Tin Oxide Surface Research Articles

Thiol Groups Reutilization on Chemical Bath Deposited Tin Oxide Surface Achieving Interface Anchoring and Defects Passivation for Enhancing the Performance and Stability of Perovskite Solar Cells.

Due to its simple process and adaptability to large-area deposition, chemical bath deposition (CBD) is one of the preparation methods for the SnO2 layer in highly efficient "n-i-p" structured perovskite solar cells (PSCs). However, the residual thioglycolic acid (TGA) on the CBD-SnO2 surface affects the stability of PSCs and the carrier transport at the CBD-SnO2/perovskite interface, hindering the further development of this method. This work demonstrates a method for the reutilization of surface groups to construct molecular bridges. This strategy utilizes the substitution reaction between the residual thiol group on the CBD-SnO2 surface and the iodine group of iodoacetamide (IAM) to form the IAM structure. The IAM structure not only assists the perovskite grain crystallization but also increases the electronic cloud density of the CBD-SnO2 surface. Consequently, the charge mobility of the CBD-SnO2 is enhanced and the energy band alignment at the CBD-SnO2/perovskite interface is optimized. A champion device with the IAM structure achieved a power conversion efficiency (PCE) of 22.41% while it maintained 80% of its original PCE after placing at 65°C in nitrogen filled atmosphere for over 300h and in an environment at 25°C and 50 ± 5% relative humidity for over 1000h, respectively.

Surface Modification of Heterojunction with Intrinsic Thin Layer Solar Cell Electrode with Organosilane.

Solar cell (SC) technologies, which are essential in the transition toward sustainable energy, utilize photovoltaic cells to convert solar energy into electricity. Of the available technologies, heterojunction with intrinsic thin-layer (HIT) solar cells offers high efficiency and reliability. The current study explored the enhancement of HIT solar cell performance through the use of 3-aminopropyltrimethoxysilane (APTMS) self-assembled monolayers (SAMs) on the surface of the cells' indium tin oxide (ITO) layer. Photoluminescence mapping revealed greater brightness and photocurrent in the HIT sample treated with APTMS SAMs, with the results indicating more favorable optical and electrical properties. The application of APTMS SAMs led to higher open-circuit voltage, fill factor, maximum power output, and efficiency by passivating the ITO surface and achieving energy level alignment, thereby enhancing the charge carrier dynamics. These findings demonstrate the potential of APTMS SAMs to improve HIT solar cell efficiency and reliability.

Single-Particle Spectroelectrochemistry: Revealing the Electrochemical Tuning Mechanism of Chemical Interface Damping in 1,2-Benzenedithiol-Adsorbed Single Gold Nanorods.

Chemical interface damping (CID) is a newly proposed plasmon damping pathway based on interfacial hot-electron transfer from metal to adsorbate molecules. However, achieving in situ tunability of CID in single gold nanorods (AuNRs) remains a considerable challenge. Here, we present the CID effect induced by benzene 1,2-dithiol (BDT) molecule adsorption on single AuNRs and the effective electrochemical tunability of CID in BDT-adsorbed AuNRs immobilized on an indium tin oxide (ITO) surface. Manipulations of the electrochemical potential alter the electron density of AuNRs, thereby influencing and tuning the localized surface plasmon resonance (LSPR) spectrum, with cathodic potential blueshifting and anodic potential redshifting. The strong adsorption of BDT on Au induced CID in single AuNRs. The potential-induced LSPR scattering spectra of BDT-adsorbed AuNRs for linear potential sweep showed a stable LSPR spectral response, irrespective of the concentrations of BDT molecules. Due to the involvement of two Au-S bonds, BDT molecules have a higher free adsorption energy and a lower desorption rate on the Au surface. This resulted in a stable LSPR spectral response for a linear electrochemical potential sweep. Furthermore, a constant anodic and cathodic potential application showed the tunability of the CID at the BDT-Au interface.

