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1.
使用尿素-氯化胆碱低共熔溶剂(UCC-DES),采用水热合成和反溶剂(乙醇)法,以化工材质ZnO粉末为原料制备了分层的球状微/纳米ZnO晶体.分析了反应时间、反溶剂的种类和含量对ZnO晶体形貌的影响以及ZnO晶体析出的原因.并将制备的分层球状ZnO微/纳米晶体应用于光催化降解甲基橙.结果表明,制备的ZnO晶体对甲基橙有良好的光催化降解性能.  相似文献   

2.
Synthesis of metal–organic framework (MOF) based on tetra-pyridyl porphyrin and palladium (II) salt resulted in the formation of palladium oxide nano-crystals. The palladium oxide nano-crystals were characterized by PXRD, TEM, HRTEM, ED, UV–Vis spectroscopy, DLS, SEM and AFM. A plausible mechanism for the in situ generation of nano-crystals has been proposed.  相似文献   

3.
We describe the effect of surface-modified hydroxyapatite (HAp) nano-crystals on biocompatibility of a new-type nanocomposite consisting of poly(ε-caprolactone) (PCL) and HAp. Surface-modified hydroxyapatite (HAp) nano-crystals were prepared by chemically grafting PCL on HAp surfaces. Time-dependent phase monitoring indicated that PCL surface-grafting contributed to the enhanced dispersion of HAp at nano-level in the PCL solution. The protein adhesion and cell experiments showed that the presence of PCL-grafted HAp nano-crystals in nanocomposites contributed to the enhanced biocompatibility. PCL-grafted HAp in nanocomposites provided more favorable environments for protein adsorption, compared with unmodified HAp. Nanocomposites containing PCL-grafted nanophase HAp showed positive effects on adhesion and proliferation of NIH3T3 fibroblasts.  相似文献   

4.
以一水合醋酸钙、浓磷酸为原料,采用湿化学合成法预先合成磷酸一氢钙(CMHP),在室温将其浸泡于定期更换的无水甲醇中,经过72 h的浸泡,CMHP转化为β-磷酸三钙(β-TCP)纳米晶。对所得样品分别进行X射线粉末衍射仪(XRD)、激光拉曼散射光谱(Raman)以及透射电镜(TEM)表征,结果表明,所得短棒状β-TCP的晶粒长度在30~60 nm之间;CMHP电离产生的氢离子通过CMHP和甲醇之间的界面层,进入甲醇本体,促使CMHP的电离以及向β-TCP的晶型转化,这种晶型转化不经过无定形态而直接转化为β-TCP纳米晶。  相似文献   

5.
采用热分解法和硫熔法分别合成了纳米Y2O2S∶Eu3+和体相Y2O2S∶Eu3+。其中硫氧化钇纳米粒子的制备是以水热法合成的Y(OH)3为前驱体,随后在激活剂和硫的共同作用下焙烧得到的。结果表明,所得Y2O2S∶Eu3+为单一纯相纳米粒子,粒径分布集中,大小约80nm,而前驱体Y(OH)3为纳米棒状,形貌上的这一巨大变化是由激活剂和硫粉在高温煅烧过程所形成的熔融物的腐蚀作用造成的。荧光光谱分析表明,Eu3+能有效地掺入硫氧化钇基质中,并具有良好的发光性能。此外,还探讨了纳米粒子的形成机理。  相似文献   

6.
Development of effective and reproducible approaches for preparing large amount of uniformly sized or narrowly size-distributed inorganic nanocrystals has remained as a great challenge in materials chemistry research in the past decade. Based upon Xiang and coworkers, work[1], in this paper we present a simple and effective approach directly utilizing solid-state double decomposition reactions at room temperature to produce nano-particles of CdS, ZnS and CaCO3 in the size range of 3-20 nm measured with x-ray diffraction. Transmission electron microscope (TEM) images of these nano-crystals confirm the existence of the aggregated "islands" of nano-crystals as the main body of the samples and the partially dispersed nano-particles in some areas. The processes of morphological variation and self-assembly of CdS nano-particles under electron beam bombardment are discussed as well.  相似文献   

