Optical fluorescent sensor based on perovskite QDs for nitric oxide gas detection.

In this paper, a new, to the best of our knowledge, optical fluorescent sensor for the sensing of nitric oxide (NO) gas is developed. The optical NO sensor based on C s P b B r 3 perovskite quantum dots (PQDs) is coated on the surface of filter paper. The C s P b B r 3 PQD sensing material can be excited with a UV LED of a central wavelength at 380 nm, and the optical sensor has been tested in regard to monitoring different NO concentrations from 0-1000 ppm. The sensitivity of the optical NO sensor is represented in terms of the ratio I N2/I 1000p p m N O , where I N2 and I 1000p p m N O represent the detected fluorescence intensities in pure nitrogen and 1000 ppm NO environments, respectively. The experimental results show that the optical NO sensor has a sensitivity of 6. In addition, the response time was 26 s when switching from pure nitrogen to 1000 ppm NO and 117 s when switching from 1000 ppm NO to pure nitrogen. Finally, the optical sensor may open a new approach for the sensing of the NO concentration in the harsh reacting environmental applications.

A Ratiometric Optical Dual Sensor for the Simultaneous Detection of Oxygen and Carbon Dioxide.

Simultaneous detection of carbon dioxide (CO2) and oxygen (O2) has attracted considerable interest since CO2 and O2 play key roles in various industrial and domestic applications. In this study, a new approach based on a fluorescence ratiometric referencing method was reported to develop an optical dual sensor where platinum (II) meso-tetrakis(pentafluorophenyl)porphyrin (PtTFPP) complex used as the O2-sensitive dye, CdSe/ZnS quantum dots (QDs) combined with phenol red used as the CO2-sensitive dye, and CdSe/ZnS QDs used as the reference dye for the simultaneous detection of O2 and CO2. All the dyes were immobilized in a gas-permeable matrix poly (isobutyl methacrylate) (PolyIBM) and subjected to excitation using a 380 nm LED. The as-obtained distinct fluorescence spectral intensities were alternately exposed to analyte gases to observe changes in the fluorescence intensity. In the presence of O2, the fluorescence intensity of the Pt (II) complex was considerably quenched, while in the presence of CO2, the fluorescence intensity of QDs was increased. The corresponding ratiometric sensitivities of the optical dual sensor for O2 and CO2 were approximately 13 and 144, respectively. In addition, the response and recovery for O2 and CO2 were calculated to be 10 s/35 s and 20 s/60 s, respectively. Thus, a ratiometric optical dual gas sensor for the simultaneous detection of O2 and CO2 was successfully developed. Effects of spurious fluctuations in the intensity of external and excitation sources were suppressed by the ratiometric sensing approach.

Resolving Cross-Sensitivity Effect in Fluorescence Quenching for Simultaneously Sensing Oxygen and Ammonia Concentrations by an Optical Dual Gas Sensor.

Simultaneous sensing of multiple gases by a single fluorescent-based gas sensor is of utmost importance for practical applications. Such sensing is strongly hindered by cross-sensitivity effects. In this study, we propose a novel analysis method to ameliorate such hindrance. The trial sensor used here was fabricated by coating platinum(II) meso-tetrakis(pentafluorophenyl)porphyrin (PtTFPP) and eosin-Y dye molecules on both sides of a filter paper for sensing O2 and NH3 gases simultaneously. The fluorescent peak intensities of the dyes can be quenched by the analytes and this phenomenon is used to identify the gas concentrations. Ideally, each dye is only sensitive to one gas species. However, the fluorescent peak related to O2 sensing is also quenched by NH3 and vice versa. Such cross-sensitivity strongly hinders gas concentration detection. Therefore, we have studied this cross-sensitivity effect systematically and thus proposed a new analysis method for accurate estimation of gas concentration. Comparing with a traditional method (neglecting cross-sensitivity), this analysis improves O2-detection error from -11.4% ± 34.3% to 2.0% ± 10.2% in a mixed background of NH3 and N2.

