Preparation and application of solvent‐modulated self‐doped N–S multicolour fluorescence carbon quantum dots

In this paper, two types of carbon quantum dot (CQDs) were prepared using biocompatible l ‐methionine as the carbon source and urea as the nitrogen source and a one‐step hydrothermal treatment. By changing the reaction solvents (deionized (DI) water and dimethylformamide (DMF)), the maximum emission of the resulting CQDs shifted from blue to red light. Specifically, the emission wavelength of the CQDs moved from 433 nm to 625 nm following embedding of a new functional group (–CONH–) on the surface of the CQDs. Photoluminescence quantum yields of the CQDs with blue and red emission reached 64% and 61%, respectively. The R‐CQDs were used to detect metal ions and a linear relationship was demonstrated between ln(F/F₀) and Fe³⁺ concentration in the range 0–0.5 mmol/L with a detection limit of 0.067 μM. Therefore these R‐CQDs have great potential as fluorescent probes for Fe³⁺ detection. We expect that the excellent water‐soluble, biocompatible and optical properties of the CQDs developed in this work mean that they will be widely used to detect biological cells.     

Fluorescence ‘off–on’ probe for lead (II) detection based on Atractylodes III CQDs and bioimaging

In this work, a type of carbon quantum dots (CQDs) with bright blue emission was readily fabricated through one-step hydrothermal treatment from Atractylodes III. We explored the surface morphology and optical properties of the CQDs using transmission electron microscopy, X-ray diffraction patterns, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy and ultraviolet–visible light spectrophotometry. The obtained CQDs possessed good photoluminescence properties, water solubility, and biocompatibility. The fluorescence quantum yield of these was 3.72%. It was found that the fluorescence intensity of CQDs was quenched by picric acid. After adding lead (II), the fluorescence could be effectively recovered. Therefore, an ‘off–on’ fluorescence probe was designed to detect lead (II) in the range 0–580 μM and the limit of detection was 0.068 μM. In addition, the experiments showed that the CQDs could be successfully used in bioimaging and as a hidden fluorescent ink.     

Europium‐activated rare earth fluoride (LnF3:Eu3+–Ln = La,Gd) nanocrystals prepared by using ionic liquid/NH4F as a fluorine source via hydrothermal synthesis

Lanthanide (Ln) fluorides are considered exceptional luminescent rigid host matrices for various optical active Ln³⁺ ions due to their high refractive index, high chemical stability and low phonon energy, leading to the low probability of non‐radiative decay, which results in higher photoluminescence quantum yield (PLQY) (usually higher than oxide hosts). In this study, Eu³⁺‐activated Ln fluorides (LnF₃:Eu³⁺–Ln = La, Gd) are synthesized by the hydrothermal method using 1‐butyl‐3‐methylimidazolium tertrafluoroborate [BMIBF₄] and NH₄F as fluorine precursors. The synthesized nanocrystals (NCs) are structurally and morphologically characterized, and their optical properties investigated using spectrofluorometry. The X‐ray diffraction (XRD) patterns of Eu³⁺‐substituted and ‐unsubstituted LnF₃ (prepared from a different fluorine source) are indexed based on the hexagonal and orthorhombic crystal structure, respectively. Average crystalline sizes are calculated using the Scherrer equation and it is found that the synthesized NCs have an average crystalline size of 12–35 nm. Transmission electron microscopy (TEM) images reveal that the NCs are well dispersed and nearly ellipsoid, with an average size of ~ 5 nm. Eu³⁺‐activated NCs show characteristic excitation and emission spectra. The emission spectra show both magnetic (⁵D₀–⁷F₁) and electric (⁵D₀–⁷F₂) dipole transition with appropriate CIE color coordinates; however, the intensity of the magnetic dipole transition is high, which is in accordance with local site symmetry. Owing to their unique size and excellent optical properties, the synthesized NCs may have potential application in the fields bio‐imaging and solar concentrators. Copyright © 2016 John Wiley & Sons, Ltd.     

Carbon quantum dots fluorescence quenching for potassium optode construction

Photophysical phenomena associated with carbon nanoparticles in combination with biocompatibility and readily functionalizable properties have attracted significant interest for sensing and imaging applications. A potassium ion optode based on the fluorescence quenching of carbon quantum dots (CQDs) was constructed. The CQDs were synthesized using a microwave method, citric acid and 2,2′‐(ethylene‐dioxy)bis(ethylamine). A quantum yield of 7.1% was calculated for the synthesized CQDs. A linear dynamic range of about one‐order of magnitude with a correlation coefficient of 0.99 was obtained. The optode was applied on real samples and a 0.60–1.60% error range was obtained relative to the ion‐selective electrode.     

