Reprecipitation Methods Research Articles

CaCl2 doping effect on optical and structural properties of halide perovskites under ligand assisted reprecipitation synthesis

The high potential of metal halide perovskite (MHP) nanocrystals with the general formula CsPbX3 (X = Cl, Br, and I) has led to the development of easy and cost-effective methods on a daily basis. The room temperature (RT) and open atmosphere ligand-assisted reprecipitation (LARP) methods were utilized to synthesize CsPbBr3 and CsPbBr2I nanocrystals (NCs). CaCl2 was used as a dopant in four different concentrations (0.25, 0.5, 0.75, and 1 % molar) to optimize the optical and electrical properties and to enhance the stability of NCs. The most optimal results were observed with 0.25 % doping for CsPbBr2I and 0.75 % doping for CsPbBr3. XRD and FE-SEM analyses revealed a cubic crystal structure for the synthesized nanocrystals. Dynamic light scattering (DLS) analysis indicated an average size of was 35–70 nm. The introduction of Ca2+ impurity, resulted in increased sizes for 0.75 % doped CsPbBr3 NCs; and increased intensity for 0.25 % doped CsPbBr2I NCs. Optical studies, including UV–vis, Fourier Transform Infrared (FTIR), and photoluminescence spectroscopies were conducted. The bandgap of CsPbBr2I and CsPbBr3 was estimated at 2.60 and 2.75 eV, respectively. The FTIR spectra suggested the effective involvement of the ligand agents oleic acid (OA) and oleylamine (OLA) in synthesis of metal halide perovskite nanocrystals. Photoluminescence spectroscopy demonstrated that the photoluminescence intensity of CsPbBr2I and CsPbBr3 varied with impurity doping, indicating an enhancement of semiconductor electronic properties under Ca2+ doping.

Enhanced photoluminescence emission intensity and stability of deep blue-emissive (Et3NH)PbBr3 perovskite nanocrystals by using metal-organic frameworks

The primary obstacle faced by researchers in the field of luminescent metal-halide perovskites is their inherent instability, prompting a shift in focus towards enhancing the stability of perovskite nanocrystals (PNCs). One of the promising approaches to address this challenge involves the utilization of metal-organic frameworks (MOFs) to fabricate PNCs@MOF composites. The present study reports a facile and low-cost colloidal strategy to prepare (Et3NH)PbBr3 PNCs followed by their encapsulation within UiO-67 to enhance their photoluminescence (PL) emission stability. The PNCs and modified UiO-67 were prepared separately via simple and efficient ligand-assisted reprecipitation (LARP) and hydrothermal methods, respectively. After modification of the UiO-67, the pore sizes experienced a substantial increase from 1.90 to 28.84 nm which significantly facilitated the localization of PNCs within the porous matrix. Under a full survey of experimental conditions, the resulting (Et3NH)PbBr3@UiO-67 composite exhibited a bright deep-blue emission at around 410 nm with an emission quantum yield of 52 %. The emission durability of the fabricated PNCs@MOF composites was assessed against temperature and long-time of storage, confirming the superior advantages of MOF even at elevated temperatures of up to 100 °C. The stable and luminous deep-blue emission displayed by the PNCs@MOF composites in this investigation, offers a promising advancement in materials development for optoelectronic applications.

Porphyrin-Based Nanomaterials for the Photocatalytic Remediation of Wastewater: Recent Advances and Perspectives

Self-organized, well-defined porphyrin-based nanostructures with controllable sizes and morphologies are in high demand for the photodegradation of hazardous contaminants under sunlight. From this perspective, this review summarizes the development progress in the fabrication of porphyrin-based nanostructures by changing their synthetic strategies and designs. Porphyrin-based nanostructures can be fabricated using several methods, including ionic self-assembly, metal–ligand coordination, reprecipitation, and surfactant-assisted methods. The synthetic utility of porphyrins permits the organization of porphyrin building blocks into nanostructures, which can remarkably improve their light-harvesting properties and photostability. The tunable functionalization and distinctive structures of porphyrin nanomaterials trigger the junction of the charge-transfer mechanism and facilitate the photodegradation of pollutant dyes. Finally, porphyrin nanomaterials or porphyrin/metal nanohybrids are explored to amplify their photocatalytic efficiency.

Influence of arylalkyl amines on the formation of hybrid CsPbBr3 nanocrystals via a modified LARP method.

