Review of the Design of Ruthenium-Based Nanomaterials and Their Sensing Applications in Electrochemistry.

In this review, ruthenium nanoparticles (Ru NPs)-based functional nanomaterials have attractive electrocatalytic characteristics and they offer considerable potential in a number of fields. Ru-based binary or multimetallic NPs are widely utilized for electrode modification because of their unique electrocatalytic properties, enhanced surface-area-to-volume ratio, and synergistic effect between two metals provides as an effective improved electrode sensor. This perspective review suggests the current research and development of Ru-based nanomaterials as a platform for electrochemical (EC) sensing of harmful substances, biomolecules, insecticides, pharmaceuticals, and environmental pollutants. The advantages and limitations of mono-, bi-, and multimetallic Ru-based nanocomposites for EC sensors are discussed. Besides, the relevant EC properties and analyte sensing approaches are also presented. On the basis of these insights, we highlighted recent results for synthesizing techniques and EC environmental pollutant sensors from the perspectives of diverse supports, including graphene, carbon nanotubes, silica, semiconductors, metal sulfides, and polymers. Finally, this work overviews the modern improvements in the utilization of Ru-based nanocomposites on the basis for electroanalytical sensors as well as suggestions for the field's future development.

A vector correlation study using a hexapole-oriented molecular beam: photodissociation dynamics of oriented isohaloethane.

The photodissociation dynamics of isohaloethane (1-bromo-2-chloro-1,1,2-trifluoroethane) at 234 nm was studied by a sliced imaging technique combined with an oriented molecular beam. The speed and angular distributions of the competitive products of spin-orbit selected Br and Cl atoms were determined by analysis of the obtained images. The anisotropic parameter, ß, was found to be 2.0 ± 0.2 for the excited state of Br(2P1/2) (Br*) and 1.2 ± 0.3 for the ground state of Br(2P3/2) (Br). The speed distributions for both Br and Br* exhibited Gaussian-like characteristics. These results indicate that Br atoms were generated by direct formation after excitation through the nσ*(C-Br) potential energy surfaces. In contrast, the angular distributions for the Cl fragments were almost isotropic, while the speed distributions displayed Boltzmann-like characteristics. This suggests that the Cl atoms may form through long-lived parent molecules after photoexcitation. The branching ratio for Br and Cl atom formation was found to be approximately 1.2, that is, Br atom formation occurred preferentially, in contrast to the case of halothane photodissociation reported in our previous work [Che et al., J. Phys. Chem. A, 2020, 124, 5288]. A vector correlation study between the laser polarization axis and the direction of the dipole moment revealed a similar tendency for all photofragments, suggesting that the fragments were formed through a common excited state of isohaloethane. The vector correlation was also studied theoretically for comparison with the experimental results. The angle between the transition dipole moment in photodissociation and the permanent dipole moment was found to be 42 ± 15°. The obtained results indicate that this vector correlation approach combined with an oriented molecular beam is a powerful tool for determining the transition dipole moments in photodissociation.

Recent Developments in Carbon-Based Nanocomposites for Fuel Cell Applications: A Review.

Carbon-based nanocomposites have developed as the most promising and emerging materials in nanoscience and technology during the last several years. They are microscopic materials that range in size from 1 to 100 nanometers. They may be distinguished from bulk materials by their size, shape, increased surface-to-volume ratio, and unique physical and chemical characteristics. Carbon nanocomposite matrixes are often created by combining more than two distinct solid phase types. The nanocomposites that were constructed exhibit unique properties, such as significantly enhanced toughness, mechanical strength, and thermal/electrochemical conductivity. As a result of these advantages, nanocomposites have been used in a variety of applications, including catalysts, electrochemical sensors, biosensors, and energy storage devices, among others. This study focuses on the usage of several forms of carbon nanomaterials, such as carbon aerogels, carbon nanofibers, graphene, carbon nanotubes, and fullerenes, in the development of hydrogen fuel cells. These fuel cells have been successfully employed in numerous commercial sectors in recent years, notably in the car industry, due to their cost-effectiveness, eco-friendliness, and long-cyclic durability. Further; we discuss the principles, reaction mechanisms, and cyclic stability of the fuel cells and also new strategies and future challenges related to the development of viable fuel cells.

