Multifunctional optical thermometry using dual-mode green emission of CaZrO3:Er/Yb/Mo perovskite phosphors.

The weak emission intensity of rare-earth element-doped dual-mode materials leads to low-sensor sensitivity, which is a challenge in optical sensor applications. The present work achieved high-sensor sensitivity and high green color purity based on the intense green dual-mode emission of Er/Yb/Mo-doped CaZrO3 perovskite phosphors. Their structure, morphology, luminescent properties, and optical temperature sensing properties have been investigated in detail. Phosphor shows a uniform cubic morphology with an average size of approximately 1 µm. Rietveld refinement confirms the formation of single-phase orthorhombic CaZrO3. Under the excitation of 975 and 379 nm, the phosphor emits pure green up and down-conversion (UC and DC) emission at 525/546 nm corresponding to 2H11/2/4S3/2-4I15/2 transitions of Er3+ ions, respectively. Intense green UC emissions were achieved because of energy transfer (ET) from the high-energy excited state of Yb3+-MoO42- dimer to the 4F7/2 level of Er3+ ion. Furthermore, the decay kinetics of all obtained phosphors confirmed ET efficiency from Yb3+-MoO42- dimer to Er3+ ions, leading to strong green DC emission. Moreover, the DC of the obtained phosphor shows that a sensor sensitivity value of 0.697% K-1 at 303 K is higher than the UC (0.667% K-1 at 313 K) because the thermal effect generated by the DC excitation source light is ignored compared with UC luminescence. CaZrO3:Er-Yb-Mo phosphor shows intense green dual-mode emission with high green color purity, 96.50% of DC and 98% of UC emissions, and high sensitivity, making it suitable for optoelectronic devices and thermal sensor applications.

A label-free and highly sensitive DNA biosensor based on the core-shell structured CeO2-NR@Ppy nanocomposite for Salmonella detection.

A core-shell cerium oxide nanorod@polypyrrole (CeO2-NR@Ppy) nanocomposite-based electrochemical DNA biosensor was studied for Salmonella detection. The core-shell CeO2-NR@Ppy nanocomposite was prepared by in situ chemical oxidative polymerization of pyrrole monomer on CeO2-NRs, which provided a suitable platform for electrochemical DNA biosensor fabrication. The immobilization of ss-DNA sequences onto nanocomposite-coated microelectrode was performed via covalent attachment method. DNA biosensor electrochemical responses were studied by cyclic voltammetry and electrochemical impedance spectroscopy with [Fe (CN)6]3-/4- as redox probe. Under optimal conditions, DNA biosensor response showed good linearity in the range of 0.01-0.4 nM with sensitivity of 593.7â€¯Ω·nM-1·cm-2. The low limit of detection and limit of quantification for the DNA biosensor were 0.084 and 0.28 nM, respectively. The proposed DNA biosensor also showed good results when used in detecting actual Salmonella samples.

Luminescence of lemon-derived carbon quantum dot and its potential application in luminescent probe for detection of Mo6+ ions.

This article reports on the first attempt of a systematic study on the synthesis of carbon dots (C-dots) for the potential applications in labeling and detection of molybdenum ion (Mo6+ ). Carbon dots (C-dots) were synthesized directly via a simple hydrothermal method using lemon juices as carbon precursor with different temperatures to control the luminescence of C-dots. The obtained C-dots had strong green light emission and the ability to use its luminescence properties as probes for Mo6+ detection application, which is based on Mo6+ induced luminescence quenching of C-dots. This analysis system exhibits strong sensitivity and good selectivity for Mo6+ ion, and a detection limit as low as 20 ppm is achieved. These results suggest that the present C-dots have potential application in optoelectronic, labeling and luminescent probing of Mo6+ ions.

Enhancing the luminescence of Eu3+ /Eu2+ ion-doped hydroxyapatite by fluoridation and thermal annealing.

This paper reports a novel way for the synthesis of a europium (Eu)-doped fluor-hydroxyapatite (FHA) nanostructure to control the luminescence of hydroxyapatite nanophosphor, particularly, by applying optimum fluorine concentrations, annealed temperatures and pH value. The Eu-doped FHA was made using the co-precipitation method followed by thermal annealing in air and reducing in a H2 atmosphere to control the visible light emission center of the nanophosphors. The intensities of the OH- group decreased with the increasing fluorine concentrations. For the specimens annealed in air, the light emission center of the nanophosphor was 615 nm, which was emission from the Eu3+ ion. However, when they were annealed in reduced gas (Ar + 5% H2 ), a 448 nm light emission center from the Eu2+ ion of FHA was observed. The presence of fluorine in Eu-doped FHA resulted in a significant enhancement of nanophosphor luminescence, which has potential application in light emission and nanomedicine.

Label-free electrochemical immunosensor based on cerium oxide nanowires for Vibrio cholerae O1 detection.

This paper developed a label-free immunosensor based on cerium oxide nanowire for Vibrio cholerae O1 detection application. The CeO2 nanowires were synthesized by hydrothermal reaction. The immobilization of Anti-V. cholerae O1 onto CeO2 nanowire-deposited sensor was performed via an amino ester, which was created by using 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide, and sulfo-N-hydroxysuccinimide. The electrochemical responses of the immunosensor were studied by electrochemical impedance spectroscopy with [Fe (CN) 6] (3-/4-) as redox probe. A linear response in electron transfer resistance for cell of V. cholerae O1 concentration was found in the range of 1.0 × 10(2)CFU/mL to 1.0 × 10(4)CFU/mL. The detection limit of the immunosensor was 1.0 × 10(2)CFU/mL. The immunosensor sensitivity was 56.82 Ω/CFU · mL(-1). Furthermore, the parameters affecting immunosensor response were also investigated, as follows: pH value, immunoreaction time, incubation temperature, and anti-V. cholerae O1 concentration.

Biosensor based on nanocomposite material for pathogenic virus detection.

This paper introduces a DNA biosensor based on a DNA/chitosan/multi-walled carbon nanotube nanocomposite for pathogenic virus detection. An easy, cost-effective approach to the immobilization of probe DNA sequences on the sensor surface was performed. Cyclic voltammograms were used to characterize the probe DNA sequence immobilization. Complementary sequence hybridization was examined by electrochemical impedance spectroscopy. Results revealed that the developed DNA sensor can detect a target DNA concentration as low as 0.01×10(-12) M. The sensitivity of the prepared sensor was 52.57 kΩ/fM. The reusability and storage stability of the DNA sensor were also investigated. Results showed that the electron-transfer resistance decreased to approximately 35% after 8 weeks and to approximately 80% after 12 weeks of storage.

DNA sensor development based on multi-wall carbon nanotubes for label-free influenza virus (type A) detection.

This paper describes the DNA immobilization using carbon multi-walled nanotubes (MWCNTs) for direct and label-free detection of influenza virus (type A). The DNA probe was attached on the sensor surface by means of covalent bonding between the amine and phosphate groups of the DNA sequence. The interaction between the DNA probe and the MWCNTs were characterized by Fourier Transform Infrared (FTIR) spectrometry, Raman spectra. The hybridization of the DNA probe and the target DNA were detected by changes in the conductance on the surface of sensors leading to the change in the output signal of the system. The results show that the DNA sensor can detect as low as 0.5 nM of the target DNA samples; the response time of DNA sensor is approximately 4 min.