Understanding the charge transfer dynamics of the Cu2WS4-CNT-FeOOH ternary composite for photo-electrochemical studies.

Ternary transition metal chalcogenide (Cu2WS4) is a semiconductor with a band gap of 2.1 eV and could be a promising candidate for photoelectrochemical water splitting and solar energy conversion applications. Despite numerous reports on ternary transition metal chalcogenides, this semiconductor's ultrafast charge transfer dynamics remain unknown. Here, we report on charge carrier dynamics in a pristine Cu2WS4 system with the aid of ultrafast transient (TA) pump-probe spectroscopy and a hot carrier transfer process from Cu2WS4 to multi-walled carbon nanotubes (CNTs) and FeOOH has been observed. Furthermore, we have explored Cu2WS4-FeOOH having a type-II composite for photo-electrochemical (PEC) water oxidation and modified this with the addition of multi-walled carbon nanotubes to expedite the charge-transfer processes and photo-anodic performance. The photo-electrochemical studies demonstrate that the Cu2WS4-CNT, Cu2WS4-FeOOH, and Cu2WS4-CNT-FeOOH provide nearly 3-, 8- and 12-fold enhancement in photocurrent density relative to the bare Cu2WS4 photo-anode at 1.23 V vs. RHE. These photo-electrochemical studies support the results obtained from the TA investigation and further prove the higher charge separation in the ternary composite system. These studies probe the excited states and provide evidence of longer charge separation in the binary and ternary composites, responsible for their remarkable photo-electrochemical performance.

Correction: Understanding the charge transfer dynamics of the Cu2WS4-CNT-FeOOH ternary composite for photo-electrochemical studies.

Correction for 'Understanding the charge transfer dynamics of the Cu2WS4-CNT-FeOOH ternary composite for photo-electrochemical studies' by Preeti Dagar et al., Phys. Chem. Chem. Phys., 2023, https://doi.org/10.1039/D3CP03498D.

NaBiF4:Yb3+,Tm3+ submicron particles as luminescent probes for in vitro imaging of cells.

Upconversion materials have attracted considerable research interest for their application in bioimaging due to their unique optical properties. NaREF4 (RE = Sc, Y, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb and Lu) based host lattice, which is widely used for upconversion, requires expensive rare-earth elements and tedious reaction conditions. Hence there is a need to develop environmentally friendly and cost effective materials for upconversion. In this study, we propose NaBiF4 as a host material for upconversion which is based on environmentally friendly and cost-effective bismuth. NaBiF4 has not been explored as an imaging probe before. We report efficient Yb3+/Tm3+ doped NaBiF4 based upconversion submicron particles which exhibit a photostable, wide upconversion emission range (NIR-to-NIR and Vis) under NIR (980 nm) excitation, and in-vitro non-cytotoxic uptake by mammalian cancer cell lines as well as bacterial cells with a high signal to background ratio. The synthesis of the chosen host material co-doped with Yb3+/Tm3+ has not been reported earlier through such a non-aqueous quaternary reverse micelle route. Here, we functionally validate these submicron particles as viable alternatives to currently available upconversion nanomaterials and highlight their potential as luminescent probes for bioimaging.

Thickness-dependent magneto-transport properties of topologically nontrivial DyPdBi thin films.

DyPdBi (DPB) is a topological semimetal which belongs to the rare-earth-based half-Heusler alloy family. In this work, we studied the thickness-dependent structural and magneto-transport properties of DPB thin films (20 to 60 nm) grown using pulsed laser deposition. The DPB thin films show (110) oriented growth on MgO(100) single crystal substrates. Longitudinal resistance data indicate metallic surface states dominated carrier transport and the suppression of semiconducting bulk state carriers for films ≤40 nm. We observe the weak antilocalization (WAL) effect and Shubnikov-de Hass (SdH) oscillations in the magneto-transport data. The presence of a single coherent transport channel (α∼ -0.50) is observed in the Hikami-Larkin-Nagaoka (HLN) fitting of WAL data. The power law temperature dependence of phase coherence length (LØ ) ∼ T-0.50 indicates the observation of the 2D WAL effect and the presence of topological nontrivial surface states for films ≤40 nm. The 60 nm sample shows semiconducting resistivity behavior at higher temperature (>180 K) and HLN fitting results (α∼ -0.72, LØ âˆ¼ T-0.68 ) indicate the presence of partial decoupled top and bottom surface states. The Berry phase ∼π is extracted for thin films ≤40 nm, which further demonstrates the presence of Dirac fermions and nontrivial surface states. Band structure parameters are extracted by fitting SdH data to the standard Lifshitz-Kosevich formula. The sheet carrier concentration and cyclotron effective mass of carriers decrease with increasing thickness (20 nm to 60 nm) from ∼1.35 × 1012 cm-2 to 0.68 × 1012 cm-2 and from ∼0.26 me to 0.12 me, respectively. Our observations suggest that samples with a thickness ≤40 nm have transport properties dominated by surface states and samples with a thickness ≥60 nm have contributions from both bulk and surface states.

