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High luminescent L-cysteine capped CdTe quantum dots prepared at different reaction times

机译:在不同反应时间内制备的高发亮L-半胱氨酸封端的CDTE量子点

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This paper reports a facile synthesis route of high luminescent L-cysteine capped CdTe quantum dots (QDs). The effect of reaction time on the growth mechanism, optical and physical properties of the CdTe QDs was investigated in order to find the suitability of them towards optical and medical applications. The representative high-resolution transmission microscopy (HRTEM) analysis showed that the as-obtained CdTe QDs appeared as spherical particles with excellent monodispersity. The images exhibited clear lattice fringes which are indicative of good crystallinity. The X-ray diffraction (XRD) pattern displayed polycrystalline nature of the QDs which correspond well to zinc blende phase of bulk CdTe. The crystallite sizes calculated from the Scherrer equation were less than 10 nm for different reaction times which were in close agreement with the values estimated from HRTEM. An increase in reaction time improved crystallinity of the sample as explained by highest peak intensity of the XRD supported by the photoluminescence emission spectra which showed high intensity at a longer growth time. It was observed that for prolonged growth time the emission bands were red shifted from about 517-557 nm for 5-180 min of reaction time due to increase in particle sizes. Ultraviolet and visible analysis displayed well-resolved absorption bands which were red shifted upon an increase in reaction time. There was an inverse relation between the band gap and reaction time. Optical band gap decreases from 3.98 to 2.59 eV with the increase in reaction time from 15 to 180 min.
机译:本文报道了高发发光L-半胱氨酸封端的CdTe量子点(QDS)的容易合成途径。研究了反应时间对CDTE QDS的生长机理,光学和物理性质的影响,以找到它们朝向光学和医疗应用的适用性。代表性的高分辨率透射显微镜(HRTEM)分析表明,AS获得的CDTE QDS出现为具有优异的单反叠性的球形颗粒。图像表现出透明的晶格边缘,其表示良好的结晶度。 X射线衍射(XRD)模式显示QD的多晶性质,其对应于散装CDTE的锌融合阶段。对于不同反应时间,从Scherrer方程计算的微晶尺寸小于10nm,不同的反应时间与HRTEM估计的值密切一致。反应时间的增加改善了样品的结晶度,如光致发光发射光谱所解释的XRD的最高峰强度,所述光致发光发射光谱在较长的生长时间下显示出高强度。观察到,对于延长的生长时间,由于颗粒尺寸的增加,发射带的红色从约517-557nm移位为5-180分钟的反应时间。紫外线和可见分析显示出良好的隔离吸收带,其红色在反应时间的增加时移位。带隙和反应时间之间存在反向关系。光带间隙从3.98到2.59eV降低,随着15-180分钟的反应时间增加。

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