STRONG LUMINESCING CdSe NANOPARTICLES BY SURFACE MODIFICATION WITH CADMIUM (II) HYDROUS OXIDE

2005 ◽  
Vol 19 (15n17) ◽  
pp. 2835-2840 ◽  
Author(s):  
XINGPING ZHOU ◽  
YOSHIO KOBAYASHI ◽  
NORIAKI OHUCHI ◽  
MOTOHIRO TAKETA ◽  
ATSUO KASUYA
Keyword(s):  
Aqueous Solution ◽  
Surface Modification ◽  
Room Temperature ◽  
Rhodamine 6G ◽  
Cdse Nanoparticles ◽  
Hydrous Oxide ◽  
Photoluminescence Quantum Yield ◽  
Photoluminescence Enhancement ◽  
Cubic Structure ◽  
Average Size

CdSe nanoparticles were prepared by simply mixing Na 2 SSeO 3 solution with CdSO 4 solution under [ Cd 2+]/[ Se 2-] ( Cd/Se ) ratio of 1.2 at room temperature. The nanoparticles had an average size of 2.3 nm and showed fairly strong photoluminescence (PL) with a peak at 539 nm. Deposition of cadmium (II) hydrous oxide on the CdSe nanoparticles increased photoluminescence quantum yield from 3.1 to 34.8%, in comparison to Rhodamine 6G aqueous solution. Both of the CdSe nanoparticles and the cadmium (II) hydrous oxide deposited on CdSe nanoparticles were characterized as of cubic structure from XRD data and the electron diffraction (ED) patterns. Also, the reason for the photoluminescence enhancement was simply elucidated.

Size-Selective Synthesis of Ultrasmall Hydrophilic CdSe Nanoparticles in Aqueous Solution at Room Temperature

2012 ◽  
pp. 125-141
Author(s):  
Yeon-Su Park ◽  
Yukihiro Okamoto ◽  
Noritada Kaji ◽  
Manabu Tokeshi ◽  
Yoshinobu Baba
Keyword(s):  
Aqueous Solution ◽  
Room Temperature ◽  
Cdse Nanoparticles ◽  
Selective Synthesis

Synthesis of Monodisperse Fe3O4 Microspheres and Effect of the Precursor Concentration

2011 ◽  
Vol 183-185 ◽  
pp. 2327-2330 ◽  
Author(s):  
De Hui Sun ◽  
De Xin Sun ◽  
Ming Xing Han
Keyword(s):  
Room Temperature ◽  
Size Range ◽  
Precursor Concentration ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
Xrd Pattern ◽  
X Ray ◽  
Magnetic Investigation ◽  
Cubic Structure ◽  
Average Size

In present work, we synthesized monodisperse Fe3O4microsphere using a free-surfactant solvothermal reduction route and investigated effect of the precursor concentration (FeCl3∙6H2O and NaAc) on microsphere sizes under other reaction conditions held constant. The morphologies, structures, and magnetism of the products were characterized by SEM, XRD, FTIR and VSM. The results showed that the Fe3O4 microsphere with a tunable average size range from 120 nm to 300 nm is composed of many Fe3O4collective nanoparticles. Their average diameters increased with increase of precursor FeCl3∙6H2O concentration but decreased with increase of precursor NaAc concentration. The X-ray diffraction (XRD) pattern confirmed that the Fe3O4microspheres belong to cubic structure. Magnetic investigation reveals that the Fe3O4microspheres have higher saturation magnetization and negligible coercivity at room temperature.

scholarly journals Facile Synthesis of Pd-Ir Nanocubes for Biosensing

2021 ◽  
Vol 9 ◽  
Author(s):  
Jiuxing Li ◽  
Yingfu Li
Keyword(s):  
Aqueous Solution ◽  
Energy Barrier ◽  
Homogeneous Nucleation ◽  
Shell Thickness ◽  
Room Temperature ◽  
Low Energy ◽  
Free Access ◽  
Facile Synthesis ◽  
Significant Step ◽  
Cubic Structure