Understanding the role of ionic flux on the polarity of the exposed surfaces of ZnO.

The role of ionic flux in controlling the polarity of the surfaces of ZnO was evaluated, both experimentally and theoretically. Zinc oxide was synthesized by controlled decomposition of zinc oxalate nanorods in the presence of ionic flux. The degree of preferred orientation for a specific plane, for the ZnO structures, was observed by calculating the texture coefficient. The presence of flux (NaCl, KCl, a mixture of NaCl-KCl and Na2SO4) during decomposition of the oxalate precursor led to the preferential growth of (112[combining macron]0) planes. The value of texture coefficient was found to be high for the (112[combining macron]0) plane when the decomposition was carried out in the presence of a mixture of NaCl and KCl when compared to their counterparts. A decrease in the value of texture coefficient for the (112[combining macron]0) plane was observed when Na2SO4 was used as a flux, which was similar to the value obtained for ZnO synthesized in the absence of flux. The observations from the analysis of texture coefficient were correlated with the photocatalytic degradation of rhodamine B dye, by making use of the fact that the nature of exposed surfaces influences the catalytic activity of a material. On-site Coulomb correlation corrected density functional theory (DFT + U)-based computational studies were performed to get theoretical insight into the role of the ionic flux in surface reconstructions. The surface energies for different ZnO surfaces were computed in the presence and absence of the ionic flux. It was revealed that the pristine (101[combining macron]0) surface is more stable compared to pristine (112[combining macron]0) by 0.04 J m-2 (surface energy), however the scenario changes in the presence of the ionic flux and (112[combining macron]0) becomes more stable by 0.03 J m-2. This indeed corroborated with our experimental observations and explained the fundamental role of ionic flux on the polarity of exposed surfaces of ZnO.

Hydrotrope-Driven Self-Assembly in CTAB/ n-Hexanol/Water/Heptane Reverse Micellar System.

Self-organization of nanoparticles into one-dimensional (1D) nanochains leads to new unpredicted physiochemical properties, which are further exploited to develop photonic or electronic devices. Thus, the controlled fabrication of 1D nanochains requires nanotemplate, which acts as building blocks for the self-assembly of nanoparticles. To address this issue, we designed a hydrotrope (sodium salicylate)-based CTAB/ n-hexanol/water/heptane reverse micellar system. Hydrotrope, herein, modulates electrostatic interactions between reverse micellar droplets and paves the way for the formation of self-assembled structures. Small-angle X-ray scattering studies were performed on the CTAB/heptane reverse micellar system by varying hydrotrope concentrations and water-to-surfactant ratios (W x). The aqueous content of the reverse micellar pool is determined from the W x value, where W x = [H2O]/[CTAB] and [CTAB] = 0.05 M. SAXS studies were performed for CTAB/heptane reverse micellar systems at three different W x values, that is, 6, 12, and 16 and represented by W6, W12, and W16, respectively. All SAXS profiles were modeled with a spherical form factor and a Baxter sticky hard sphere structure factor. The interaction between droplets was predicted in terms of stickiness parameter. The effect of W x on the formation of self-assembled structures and forces governing the assembly has been discussed in detail. For the W6 system, the electrostatic repulsion between reverse micellar droplets decreases, resulting in the formation of the 1D chain-like assembly of nanodroplets. In the case of the W12 system, the dual feature of the hydrotrope has been observed, it increases the size of the reverse micellar system and reduces electrostatic repulsion between droplets because of which the formation of chain-like assemblies cannot be determined with accuracy. For the W16 system, the decrease in micellar size with the increase in the hydrotrope concentration has been observed. Thus, our reverse micellar templates may provide a comprehensive method for the fabrication of high aspect ratio 1D nanochains of a variety of materials and harnessing their collective properties for magnetic, catalytic, and opto-electronic applications.