7.
以巯基乙酸为稳定剂,通过控制反应温度、反应时间及pH值,在水相中合成了稳定的受激发出紫光、蓝光、绿光、黄光和红光的CdS量子点;通过紫外可见吸收光谱、荧光光谱和X射线衍射谱(XRD)对产物的光学性能和晶体结构进行了表征,结果表明所合成的CdS量子点分散性较好,量子产率为8%,为立方晶型,粒径约1 nm;利用荧光倒置显微镜观察了量子点在洋葱内表皮细胞膜上聚集及受激发射荧光行为,实现细胞膜初步标记.  相似文献   

8.
Electronic structure of Mg9O9 and Mg9O8 clusters modeling nano-crystalline powders of magnesium oxide has been analyzed within the frames of the density functional theory (DFT). In the framework of time-dependent DFT method (TD-DFT), the relationship between the surface and bulk properties of nano-crystals is analyzed based on variations in the density of electronic states (DOS) and changes of electronic spectra. The spectroscopy of spatial defects like low-coordinated oxygen ions and of surface point defects like F+- and F-centers is investigated. Optical properties of the nano-sized crystalline magnesium oxide are characterized by a spectrum of absorption bands in the range of 1-5 eV. Point defects such as F-centers absorb light in the range of 1.2-1.5 eV. Spatial defects OLC in nano-crystals generate absorption bands in the range of 2.5-5.0 eV. According to calculations, there is no direct relation between coordination numbers of surface ions and excitation energies. Theoretical excitation energies are compared with experimental optical properties of the F+- and F-centers.  相似文献   

9.
Eu3+ doped transparent glass ceramics embedding SnO2 nano-crystals were prepared by melt quenching and subsequent heating. Site selective excitation experiments revealed that some Eu3+ ions were incorporated in the SnO2 lattices by substituting Sn4+ ions, whereas the rest located in the oxide glassy matrix. Interestingly, it is found that the Eu3+ ions residing in the SnO2 lattices exhibited much longer luminescent decay lifetime than those in the glassy matrix. Measurements on the photoluminescence excitation and photoluminescence spectra demonstrated the occurrence of energy transfer from the SnO2 nano-crystals to the Eu3+ ions. The influences of Eu3+ content, and furthermore, their location on the energy transfer process were discussed.  相似文献   

10.
Transparent BaF2-SiO2 glass ceramics doped with different content of Er3+ were prepared by sol-gel method. The microstructural evolution of the samples was studied with X-ray diffraction (XRD), transmission electron microscope (TEM), absorption and infrared spectra (IR). BaF2 nano-crystals with 2-15 nm in size, depending on the crystallization temperature, distributed homogeneously among the amorphous silica matrix. The BaF2 lattice parameters decreased with the increasing of Er3+ doping, indicating the incorporation of Er3+ into nano-crystals, which was further confirmed by energy dispersive X-ray spectroscopy (EDS) and absorption spectra analysis. The upconversion emissions of Er3+ emerged under the excitation at 980 nm for glass ceramic heat-treated at 800 °C.  相似文献   

11.
吴友吉  李涛  金盈  王芬华 《合成化学》2016,24(12):1075-1078
以纳米氧化锡为添加粒子,与偕胺肟化处理后的聚丙烯腈纤维反应,制得纳米氧化锡/偕胺肟复合纤维(1),其结构及形貌经XRD, SEM和EDX表征。并研究了1对大肠杆菌和金黄色葡萄球菌的抑菌性能。结果表明:在纤维表面生成了四方晶系的纳米氧化锡,1对受试菌种具有良好的抑菌性能。  相似文献   

12.
In this paper, the spectroscopic properties of Nd(3+) doped transparent oxyfluoride glass ceramics containing LaF(3) nano-crystals were systematically studied. The formation and distribution of LaF(3) nano-crystals in the glass matrix were investigated by X-ray diffraction (XRD) and transmission electron microscopy (TEM). Based on Judd-Ofelt theory, the intensity parameters Omega(t) (t=2, 4, 6), spontaneous emission probability, radiative lifetime, radiative quantum efficiency, width of the emission line and stimulated emission cross-section of Nd(3+) were evaluated. Particularly, the effect of Nd(3+) doping level on them was discussed. With the increase of Nd(3+) concentration in the glass ceramic, the experimental luminescence lifetime, radiative quantum efficiency and stimulated emission cross-section vary from 353.4 micros, 78.3% and 1.86 x 10(-20)cm(2) to 214.7 micros, 39.9% and 1.52 x 10(-20)cm(2), respectively. The comparative study of Nd(3+) spectroscopic parameters in different hosts suggests that the investigated glass ceramic system is potentially applicable as laser materials for 1.06 microm emission.  相似文献   

