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采用反胶束法合成镱铥共掺杂的氟化镧纳米粒子.这种反胶束是由微乳液作为合成媒介,这些分散的纳米粒子在化学成分、尺寸分布上是可控的.产物形貌经场发射扫描电镜和透射电镜表征.固态样品分散在乙醇中,在未经超声处理时,样品表现为玉米棒样的聚集.棒的平均直径和长度分别为110,575nm.我们认为这种大量纳米粒子聚集成良好超结构是由于溶剂挥发,分子交叉链接或者表面活性剂分子附着于纳米粒子特殊晶面造成的.当样品经过超声处理后,由于超声振动破坏了上述因素,玉米棒形貌的聚集体转为大量纳米粒子.单个粒子的高分辨电镜显示出该纳米粒子的单晶结构.并且晶面间距约为0.366nm,与纯氟化镧六角相[002]晶面相一致.样品在300℃退火30min后的透射电镜照片显示纳米粒子的平均直径大约为35nm,这与XRD结果相吻合.并且,这些纳米粒子表现出了良好的单分散性,并且在978nm二极管激发下,纳米粒子呈现出亮蓝色上转换发光,这种上转换荧光粉在光电子或生物检测中有潜在的应用前景.  相似文献   

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利用核壳结构实现纳米颗粒的多色上转换发光   总被引:1,自引:1,他引:0       下载免费PDF全文
将多色荧光标记技术应用于生物信息检测可实现快速、实时、同步大规模检测目标生物分子的目的,利用上转换纳米粒子作为多色荧光探针可有效地避免生物组织自荧光对检测信号的影响。本文制备了具有核-壳结构的稀土氟化物纳米粒子,并通过在核与壳不同位置共掺杂不同浓度的敏化离子和发光离子来改变发光离子各发射峰之间的相对强度。利用不同颜色和强度的发射光谱实现了纳米粒子的多色上转换发光。利用透射电子显微镜成像、X射线衍射分析、发光光谱等测量手段对多色上转换发光纳米粒子进行了形貌、结构和上转换发光性质的表征。实验结果表明,具有核-壳结构的纳米粒子尺寸小于30 nm,呈球形。在980 nm红外光激发下,纳米粒子呈现从红色到蓝紫色的颜色可变的上转换发光。  相似文献   

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纳米NaY1-x-yF4:Yby3+, Tmx3+材料的上转换光学特性   总被引:1,自引:1,他引:0  
用水热法合成了NaY1-x-yF4:Yby3+,Tmx3+上转换纳米粒子材料。实验发现,样品的粒径多数在100nm以内;当加热温度180℃、反应时间120min、稀土离子Tm3+的摩尔分数为0.04%时,所制备的纳米材料在980nm半导体激光激发下,其主要上转换发光的辐射峰值位于476.54nm处。  相似文献   

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The behavior of iron nanoparticles is heavily influenced by their highly reactive surfaces. A better understanding of organic ligand/particle interactions must be achieved in order to synthesize iron nanoparticles with magnetic saturations (σ sat) equivalent to bulk iron. Even when synthesized using careful, air‐free chemistry techniques and ligands more weakly interacting than those often reported in the literature, the magnetic saturation of iron nanoparticles generally only approaches, but not equals, the magnetic saturation of bulk iron. Here, iron nanoparticles are synthesized using Schlenk line chemistry methods and two different weakly interacting ligands: 2,4‐pentanedione and hexaethylene glycol monododecylether. These particles have saturation magnetizations slightly lower than bulk iron, which is believed to be caused by interactions between the passivating ligands and the surface of the nanoparticles. Using X‐ray absorption fine structure studies, it is shown that oxidized species of iron exist at the nanoparticles’ surface and can be attributed to iron/ligand interaction. The percentage of oxidized species scales with the surface to volume ratio of the nanoparticles, and therefore appears limited to the nanoparticle surface. X‐ray absorption fine structure analysis also shows that the nanoparticles have an expanded crystalline lattice, which can further impact their magnetic properties.  相似文献   

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The Er3+ codoped with CdS nanoparticles in sol-gel glass with an average particle size of about 10 nm have been synthesized by sol-gel method. The green and red up-conversion emissions centered at about 534, 560 and 680 nm, corresponding to the 2H11/24I15/2, 4S3/24I15/2 and 4F9/24I15/2 transitions of Er3+, respectively; were detected by a 800 nm excitation. The two-photon absorption process is involved in the green and red up-conversion emissions.  相似文献   

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利用温和的溶剂热方法合成了具有上转换发光性能的Yb3+-Tm3+和Yb3+-Er3+共掺的纳米NaYGdF4。在该体系中,通过调节Gd3+在基质中的掺杂量可以有效地控制产物的相变、尺寸以及上转换荧光性能。XRD和TEM分析结果表明,Gd3+的掺入在促进NaYF4纳米颗粒由立方相到六方相转变的同时有助于减小其尺寸。上转换光谱研究表明,在Yb3+-Tm3+和Yb3+-Er3+共掺体系中,可通过优化Gd3+的掺杂量来有效提高产物的上转换荧光强度。同时,通过研究Tm3+和Er3+在不同可见光波段的发光强度与泵浦功率的关系探讨了上转换发光的机制。  相似文献   

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当用582.6nm的黄色激激发Nd^3+:LaCl的^2G7/2+^4G5/2能级时,观察到了^4D3/2和^2G9/2能级的兰光和紫外发射。研究表明,^2D3/2上转换的机理是能量传递和激发态吸收而^2G9/2则是由于^4G5/2+^G5/2→^2G9/2+^F7/2交叉驰豫过程。通过对12K下^4D3/2→^4I11/2荧光衰减曲线的分析, 得到 能量传递几率为wt1=1468s^-1。测量和讨论了Nd^3+:LaCl3和NdCl3主要发光能级室温和12K下的寿命。  相似文献   

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Yu  Dezhong  Zha  Zhonghui  Tang  Sheng  Qiu  Yuan  Liu  Dong 《Journal of fluorescence》2022,32(4):1289-1297
Journal of Fluorescence - Upconversion nanoparticles (UCNPs) have achieved considerable success in protein sensing in vitro. And aptamer is one of the most frequently used biomolecules to modify...  相似文献   

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CaTiO3:Er3+ (5%) nanocrystals were obtained by sol–gel method under acidic conditions. The sizes of nanocrystals were 40 nm. Strong green anti-Stokes emission was observed after excitation of the 4I9/2 and 4I11/2 level. The emission is due to excited state absorption (ESA) and energy transfer upconversion (ETU).  相似文献   

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