Correction: Understanding the role of co-surfactants in microemulsions on the growth of copper oxalate using SAXS.

Correction for 'Understanding the role of co-surfactants in microemulsions on the growth of copper oxalate using SAXS' by Sunaina et al., Phys. Chem. Chem. Phys., 2019, 21, 336-348.

New process for conversion of hazardous industrial effluent of ceramic industry into nanostructured sodium carbonate and their application in textile industry.

Increase in industrialization as a tool to become global leader has led to an exponential rise in environmental pollution. The present study describes a process developed to extract nanocrystalline sodium carbonate from chemical industry effluents, which contributes to wealth creation from hazardous waste. Sodium carbonate is a high demand product because of its applications in detergents, dyeing, glass, and paper manufacturing. In the present work, we have extracted nanostructured sodium carbonate using industrial waste (alkaline solution of silicates, obtained from ceramic industry) and carbon dioxide (a major component of flue gas effluent from power plants). Here we have collected waste from ceramic industries, which is highly corrosive (pH 13-14) and disposal of such waste is dangerous to the environment and needs to be taken special care. Pure carbon dioxide has been purged in collected industrial waste to get nanoparticles and flakes structure of sodium carbonate at room temperature. The use of the nanostructured sodium carbonate in the dyeing of textiles was encouraging. Significantly, higher dyeing efficacy was observed compared to the fabric dyed in the absence of sodium carbonate (Na2CO3). The nanocrystalline particles show much better color strength than bulk sodium carbonate when K/S value was compared. Na2CO3 with the minimum particle size (26 nm) results in the maximum color strength (K/S = 14.49).

Design and Comparative Studies of Z-Scheme and Type II Based Heterostructures of NaNbO3/CuInS2/In2S3 for Efficient Photoelectrochemical Applications.

Here, we report the fabrication of a new Z-scheme based core/shell/shell heterostructure of NaNbO3/CuInS2/In2S3 (core/shell/shell) for photoelectrochemical (PEC) water splitting and also for degradation of organic pollutants. We have also performed a comparative study with a modified heterostructure of NaNbO3/In2S3/CuInS2 having Type II band alignment. The PEC measurements under visible light irradiation show increased photocatalytic performance for the NaNbO3/CuInS2/In2S3 heterostructures as revealed by a high current density of ∼6.72 mA/cm2 at -1.0 V versus Ag/AgCl and low photocurrent onset potential of ∼ -110 mV in comparison to the Type II system (∼1.63 mA/cm2 and -180 mV vs Ag/AgCl). Mott-Schottky plots confirmed the n-p-n type heterojunction formation in the NaNbO3/CuInS2/In2S3 heterostructure which reduces the charge carrier recombination (revealed by PL intensity and short lifetime). The Z-scheme based system also exhibits excellent degradation efficiency (∼99.6%) of organic pollutants. This work shows that the Z-scheme charge separation mechanism in NaNbO3/CuInS2/In2S3 nanostructures is more efficient than the Type II based on NaNbO3/In2S3/CuInS2.

Understanding the role of co-surfactants in microemulsions on the growth of copper oxalate using SAXS.

This study is an effort to understand the mechanism of the effect of the chain length of co-surfactants on the growth of copper oxalate inside the core of reverse micelles using small angle X-ray scattering (SAXS). In this study, we have used two different kinds of co-surfactants viz. 1-butanol (C4) and 1-octanol (C8) for the formation of the microemulsions. Time-dependent SAXS studies were carried out for these two systems. The data were analyzed using both the model-independent approach and model-dependent approach. For microemulsions containing only water inside the core of reverse micelles (no ions), the shape of the reverse micelles was observed to be ellipsoid and spherical in nature for 1-butanol and 1-octanol respectively. For a system containing copper oxalate nanostructures, the fitting was carried out using the ellipsoidal core-shell model for reverse micelles and spheres, ellipsoids and cylinders for copper oxalate nanostructures with 1-butanol as the co-surfactant. With 1-octanol as the co-surfactant, the two contributions that were used were the spherical core-shell model for reverse micelles and spheres for copper oxalate nanostructures. Based on the analysis of SAXS data, a growth mechanism has been proposed. The study discussed here could open the field of understanding the growth mechanism of complex nanostructures formed using the microemulsion route.

Nanocatalysts for hydrogen evolution reactions.