Perovskite nanocrystals have attracted much attention in the last ten years due to their different applications, especially in the photovoltaic domain and LED performance. In this large family of perovskite nanocrystals, CsPbBr3 nanocrystals are attractive nanomaterials because they are good candidates for obtaining green emissions and exploring new synthesis routes. In this context, controlling the nanometric scale's morphology, particularly the size and monodispersity, is fundamental for exploring their photophysical properties and final applications. Currently, the nanometric size of nanocrystals is ensured by the presence of oleic acid and oleylamine molecules, in using Hot Injection (HI) or ligand-assisted reprecipitation (LARP) methods. If oleic acid plays a fundamental role, oleylamine can be easily substituted by other amino molecules, opening the way for the functionalization of CsPbBr3 nanocrystals and the obtention of new hybrid perovskite nanocrystal families. In this article, we describe the synthesis, by soft chemistry, of a new family of hybrid organic-inorganic CsPbBr3 nanocrystals, functionalized by aryl-alkylamine (AAA) molecules, through the modified LARP method. We highlight the mechanism for cutting submicron crystals into nanocrystals, using aryl-alkylamine molecules like scissors. The impact of these amino molecules on the final nanocrystals leads to different nanocrystal morphologies (nanocubes, nanosheets, or nanorods) and structures (monoclinic, rhombohedral, or tetragonal). In addition, this modified LARP method highlights, under certain experimental conditions, an unexpected formation of PbO ribbons.

A Review of Organic Dye Based Nanoparticles: Preparation, Properties, and Engineering/Technical Applications

Abstract: Organic dye-based nanoparticles (ODNPs) are fabricated with desired morphologies using laser ablation, reprecipitation, ion association, and self-assembly methods. Primitively, this review introduces the theory of the molecular origins of dye aggregation, manifestations of the formations of monomer to J-dimer, H-dimer, and oblique dimer (mixed J and H dimer) in ODNPs. Although, organic dye nanoparticles have better basic properties than their monomer counterparts. These nanoparticles are suitable candidates for many engineering and technical applications. Furthermore, we have discussed OLEDs, optoelectronics, sensing, environmental, light-harvesting antennas, cryptography, and biomedical imaging applications. The conclusion made from the critical review analysis opens up a new horizon for the future development of ODNPs applications.

Fabrication of a GUMBOS-based ratiometric organo nanosensor for selective and sensitive detection of perchlorate ions that works in 100% water

This work intends to develop sensitive and easily applicable ionic liquids (ILs)-based fluorimetric sensors for detecting the explosive perchlorate (ClO4-) anions in the presence of other hazards and interferents. We have designed and developed an IL-compromising pyrene butyrate anion-based fluorophoric group of uniform materials based on organic salts (GUMBOS), PBIL, from sodium pyrene butyrate and trihexyltetradecylphosphonium chloride (P66614Cl) by simple ion exchange mechanism. Using reprecipitation methods, pyrene-based water-suspended nano-GUMBOS, nPBIL, has been fabricated and characterized by numerous analytical methods. The fabricated nano-GUMBOS display bright cyan color photoluminescence due to the excimer-like emission confirmed from the color chromaticity diagram. Interestingly, due to the addition of ClO4- ions, there is a blue shift in the UV–visible absorption spectrum of the nPBIL solution with a simultaneous decrease in Mie-scattering. Consequently, there is a continuous decrease in the excimer-like emission of nPBIL with the synchronized increase in monomeric emission. We can conclude from both UV–visible absorption and emission spectra that the ClO4- ion displaces the anionic pyrene butyrate moiety of our nPBIL due to its high polarizability. The limit of detection (LOD) of the as-fabricated sensor is estimated to be 7.17 nM which is very much lower than the US Environmental Protection Agency (USEPA) predicted permeable level of perchlorate in drinking water (15 μgL−1). An efficient test kit has been fabricated and demonstrated for on-site detection of ClO4- ions in remote areas. This ion exchange-mediated substance release from such nano-GUMBOS systems is a distinctive and innovative way to design and develop efficient sensors for precisely detecting and quantifying ClO4- ions.