Development of Palladium on Bismuth Sulfide Nanorods as a Bifunctional Nanomaterial for Efficient Electrochemical Detection and Photoreduction of Hg(II) Ions.

A nanocomposite containing palladium nanoparticles embedded on bismuth sulfide nanorods (Pd@Bi2S3) was synthesized based on a solvothermal method. The structural features, composition, and morphology were characterized by XRD, FT-IR, FE-SEM-EDS, FE-TEM, HAADF-STEM, XPS, N2 physisorption, and UV-vis. Further electrochemical measurements by EIS, CV, DPV, and LSV techniques were done. It revealed that Pd@Bi2S3/GCE were exploited as electrochemical sensors for the detection of toxic mercuric ions (Hg2+), which provides a wide linear range of 0.049-445 µM, excellent sensitivity of 1.17 µA µM-1 cm-2, and detection limit of 13.5 nM. The modified electrode has also been successfully applied for the detection of Hg2+ in sea fish, river fish, and water samples. The Pd@Bi2S3/GCE signifies a robust, usability, and highly effective method for trace level detection of Hg2+ ions. Furthermore, these Pd@Bi2S3 bifunctional catalysts were discovered to have good photoreduction activity for Hg2+ ions upon the visible-light irradiation.

Photodissociation of CH2BrCHBrC(O)Cl at 248 nm: probing Br2 as the primary fragment using cavity ring-down spectroscopy.

The photodissociation of 2,3-dibromopropionyl chloride (CH2BrCHBrC(O)Cl, 2,3-DBPC) at 248 nm was carried out to study Br2 as the primary molecular product in the B3Π+0u ← X1Σ+g transition using cavity ring-down absorption spectroscopy. The rotational spectra (v'' = 0-2) were acquired and assigned with the aid of spectral simulation. It is verified that the obtained Br2 fragment is attributed to the one-photon dissociation of 2,3-DBPC and is free from contributions of secondary reactions. The vibrational ratio of the Br2 population of v(0):v(1):v(2) is equal to 1:(0.58 ± 0.12):(0.23 ± 0.09), corresponding to the Boltzmann vibrational temperature of 623 ± 38 K. The quantum yield of Br2 eliminated from 2,3-DBPC is estimated to be 0.09 ± 0.04. The dissociation pathways of 2,3-DBPC and its potential energy surfaces were calculated using density functional theory. By employing the CCSD(T)//M062X/6-31+g(d,p) level of theory, transition state barriers and corresponding reaction energies were calculated for the Br, Cl, Br2, BrCl, HBr and HCl elimination channels. The unimolecular rate constant for Br2 elimination was determined to be 2.09 × 105 s-1 using Rice-Ramsperger-Kassel-Marcus (RRKM) theory, thus explaining the small quantum yield of the Br2 channel.

Probing BrCl from photodissociation of CH2BrCl and CHBr2Cl at 248 nm using cavity ring-down spectroscopy.

Photodissociation of di- and tri-halogenated methanes including CH2BrCl and CHBr2Cl at 248 nm was investigated using cavity ringdown absorption spectroscopy (CRDS). The spectra of the BrCl(v'' = 2, 3) and Br2(v'' = 1, 2) fragments were probed over the wavelength range of 594.5-596 nm in the B3Π+0u ← X1Σ+g and B3Π (0+) ← X1Σ+ transitions, respectively. Their corresponding spectra were simulated for assignment of rotational lines at a given vibrational level. The quantum yields for Br2 eliminated from CHBr2Cl and BrCl from CH2BrCl were determined to be 0.048 ± 0.018 and 0.037 ± 0.014, respectively. The photodissociation of CHBr2Cl yielded only the Br2 fragment, but not the BrCl fragment in the experiments. An ab initio theoretical method based on the CCSD(T)//B3LYP/6-311g(d,p) level was employed to evaluate the potential energy surface for the dissociation pathways to produce Br2 and BrCl from CHBr2Cl, which encountered a transition state barrier of 445 and 484 kJ mol-1, respectively. The corresponding RRKM rate constants were calculated to show that the branching ratio of (Br2/BrCl) is ∼20. The BrCl spectrum is expected to be obscured by the much larger Br2 spectrum, explaining why BrCl fragments cannot be detected in the photolysis of CHBr2Cl.