Hydrogen fuel is among the cleanest renewable resources and is the best alternative to fossil fuels for the future. Hydrogen can be best produced by means of electrolysis or photoelectrolysis of water among the various routes available for hydrogen production. So far, Pt has been recognized as the best electrode material for electrochemical hydrogen production. However, the cost of the catalyst, activity, and durability make Pt-catalyzed hydrogen production unsuitable on a commercial scale. It has hence become imperative to explore low-cost, highly active and durable HER catalysts to replace platinum as a catalyst. This perspective provides key concepts and the current status of the research on the properties of nanocatalysts that influence the hydrogen evolution reaction. Important structural features controlling the surface chemistry (i.e. facets, defects, dopants), nature of supports (graphene, CNTs, black phosphorus), role of heteroatoms, media and morphology are the key points of discussion in this perspective.

Unconventional superconductivity at mesoscopic point contacts on the 3D Dirac semimetal Cd3As2.

Three-dimensional (3D) Dirac semimetals exist close to topological phase boundaries which, in principle, should make it possible to drive them into exotic new phases, such as topological superconductivity, by breaking certain symmetries. A practical realization of this idea has, however, hitherto been lacking. Here we show that the mesoscopic point contacts between pure silver (Ag) and the 3D Dirac semimetal Cd3As2 (ref. ) exhibit unconventional superconductivity with a critical temperature (onset) greater than 6 K whereas neither Cd3As2 nor Ag are superconductors. A gap amplitude of 6.5 meV is measured spectroscopically in this phase that varies weakly with temperature and survives up to a remarkably high temperature of 13 K, indicating the presence of a robust normal-state pseudogap. The observations indicate the emergence of a new unconventional superconducting phase that exists in a quantum mechanically confined region under a point contact between a Dirac semimetal and a normal metal.

Hydrotrope induced structural modifications in CTAB/butanol/water/isooctane reverse micellar systems.

Designing nanostructures of desired morphology calls for development of new synthetic protocols to stimulate structural alterations in templates, modulating the architecture of nano-metric structures. The present study is an endeavor to investigate structural modifications in reverse micellar nanotemplates of a cationic surfactant system, CTAB/butanol/water/isooctane, as a function of hydrotrope concentration (sodium salicylate) and amount of water loading, Wx, in the micellar pool by synchrotron small-angle X-ray scattering. The micellar structural transition from a one-dimensional cylinder to a prolate ellipsoid can be controlled by tuning the water-to-surfactant molar ratio while the hydrotrope modulates growth of the micellar droplets. The inter-micellar interactions in these systems could be best represented by the Polymer Reference Interaction Site (PRISM) model at lower water content in the reverse micellar pool and by the Macroion model at higher water loadings. The location of the hydrotrope inside the micellar assembly and its interaction with different components of the reverse micellar system is probed with the help of 1H NMR studies. The formation and tuning of anisotropic cylindrical/ellipsoidal reverse micellar droplets suggest promising application of such aggregates as "tunable soft templates" for fabricating fascinating nanostructures.

The mechanism of nanoparticle-mediated enhanced energy transfer during high-intensity focused ultrasound sonication.

In this combined experimental and theoretical research, magnetic nano-particle (mNP) mediated energy transfer due to high intensity-focused ultrasound (HIFU) sonication has been evaluated. HIFU sonications have been performed on phantoms containing three different volume percentages (0%, 0.0047%, and 0.047%) of mNPs embedded in a tissue mimicking material (TMM). A theoretical model has been developed to calculate the temperature rise in the phantoms during HIFU sonication. It is observed from theoretical calculation that the phonon layer at the interface of the mNPs and TMM dominates the attenuation for higher (0.047%) concentration. However, for a lower concentration (0.0047%) of mNPs, intrinsic absorption is the dominating mechanism. Attenuation due to the viscous drag becomes the dominating mechanism for larger size mNPs (>1000 nm). At a higher concentration (0.047%), it is observed from theoretical calculations that the temperature rise is 25% less for gold nano-particles (gNPs) when compared to mNPs. However, at lower concentrations (0.0047% and 0.002%), the difference in temperature rise for the mNPs and gNPs is less than 2%.

Cu-Based Nanocomposites as Multifunctional Catalysts.