Photolytic decomposition of PFOS by electrospun nanofiber composites of Fe(III)/PVDF Under UV-C light

Per- and polyfluoro alkyl substances (PFAS) are emerging pollutants that have contaminated various water streams of the world. Besides polluting the environment, it is related to several human diseases, including cancer. Various methods have been proposed to remove PFAS from water streams including, photocatalytic or photolytic decomposition of PFAS which decomposes PFAS in a quasi-perpetual fashion and does not generate secondary pollution. In this work, perfluoroctane sulfonic acid (PFOS) is used as a model PFAS to study its photolytic decomposition by nanofiber composites (NFC) of Fe (III) and polyvinylidene fluoride (PVDF) under ultraviolet (UV)-C light. The nanofiber composite was fabricated using an electrospinning technique with PVDF and iron precursor on the conductive surface of indium tin oxide (ITO) coated polyethylene terephthalate (PET) film. The composite was characterized with SEM-EDX, AFM, XRD, and TGA. It was found that a significant amount, 70 % of aqueous PFOS solution is decomposed by the composites in the presence of traces of hydrogen peroxide and UV-C light. The kinetics of PFOS degradation was fit with pseudo-first order rate constant of 0.056 hr−1. It is proposed that PFOS binds with Fe(III) to form an unstable complex that is decomposed under UV-C light and Fe(III) is reduced Fe(II). Hydrogen peroxide provides the simultaneous benefits of further decomposing the PFOS complex and regenerating Fe(III). The overall results suggest that this nanofiber composite can be used for the photolytic decomposition of PFOS. It is also revealed that two composite mats showed the optimal performance and the increase in concentration of hydrogen peroxide increased the degradation of PFOS monotonically.

Mechanical reconfigurable infrared filter for stress sensing applications

In this study, we introduce a novel tunable infrared filter design aimed at stress sensor applications such as health monitoring, advanced robotics and industrial automation. The design utilizes a double-layer plasmonic frequency-selective surface (FSS) of indium tin oxide (ITO) with an aerogel inter-space region. The unique feature of this design is its ability to control the transmission pattern based on the stress exerted, which alters the distance between the two filter layers. Our approach employs both numerical simulations and a simplified model grounded in equivalent circuit theory and the transfer matrix method for accurate transmission pattern estimation where the sensor achieved a sensitivity of 20nm/MPa for average stress of 14MPa and spectrum range (λ>800nm\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$\\lambda >800 nm$$\\end{document}). The work provides an in-depth analysis of how layer dimensions and inter-layer distance influence both transmission and force, taking into account the elastic properties of the inter-space material.

Signal-on sensor using MOF-MoS2 with high-performance photoelectrochemical activity for specific detection of Hg2+

Mercury is a common, bioaccumulative, and highly toxic pollutant, and its harmful effects on the human body and environment should not be underestimated. In this study, an enzyme-free photoelectrochemical (PEC) analysis method based on signal-on detection was developed using a novel photoelectrochemically active material, metal–organic framework (MOF)-MoS2, for the specific detection of Hg2+. Driven by visible light, MOF-MoS2 can be used as a PEC sensitizer and Hg2+ recognition probe. With the addition of Hg2+, the active sulfur sites on the MOF-MoS2/F-doped tin oxide surface specifically combined to yield HgS, which was further used for signal amplification and specifically turned on the photocurrent response of the electrode. In addition, the p–n junction formed between the MOF-MoS2/HgS complexes triggered the development of MOF-MoS2 composites in the direction of electron–hole separation, leading to an increase in optoelectronic signals. Importantly, the PEC sensor detected Hg2+ over a wide linear range from 0.01 to 1000 nM, with a limit of detection of 0.25 pM. The fabricated sensor exhibited good stability, excellent reproducibility, and specificity. The PEC platform may provide new insights into the non-intrusive detection of Hg2+ in human and water samples.

Enhanced Performance of P-Channel CuIBr Thin-Film Transistor by ITO Surface Charge-Transfer Doping.