Temperature effect on water dynamics in tetramer phosphofructokinase matrix and the super-arrhenius respiration rate.

Advances in understanding the temperature effect on water dynamics in cellular respiration are important for the modeling of integrated energy processes and metabolic rates. For more than half a century, experimental studies have contributed to the understanding of the catalytic role of water in respiration combustion, yet the detailed water dynamics remains elusive. We combine a super-Arrhenius model that links the temperature-dependent exponential growth rate of a population of plant cells to respiration, and an experiment on isotope labeled 18O2 uptake to H218O transport role and to a rate-limiting step of cellular respiration. We use Phosphofructokinase (PFK-1) as a prototype because this enzyme is known to be a pacemaker (a rate-limiting enzyme) in the glycolysis process of respiration. The characterization shows that PFK-1 water matrix dynamics are crucial for examining how respiration (PFK-1 tetramer complex breathing) rates respond to temperature change through a water and nano-channel network created by the enzyme folding surfaces, at both short and long (evolutionary) timescales. We not only reveal the nano-channel water network of PFK-1 tetramer hydration topography but also clarify how temperature drives the underlying respiration rates by mapping the channels of water diffusion with distinct dynamics in space and time. The results show that the PFK-1 assembly tetramer possesses a sustainable capacity in the regulation of the water network toward metabolic rates. The implications and limitations of the reciprocal-activation-reciprocal-temperature relationship for interpreting PFK-1 tetramer mechanisms are briefly discussed.

Internet of Things-Enabled Aggregation-Induced Emission Probe for Cu2+ Ions: Comprehensive Investigations and Three-Dimensional Printed Portable Device Design.

Herein, we have developed a novel aggregation-induced emission (AIE) probe and three-dimensional (3D) printed portable device for copper (Cu2+) sensing in an aqueous medium. A ubiquitous synthetic route has been employed to devise the anthracene-conjugated imidazo[1,5-a]pyridine (TL19) probe as a unique anchor for Cu2+ ions. The TL19 is meticulously characterized through pivotal spectroscopic techniques, and the satisfactory results were obtained. The solvatochromic analysis and density functional theory calculations cohesively reveal that the TL19 exhibits the intramolecular charge transfer transition upon photoexcitation. Intriguingly, the TL19 exhibits spherically shaped nanoaggregates and enhanced fluorescence in DMSO/water (10:90) mixtures. This fluorescent nanoaggregate instantaneously responded toward the detection of Cu2+ via a deaggregation mechanism. The detection limit is found to be 9 pM in an aqueous medium. Further, the detection of Cu2+ in the HeLa cells has also been achieved due to bright green fluorescence, photostability, and biocompatibility nature of TL19 aggregates. On the other hand, an internet of things (IoT)-embedded 3D printed portable device is constructed for the detection of Cu2+ ions in real water samples. The Cu2+ detection is achieved through an IoT device, and results were acknowledged through an android application in 3.32 s round-trip time. Thus, the IoT-enabled AIE probe could be a prospective device for Cu2+ detection in a constrained environment.

Gold Nanoparticle Embedded on a Reduced Graphene Oxide/polypyrrole Nanocomposite: Voltammetric Sensing of Furazolidone and Flutamide.