Preparation of carbon quantum dots based on starch and their spectral properties

A simple method for the synthesis of water‐soluble carbon quantum dots (CQDs) has been developed based on chemical oxidation of starch. The structures and optical properties of the CQDs were characterized by ultraviolet–visible (UV–Vis) spectroscopy, photoluminescence spectroscopy (PL) and transmission electron microscopy. The CQDs were found to emit bright blue fluorescence and disperse uniformly. The effects of ambient temperature, light and pH on the properties of CQDs were studied. The CQDs exhibited good chemical stability, good photostability and pH sensitivity. Furthermore, the interaction between CQDs and bovine serum albumin (BSA) was investigated. Copyright © 2014 John Wiley & Sons, Ltd.     

Luminescence investigation of a cerium‐doped yttrium vanadate phosphor

Cerium (Ce³⁺)‐doped (1, 3, and 7 mol%) yttrium vanadate phosphors were prepared using a co‐precipitation technique. The structural and optical properties of the synthesized samples were studied using X‐ray diffraction (XRD), Fourier transform infrared spectroscopy, scanning electron microscopy (SEM), high‐resolution transmission electron microscopy (HR‐TEM), optical absorption, and photoluminescence (PL) spectroscopy techniques. The tetragonal structure and the formation of the nanosized crystallites in the YVO₄:Ce phosphor were confirmed using XRD analysis. HR‐TEM morphology showed rod‐like nanoparticles of different sizes. Optical absorption spectra demonstrated strong absorption bands at 268 and 276 nm. PL spectra showed strong peaks at 546, 574, and 691 nm following excitation at 300 nm. The calculated CIE chromaticity coordinates demonstrated that YVO₄:Ce could be used as a novel phosphor for the development of light‐emitting diode lamps.     

Tunable excitation properties of ZnCdS:Mn/ZnS quantum dots for cancer imaging

Water‐soluble ZnS:Mn quantum dots (QDs) were synthesized using a hydrothermal method with 3‐mercaptopropionic acid as stabilizer. The optical properties of ZnS:Mn QDs were thoroughly investigated by tuning the doping concentration of Mn²⁺ and the Zn/S precursor ratio, to obtain an optimal parameter for QDs with excellent fluorescence characteristics. ZnS:Mn QDs excited at only one wavelength, however, which seriously limited their further application. Here, a trace Cd ion was doped into a ZnS host, resulting in QD excitation covering a wide adjustable waveband. Furthermore, when a ZnS shell was coated onto the surface of the ZnCdS:Mn QDs, photoluminescence intensity and stability were further enhanced. After coupling with an anti‐CK 19 antibody, the ZnCdS:Mn/ZnS core/shell QDs were able to function by labeling cancer cells, indicating that they could be considered as a suitable bio‐probe for cells and tissue imaging.     

Blue organic light‐emitting diodes based on fluorene‐bridged quinazoline and quinoxaline derivatives

Two blue emitters based on fluorene‐bridged quinazoline and quinoxaline derivatives were prepared via the Suzuki reaction. Their photoluminescent properties were investigated. Furthermore, theoretical studies on these materials using the density functional theory calculation were conducted. To explore their electroluminescent properties, multilayered organic light‐emitting diodes were fabricated with the following device structure: indium–tin–oxide (180 nm)/4,4′‐bis(N‐(1‐naphthyl)‐N‐phenylamino)biphenyl (50 nm)/blue emitting materials ( 1 and 2 ) (30 nm)/bathophenanthroline (35 nm)/8‐hydroxy‐quinolinato lithium (2 nm)/Al (100 nm). Two devices showed efficient blue emission with the external quantum efficiencies of 1.58% and 1.30%, respectively, at 20 mA/cm², and Commission Internationale dÉclairage coordinates of (0.18, 0.24) and (0.19, 0.27) at 6.0 V. These results suggest that the self‐aggregation properties of emitters would have considerable effects on their photoluminescent and electroluminescent properties.     