13.
High yield of nickel ferrite nano-octahedra with size distribution from 40 to 90 nm were synthesized through a simple hydrothermal method. The formation of faceted octahedra enclosed by {111} planes implies the much faster growth rate along 〈100〉 over 〈111〉 for face-centered cubic phase during hydrothermal process. Magnetic measurements indicated that the sample is soft-magnetic materials with much lower coercivity and much higher saturation magnetization compared to the nickel ferrite nano-crystals with similar size distribution but irregular shapes reported earlier.  相似文献   

14.
<正>Upconversion(UC)phosphor Tm~(3+)doped YF_3 nano-crystals were prepared by hydrothermal method under different conditions and characterized by Field Transmission electron microscopy(TEM),Scanning electron microscopy(SEM)and X-ray diffraction(XRD).Their UC luminescence properties were studied by fluorescence spectrophotometer with 980 nm diode laser excitation,and impact of different grain sizes and morphology on the UC luminescence intensity was discussed.The fluorescence decay lifetime was calculated by Multi-exponential function fitting method.Results show that UC emission intensity was enhanced with the reduction of grain size,and the decay lifetime is 0.60 us.  相似文献   

15.
将实验室合成的聚苯乙烯乳胶微球(PS)加入制备方钠石(SOD)沸石的前驱体凝胶中,在45℃条件下制得干凝胶,随后采用"蒸汽相转化"法制备了大块状SOD沸石材料。对影响多级SOD沸石形成因素进行了详细讨论。采用X射线衍射(XRD)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、N_2吸附-脱附和压汞技术等表征手段对制备的材料进行了详细表征。结果表明通过"蒸汽相转化"法制备的大块状SOD沸石由球状多晶聚集体构成,这些球状多晶聚集体又是由粒径为50~100 nm的初级纳米晶粒组成,在初级纳米晶粒上和纳米晶粒之间形成了2~50 nm介孔结构以及由脱除PS微球形成的50~300 nm的大孔结构。  相似文献   

16.
将实验室合成的聚苯乙烯乳胶微球(PS)加入制备方钠石(SOD)沸石的前驱体凝胶中,在45℃条件下制得干凝胶,随后采用“蒸汽相转化”法制备了大块状SOD沸石材料。对影响多级SOD沸石形成因素进行了详细讨论。采用X射线衍射(XRD)、扫描电子显微镜(SEM)、透射电子显微镜(TEM)、N2吸附-脱附和压汞技术等表征手段对制备的材料进行了详细表征。结果表明通过“蒸汽相转化”法制备的大块状SOD沸石由球状多晶聚集体构成,这些球状多晶聚集体又是由粒径为50~100 nm的初级纳米晶粒组成,在初级纳米晶粒上和纳米晶粒之间形成了2~50 nm介孔结构以及由脱除PS微球形成的50~300 nm的大孔结构。  相似文献   