A new electrochemical sensor has been constructed based on the in situ preparation of gold nanoparticle embedded on reduced graphene oxide and polypyrrole nanotube (AuNP@rGO/PPyNT) composite through a nanosecond laser-induced heating technique. The as-prepared composite is used for individual as well as the simultaneous electrochemical determination of chemotherapy drug (furazolidone, FU) and anticancer drug (flutamide, FLT). The composite was analyzed by X-ray Diffraction, scanning electron microscopy/energy-dispersive X-ray analysis, transmission electron microscopy, Raman spectrometry, and X-ray photoelectron spectroscopy analysis, thus confirming the successful synthesis of this composite and its physical features. The modified AuNP@rGO/PPyNT electrode was examined through cyclic voltammetry and differential pulse voltammetry (DPV) methods in pH 7.0 for the determination of FU and FLT in individual, simultaneous, and mixed systems. The fabricated sensor showed wide linear responses (0.01-1080.11 µM and 0.01-1214.11 µM) of analytes, with the lower limits of detection of 2.3 and 2.45 nM and higher sensitivity of 53.75 and 50.06 µA µM-1 cm-2, respectively. Furthermore, the constructed sensor demonstrates higher stability, reproducibility, and repeatability, and is effectively applied for the analysis of FU and FLT content in the human serum sample analysis with satisfactory recovery.

Ultrafine Bi-Sn nanoparticles decorated on carbon aerogels for electrochemical simultaneous determination of dopamine (neurotransmitter) and clozapine (antipsychotic drug).

This present study describes the synthesis of ultrafine Bi-Sn nanoparticles decorated on carbon aerogels (Bi-Sn NP/CAG) as a nanocomposite for the electrochemical simultaneous determination of dopamine (DA) and clozapine (CLZ). The typical characterization techniques, such as XRD, Raman, BET, FT-IR, TGA, XPS, and FE-SEM/TEM, showed useful insights into the crystal phase and morphology of Bi-Sn NP/CAG. Integrated Bi-Sn NP/CAG built into a cost-effective screen printed carbon electrode (SPCE) offers a high electrochemical surface area (ECSA) compared to unmodified, Bi-Sn, and CAG/SPCEs, such that it favourably allowed the binding of DA and CLZ molecules onto the surface at the Bi-Sn/CAG, which was demonstrated by cyclic and differential pulse voltammetry techniques. As a result, the DA and CLZ sensing exhibited low detection limits (DL, 4.6 and 97.6 nM (S/N = 3)), and sensitivity (3.402 and 0.4 µA µM-1 cm-2) over a wide linear range (0.02-97.59 and 0.5-2092 µM), respectively. To go a step further, the Bi-Sn NP/CAG/SPCE was applied for the simultaneous determination of DA and CLZ which featured lower DL (23.1 and 31.3 nM (S/N = 3)), and sensitivity (0.4979 and 0.04 µA µM-1 cm-2) over a wide linear range (2-182 and 10-910 µM), respectively. The selectivity for DA and CLZ in the presence of a 10-fold concentration of their potentially interfering active species was demonstrated. Finally, this sensing methodology enables the rapid electrochemical determination of the amount of DA and CLZ in a rat brain region serum sample with successful recovery outcomes.

Carbon Dot Nanoparticles Exert Inhibitory Effects on Human Platelets and Reduce Mortality in Mice with Acute Pulmonary Thromboembolism.

The inhibition of platelet activation is considered a potential therapeutic strategy for the treatment of arterial thrombotic diseases; therefore, maintaining platelets in their inactive state has garnered much attention. In recent years, nanoparticles have emerged as important players in modern medicine, but potential interactions between them and platelets remain to be extensively investigated. Herein, we synthesized a new type of carbon dot (CDOT) nanoparticle and investigated its potential as a new antiplatelet agent. This nanoparticle exerted a potent inhibitory effect in collagen-stimulated human platelet aggregation. Further, it did not induce cytotoxic effects, as evidenced in a lactate dehydrogenase assay, and inhibited collagen-activated protein kinase C (PKC) activation and Akt (protein kinase B), c-Jun N-terminal kinase (JNK), and p38 mitogen-activated protein kinase (MAPK) phosphorylation. The bleeding time, a major side-effect of using antiplatelet agents, was unaffected in CDOT-treated mice. Moreover, our CDOT could reduce mortality in mice with ADP-induced acute pulmonary thromboembolism. Overall, CDOT is effective against platelet activation in vitro via reduction of the phospholipase C/PKC cascade, consequently suppressing the activation of MAPK. Accordingly, this study affords the validation that CDOT has the potential to serve as a therapeutic agent for the treatment of arterial thromboembolic disorders.

