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作 者:赵文华 魏智强 朱学良[2] 张旭东 冯旺军[2] 姜金龙[2] Zhao Wenhua 1,2, Wei Zhiqiang 1,2, Zhu Xueliang 2, Zhang Xudong 2 Feng WanRjun 2, Jiang Jinlong 2(1. State Key Laboratory of Advanced Processing and Recycling Nonferrous Metals, Lanzhou 730050, China;2. Lanzhou University of Technology, Lanzhou 730050, China)
机构地区:[1]省部共建有色金属先进加工与再利用国家重点实验室,甘肃兰州730050 [2]兰州理工大学,甘肃兰州730050
出 处:《稀有金属材料与工程》2018年第10期3148-3154,共7页Rare Metal Materials and Engineering
基 金:国家自然科学基金(51261015);甘肃省自然科学基金(1308RJZA238)
摘 要:以乙二胺为修饰剂,采用水热法合成了不同掺杂浓度的Zn_(1-x)Co_xS(x=0.00,0.01,0.03,0.05,0.07)纳米棒,并通过X射线衍射(XRD)、场发射扫描电子显微镜(FESEM)、高分辨透射电子显微镜(HRTEM)、X射线能量色散分析谱仪(EDS)、紫外-可见吸收光谱(UV-vis)、光致发光光谱(PL)和傅里叶红外光谱(FT-IR)对样品的晶体结构、形貌和光学性能进行表征。结果表明,所有样品都具有结晶良好的六方纤锌矿结构,样品中掺杂的Co^(2+)以替代Zn^(2+)的形式进入到ZnS晶格中。形貌为一维的纳米棒状,分散性良好。随着Co掺杂量的增加,晶胞体积逐渐减小,晶粒尺寸增大,晶格常数发生收缩。UV-vis光谱发现掺杂样品的光学带隙发生了红移现象。PL谱图表明样品存在紫光(402 nm)、蓝光(470 nm)、黄光(600 nm)和红外光(826 nm)4个明显的发光峰,随着Co掺杂浓度的增加,发光强度呈减小趋势。红外光谱的吸收峰位并没有随着掺杂浓度的增加而发生变化。Co-doped Zn1-xCoxSx=0,0.01,0.03,0.05,0.07)nanorods were synthesized by a hydrothermal method using ethylenediamine as a modifier.The crystal microstructure,morphology and optical properties of the sample were characterized by X-ray diffraction(XRD),field emission scanning electron microscopy(FESEM),high-resolution transmission electron microscopy(HRTEM),X-ray energy dispersive spectrometry(EDS),ultraviolet-visible diffuse reflectance spectroscopy(UV-vis DRS),photoluminescence spectra(PL)and Fourier transform infrared spectroscopy(FT-IR).The results show that all the samples synthesized by this method possess wurtzite structure with good crystallization,which indicates that all Co2+successfully replaces the lattice sites of Zn-(2+)to generate single-phase Zn_(1-x)Co_xS.The morphology is one-dimensional rod-like shape with good dispersion.The grain size increases,the cell volume decreases and the lattice constant shrinks with the increase of Co content.The UV-vis spectra reveal that the red shift of band gap occurs in the doped Zn_(1-x)Co_xS nanorods compared with the pure ZnS.The PL spectra show that the samples have obvious violet(402 nm),blue(470 nm,yellow(600 nm)and infrared(826 nm)emission peaks,and the luminescence intensity decreases with the increase of the Co doping concentration.The FT-IR spectrum shows that the absorption peak position does not change with the increase of the Co doping concentration.
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