Ionic liquids-based organo nano-fluorosensor for fast and selective detection of sarin gas surrogate, diethylchlorophosphate

This work intends to develop a sensitive and easily applicable ionic liquid (IL) based fluorimetric sensor for detecting sarin surrogate, diethylchlorophosphate (DCP) in solution and gas phases, respectively. We have designed and synthesized a pyrene butyrate anion-based IL (PBIL) from the sodium salt of pyrene butyrate and trihexyltetradecylphosphonium chloride (P66614Cl) by a simple ion exchange mechanism. By utilizing reprecipitation methods, PBIL-based nanoparticles, nPBIL, has been fabricated. Various conventional analytical techniques have confirmed the formations of PBIL and nPBIL. The as-prepared nPBIL shows a structured emission band from 300 to 420 nm along with an excimer-like emission range from 420 nm to 600 nm and displays bright cyan color photoluminescence because of the stacking of pyrene moieties in a nanocrystalline fashion. Interestingly, due to the introduction of DCP in the water-suspended nPBIL, there is a slight (6 nm) blue shift in the UV–visible absorption spectra with an immediate reduction in Mie-scattering. Simultaneously, there is a gradual decrease in excimer-like emission with a synchronized increase in monomeric emission with the steady introduction of DCP in the water-suspended solution of nPBIL due to the formation of a phosphorylated product. The limit of detection (LOD) utilizing our as-fabricated organo nanosensor, nPBIL, towards the detection of DCP is estimated to be 7.32 µM and found to be superior to many chemosensors available in the literature. An nPBIL-stained test kit experiment has also been demonstrated as a carriable and visible photonic device for the on-site detection of DCP within the assembly of other analogous harmful analytes. Also, a dip-stick analysis has been performed for selective recognization of DCP vapor. The effectiveness of nPBIL in identifying and quantifying DCP demonstrated its potential for usage as a photonic device for practical sample investigation.

Lead-Free, Luminescent Perovskite Nanocrystals Obtained through Ambient Condition Synthesis.

Heterovalently substituting toxic lead is an increasingly popular design strategy to obtain environmentally sustainable variants of the exciting material class of halide perovskites. Perovskite nanocrystals (NCs) obtained through solution-based methods exhibit exceedingly high optical quality. Unfortunately, most of these synthesis routes still require reaction under inert gas and at very high temperatures. Herein a novel synthesis routine for lead-free double perovskite (LFDP) NCs is presented. An approach based upon the hot injection and ligand-assisted reprecipitation (LARP) methods to achieve a low-temperature and ambient atmosphere-based synthesis for manganese-doped Cs2 NaBiCl6 NCs is presented. Mn incorporation is critical for the otherwise non-emissive material, with a 9:1 Bi:Mn precursor ratio maximizing the bright orange photoluminescence (PL) and quantum yield (QY). Higher synthesis temperatures slightly increase the material's performance, yet NCs synthesized at room temperature are still emissive, highlighting the versatility of the synthetic approach. While the material's indirect bandgap limits its appeal for optoelectronics, this feature could benefit photocatalysis due to longer carrier lifetimes. Moreover, the developed synthesis is facile and can rapidly be adapted to other more viable material compositions and up-scaled to realize applications directly.

Facile low-energy and high-yield synthesis of stable α-CsPbI3 perovskite quantum dots: Decomposition mechanisms and solar cell applications

CsPbI3 perovskite quantum dots (PQDs) are considered promising building blocks for photovoltaic and optoelectronic devices. Although ligand-assisted reprecipitation methods have been developed for low-temperature and open-air synthesis of various PQDs, the resulting CsPbI3 PQDs are easily decomposed during purification with non-solvents. Herein, we report a facile low-energy and high-yield synthetic route to produce stable α-CsPbI3 PQDs, which includes a pre-centrifugation step to eliminate the undesirable residues without using any non-solvent. After pre-centrifugation and separation from the residues, the CsPbI3 PQDs in the supernatant can be safely washed twice with a typical non-solvent. To understand the adverse effects of the residues, the decomposition mechanisms of the PQDs are studied in depth by combinatorial analysis of crystallinity, surface reactions, and desorption energy calculations on the (100), (110), and (111) facets. As a result, unreacted Cs+ ions and oleic acids in the precipitated residues are found to induce desorption of surface constituents and undesired phase transitions. The facile low-energy synthesis can be scaled-up to 1 L of crude solution, facilitating preparation of dense PQD solutions. CsPbI3 PQD-based solar cells fabricated through layer-by-layer coating with the dense solution exhibit a power conversion efficiency of 8.28 %.