Optical sensor for dual sensing of oxygen and carbon dioxide based on sensing films coated on filter paper.

An optical sensor for the dual sensing of oxygen (O2) and carbon dioxide (CO2) based on sensing films coated on filter paper is proposed. Ethyl cellulose (EC) doped with platinum(II) meso-tetrakis(pentafluorophenyl)porphyrin (PtTFPP) and 7-amino-4-trifluoromethyl coumarin serve as the oxygen sensing material and reference blue emission dye for the pH indicator, respectively. The CO2 sensing layer includes the pH-sensitive fluorescent indicator 1-hydroxy-3,6,8-pyrenetrisulfonic acid trisodium salt immobilized within the EC. The O2- and CO2-sensitive materials can both be excited with a 405 nm LED, and the two emission wavelengths can be detected separately. The experimental result reveals that the optical O2 and CO2 sensors have sensitivities of IN2 /I100%O2 =22.8 and IN2 /I100%CO2 =3.6, respectively. The response times of the optical O2 sensor were 15 s upon switching from nitrogen to O2 and 41 s when moving from O2 to nitrogen (N2). The response times of the optical CO2 sensor were 7 s upon switching from 100% N2 to 100% CO2 and 39 s when moving from 100% CO2 to 100% N2. The proposed optical dual sensor can be used for the simultaneous sensing of O2 and CO2 concentrations in environmental applications.

Ratiometric optical fiber sensor for dual sensing of copper ion and dissolved oxygen.

This paper develops a new ratiometric optical dual sensor for Cu2+ ions and dissolved oxygen (DO) incorporating a sol-gel matrix doped with palladium tetrakis pentafluorophenyl porphine as the oxygen-sensitive material, CdSe quantum dots as the Cu2+ ion-sensing material, and 7-amino-4-trifluoromethyl coumarin as the Cu2+ /DO practically independent fluorescent dye. The feasibility of coating an optical fiber with the sensing film to fabricate a ratiometric optical fiber dual sensor is investigated. Using an LED with a central wavelength of 405 nm as an excitation source, it is shown that the emission wavelengths of the Cu2+ ion-sensitive, DO-sensitive dye and the reference dye have no spectral overlap and therefore permit Cu2+ ion and DO concentration to be measured using a ratiometric-based method. The ratiometric optical fiber dual sensor has been tested with regard to monitoring different Cu2+ ion (0-10 µM) and DO concentrations (0-38 mg/L). The results show that the luminescence properties of the Cu2+ ion sensor are independent of the presence of the oxygen sensor and have a uniquely good linear response in the 0-10 µM range. The proposed ratiometric sensing approach presented in this study has the advantage of suppressing spurious fluctuations in the intensity of the excitation source.

Portable optical oxygen sensor based on time-resolved fluorescence.

A new, simple signal processing, low-cost technique for the fabrication of a portable oxygen sensor based on time-resolved fluorescence is described. The sensing film uses the oxygen sensing dye platinum meso-tetra (pentfluorophenyl) porphyrin (PtTFPP) embedded in a polymer matrix. The ratio τ0/τ100 measures sensitivity of the sensing film, where τ0 and τ100 represent the detected fluorescence lifetimes from the sensing film exposed to 100% nitrogen and 100% oxygen, respectively. The experimental results reveal that the PtTFPP-doped oxygen sensor has a sensitivity of 2.2 in the 0%-100% range. A preparation procedure for coating the photodiodes with the oxygen sensor film that produces repetitive and reliable sensing devices is proposed. The developed time-resolved optical oxygen sensor is portable, low-cost, has simple signal processing, and lacks optical filter elements. It is a cost-effective alternative to traditional electrochemical-based oxygen sensors and provides a platform for other optical based sensors.

A novel optical dual sensor based on a coaxial electrospinning method for simultaneous sensing of oxygen and ammonia.