Herein, we report the synthesis of Cu/Cu2 O nanocomposites by a one-step hydrothermal process at 180 °C, for which the resulting morphology is dependent on the hydrothermal reaction time (24, 72, and 120 h). With a longer reaction time of 120 h, a rod-shape morphology is obtained, whereas at 72 and 24 h assemblies of nanoparticles are obtained. The rod-shaped (120 h) particles of the Cu/Cu2 O nanocomposites show a much higher efficiency (6.3 times) than the agglomerates and 2.5 times more than the assemblies of nanoparticles for the hydrogen-evolution reaction. During the oxygen-evolution reaction, the nanorods produce a current that is 5.2 and 3.7 times higher than that produced by the agglomerated and assembled nanoparticles, respectively. The electrocatalysts are shown to be highly stable for over 50 cycles. As catalysts for organic synthesis, a 100 % yield is achieved in the Sonogashira cross-coupling reaction with the nanorods, which is higher than with the other nanocomposite particles. This result demonstrates the significant enhancement of yield obtained with the nanorods for cross-coupling reactions.

Probing the Crystal Structure, Composition-Dependent Absolute Energy Levels, and Electrocatalytic Properties of Silver Indium Sulfide Nanostructures.

The absolute electronic energy levels in silver indium sulfide (AIS) nanocrystals (NCs) with varying compositions and crystallographic phases have been determined by using cyclic voltammetry. Different crystallographic phases, that is, metastable cubic, orthorhombic, monoclinic, and a mixture of cubic and orthorhombic AIS NCs, were studied. The band gap values estimated from the cyclic voltammetry measurements match well with the band gap values calculated from the diffuse reflectance spectra measurements. The AIS nanostructures were found to show good electrocatalytic activity towards the hydrogen evolution reaction (HER). Our results clearly establish that the electronic and electrocatalytic properties of AIS NCs are strongly sensitive to the composition and crystal structure of AIS NCs. Monoclinic AIS was found to be the most active HER electrocatalyst, with electrocatalytic activity that is almost comparable to the MoS2 -based nanostructures reported in the literature, whereas cubic AIS was observed to be the least active of the studied crystallographic phases and compositions. In view of the HER activity and electronic band structure parameters observed herein, we hypothesize that the Fermi energy level of AIS NCs is an important factor that decides the electrocatalytic efficiency of these nanocomposites. The work presented herein, in addition to being the first of its kind regarding the composition and phase-dependence of electrochemical aspects of AIS NCs, also presents a simple solvothermal method for the synthesis of different crystallographic phases with various Ag/In molar ratios.

Design of porous silica supported tantalum oxide hollow spheres showing enhanced photocatalytic activity.

Silica-supported tantalum oxide (ST) hollow spheres were designed for photocatalytic applications in the UV range of 4.1 to 4.8 eV. These nanostructures with a variable diameter of 100-250 nm and shell thickness of 24-58 nm were obtained by the hydrothermal treatment of tantalum isopropoxide and tetraethylorthosilicate at 120 °C for 48 h in the presence of cetyl trimethyl ammonium bromide, which was used as a capping agent. The maximum observed surface area was found to be 610 m(2)/g and pore size distribution of ST hollow spheres varied from 13.4 to 19.0 nm. Lewis acidity of silica and the contact area between SiO2 and Ta2O5 plays a crucial role in controlling the photocatalytic properties of the ST hollow spheres. We observe a remarkable 6× enhancement in the photoactivity of silica-supported tantalum oxide hollow spheres compared to pure Ta2O5.

Band gap engineering of ZnO using core/shell morphology with environmentally benign Ag2S sensitizer for efficient light harvesting and enhanced visible-light photocatalysis.