The process development and optimization of p-type semiconductors and p-channel thin-film transistors (TFTs) are essential for the development of high-performance circuits. In this study, the Br-doped CuI (CuIBr) TFTs are proposed by the solution process to control copper vacancy generation and suppress excess holes formation in p-type CuI films and improve current modulation capabilities for CuI TFTs. The CuIBr films exhibit a uniform surface morphology and good crystalline quality. The on/off current (ION/IOFF) ratio of CuIBr TFTs increased from 103 to 106 with an increase in the Br doping ratio from 0 to 15%. Furthermore, the performance and operational stability of CuIBr TFTs are significantly enhanced by indium tin oxide (ITO) surface charge-transfer doping. The results obtained from the first-principles calculations well explain the electron-doping effect of ITO overlayer in CuIBr TFT. Eventually, the CuIBr TFT with 15% Br content exhibits a high ION/IOFF ratio of 3 × 106 and a high hole field-effect mobility (μFE) of 7.0 cm2 V-1 s-1. The band-like charge transport in CuIBr TFT is confirmed by the temperature-dependent measurement. This study paves the way for the realization of transparent complementary circuits and wearable electronics.

Label-Free Electrochemical Dopamine Biosensor Based on Electrospun Nanofibers of Polyaniline/Carbon Nanotube Composites.

The development of conducting polymer incorporated with carbon materials-based electrochemical biosensors has been intensively studied due to their excellent electrical, optical, thermal, physical and chemical properties. In this work, a label-free electrochemical dopamine (DA) biosensor based on polyaniline (PANI) and its aminated derivative, i.e., poly(3-aminobenzylamine) (PABA), composited with functionalized multi-walled carbon nanotubes (f-CNTs), was developed to utilize a conducting polymer as a transducing material. The electrospun nanofibers of the composites were fabricated on the surface of fluorine-doped tin oxide (FTO)-coated glass substrate under the optimized condition. The PANI/f-CNTs and PABA/f-CNTs electrospun nanofibers were characterized by attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and transmission electron microscopy (TEM), which confirmed the existence of f-CNTs in the composites. The electroactivity of the electrospun nanofibers was investigated in phosphate buffer saline solution using cyclic voltammetry (CV) before being employed for label-free electrochemical detection of DA using differential pulse voltammetry (DPV). The sensing performances including sensitivity, selectivity, stability, repeatability and reproducibility of the fabricated electrospun nanofiber films were also electrochemically evaluated. The electrochemical DA biosensor based on PANI/f-CNTs and PABA/f-CNTs electrospun nanofibers exhibited a sensitivity of 6.88 µA·cm-2·µM-1 and 7.27 µA·cm-2·µM-1 in the linear range of 50-500 nM (R2 = 0.98) with a limit of detection (LOD) of 0.0974 µM and 0.1554 µM, respectively. The obtained DA biosensor showed great stability, repeatability and reproducibility with precious selectivity under the common interferences, i.e., glucose, ascorbic acid and uric acid. Moreover, the developed electrochemical DA biosensor also showed the good reliability under detection of DA in artificial urine.

In situ Blending For Co-Deposition of Electron Transport and Perovskite Layers Enables Over 24% Efficiency Stable Conventional Solar Cells.

Simplifying the manufacturing processes of multilayered high-performance perovskite solar cells (PSCs) is yet of vital importance for their cost-effective production. Herein, an in situ blending strategy is presented for co-deposition of electron transport layer (ETL) and perovskite absorber by incorporating (3-(7-butyl-1,3,6,8-tetraoxo-3,6,7,8-tetrahydrobenzo- [lmn][3,8]phenanthrolin-2(1H)-yl)propyl)phosphonic acid (NDP) into the perovskite precursor solutions. The phosphonic acid-like anchoring group coupled with its large molecular size drives the migration of NDP toward indium tin oxide (ITO) surface to form a distinct ETL during perovskite film forming. This strategy circumvents the critical wetting issue and simultaneously improves the interfacial charge collection efficiencies. Consequently, n-i-p PSCs based on in situ blended NDP achieve a champion power conversion efficiency (PCE) of 24.01%, which is one of the highest values for PSCs using organic ETLs. This performance is notably higher than that of ETL-free (21.19%) and independently spin-coated (21.42%) counterparts. More encouragingly, the in situ blending strategy dramatically enhances the device stability under harsh conditions by retaining over 90% of initial efficiencies after 250h in 100°C or 65% humidity storage. Moreover, this strategy is universally adaptable to various perovskite compositions, device architectures, and electron transport materials (ETMs), showing great potential for applications in diverse optoelectronic devices.