The coaxial electrospinning method is widely used in a wide range of applications, including medical devices and sensing technology. This study proposes a novel optical dual sensor for simultaneous detection of oxygen (O2) and ammonia (NH3) based on coaxial electrospinning method to produce core-shell fiber membrane doped fluorescent dyes. The O2 (core) and NH3 (shell) sensitive dye membranes were successfully fabricated using coaxial electrospinning method by dissolving a polymer matrix, cellulose acetate (CA), with platinum (II) meso-tetrakis (pentafluorophenyl) porphyrin (PtTFPP) and Eosin-Y, respectively. The optical dual sensor was illuminated by an UV LED to monitor the intensity change and wavelength shift in the presence of selected analyte gases. The experimental data show that the sensitivities of optical dual sensor were found to be 6.4 and 3.2 for O2 and NH3, respectively. The response and recovery times of O2 and NH3 sensing probes were measured to be 12 s/29 s and 65 s/66 s, respectively. Also, when exposed to NH3 gas gradually from 0 to 500 ppm, the wavelength shift data of Eosin-Y was started at 569.5 nm, 573.9 nm, 578.4 nm, 579.4 nm, 580.8 nm, and 582.2 nm, respectively. In applications, the proposed optical dual sensor based on coaxial electrospinning method can detect O2 and NH3 gases simultaneously.

Strongly Improving the Sensitivity of Phosphorescence-Based Optical Oxygen Sensors by Exploiting Nano-Porous Substrates.

Sensitivity is one of the crucial factors in determining the quality of a fluorescence/phosphorescence-based gas sensor, and is estimated from the measurement of responses (I0/I, where I0 and I refer to the measured optical intensity of a sensor in absence and presence of analyte molecules) at various concentrations of analytes. In this work, we demonstrate phosphorescence-based optical oxygen sensors fabricated on highly porous anodic aluminum oxide (AAO) membranes showing dramatically high response. These sensors exploit the enormous surface area of the AAO to facilitate the effective interaction between the sensing molecules and the analytes. We spin-coat an AAO membrane (200 nm pore diameter) with a platinum-based oxygen sensing porphyrin dye, platinum(II) meso-tetrakis (pentafluorophenyl) porphyrin (PtTFPP), to fabricate a sensor exhibiting I0/I ~400 at 100% oxygen atmosphere. To address the generality of the AAO membrane, we fabricate a separate sensor with another porphyrin dye, platinum octaethylporphyrin (PtOEP), which exhibits an even higher I0/I of ~500. Both of these sensors offer the highest responses as an optical oxygen sensor hitherto reported. SEM and EDS analysis are performed to realize the effect of the increased surface area of the AAO membrane on the enhanced sensitivity.

Ingenious Fabrication of Ag-Filled Porous Anodic Alumina Films as Powerful SERS Substrates for Efficient Detection of Biological and Organic Molecules.

Surface-enhanced Raman scattering (SERS) has been widely used to effectively detect various biological and organic molecules. This detection method needs analytes adsorbed onto a specific metal nanostructure, e.g., Ag-nanoparticles. A substrate containing such a structure (called SERS substrate) is user-friendly for people implementing the adsorption and subsequent SERS detection. Here, we report on powerful SERS substrates based on efficient fabrication of Ag-filled anodic aluminum oxide (AAO) films. The films contain many nanopores with small as-grown inter-pore gap of 15 nm. The substrates are created by electrochemically depositing silver into nanopores without an additional pore widening process, which is usually needed for conventional two-step AAO fabrication. The created substrates contain well-separated Ag-nanoparticles with quite a small inter-particle gap and a high number density (2.5 × 1010 cm-2). We use one-step anodization together with omitting additional pore widening to improve the throughput of substrate fabrication. Such substrates provide a low concentration detection limit of 10-11 M and high SERS enhancement factor of 1 × 106 for rhodamine 6G (R6G). The effective detection of biological and organic molecules by the substrate is demonstrated with analytes of adenine, glucose, R6G, eosin Y, and methylene blue. These results allow us to take one step further toward the successful commercialization of AAO-based SERS substrates.