Quantum‐Confined Dodecahedron CsPbBr3 Quantum Dots by A Sequential Post‐Treatment Strategy for Efficient Blue PeLEDs

AbstractCsPbBr3 quantum dots (QDs) prepared through traditional hot‐injection and room temperature reprecipitation methods are usually hexahedral (nanoplate/cube) and green‐emitting. These methods severely obstruct the development of blue perovskite‐based light‐emitting diodes (PeLEDs) because the resultant QDs always suffer unachievable morphology regulation. Here, highly efficient blue‐emitting rhombic dodecahedron CsPbBr3 QDs (CsPbBr3 <12> QDs) are obtained by regulating morphological transformation for the first time through a novel and facile sequential post‐treatment strategy. Hydrobromide (‐NH3+) with stronger adsorption energy promotes the morphology transform of QDs from nanoplate to cube by substituting oleylamine in the first step. Then, polar solvent vapor eliminates PbX64− and led to the (112) crystal plane of the cube QDs being exposed, which is effectively stabilized by ‐NH3+ to realize morphology transition from cube to the dodecahedron. Highly efficient 12‐faceted dodecahedrons are endowed with significantly enhanced photoluminescence quantum yield of 89.8% at 476 nm as well as uniform size distribution and mono‐dispersity. The target blue PeLEDs achieve the maximum external quantum efficiency of 6.6% (480 nm) and excellent spectrum stability. This study provides a new strategy to prepare blue‐emitting CsPbBr3 <12> QDs by delicate control toward the growth and polyhedron process of crystal.

Effect of silica encapsulation on the stability and photoluminescence emission of FAPbI3 nanocrystals for white-light-emitting perovskite diodes

The α-FAPbI 3 perovskite nanocrystals exhibit interesting optical properties, which make them attractive for versatile optoelectronic applications; however, the spontaneous phase transformation to the non-perovskite phase (δ-FAPbI 3 ) in humid conditions requires a new strategy to improve the phase stability of the material. We employed 3-Aminopropyl triethoxysilane (APTES)-assisted reprecipitation and sol-gel methods at ambient temperature to prepare stable α-FAPbI 3 nanocrystals embedded in a silica matrix. Transmission electron microscopy (TEM) and X-ray diffraction analysis determined that ultrafine perovskite nanocrystals (11.5 ± 3 nm) were uniformly distributed in a silica matrix. Investigations of the optical properties of the synthesized materials revealed that about 94% of the photoluminescence (PL) emission of silica-encapsulated FAPbI 3 nanocrystals was preserved under humid conditions (60%) after at least a month, while the PL emission of untreated FAPbI 3 was significantly decayed after few days. The thermal analysis also determined that the thermal stability of FAPbI 3 nanocrystals was improved by silica encapsulation. The red-emitting silica-encapsulated FAPbI 3 nanocrystals with a wavelength of 720 nm were used to fabricate white light-emitting diodes (LEDs) in a vertical structure consisting of a blue-chip, PMMA/CsPbBr 3 QDs, and PMMA/FAPbI 3 -SiO 2 QDs. Stable perovskite-based white LEDs with a color gamut of 144% NTSC were fabricated, which was better than many phosphor-based and perovskite-based LEDs. The synthesized composite perovskite nanocrystals could be used for next-generation optoelectronic devices. • Synthesis of silica-encapsulated FAPbI 3 quantum dots at ambient temperature by a combined LARP and sol-gel process. • Minor PL intensity loss in the humidified atmosphere after few months. • WLEDs with a high color gamut of 144% NTSC. • A pure red LED with coordination (0.729, 0.270).

Enhanced Air Stability of Perovskite Quantum Dots by Manganese Passivation

Organic-inorganic perovskite quantum dots (PeQDs) have attracted attention due to their excellent optical properties, e.g., high photoluminescence quantum yields (PLQYs; >70%), a narrow full width at half maximum (FWHM; 25 nm or less), and color tunability adjusted by the halide components in an entire tunability (from 450 nm to 730 nm). On the other hand, PeQD stability against air, humidity, and thermal conditions has still not been enough, which disturbs their application. To overcome these issues, with just a focus on the air stability, Mn2+ ion passivated perovskite quantum dots (Mn/MAPbBr3 QDs) were prepared. Mn2+ could be expected to contract the passivating layer against the air condition because the Mn2+ ion was changed to the oxidized Mn on PeQDs under the air conditions. In this research, Mn/MAPbBr3 QDs were successfully prepared by ligand-assisted reprecipitation (LARP) methods. Surprisingly, Mn/MAPbBr3 QD films showed more than double PLQY stability over 4 months compared with pure MAPbBr3 ones against the air, which suggested that oxidized Mn worked as a passivating layer. Improving the PeQD stability is significantly critical for their application.