Boron and nitrogen co‐doped carbon dots as a sensitive fluorescent probe for the detection of curcumin

In this present study, a fluorescent probe was developed to detect curcumin, which is derived from the rhizomes of the turmeric. We used a simple and economical way to synthesize boron and nitrogen co‐doped carbon dots (BNCDs) by microwave heating. The maximum emission wavelength of the BNCDs was 450 nm at an excitation wavelength of 360 nm. The as‐prepared BNCDs were characterized by multiple analytical techniques such as transmission electron microscopy, X‐ray photoelectron spectroscopy, X‐ray diffraction, and infrared spectroscopy. The synthesized carbon nanoparticles had an average particle diameter of 4.23 nm. The BNCDs exhibited high sensitivity to the detection of curcumin at ambient conditions. The changes of BNCDs fluorescent intensity show a good linear relationship with the curcumin concentrations in the range 0.2–12.5 μM. This proposed method has been successfully applied to detect the curcumin in urine samples with the recoveries of 96.5–105.5%.     

Effect of CaCN2 on the preparation of CaAlSiN3:Eu2+ phosphors

Highly efficient red‐emitting phosphors, CaAlSiN₃:Eu²⁺, were successfully prepared by the solid‐state method using calcium cyanide (CaCN₂) as the single calcium source. The influences of crystallization temperature, crystallization time, calcination mode and compounds ratio on the photoluminescent properties were investigated. The CaAlSiN₃:Eu²⁺ phosphors were obtained with 1 mol% CaCN₂ by a two‐step calcination procedure at 900°C for 2 h and subsequently at 1600°C for 8 h. The CaAlSiN₃:Eu²⁺ phosphors showed the strongest luminescent intensity at 660 nm when excited by 468 nm. With an increase in crystallization time, the maximum wavelength of the emission was shifted from 644 nm to 660 nm.     

Copper nanoclusters: an efficient fluorescence sensing platform for quinoline yellow

Fluorescence quenching behavior of artificial food colorant quinoline yellow (QY), on interaction with l ‐cysteine stabilized copper nanoclusters (l ‐Cys‐CuNCs) is investigated in this work. For this purpose, l ‐cysteine stabilized CuNCs were synthesized and characterized using various analytical techniques. Results demonstrated that the synthesized probe (size ~2 nm) had very promising optical features such as bright blue fluorescence, significant quantum yield and excellent photostability. l ‐Cys‐CuNCs can function as a fluorescence sensor by selectively sensing QY among other yellow colorants, giving a detection limit as low as 0.11 μM. The developed sensor exhibited a linear concentration range from 5.50 to 0.20 μM. The developed fluorescence assay was successfully applied for testing commercial samples, thereby making this sensing strategy significant for quality control of food stuffs.     

Rapid and visual detection for hypochlorite of an AIE enhanced fluorescence probe

In this paper, a new ‘turn‐on' fluorescence probe for the rapid, sensitive, and visual detection of hypochlorite is reported. The push–pull type trianiline–tricyanofuran‐based fluorescent probe was prepared using a condensation reaction between tricyanofuran and the thiophene–trianiline derivative that had high quantum yields and showed aggregation‐induced emission enhanced properties. Upon exposure to hypochlorite, prominent fluorescence enhancement of the probe was observed via the release of the fluorophore from the probe. The probe showed a ratiometric absorption change at 315 nm and 575 nm. Importantly, the probe showed an excellent detection limit for hypochlorite at 1.2 × 10^?7 M in solution and it was successfully applied for monitoring hypochlorite in waste water by test strip. This work reports a new fluorescence analytical sensing method for hypochlorite that has potential practical value in environmental monitoring and biological discrimination.     

2‐(4‐Ethoxy phenyl)‐4‐phenyl quinoline organic phosphor for solution processed blue organic light‐emitting diodes