Band gap engineering offers tunable optical and electronic properties of semiconductors in the development of efficient photovoltaic cells and photocatalysts. Our study demonstrates the band gap engineering of ZnO nanorods to develop a highly efficient visible-light photocatalyst. We engineered the band gap of ZnO nanorods by introducing the core/shell geometry with Ag2S sensitizer as the shell. Introduction of the core/shell geometry evinces great promise for expanding the light-harvesting range and substantial suppression of charge carrier recombination, which are of supreme importance in the realm of photocatalysis. To unveil the superiority of Ag2S as a sensitizer in engineering the band gap of ZnO in comparison to the Cd-based sensitizers, we also designed ZnO/CdS core/shell nanostructures having the same shell thickness. The photocatalytic performance of the resultant core/shell nanostructures toward methylene blue (MB) dye degradation has been studied. The results imply that the ZnO/Ag2S core/shell nanostructures reveal 40- and 2-fold enhancement in degradation constant in comparison to the pure ZnO and ZnO/CdS core/shell nanostructures, respectively. This high efficiency is elucidated in terms of (i) efficient light harvesting owing to the incorporation of Ag2S and (ii) smaller conduction band offset between ZnO and Ag2S, promoting more efficient charge separation at the core/shell interface. A credible photodegradation mechanism for the MB dye deploying ZnO/Ag2S core/shell nanostructures is proposed from the analysis of involved active species such as hydroxyl radicals (OH(•)), electrons (e(-)(CB)), holes (h(+)(VB)), and superoxide radical anions (O2(•-)) in the photodegradation process utilizing various active species scavengers and EPR spectroscopy. The findings show that the MB oxidation is directed mainly by the assistance of hydroxyl radicals (OH(•)). The results presented here provide new insights for developing band gap engineered semiconductor nanostructures for energy-harvesting applications and demonstrate Ag2S to be a potential sensitizer to supersede Cd-based sensitizers for eco-friendly applications.

The iron-age of superconductivity: structural correlations and commonalities among the various families having -Fe-Pn- slabs (Pn = P, As and Sb).

The fascination of mankind towards a sudden change of a property, like colour, shape, elasticity, viscosity, electrical conductivity and magnetism, is well known. If the change in property is such that it leads to disapperance of an existing property or development of a new property then the effect is magical. It is for this reason that superconductivity remains an enigma for scientists for over a century after Kammerlingh Onnes discovered that the electrical resistance of mercury falls to zero below a temperature of 4.2 K. Since then scientists have been enchanted by superconductivity. Over these hundred years attempts have been made to discover materials which show this effect at higher temperatures. After a very exciting period of Cu oxide superconductors (1986-1993) there has been a lull in the search for high T(c) materials. The discovery of superconductivity in 2008 at 26 K in LaOFeAs (F-doped) has renewed the excitement in the field of superconductivity. This breakthrough in an Fe-containing compound led to the discovery of several new families of Fe-based superconductors having either pnictogens (P, As) or chalcogen (Se, Te) of the type AFFeAs (A = alkaline-earth metal), AFe(2)As(2), AFeAs (A = alkali metals), A(3)M(2)O(5)Fe(2)As(2) (M = transition metals) and A(4)M(2)O(6)Fe(2)As(2). This review article discusses in detail the structural aspects of these new Fe-based superconductors which primarily consist of edge-shared distorted FeX(4) (X = pnictogen and chalcogen) tetrahedra and these tetrahedral layers are reponsible for enabling superconductivity. Extremely large upper critical field (>200 Tesla) of these superconductors make them promising for high field application. Structural commonalities and differences among different families of these superconductors have been outlined. We also discuss the common features and differences with the copper-oxide based superconductors. Here we have discussed all the Fe-based oxypnictide families (like LnOFePn, AFe(2)Pn(2), AFFePn and A(4)M(2)M'Fe(2)As(2)O(6)etc.) known today and have also included the phosphides and antimonides other than the arsenides. We have in addition discussed in detail the various factors like pressure, hole and electron doping, transition metal doping, which have not been reviewed earlier.

Plasmon enhanced fluoro-immunoassay using egg yolk antibodies for ultra-sensitive detection of herbicide diuron.

Plasmon enhanced fluorescence immunoassay (PEFI) format has been reported in developing a sensitive heterogeneous fluoroimmunoassay for monitoring the phenylurea herbicide diuron. Computer-assisted molecular modeling was carried out to study the conformational and electrostatic effects of synthesized hapten for producing highly specific egg yolk antibody against a phenyl urea herbicide diuron. The generated antibodies were labeled with fluorescein isothiocyanate at different molar ratios and used as tracer in the developed fluorescence based immunoassay. The sensitivity of the assay format was enhanced by using silver nanoparticles tagged with bovine serum albumin as a new blocking reagent in the developed PEFI format. Enhancer treatment on the developed immunoassay showed a significant improvement of fluorescence signal intensity with approximately 10 fold increase in assay sensitivity. The immunoassay has a detection limit of 0.01 ng mL(-1) with good signal precision (~2%) in the optimum working concentration range between 1 pg mL(-1) to 10 µg mL(-1) of diuron. These findings facilitate high throughput fluorescence-based processes that could be useful in biology, drug discovery and compound screening applications.