of CdS NP cores in the apoferritin cavity. These synthesized CdS NPs with different photoluminescence properties will be applicable in a wide variety of nano-applications.
通过缓慢化学反应合成和两步合成方案,在马脾脱铁铁蛋白(HsAFr)的腔内进行了硫化镉(CdS)纳米颗粒(NP)核的简单尺寸控制合成。我们发现CdS NP核的合成速度较慢,并且当氨水浓度较低时,在脱铁铁蛋白腔内会形成过早的CdS NP核。事实证明,控制氨水浓度可以控制CdS NP核的合成,并成功制备出尺寸可控的CdS NP核,其直径为4.7至7.1纳米,尺寸分散性窄。X射线粉末衍射(XRD)、能量色散光谱(EDS)分析和高分辨率透射电子显微镜(HR-TEM)观察表明,所获得的CdS NP核为立方多晶NP,其光致发光随直径呈现红移。通过对重组脱铁铁蛋白中CdS NP核合成的研究,发现脱铁铁蛋白的zeta电位对于CdS NP核在脱铁铁蛋白腔内的生物矿化很重要。这些具有不同光致发光特性的合成CdS NPs将适用于各种纳米应用。