This paper reports the synthesis and characterization of 2‐(4‐ethoxyphenyl)‐4‐phenyl quinoline (OEt‐DPQ) organic phosphor using an acid‐catalyzed Friedlander reaction and the preparation of blended thin films by molecularly doping OEt‐DPQ in poly(methyl methacrylate) (PMMA) at different wt%. The molecular structure of the synthesized phosphor was confirmed by Fourier transform infra‐red (FTIR) spectroscopy and nuclear magnetic resonance spectra (NMR). Surface morphology and percent composition of the elements were assessed by scanning electron microscopy (SEM) and energy dispersive analysis of X‐rays (EDAX). The thermal stability and melting point of OEt‐DPQ and thin films were probed by thermo‐gravimetric analysis (TGA)/differential thermal analysis (DTA) and were found to be 80°C and 113.6°C, respectively. UV–visible optical absorption spectra of OEt‐DPQ in the solid state and blended films produced absorption bands in the range 260–340 nm, while photoluminescence (PL) spectra of OEt‐DPQ in the solid state and blended thin films demonstrated blue emission that was registered at 432 nm when excited at 363–369 nm. However, solvated OEt‐DPQ in chloroform, tetrahydrofuran or dichloromethane showed a blue shift of 31–43 nm. Optical absorption and emission parameters such as molar extinction coefficient (ε), energy gap (E_g), transmittance (T), reflectance (R), refractive index (n), oscillator energy (E₀) and oscillator strength (f), quantum yield (φ_f), oscillator energy (E₀), dispersion energy (E_d), Commission Internationale de l'Éclairage (CIE) co‐ordinates and energy yield fluorescence (E_F) were calculated to assess the phosphor's suitability as a blue emissive material for opto‐electronic applications such as organic light‐emitting diodes (OLEDs), flexible displays and solid‐state lighting technology.     

Enhanced fluorescence of tetrasulfonated zinc phthalocyanine by graphene quantum dots and its application in molecular sensing/imaging

When excited at 435 nm, tetra‐sulfonate zinc phthalocyanine (ZnPcS₄) emitted dual fluorescence at 495 and 702 nm. The abnormal fluorescence at 495 nm was experimentally studied and analyzed in detail for the first time. The abnormal fluorescence at 495 nm was deduced to originate from triplet–triplet (T–T) energy transfer of excited phthalocyanine (³*ZnPcS₄). Furthermore, graphene quantum dots (GQDs) enhanced the 495 nm fluorescence quantum yield (Q) of ZnPcS₄. The fluorescence properties of ZnPcS₄–GQDs conjugate were retained in a cellular environment. Based on the fluorescence of ZnPcS₄–GQDs conjugate, we designed and prepared an Apt29/thrombin/Apt15 sandwich thrombin sensor with high specificity and affinity. This cost‐saving, simple operational sensing strategy can be extended to use in sensing/imaging of other biomolecules.     

Highly luminescent S,N co‐doped carbon quantum dots‐sensitized chemiluminescence on luminol–H2O2 system for the determination of ranitidine

S,N co‐doped carbon quantum dots (N,S‐CQDs) with super high quantum yield (79%) were prepared by the hydrothermal method and characterized by transmission electron microscopy, photoluminescence, UV–Vis spectroscopy and Fourier transformed infrared spectroscopy. N,S‐CQDs can enhance the chemiluminescence intensity of a luminol–H₂O₂ system. The possible mechanism of the luminol–H₂O₂–(N,S‐CQDs) was illustrated by using chemiluminescence, photoluminescence and ultraviolet analysis. Ranitidine can quench the chemiluminescence intensity of a luminol–H₂O₂–N,S‐CQDs system. So, a novel flow‐injection chemiluminescence method was designed to determine ranitidine within a linear range of 0.5–50 μg ml^?1 and a detection limit of 0.12 μg ml^?1. The method shows promising application prospects.     

Synthesis,characterization and thermoluminescence studies of (ZnS)1‐x(MnTe)x nanophosphors

The present paper reports the thermoluminescence (TL) of (ZnS)_1‐x(MnTe)_x nanophosphors that were prepared by a wet chemical synthesis method. The structure investigated by X‐ray diffraction patterns confirms the formation of a sphalerite phase whose space group was found to be F 3m. From XRD, TEM and SEM analyses the average sizes of the particles were found to be 12 nm, 11 nm and 15 nm, respectively. Initially the TL intensity increased with increasing values of x because the number of luminescence centres increased; however, for higher values of x the TL intensity decreased because of the concentration quenching. Thus the TL, mechanoluminescence and photoluminescence intensities are optimum for a particular value of x, that is for x = 0.05. Thermoluminescence of the (ZnS)_1‐x (MnTe)_x nanophosphor has not been reported previously. There were two peaks seen in the thermoluminescence glow curves in which the first peak lay at 105–100 °C and the second peak lay at 183.5–178.5 °C. The activation energies for the first and second peaks were found to be 0.45 eV and 0.75 eV, respectively.     