Volcanic Eruption in the Nanoworld: Efficient Oxygen Exchange at the Si/SnO2 Interface.

Here, a phenomenon of efficient oxygen exchange between a silicon surface and a thin layer of tin dioxide during chemical vapor deposition is presented, which leads to a unique Sn:SiO2 layer. Under thermodynamic conditions in the temperature range of 725-735°C, the formation of nanostructures with volcano-like shapes in "active" and "dormant" states are observed. Extensive characterization techniques, such as electron microscopy, X-ray diffraction, synchrotron radiation-based X-ray photoelectron, and X-ray absorption near-edge structure spectroscopy, are applied to study the formation. The mechanism is related to the oxygen retraction between tin(IV) oxide and silicon surface, leading to the thermodynamically unstable tin(II)oxide, which is immediately disproportionate to metallic Sn and SnO2 localized in the SiO2 matrix. The diffusion of metallic tin in the amorphous silicon oxide matrix leads to larger agglomerates of nanoparticles, which is similar to the formation of a magma chamber during the natural volcanic processes followed by magma eruption, which here is associated with the formation of depressions on the surface filled with metallic tin particles. This new effect contributes a new approach to the formation of functional composites but also inspires the development of unique Sn:SiO2 nanostructures for diverse application scenarios, such as thermal energy storage.

Dielectric Properties of a Ferroelectric Nematic Material: Quantitative Test of the Polarization-Capacitance Goldstone Mode.

The recently discovered ferroelectric nematic (N_{F}) liquid crystals (LC) have been reported to show an extraordinarily large value of the real part of the dielectric constant (ϵ^{'}>10^{3}) at low frequencies. However, it was argued by Clark etal. in Phys. Rev. Res. 6, 013195 (2024)PPRHAI2643-156410.1103/PhysRevResearch.6.013195 that what was measured was the capacitance of the insulating layer at LC or electrode surface and not that of the liquid crystal. Here we describe the results of dielectric spectroscopy measurements of an N_{F} material in cells with variable thickness of the insulating layers. Our measurements quantitatively verify the model by Clark etal. Additionally, our measurements in cells with bare conducting indium tin oxide surface provide a crude estimate of ϵ_{⊥}∼10^{2} in the N_{F} phase.

Optimizing luminous efficiency in polymer light-emitting diodes through anode oxygen-plasma treatment under diverse pressure conditions

This study investigates the impact of oxygen-plasma (O2-plasma) treatment on the microscale electrical properties of indium tin oxide (ITO) surfaces for enhancement of the luminous efficiency of polymer light-emitting diodes (PLEDs). Significant effects on conductivity distribution were observed when treatment was performed at pressures exceeding 0.4 Torr. ITO-6, the ITO treated with O2-plasma at 0.6 Torr, emerged as the preferred anode substrate for PLEDs, displaying a 72.5 % coverage of stable-conductive regions. When utilized as the anode in PLED, it exhibited a remarkable 209 % increase in average current efficiency and a 184 % enhancement in electroluminescent intensity compared to the reference PLED. These findings provide valuable insights for optimizing PLEDs through surface modification of ITO.