Displaying extremely high peroxidase-like activity and uniform cubic structure enclosed by (100) facets, Pd-Ir nanocubes are an attractive nanomaterial for bioanalysis. However, there exists a great challenge to deposit atomic layers of Ir on the surface of Pd nanocubes due to the relatively low energy barrier of homogeneous nucleation of Ir atoms compared to heterogeneous nucleation. Here, a simple and surfactant-free approach is presented to synthesize Pd-Ir nanocubes with atomic Ir shell thickness in an aqueous solution at room temperature. Biomolecules such as antibodies and nucleic acids have free access to the surface of Pd-Ir nanocubes. Applications of Pd-Ir nanocubes in immunoassays and aptamer-based biosensors are realized, exploiting the excellent peroxidase activity and fluorescence quenching ability of Pd-Ir nanocubes. This work makes a significant step forward towards the practical utility of Pd-Ir nanocubes in bioanalysis.

Preparation of BSA Nanoparticles by Desolvation Technique Using Acetone as Desolvating Agent

2012 ◽  
Vol 5 (1) ◽  
pp. 1643-1647
Author(s):  
Krishna Sailaja A ◽  
Amareshwar P
Keyword(s):  
Aqueous Solution ◽  
Standard Deviation ◽  
Process Parameters ◽  
Self Assembly ◽  
Size Control ◽  
Polymeric Materials ◽  
Preparation Condition ◽  
Assembly Process ◽  
Average Size

In order to see the functionality and toxicity of nanoparticles in various food and drug applications, it is important to establish procedures to prepare nanoparticles of a controlled size. Desolvation is a thermodynamically driven self-assembly process for polymeric materials. In this study, we prepared BSA nanoparticles using the desolvation technique using acetone as desolvating agent. Acetone was added intermittently into 1% BSA solution at different pH under stirring at 700 rpm. Amount of acetone added, intermittent timeline of acetone addition, and pH of solution were considered as process parameters to be optimized. The effect of the process parameters on size of the nanoparticles was studied. The results indicated that the size control of BSA nanoparticles was achieved by adding acetone intermittently. The standard deviation of average size of BSA nanoparticles at each preparation condition was minimized by adding acetone intermittently. The intermittent addition in polymeric aqueous solution can be useful for size control for food or drug applications.  

scholarly journals Practical Synthesis of 2-Iodosobenzoic Acid (IBA) without Contamination by Hazardous 2-Iodoxybenzoic Acid (IBX) under Mild Conditions

Molecules ◽  
2021 ◽  
Vol 26 (7) ◽  
pp. 1897
Author(s):  
Hideyasu China ◽  
Nami Kageyama ◽  
Hotaka Yatabe ◽  
Naoko Takenaga ◽  
Toshifumi Dohi
Keyword(s):  
Aqueous Solution ◽  
Room Temperature ◽  
Practical Method ◽  
Hypervalent Iodine ◽  
Mild Conditions ◽  
Sequential Procedures ◽  
Iodine Compounds ◽  
Practical Synthesis ◽  
Iodosobenzoic Acid ◽  
Lower Temperature

We report a convenient and practical method for the preparation of nonexplosive cyclic hypervalent iodine(III) oxidants as efficient organocatalysts and reagents for various reactions using Oxone® in aqueous solution under mild conditions at room temperature. The thus obtained 2-iodosobenzoic acids (IBAs) could be used as precursors of other cyclic organoiodine(III) derivatives by the solvolytic derivatization of the hydroxy group under mild conditions of 80 °C or lower temperature. These sequential procedures are highly reliable to selectively afford cyclic hypervalent iodine compounds in excellent yields without contamination by hazardous pentavalent iodine(III) compound.

scholarly journals Self-assembly induced luminescence of Eu3+-complexes and application in bioimaging

2021 ◽  
Author(s):  
Ping-Ru Su ◽  
Tao Wang ◽  
Pan-Pan Zhou ◽  
Xiao-Xi Yang ◽  
Xiao-Xia Feng ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Rare Earth ◽  
Luminescence Intensity ◽  
Self Assembly ◽  
Room Temperature ◽  
Molecular Motion ◽  
Proof Of Concept ◽  
Room Temperature Phosphorescence ◽  
New Strategy ◽  
Size Controlled