Photostability of quantum dot micelles under ultraviolet irradiation

Phospholipid quantum dot micelles are useful for bio‐applications because of their amphiphilicity and exceptional biocompatibilities. We investigated the uptake of phospholipid [polyethylene glycol (PEG), biotin, and folic acid terminated] modified CdSe/ZnS quantum dot micelles by cancer cells and its photostability under ultrviolet light in the C spectrum (UV‐C) (254 nm) or UV‐A (365 nm) light irradiation. The stability of micelles to the exposure of UV‐C and UV‐A light was assessed. Biotin‐modified quantum dot micelles give photoluminescence enhancement under UV‐C light irradiation. Folate modified micelle under UV‐C and UV‐A results show considerable photoluminescence enhancement. Photoluminescence lifetime measurements showed 7.04, 8.11 and 11.42 ns for PEG, folate, and biotin terminated phospholipid micelles, respectively. Folate and biotin‐modified quantum dot micelles showed excellent uptake by HeLa cells under fluorescence confocal microscopy. Phospholipid CdSe/ZnS quantum dot micelles can be potentially used for diagnosis and treatment of cancer in the future.     

Microwave‐assisted sintering synthesis of greenish‐yellow emitting Sr2SiO4:Eu2+ phosphors

Europium ion (Eu²⁺) doped Sr₂SiO₄ phosphors with greenish‐yellow emission were synthesized using microwave‐assisted sintering. The phase structure and photoluminescence (PL) properties of the obtained phosphor samples were investigated. The PL excitation spectra of the Sr₂SiO₄:Eu²⁺ phosphors exhibited a broad band in the range of 260 nm to 485 nm with a maximum at 361 nm attributed to the 5f‐4d allowed transition of the Eu²⁺ ions. Under an excitation at 361 nm, the Sr₂SiO₄:Eu²⁺ phosphor exhibited a greenish‐yellow emission peak at 541 nm with an International‐Commission‐on‐Illumination (CIE) chromaticity of (0.3064, 0.4772). The results suggest that the microwave‐assisted sintering method is promising for the synthesis of phosphors owing to the decreased sintering time without the use of additional reductive agents.     

The characterization of plant species using first‐derivative fluorescence spectra

Plants are one of the most important parts of the ecological system and demand a reliable method for accurate classification. In this study, the first‐derivative fluorescence spectral curves (FDFSCs) based on laser‐induced fluorescence technology were proposed for the characterization of plant species. The measurement system is mainly composed of a spectrometer, an excitation light source (the two excitation wavelengths are 460 and 556 nm, respectively), and an intensified charge‐coupled device camera. FDFSCs were calculated from the deviation between the fluorescence values at each wavelength, plus and minus one band, divided by the wavelength range. Principal component analysis was utilized to analyze the FDFSCs by extracting the main attributes and reducing the dimensionality of variables. A support vector machine was used to evaluate FDFSC performance for the identification of plant species. Plant species that are difficult to distinguished by the naked eye, can be identified effectively using the proposed FDFSCs. For the 556 nm and 460 nm excitation wavelengths, the overall identification rates of the six plant species evaluated were 93.3% and 91.7%, respectively. Experimental results demonstrated that the combination of the FDFSCs with multivariate analysis could provide a simple and reliable method for the characterization of plant species.     

Study of luminescence properties of dysprosium‐doped CaAl12O19 phosphor for white light‐emitting diodes

Dy³⁺‐doped CaAl₁₂O₁₉ phosphors were synthesized utilizing a combustion method. Crystal structure and morphological examinations were performed respectively using X‐ray diffraction (XRD) and scanning electron microscopy (SEM) techniques to identify the phase and morphology of the synthesized samples. Fourier transform infrared spectroscopy (FTIR) estimations were carried out using the KBr method. Photoluminescence properties (excitation and emission) were recorded at room temperature. CaAl₁₂O₁₉:Dy³⁺ phosphor showed two emission peaks respectively under a 350‐nm excitation wavelength, centered at 477 nm and 573 nm. Dipole–dipole interaction via nonradiative energy shifting has been considered as the major cause of concentration quenching when Dy³⁺ concentration was more than 3 mol%. The CIE chromaticity coordinates positioned at (0.3185, 0.3580) for the CaAl₁₂O₁₉:0.03Dy³⁺ phosphor had a correlated color temperature (CCT) of 6057 K, which is situated in the cool white area. Existing results point out that the CaAl₁₂O₁₉:0.03Dy³⁺ phosphor could be a favorable candidate for use in white light‐emitting diodes (WLEDs).