17.
半导体纳米晶具有独特的量子限域效应以及新颖的尺寸和形貌依赖特性,已被证实是在低成本高性能光伏器件、光致及电致发光二极管、生物成像、光催化等领域非常具有潜力的新型材料.其中,II-VI族与I-III-VI族半导体纳米晶由于其优异的性能在过去的数十年中引起了广泛的关注.过去数十年对于II-VI族半导体纳米晶的研究已经十分成熟,然而几乎所有的传统II-VI族半导体纳米晶都含有对环境有害的元素,对人体和环境造成不可逆转的伤害,从而限制了II-VI族半导体纳米晶的进一步应用.与二元II-VI族纳米晶相比,大部分三元I-III-VI族纳米晶不含镉和铅等重金属元素,因而具有低毒性的特点,并且其带隙窄、吸光收系数大、斯托克斯位移大、自吸收小以及发光波长在近红外区,所以有望使其成为新一代荧光纳米晶材料.例如,CuInS_2的带隙为1.53 eV,与太阳光谱匹配且其吸光系数较大,在10.5cm.~1左右,从而使其成为制备太阳能电池的一种优秀材料.另一方面,I-III-VI族纳米晶在可见光和近红外范围内呈现与尺寸相关的发光,它们的荧光量子产率在包覆ZnS壳后可超过50%,因而在照明,显示和生物成像领域具广泛应用的潜力.水溶性的I-III-VI族量子点粒径尺寸可以小于10 nm,可以减小纳米颗粒通过肾清除的淘汰率,并且具有高荧光性能和耐光性的特点,因此成为进行生物成像工作的优秀材料.与此同时,I-III-VI族纳米晶在光催化领域也展现了巨大的发展前景.本综述主要关注I-III-VI族纳米晶的合成,性质及应用.首先,我们概述了不同的化学合成方法,并列举讨论了一些经典的工作,根据纳米晶的种类分类统计了主要合成方法、形貌及尺寸.第二部分,我们讨论了它们的光物理和电子特性,解释了纳米晶的"donor-acceptor pair"(DAP)结合机理,概述了I-III-VI族纳米晶的磁光现象.接下来,我们概述了I-III-VI族纳米晶主要的应用领域,着重总结了在太阳能电池领域、半导体发光二极管领域、生物成像领域以及光催化制氢领域的研究进展.最后,我们会讨论半导体纳米晶的应用前景,以及它的机遇和挑战.  相似文献   

18.
In this paper, a cellulase pretreatment was studied prior to the acid hydrolysis to decrease the total acid usage during the cellulose nano-crystals (CNC) preparation from a bleached softwood kraft pulp. Cellulase pretreatment facilitates the subsequent acid hydrolysis to produce CNC with similar quality to that of the control, but at a lower sulfuric acid concentration. The underline mechanism is that cellulase pretreatment led to the formation of more carbonyl groups which can be oxidized into carboxyl groups in the subsequent acid hydrolysis, furthermore, more hydroxyl groups are exposed, thus esterification into sulfonic groups can be enhanced. The results showed that with a cellulase dosage of 4.8 u/g (based on dry pulp) in the pretreatment stage, the sulfuric acid concentration can be decreased from 64 to 40 wt% without compromising the quality of resulting CNC particles. Other results from charge properties, Fourier transform infrared spectroscopy (FT-IR) and transmission electron microscopy (TEM) analyses also supported the conclusions.  相似文献   

19.
The structural and thermal properties of polyhydroxybutyrate (PHB) gels in dimethylformamide (DMF) are presented and discussed. The dilute and semi-dilute mixed PHB/DMF system undergoes a phase separation on cooling at a temperature Tgel, producing a gel in which the crystalline fraction is of the order of 50-60% and the diffraction pattern is that of disperse nano-crystals, with the same unit cell of the pure crystalline PHB. Upon heating, two melting peaks are normally observed at Tm1 and Tm2 (always higher than Tgel). Shapes of the peaks, temperatures and enthalpies of melting depend slightly on scanning rate on heating but on the procedure of gel preparation. Reproducibility and reversibility have always been found with repeated thermal cycles. A thermodynamic phase diagram is therefore constructed and discussed, although the morphology of the system may be subject to the experimental conditions under which the gel is prepared.  相似文献   

20.
高温高压下氧化锌纳米晶的晶粒演化动力学   总被引:3,自引:0,他引:3  
邵光杰  秦秀娟  刘日平  王文魁 《化学学报》2006,64(16):1649-1653
用GS-1B型六面顶压机研究了ZnO纳米晶高温高压下的晶粒演化动力学, 用MDI/JADE5 X射线衍射仪(Cu靶)和XL30S-FEG场发射扫描电子显微镜对高压样品的相组成、晶粒尺寸及微观形貌进行了表征. 实验发现300 ℃(包括300 ℃)以下, ZnO纳米材料中晶粒生长速率随着压力的升高先增大后减小, 1~3 GPa烧结体晶粒尺寸随着压力的升高而增大, 4~6 GPa烧结体晶粒尺寸随着压力的升高而减小. 利用高压下晶粒生长速率方程求出1~3 GPa, 4~6 GPa的激活体积分别为-5.82, 9.66 cm3/mol. 400 ℃(包括400 ℃)以上, 1~6 GPa烧结体的晶粒尺寸随着压力的升高而不断增大.  相似文献   

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