Seed‐Mediated Synthesis of Colloidal 2D Halide Perovskite Nanoplatelets

AbstractColloidal synthesis of two‐dimensional lead halide perovskite nanoplatelets (2D LHP NPLs) with a general formula of L2[APbX3]n−1PbX4 has been widely performed by using hot‐injection or ligand assisted reprecipitation methods. Herein, for the first time, we report on seed‐mediated synthesis of two and three monolayers (n=2, 3) lead halide perovskite nanoplatelets without using A‐site cation halide salt (AX; A=Cesium, methylammonium, formamidinium and, X=Cl, Br, I) and long chain alkylammonium halide salts (LX; L=oleylammonium, octylammonium, butylammonium and, X=Cl, Br, I). The nanocrystal seeds have been prepared by reacting lead (II) halide salt and coordinating ligands in a nonpolar solvent and then they have been reacted with cesium oleate, formamidinium oleate or methylamine. Our facile synthesis route enabling further understanding of the growth dynamics of LHP NPLs provides highly stable, monodisperse NPLs with very narrow absorption and emission linewidths (min. 68 meV), and high PLQY (max. 37.6%).

Indocyanine Green-Based Theranostic Nanoplatform for NIR Fluorescence Image-Guided Chemo/Photothermal Therapy of Cervical Cancer

PurposeIndocyanine green (ICG) is a favorable fluorescence nanoprobe for its strong NIR-I fluorescence emission and good photothermal capabilities. However, the stability and tumor targeting ability of ICG is poor, which limits its further applications. To further improve the photothermal and therapeutic efficiency of ICG, bovine serum albumin (BSA) was utilized to encapsulate the ICG and the chemotherapeutic drug doxorubicin (DOX) was loaded to form the BSA@ICG-DOX theranostic nanoplatform.MethodsIn this study, ICG-loaded BSA nanoparticles (NPs) and the BSA@ICG-DOX NPs were fabricated using reprecipitation methods. Next, the tumour inhibition ability and biocompatibility of the NPs were evaluated. A subcutaneous xenografted nude mice model was established and imaging guided synergetic therapy was performed with the assistance of BSA@ICG-DOX NPs under 808 nm laser irradiation.ResultsThe BSA@ICG NPs exhibited strong NIR-I fluorescence emission, excellent photothermal properties, biocompatibility, and tumor targeting ability. To further improve the therapeutic efficiency, the chemotherapeutic drug doxorubicin (DOX) was loaded into the BSA@ICG NPs to form the BSA@ICG-DOX theranostic nanoplatform. The BSA@ICG-DOX NPs were spherical with an average size of ~194.7 nm. The NPs had high encapsulation efficiency (DOX: 19.96% and ICG: 60.57%), and drug loading content (DOX: 0.95% and ICG: 3.03%). Next, excellent NIR-I fluorescence and low toxicity of the BSA@ICG-DOX NPs were verified. Targeted NIR-I fluorescence images were obtained after intravenous injection of the NPs into the subcutaneous cervical tumors of the mice.ConclusionTo improve the anti-tumor efficiency of the ICG@BSA NPs, the chemotherapeutic drug DOX was loaded into the BSA@ICG NPs. The NIR excitation/emission and targeted BSA@ICG-DOX NPs enables high-performance diagnosis and chemo/photothermal therapy of subcutaneous cervical tumors, providing a promising approach for further biomedical applications.

Comparison and evaluation of the quick purification methods of methamphetamine hydrochloride from dimethyl sulfone for spectroscopic identification

Methods to quickly purify methamphetamine hydrochloride from the cutting agent dimethyl sulfone for subsequent identification of confiscated crystalline samples using infrared absorption spectroscopy were compared and evaluated. Although sequential solvation and reprecipitation methods were simple, spectral contamination from dimethyl sulfone was inevitable and might affect the interpretation of the spectra. In addition, methamphetamine hydrochloride and dimethyl sulfone could form a solid solution because of solvation of both crystals into a single solution layer. By contrast, sublimation was an effective method for separation of methamphetamine hydrochloride and dimethyl sulfone. Sublimation combined with infrared absorption spectroscopy enabled rapid identification of crystalline methamphetamine hydrochloride.