Abstract Design and engineering of highly efficient emitting materials with assembly-induced luminescence, such as room temperature phosphorescence (RTP) and aggregation-induced emission (AIE), have stimulated extensive efforts. Here, we propose a new strategy to obtain size-controlled Eu3+-complex nanoparticles (Eu-NPs) with self-assembly induced luminescence (SAIL) characteristics without encapsulation or hybridization. Compared with previous RTP or AIE materials, the SAIL phenomena of increased luminescence intensity and lifetime in aqueous solution for the proposed Eu-NPs are due to the combined effect of self-assembly in confining the molecular motion and shielding the water quenching. As a proof of concept, we also show that this system can be further applied in bioimaging, temperature measurement and HClO sensing. The SAIL activity of the rare-earth (RE) system proposed here offers a further step forward on the roadmap for the development of RE light conversion systems and their integration in bioimaging and therapy applications.

Room temperature synthesis of Sn2+ doped highly luminescent CsPbBr3 quantum dots for high CRI white light-emitting diodes

Nanoscale ◽  
2021 ◽  
Author(s):  
Dongdong Yan ◽  
Qionghua Mo ◽  
Shuangyi Zhao ◽  
Wensi Cai ◽  
Zhigang Zang
Keyword(s):  
Quantum Dots ◽  
Quantum Yield ◽  
White Light ◽  
Room Temperature ◽  
Temperature Synthesis ◽  
Light Emitting ◽  
Photoluminescence Quantum Yield ◽  
Hot Injection ◽  
White Light Emitting Diodes ◽  
Cspbbr3 Quantum Dots

With a high photoluminescence quantum yield (PLQY) being able to exceed 90% for those prepared by hot injection method, CsPbBr3 quantum dots (QDs) have attracted intensive attentions for white light-emitting...

scholarly journals Room Temperature Syntheses of ZnO and Their Structures

Symmetry ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 733
Author(s):  
Domenica Donia ◽  
Elvira Maria Bauer ◽  
Mauro Missori ◽  
Ludovica Roselli ◽  
Daniele Cecchetti ◽  
...  
Keyword(s):  
Room Temperature ◽  
Direct Synthesis ◽  
Threshold Value ◽  
Rietveld Analysis ◽  
Synthesis Temperature ◽  
Density Variation ◽  
Controlled Synthesis ◽  
Sem Images ◽  
Aqueous Solvent ◽  
Average Size

ZnO has many technological applications which largely depend on its properties, which can be tuned by controlled synthesis. Ideally, the most convenient ZnO synthesis is carried out at room temperature in an aqueous solvent. However, the correct temperature values are often loosely defined. In the current paper, we performed the synthesis of ZnO in an aqueous solvent by varying the reaction and drying temperatures by 10 °C steps, and we monitored the synthesis products primarily by XRD). We found out that a simple direct synthesis of ZnO, without additional surfactant, pumping, or freezing, required both a reaction (TP) and a drying (TD) temperature of 40 °C. Higher temperatures also afforded ZnO, but lowering any of the TP or TD below the threshold value resulted either in the achievement of Zn(OH)2 or a mixture of Zn(OH)2/ZnO. A more detailed Rietveld analysis of the ZnO samples revealed a density variation of about 4% (5.44 to 5.68 gcm−3) with the synthesis temperature, and an increase of the nanoparticles’ average size, which was also verified by SEM images. The average size of the ZnO synthesized at TP = TD = 40 °C was 42 nm, as estimated by XRD, and 53 ± 10 nm, as estimated by SEM. For higher synthesis temperatures, they vary between 76 nm and 71 nm (XRD estimate) or 65 ± 12 nm and 69 ± 11 nm (SEM estimate) for TP =50 °C, TD = 40 °C, or TP = TD = 60 °C, respectively. At TP = TD = 30 °C, micrometric structures aggregated in foils are obtained, which segregate nanoparticles of ZnO if TD is raised to 40 °C. The optical properties of ZnO obtained by UV-Vis reflectance spectroscopy indicate a red shift of the band gap by ~0.1 eV.

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