UV Photodissociation of Halothane in a Focused Molecular Beam: Space-Speed Slice Imaging of Competitive Bond Breaking into Spin-Orbit-Selected Chlorine and Bromine Atoms.

A molecular beam of halothane (2-bromo-2-chloro-1,1,1-trifluoroethane) is focused by a hexapolar electrostatic field and photolyzed by UV laser radiation at 234 nm. Angular and speed distributions of chlorine and bromine photofragments emitted from halothane are measured for both spin-orbit states independently. Although the dissociation energy of the C-Cl bond is larger than that of C-Br, the relative yield of Cl to Br was found to be approximately 2. Measured speed and angular distributions of atomic fragments show distinct kinetic energy release and scattering characteristics: for bromine, observed fast and aligned fragments exhibit a signature of a direct mode of dissociation for the C-Br bond, via the electronically excited potential energy surface denoted nσ*(C-Br), of repulsive nature; for chlorine, a variation in the features is observed for the dissociation pathway through nσ*(C-Cl), from a modality similar to the bromine case, leading to fragments with appreciable kinetic energy release and pronounced directionality, to a modality involving slow products, nearly isotopically distributed. The origin of this behavior can be attributed to nonadiabatic interaction operating between the nσ*(C-Br) and nσ*(C-Cl) surfaces. These results are not only relevant for a detailed understanding of adiabatic versus diabatic coupling mechanisms in the manifold of excited states populated by photon absorption, but they also point out the possibility of selectively inducing specific dissociation pathways, even when involving energetically unfavorable outcomes, such as, in this case, the prevailing rupture of the stronger C-Cl bond against that of the weaker C-Br bond.

An overview of palladium supported on carbon-based materials: Synthesis, characterization, and its catalytic activity for reduction of hexavalent chromium.

Palladium plays a pivotal role in most of the industrial heterogeneous catalysts, because of its unique properties such as well-defined structure, great intrinsic carrier, outstanding electronic, mechanical and thermal stability. The combination of palladium and various porous carbons (PCs) can widen the use of heterogeneous catalysts. This review highlights the advantages and limitations of carbon supported palladium-based heterogeneous catalyst in reduction of toxic hexavalent chromium (Cr(VI)). In addition, we address recent progress on synthesis routes for mono and bimetallic palladium nanoparticles supported by various carbon composites including graphene-based materials, carbon nanotubes, mesoporous carbons, and activated carbons. The related reaction mechanisms for the Cr(VI) reduction are also suggested. Finally, the challenge and perspective are proposed.

Photochemically Synthesized Ruthenium Nanoparticle-Decorated Carbon-Dot Nanochains: An Efficient Catalyst for Synergistic Redox Reactions.

Ruthenium nanoparticle (NP)-decorated carbon dots (Ru/C-dots) were fabricated as a potential catalyst in the application of both oxidation and reduction. The photochemical method was used to synthesize Ru/C-dot nanohybrids. The as-prepared Ru/C-dots exhibited a core-shell-based nanochain structure, in which the spherical nature of C-dots further evolved to a layer structure to homogeneously encapsulate Ru NPs. Such Ru/C-dots have excellent catalytic properties, which were demonstrated in the oxidation of flavonoids and concomitantly reduction of inorganic complex and organic dyes, each yielding a high catalytic rate constant. We also proposed an appropriate catalytic mechanism for each reaction. Higher catalytic activity was achieved by the synergistic effect of the encapsulated Ru NPs and the C-dots layer. Further, this nanohybrid was successfully applied to inspect a real aqueous sample. We anticipated that Ru/C-dots nanohybrid may open up a broad platform for the design of efficient multifunctional catalysts.