Morphology, photophysics and optoelectronics of P3HT nanoparticles and TiO2 nanorods composite

Morphology and photophysics of polymers are critical to the performance of organic optoelectronics. In this work, poly(3-thiophene) (P3HT) nanoparticles were successfully fabricated by the miniemulsion and reprecipitation methods. The P3HT nanoparticles demonstrated uniform distribution with the domain size of [Formula: see text][Formula: see text]40 nm. The photophysics of P3HT nanoparticles was investigated by absorption and steady-state and time-resolved PL spectroscopy. P3HT nanoparticles showed more ordered and longer conjugation length than pristine P3HT. At the same time, P3HT nanoparticles showed aggregate species which are favorable for interchain charge transfer. The organic/inorganic hybrid photodetectors based on P3HT and TiO2 nanorods were fabricated. The superior performance of the photodetector based on P3HT nanoparticle and TiO2 nanorods comes from the efficient charge transfer and large donor/acceptor interface.

Synthesis and Characterization of Porphyrin-Based GUMBOS and NanoGUMBOS as Improved Photosensitizers

Porphyrin-based GUMBOS and nanoGUMBOS were synthesized for potential application as improved photosensitizing materials. In this study, porphyrin dyes [meso-tetra(4-carboxyphenyl)porphine (TCPP) and zinc(II) meso-tetra(4-carboxyphenyl)porphine (Zn-TCPP)] were selected as anions, and trihexyltetradecylphosphonium (P66614) was employed as a cation. The resulting [P66614]4[TCPP] and [P66614]4[Zn-TCPP] GUMBOS (group of uniform materials based on organic salts) provided high photostability and excellent thermal stability for these compounds. NanoGUMBOS, i.e., nanomaterials derived from GUMBOS, were synthesized using reprecipitation and ion association methods. The surface charges of these nanoparticles were tuned from positive to negative through use of an ion association synthetic method without the need for additives or stabilizers. When compared to the parent dyes, nanoGUMBOS exhibited excellent photodynamic properties for potential applications as photosensitizers. Evaluation of the electrochemical propert...

Two‐Photon Imaging of a Cellular Line Using Organic Fluorescent Nanoparticles Synthesized by Laser Ablation

A comparative study of the optical properties of organic fluorescent nanoparticles fabricated by laser ablation (NPs‐LA), reprecipitation (NPs‐RP), and microemulsion (NPs‐ME) methods is presented. These nanoparticles contain a fluorene‐based p‐conjugated molecule (BT2). Distinctive electronic transitions are observed in samples due to the specific way in which the molecule BT2 is assembled in each type of nanoparticles; for instance, transitions involved in absorption and emission spectra of NPs‐LA result in blueshifting with respect to the molecular solution of BT2, whereas redshifting is observed in NPs‐RP and NPs‐ME. Further, the results show that under infrared excitation, the aqueous suspensions of NPs‐LA exhibit the highest fluorescence induced by two‐photon absorption (≈790 GM at 740 nm), as well as the best photostability, compared with aqueous suspensions of NPs‐RP and NPs‐ME. The nanoparticles synthetized by the three aforementioned methods are employed as exogenous agents for the visualization of human cervical cancer cell line (HeLa) using confocal and two‐photon microscopy. Under similar experimental conditions, it is found that microscopy images of the best quality are obtained with NPs‐LA. These results show that laser ablation is a suitable technique for the fabrication of organic fluorescent nanoparticles used as contrast agents for in vitro fluorescence microscopy.

Charge generation and morphology in P3HT:PCBM nanoparticles prepared by mini-emulsion and reprecipitation methods.

Organic semiconductor nanoparticles provide a potentially scalable approach for photovoltaics that can be processed from aqueous media. Particles of poly(3-hexylthiophene) (P3HT):phenyl-C61-butyric acid methyl ester (PCBM) were prepared using two techniques; those produced by a mini-emulsion method contained greater amounts of crystalline P3HT domains with charge generation resembling phase-separated annealed solvent-cast films.

Fluorometric appraisal of HSO4−in aqueous media and daily utilities using organic–inorganic nanohybrids

Receptor 1 based on rhodamine dye was designed and characterized using 1H, 13C NMR and mass spectroscopy like spectroscopic techniques. Re-precipitation methods have been used for developing nano-aggregates of 1 (N1) in aqueous medium, which were further used for preparation of inorganic–organic hybrid nanomaterial (H1) i.e. by coating organic nanoparticles with gold nanoparticles. Changes in the photophysical profile by anion binding of N1 and H1 were evaluated using fluorescence spectroscopy. No selectivity was perceived with nano-aggregates (N1) for any anion. However, the hybrid nanomaterial (H1) selectively recognized HSO4− through enhancement of fluorescence emission intensity in aqueous medium. Thus, the hybrid nanomaterial (H1) has been established for sensing of HSO4− and was considered for various parameters like rapid response, good stability in water and is validated for determination of HSO4− ions in daily use items.