Hierarchical self-constructed molecular layers of small bifunctional molecules with strong molecular dipole moments for improvement of quantum efficiency in inorganic quantum dots

Hierarchically structured self-assembled molecular layers are functionally versatile and structurally tunable, which are nanoscale molecular building blocks with a wide range of applications from biosensing systems to optoelectronic devices. Herein, we present a facile and effective strategy to fabricate hierarchical self-constructed molecular layers comprising small bifunctional molecules with strong molecular dipole moments for improvement of quantum efficiency in inorganic quantum dots (QDs) by using the cooperative interfacial self-assembly of hydrophilic bifunctional molecules on the polar electrode surface. The spontaneous construction of nanostructured molecular layers with different molecular dipole moments was simply achieved through solution-dipping and in situ interfacial self-organization of 3-mercaptopropionic acid or 1-propanethiol molecules on the surface of indium tin oxide (ITO) anode. It is experimentally revealed that these functional molecules formed uniform and ultrathin self-constructed molecular nanolayers on the ITO surface via covalent bonding, where bifunctional 3-mercaptopropionic acid molecules induced a polar molecular surface of thiol groups with strong dipole moments, whereas 1-propanethiol molecules formed a relatively hydrophobic surface of short alkyl chains with weak dipole moments. In addition, the nanoscale ultrathin nature of these molecular layers afforded high visible light transmittance comparable to that of pristine ITO substrate. The electro-optical properties of the QD cells revealed that hierarchical self-constructed molecular nanolayer with strong molecular dipole moments exhibited superior current and luminescent properties with a 162% improvement in external quantum efficiency relative to those of a conventional QD device without molecular layer. Furthermore, the self-assembled molecular nanolayer of 3-mercaptopropionic acid exhibited a higher luminescent efficiency than 1-propanethiol-based nanolayer owing to the increased hole mobility of thiol-based molecular layer with strong dipole moments.

Exploring the Use of a Lipopeptide in Dipalmitoylphosphatidylcholine Monolayers for Enhanced Detection of Glyphosate in Aqueous Environments.

The growing reliance on pesticides for pest management in agriculture highlights the need for new analytical methods to detect these substances in food and water. Our research introduces a SPRWG-(C18H37) lipopeptide (LP) as a functional analog of acetylcholinesterase (AChE) for glyphosate detection in environmental samples using phosphatidylcholine (PC) monolayers. This LP, containing hydrophilic amino acids linked to an 18-carbon aliphatic chain, alters lipid assembly properties, leading to a more flexible system. Changes included reduced molecular area and peak pressure in Langmuir adsorption isotherms. Small angle X-ray scattering (SAXS) and atomic force microscopy (AFM) analyses provided insights into the LP's structural organization within the membrane and its interaction with glyphosate (PNG). Structural and geometric parameters, as derived from in silico molecular dynamics simulations (MD), substantiated the impact of LP on the monolayer structure and the interaction with PNG. Notably, the presence of the LP and glyphosate increased charge transfer resistance, indicating strong adherence of the monolayer to the indium tin oxide (ITO) surface and effective pesticide interaction. A calibration curve for glyphosate concentration adjustment revealed a detection limit (LOD) of 24 nmol L-1, showcasing the high sensitivity of this electrochemical biosensor. This LOD is significantly lower than that of a similar colorimetric biosensor in aqueous media with a detection limit of approximately 0.3 μmol L-1. Such an improvement in sensitivity likely stems from adding a polar residue to the amino acid chain of the LP.

A Dopamine Detection Sensor Based on Au-Decorated NiS2 and Its Medical Application.

This article reports a simple hydrothermal method for synthesizing nickel disulfide (NiS2) on the surface of fluorine-doped tin oxide (FTO) glass, followed by the deposition of 5 nm Au nanoparticles on the electrode surface by physical vapor deposition. This process ensures the uniform distribution of Au nanoparticles on the NiS2 surface to enhance its conductivity. Finally, an Au@NiS2-FTO electrochemical biosensor is obtained for the detection of dopamine (DA). The composite material is characterized using transmission electron microscopy (TEM), UV-Vis spectroscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. The electrochemical properties of the sensor are investigated using cyclic voltammetry (CV), differential pulse voltammetry (DPV), and time current curves in a 0.1 M PBS solution (pH = 7.3). In the detection of DA, Au@NiS2-FTO exhibits a wide linear detection range (0.1~1000 μM), low detection limit (1 nM), and fast response time (0.1 s). After the addition of interfering substances, such as glucose, L-ascorbic acid, uric acid, CaCl2, NaCl, and KCl, the electrode potential remains relatively unchanged, demonstrating its strong anti-interference capability. It also demonstrates strong sensitivity and reproducibility. The obtained Au@NiS2-FTO provides a simple and easy-to-operate example for constructing nanometer catalysts with enzyme-like properties. These results provide a promising method utilizing Au coating to enhance the conductivity of transition metal sulfides.

