Type-tunable amplified spontaneous emission from core-seeded CdSe/CdS nanorods controlled by exciton-exciton interaction

Cataloged from PDF version of article.Type-tunable optical gain performance of core-seeded CdSe/CdS nanorods is studied via two-photon optical pumping. Controlling the exciton-exciton interaction by varying the core and shell size, blue-shifted and red-shifted modes of amplified spontaneous emission are systematically demonstrated and their type attributions are verified by time-resolved emission kinetics

Observation of Biexcitons in Nanocrystal Solids in the Presence of Photocharging

Cataloged from PDF version of article.T In nanocrystal quantum dots (NQDs), generating multiexcitons offers an enabling tool for enhancing NQD-based devices. However, the photocharging effect makes understanding multiexciton kinetics in NQD solids fundamentally challenging, which is critically important for solid-state devices. To date, this lack of understanding and the spectral temporal aspects of the multiexciton recombination still remain unresolved in solid NQD ensembles, which is mainly due to the confusion with recombination of carriers in charged NQDs. In this work, we reveal the spectral temporal behavior of biexcitons (BXs) in the presence of photocharging using near-unity quantum yield CdSe/CdS NQDs exhibiting substantial suppression of Auger recombination. Here, recombinations of biexcitons and single excitons (Xs) are successfully resolved in the presence of trions in the ensemble measurements of time-correlated single-photon counting at variable excitation intensities and varying emission wavelengths. The spectral behaviors of BXs and Xs are obtained for three NQD samples with different core sizes, revealing the strength tunability of the X X interaction energy in these NQDs. The extraction of spectrally resolved X, BX, and trion kinetics, which are otherwise spectrally unresolved, is enabled by our approach introducing integrated time-resolved fluorescence. The results are further experimentally verified by cross-checking excitation intensity and exposure time dependencies as well as the temporal evolutions of the photoluminescence spectra, all of which prove to be consistent. The BX and X energies are also confirmed by theoretical calculations. These findings fill an important gap in understanding the spectral dynamics of multiexcitons in such NQD solids under the influence of photocharging effects, paving the way to engineering of multiexciton kinetics in nanocrystal optoelectronics, including NQD-based lasing, photovoltaics, and photodetection

Colloidal Nanoplatelet/Conducting Polymer Hybrids: Excitonic and Material Properties

Here we present the first account of conductive polymer/colloidal nanoplatelet hybrids. For this, we developed DEH-PPV-based polymers with two different anchor groups (sulfide and amine) acting as surfactants for CdSe nanoplatelets, which are atomically flat semiconductor nanocrystals. Hybridization of the polymers with the nanoplatelets in the solution phase was observed to cause strong photoluminescence quenching in both materials. Through steady-state photoluminescence and excitation spectrum measurements, photoluminescence quenching was shown to result from dominant exciton dissociation through charge transfer at the polymer/nanoplatelet interfaces that possess a staggered (i.e., type II) band alignment. Importantly, we found out that sulfide-based anchors enable a stronger emission quenching than amine-based ones, suggesting that the sulfide anchors exhibit more efficient binding to the nanoplatelet surfaces. Also, shorter surfactants were found to be more effective for exciton dissociation as compared to the longer ones. In addition, we show that nanoplatelets are homogeneously distributed in the hybrid films owing to the functional polymers. These nanocomposites can be used as building blocks for hybrid optoelectronic devices, such as solar cells. © 2016 American Chemical Society

Type-II Colloidal Quantum Wells: CdSe/CdTe Core/Crown Heteronanoplatelets

Solution-processed quantum wells, also known as colloidal nanoplatelets (NPLs), are emerging as promising materials for colloidal optoelectronics. In this work, we report the synthesis and characterization of CdSe/CdTe core/crown NPLs exhibiting a Type-II electronic structure and Type-II specific optical properties. Here, based on a core-seeded approach, the CdSe/CdTe core/crown NPLs were synthesized with well-controlled CdTe crown coatings. Uniform and epitaxial growth of CdTe crown region was verified by using structural characterization techniques including transmission electron microscopy (TEM) with quantitative EDX analysis and X-ray diffraction (XRD). Also the optical properties were systematically studied in these Type-II NPLs that reveal strongly red-shifted photoluminescence (up to similar to 150 nm) along with 2 orders of magnitude longer fluorescence lifetimes (up to 190 ns) compared to the Type-I NPLs owing to spatially indirect excitons at the Type-II interface between the CdSe core and the CdTe crown regions. Photoluminescence excitation spectroscopy confirms that this strongly red-shifted emission actually arises from the CdSe/CdTe NPLs. In addition, temperature-dependent time-resolved fluorescence spectroscopy was performed to reveal the temperature-dependent fluorescence decay kinetics of the Type-II NPLs exhibiting interesting behavior. Also, water-soluble Type-II NPLs were achieved via ligand exchange of the CdSe/CdTe core/crown NPLs by using 3-mercaptopropionic acid (MPA), which allows for enhanced charge extraction efficiency owing to their shorter chain length and enables high quality film formation by layer-by-layer (LBL) assembly. With all of these appealing properties, the CdSe/CdTe core/crown heterostructures having Type-II electronic structure presented here are highly promising for light-harvesting applications

Level of residual monomer released from orthodontic acrylic materials

Objective: To quantify, with high-pressure liquid chromatography (HPLC), the amount of residual monomer leached from different orthodontic acrylic materials prepared with two different manipulation methods.Materials and Methods: Eighty cylindrical specimens (5 x 25 mm) were divided into eight groups (n = 10). The specimens were prepared with four acrylic materials Orthocryl Neon Blue (Dentaurum), Orthocryl EQ (Dentaurum), Orthoplast (Vertex), and 0-80 (Imicryl) and with two different manipulation methods: doughing and spray-on. HPLC measurements were made at intervals of 2 hours, 6 hours, 1 day, 1 week, and 3 months. One-way analysis of variance (ANOVA) and Tukey's honestly significant difference multiple-comparison test were used to assess the amount of monomer eluted from the various groups. To assess the differences within each group over the various periods, repeated-measures ANOVA and paired t-tests were used.Results: Statistically significant differences were found within the groups in the amount of residual monomer in the specimens at different time intervals (P < .001). HPLC showed statistically significant differences among the groups (P < .05) in the amount of eluted monomer. Evaluation of the manipulation techniques showed that the monomer release rate was higher in the specimens prepared with the doughing method. When the four acrylic materials were compared, the specimens made from Orthoplast (Vertex) showed the highest rate of monomer release with both manipulation techniques.Conclusion: The spray-on method can be recommended to clinicians for the preparation of orthodontic appliances

Circulating testosterone regulates the local GnRH-II expression in peripheral lymphocytes: An in vivo interaction in patients with idiopathic hypogonadotrophic hypogonadism (IHH).

Sensor networks are often deployed with the purpose of providing data to large-scale information management and GIS systems, or to collect measurements for specific scientific experiments. The benefits of such use are clear and widely accepted. The reuse of observations in low-cost, lightweight, web applications and mashups is a further compelling use case for sensor networks, but requires provision of data through simple mechanisms, readily accessible, that are quick to develop with. To enable the latter while maintaining support for larger applications and, to increase information utility, links to and from other datasets, we propose a domain-driven approach that embodies REST and Linked Data principles using a common semantic framework that underpins a separation of concerns between domain models, sensor observation infrastructure, and Application Programming Interfaces (APIs) while maintaining information consistency. We describe a reusable, reconfigurable, web service that realises this design and can be deployed to provide access to multiple sources of sensor information, including databases and streaming data, with flexible semantic configuration of the API and domain mapping