Roaming Dynamics and Conformational Memory in Photolysis of Formic Acid at 193 nm Using Time-resolved Fourier-transform Infrared Emission Spectroscopy.

In photodissociation of trans-formic acid (HCOOH) at 193 nm, we have observed two molecular channels of CO + H2O and CO2 + H2 by using 1 µs-resolved Fourier-transform infrared emission spectroscopy. With the aid of spectral simulation, the CO spectra are rotationally resolved for each vibrational state (v = 1-8). Each of the resulting vibrational and rotational population distributions is characteristic of two Boltzmann profiles with different temperatures, originating from either transition state pathway or OH-roaming to form the same CO + H2O products. The H2O roaming co-product is also spectrally simulated to understand the interplay with the CO product in the internal energy partitioning. Accordingly, this work has evaluated the internal energy disposal for the CO and H2O roaming products; especially the vibrational-state dependence of the roaming signature is reported for the first time. Further, given a 1 µs resolution, the temporal dependence of the CO/CO2 product ratio at v ≥ 1 rises from 3 to 10 of study, thereby characterizing the effect of conformational memory and well reconciling with the disputed results reported previously between absorption and emission methods.

Non-invasive and Time-dependent Blood-sugar Monitoring via Breath-derived CO2 Correlation Using Gas Chromatograph with a Milli-whistle Gas Analyzer.

A clear and positive correlation between the CO2 concentration and the blood-sugar level has been observed via a non-invasive and time-dependent monitoring of CO2 concentration from human breath, which is carried out by using a home-made gas chromatography (GC)/milli-whistle compact analyzer. The time-dependent sampling of the CO2 concentration correlated between 5.0 to 5.6% (1% = 104 ppm) in accordance with blood-sugar level variations of 80 to 110 mg/dL. The analytical method results in a rapid, continuous and non-invasive determination of blood-sugar level via measurement of the CO2 concentration exhaled from the lungs.

Ligusticum Striatum-Derived Carbon Dots as Nanocarriers to Deliver Methotrexate for Effective Therapy of Cancer Cells.

Ligusticum striatum herb-derived carbon dots (C-dots) were adopted as a drug carrier to deliver methotrexate (MTX). MTX is a folate antagonist drug for chemotherapy of cancer. The MTX was conjugated with C-dots to form the MTX/C-dot complex through non-covalent bonding. The efficiency of drug loading and release of MTX/C-dots was evaluated, showing a high drug loading (85.9%) capability of C-dots. The MTX/C-dots exhibited pH-dependent MTX release behavior in which high efficiency (∼69%) was obtained at pH 5.0 with respect to the value of ∼47% at pH 7.4. The cell viabilities of MTX/C-dots and bare C-dots were evaluated in HeLa and human normal fibroblasts (NHF) cells. The C-dots possess less toxicity, whereas MTX/C-dots showed high cytotoxicity compared to that of bare MTX in HeLa cells. The content of the folate receptor is higher (1.56 times) in HeLa cells than that of NHF cells such that a dense binding between the MTX and folate receptor reduces the cell viability. This finding confirms that the MTX/C-dots had a higher cellular uptake, signifying the excellent drug carrier property of C-dots. In addition, the fluorescence bioimaging measurements were examined in HeLa cells to demonstrate the drug delivery efficacy of MTX/C-dots by using confocal fluorescence microscopy. Accordingly, the MTX/C-dots demonstrate their potential in the bioimaging and drug delivery system resulting from fascinating features including photoluminescence, good biocompatibility, and proficient cellular uptake and drug release. It is believed that the MTX/C-dot nanocarrier might hold great potential for cancer chemotherapeutic applications.