Redox behavior of unsubstituted cobalt phthalocyanine in nanostructured Langmuir-Schaefer films

Although the properties of unsubstituted metal tetrapyrroles in solutions have received attention in numerous work, the physico-chemistry of their thin films remains poorly investigated. In this work, we constructed thin films of unsubstituted cobalt phthalocyanine on the surface of quartz plates and indium tin oxide (ITO) electrodes using the Langmuir-Schaefer (LS) and drop casting techniques. In LS films, CoPc species are involved in strong intermolecular interactions, which result in formation of CoPc nanostructures and prominent changes in the ultraviolet-visible spectrum. Electrochemical reduction of CoPc in LS films at −0.9 V (versus silver chloride electrode) results in formation of Co(I) species. In contrast to the highly reactive nature of Co(I)Pc in solution, these species generated in thin films are relatively resistant to dioxygen due to the dense packing of CoPc units. These findings can further the development of CoPc-based resistive sensors utilizing not only common Co(II), but also Co(I) species, which may possess different sensitivity toward analytes.

Photoelectrochemical water oxidation reaction for coated and meta-chemical surface electrodes with Na3[Ru2(μ-CO3)4]

The most economical and efficient method to produce green hydrogen relies on electrochemistry, the electricity for which is of a green origin, and on photocatalytic water splitting. The latter technology involves the use of a photocatalyst or a photo-electrocatalyst to transform solar energy into chemical energy. Vast efforts have thus been dedicated to the pursuit of such a catalyst.The current study focused on the development of a heterogeneous photoelectrochemical system in which the Na3[Ru2(μ-CO3)4] complex was used as a WOC. To that end, two types of electrodes were prepared: coated indium tin oxide (ITO) and meta-chemical surface (MCS) electrodes. Under 420 nm illumination, both electrode types exhibited higher catalytic currents than were observed without light.Our novel application of the Na3[Ru2(μ-CO3)4] complex as a catalyst in the photoelectrochemical water oxidation reaction requires minute amounts of the complex. The study findings add to the knowledge about the water-splitting process, and ultimately, they may facilitate the broader adoption of hydrogen as an environmentally friendly and increasingly accessible energy source.

A facile electrochemical aptasensor for chloramphenicol detection based on synergistically photosensitization enhanced by SYBR Green I and MoS2

This study reports the development of a photocatalytic electrochemical aptasensor for the purpose of detecting chloramphenicol (CAP) antibiotic residues in water by utilizing SYBR Green I (SG) and chemically exfoliated MoS2 (ce-MoS2) as synergistically signal-amplification platforms. The Au nanoparticles (AuNPs) were electrodeposited onto the surface of an indium tin oxide (ITO) electrode. After that, the thiolate-modified cDNA, also known as capture DNA, was combined with the aptamer. Subsequently, photosensitized SG molecules and ce-MoS2 nanomaterial were inserted into the groove of the resultant double-stranded DNA (dsDNA). The activation of the photocatalytic process upon exposure to light resulted in the generation of singlet oxygen. The singlet oxygen effectively split the dsDNA, resulting in significant enhancement in the current of [Fe(CN)6]3-/4-. When the CAP was present, both SG molecules and ce-MoS2 broke away from the dsDNA, which turned off the photosensitization response, leading to significant reduction in the current of [Fe(CN)6]3-/4-. Under the optimal conditions, the aptasensor exhibited a linear relationship between the current of [Fe(CN)6]3-/4- with logarithmic concentrations of CAP from 20 to 1000 nM, with a detection of limit (3σ) of 3.391 nM. The aptasensor also demonstrated good selectivity towards CAP in the presence of interfering antibiotics, such as tetracycline, streptomycin, levofloxacin, ciprofloxacin, and sulfadimethoxine. Additionally, the results obtained from the analysis of natural water samples using the proposed aptasensor were consistent with the findings acquired through the use of a liquid chromatograph-mass spectrometer. Therefore, with its simplicity and high selectivity, this aptasensor can potentially detect alternative antibiotics in environmental water samples by replacing the aptamers based on photosensitization.

An AuNPs/Co3O4 nanocubic cage–based electrochemiluminescent immunosensor for Corin: A biomarker of stroke

Stroke, or cerebral apoplexy, is a paroxysmal disease that seriously threatens the neurological functions of middle-aged and older men, resulting in high rates of disability and mortality. The blood level of Corin can accurately predict the risk and subtype of stroke. Herein, an immunosensor was developed utilizing a nanocomposite of Au nanoparticles and Co3O4 nanocubic cages (AuNPs/Co3O4NcC) as the sensing substrate, with luminol serving as the sensing probe for Corin detection. Through the application of 3-aminopropyltrimethoxysilane, AuNPs/Co3O4NcC was affixed to the surface of indium tin oxide (ITO)-coated glass, considerably enhancing the electrochemiluminescence (ECL) performance of luminol due to its peroxidase-like activity. To confer biological specificity by immobilizing the Corin antibody on this substrate and to block residual active sites with bovine serum albumin, an immunosensor was developed. The capture of Corin protein by the antibody through an immune reaction, leading to its binding on the sensor, resulted in a decreased ECL signal. Under optimized conditions, the proposed ECL immunosensor demonstrated a broad linear response range from 1 pg/mL to 4800 pg/mL and a low detection limit of 0.26 pg/mL. This ECL immunosensor is characterized by its specificity, stability, and reproducibility and can detect Corin in real blood samples.

A method to partition boiling heat transfer mechanisms using synchronous through-substrate high-speed visual and infrared measurements

Heat transfer during boiling involves a variety of transport mechanisms. Available experimental techniques cannot yet fully delineate these mechanisms which has contributed to a long-standing, persistent challenge of constructing accurate mechanistic models for boiling. In this work, we develop a method to identify and distinguish between the individual heat transfer mechanisms that occur during boiling using synchronous, through-substrate, high-speed visual and infrared measurements. Local heat fluxes are deduced from temperature measurements and a synchronized set of binarized phase maps are obtained from processing high-speed visual measurements. Experimental pool boiling investigation of HFE-7100 fluid on an indium tin oxide surface revealed four distinct heat transfer signatures in the heat flux maps corresponding to liquid convection, contact line evaporation, vapor convection, and local microconvection due to rewetting during boiling. To classify these regions, pixel-wise binary and morphological operations are performed on the phase maps of the entire surface. In contrast with prior partitioning techniques which use standalone heat flux measurements, our synchronous high-resolution visualization enables the region classification around fine bubble footprints that otherwise would not be detected with heat flux maps alone. The heat fluxes and superheats are then partitioned into their underlying mechanisms using classified regions from the phase maps. Analysis of the nucleate boiling regime data shows that different mechanisms contribute in varying degrees to the overall heat transfer at different points along the boiling curve: for the surface-fluid combination studied, single-phase liquid heat transfer is the primary contributor at low heat fluxes while at high heat fluxes, contact line evaporation contributed the most. We further employ the experimental approach to partitioning dynamic processes resulting from step increases in heat input demonstrating its potential for investigating transient phenomena such as dryout. The experimental and post-processing method introduced in this study is the first to delineate partitioning between different heat transfer mechanism regions in the presence of multiple interacting bubbles over the entire surface throughout the boiling curve in both steady and transient operating conditions.