Recent Advances in Functionalized Carbon Dots toward the Design of Efficient Materials for Sensing and Catalysis Applications.

Since the past decade, enormous research efforts have been devoted to the detection/degradation and quantification of environmental toxic pollutants and biologically important molecules due to their ubiquitous necessity in the fields of environmental protection and human health. These fields of sensor and catalysis are advanced to a new era after emerging of nanomaterials, especially, carbon nanomaterials including graphene, carbon nanotube, carbon dots (C-dots), etc. Among them, the C-dots in the carbon family are rapidly boosted in the aspect of synthesis and application due to their superior properties of chemical and photostability, highly fluorescent with tunable, non/low-toxicity, and biocompatibility. The C-dot-based functional materials have shown great potential in sensor and catalysis fields for the detection/degradation of environmental pollutants. The major advantage of C-dots is that they can be easily prepared from numerous biomass/waste materials which are inexpensive and environment-friendly and are suitable for a developing trend of sustainable materials. This review is devoted to the recent development (since 2017) in the synthesis of biomass- and chemical-derived C-dots as well as diverse functionalization of C-dots. Their capability as a sensor and catalyst and respective mechanism are summarized. The future perspectives of C-dots are also discussed.

Three-dimensional zinc oxide nanostars anchored on graphene oxide for voltammetric determination of methyl parathion.

The two-step microwave method was used to synthesize zinc oxide nanostars linked to graphene oxide (GO) nanosheets. The material was used to modify a screen printed carbon electrode (SPCE) and then explored as a binder-free electrocatalyst for the electrochemical determination of methyl parathion (MP). The morphology and crystallinity of the material were characterized by various techniques. The modified SPCE shows extraordinary electrochemical performances for sensitive determination of MP. Figures of merit include (a) a wide linear dynamic range (0.03-670 µM), (b) a low detection limit (1.2 nM; at S/N = 3), (c) a comparably low working voltage (-0.69 V vs. Ag/AgCl); and (d) an excellent sensitivity (16.5 µA µM-1 cm-2) that surpasses other modified electrodes. The sensor was successfully applied to the determination of MP, even in the presence of other common electroactive interference, in (spiked) fruits and vegetables. Graphical abstractGraphene oxide anchored three-dimensional zinc oxide nanostars were used to coat electrode for the sensing of methyl parathion (MP) by voltammetry.

Pyrene-Based Chemosensor for Picric Acid-Fundamentals to Smartphone Device Design.

Developing a fluorescent probe for the selective and sensitive detection of explosives is a topic of continuous research interest. Additionally, underlying the principles behind the detection mechanism is indeed providing substantial information about the design of an efficient fluorescence probe. In this context, a pyrene-tethered 1-(pyridin-2-yl)imidazo[1,5-a]pyridine-based fluorescent probe (TL18) was developed and employed as a fluorescent chemosensor for nitro explosives. The molecular structure of TL18 was well-characterized by NMR and EI-MS spectrometric techniques. UV-visible absorption, steady-state, and time-resolved fluorescence spectroscopic techniques have been employed to explicate the photophysical properties of TL18. The fluorescent nature of the TL18 probe was explored for detection of nitro explosives. Intriguingly, the TL18 probe was selectively responsive to picric acid over other explosives. The quantitative analysis of the fluorescence titration studies of TL18 with picric acid proved that the probe achieved a detection limit of 63 nM. Further, DFT and QTAIM studies were used to establish the nature of the sensing mechanism of TL18. The hydrogen-bonding interactions are the reason for the imperative sensing property of TL18 for picric acid. Thus, our experimental and theoretical studies provide an adequate and appropriate prerequisite for an efficient fluorescent probe. Furthermore, a smartphone-interfaced portable fluorimeter module is developed to facilitate sensitive and real-time sensing of picric acid. This portable module was capable of detecting picric acid down to 99 nM. Eventually, these studies will have a significant impact on development and application of a new class of chemosensors for detection of explosives.