Enhanced electrochemiluminescent of lucigenin at an electrically heated cylindrical microelectrode

In this paper, an ECL detection system equipped with an electrically heating controlled cylindrical microelectrode (HME) was used to study the ECL behavior of lucigenin. The ECL intensity of lucigenin would be increased at elevated electrode temperature but the noise had not been increased. It was found that ECL intensity at higher temperature of electrode surface (80 °C) was more than two magnitudes stronger than that at the room temperature (22 °C). The detection limit for ECL of lucigenin on a HME is much lower than that on an electrode without heating, based on which, it is possible to establish a more sensitive method for measurement of ECL by using a HME. The heating of electrode has been used to renew the electrode, which avoid the tedious work for refreshing the electrode surface. The reproducibility of lucigenin ECL system at HME is satisfactory.     

ToF-secondary ion mass-spectrometric study of copper deposition and stripping on directly heated screen-printed gold electrodes

We report about a new kind of directly heated gold electrode. All electrodes including a directly heated gold loop electrode, a Ag pseudo reference, and a carbon counter electrode have been screen-printed on a ceramic alumina substrate. Thermal behaviour was studied by potentiometry using either an external or the integrated reference electrode. Stripping voltammetric copper signals were greatly improved at elevated deposition temperature. Secondary ion mass spectrometric studies (ToF-SIMS) revealed that different negative ionic species of copper complexes can be found on the gold electrode surface as a result of ion bombardment during SIMS analysis like Cu^?, CuCl^? and CuCl₂ ^?. SIMS surface imaging using a fine focussed ion beam over the surface allowed us to obtain ion images (chemical maps) of the analyzed sample. SIMS depth profile analysis of the gold loop electrode was performed after copper deposition at room temperature (23 °C) and at 60 °C. CuCl₂ ^? ion was used for the depth profile studies as it has shown the highest intensity among other observed species. Surface spectroscopic analysis, surface imaging and depth profile analysis have shown that the amount of deposited copper species on the gold loop electrode was increased upon increasing electrode temperature during the deposition step. Therefore, the presence of chloride in the solution will hinder underpotential deposition of Cu(0) and lead to badly defined and resolved stripping peaks.     

Detection of hypoxanthine based on the electrochemiluminescent of 6-(4-methoxyphenyl)-2-methylimidazo[1,2-a]pyrazin-3(7H)-one on the electrically heated indium–tin-oxide electrode

An electrochemiluminescent (ECL) enzyme biosensor was developed for detection of hypoxanthine based on ECL of 6-(4-methoxyphenyl)-2-methylimidazo[1,2-a]pyrazin-3(7H)-one (MCLA). The xanthine oxidase (XOD) was modified on the heated indium–tin-oxide (ITO) electrode, and the ECL enzyme biosensor was found to be electrode temperatures depend, this was because that both the diffusion and convection of compounds near the electrode surface and the catalytic reaction of immobilized enzyme were affected by the temperature of electrode (T_e). In this work, the highest sensitivity was gained when T_e was 36 °C. Under the optimum condition, the linear response range of hypoxanthine (HX) was found to be 0.3–27 μmol/L, and the detection limit (defined as the concentration that could be detected at the signal-to-noise ration of 3) was 0.15 μmol/L.     

A new electrochemiluminescent detection system equipped with an electrically controlled heating cylindrical microelectrode

A new electrochemiluminescent (ECL) detection system equipped with an electrically controlled heating cylindrical microelectrode (HME) was developed in this paper. The cylindrical microelectrode made of platinum wire (25 μm in diameter, 6 mm in long) was used as the working electrode of the ECL detection system, the temperature of the electrode could be controlled electrically. The Ru(bpy)₃²⁺-ECL and Ru(bpy)₃²⁺-C₂O₄²⁻-ECL systems were used to evaluate this ECL detection system. The detection limit for oxalate was found to be 3.0 × 10⁻⁴ mol/L when T_e (temperature of the HME) was 22 °C, and found to be 3.0 × 10⁻⁶ mol/L at 80 °C, which indicates that the detection limit can be improved greatly at higher T_e, based on which, it is possible to establish a more sensitive method for measurement of ECL by using a heated microelectrode.     

Fabrication of a New Electrochemiluminescent Sensing Interface Based on Zinc Oxide Nanorod

A new electrochemiluminescence (ECL) sensing interface was established based on the zinc oxide nanorod in this paper. Firstly, the zinc oxide (ZnO) nanorod was prepared on an indium tin oxide (ITO) electrode surface by the method of constant current cathodic electrodeposition, on which the Nafion film was then modified, and finally ruthenium(II) tris(bipyridine) (Ru(bpy)₃²⁺) was immobilized at the ZnO nanorod/Nafion composite‐modified electrode. The sensing interface shows well ECL behaviors and perfect stability after being constant temperature treatment at 80 °C. The composite electrode was characterized by EIS, SEM and XRD. The results showed that the good stability maybe related to the water content of Nafion film.     

A New Heated Nickel Oxyhydroxide Covered Nickel Wire Electrode and Its Improved Electrocatalytic Oxidation for Methanol

A new heated nickel oxyhydroxide covered nickel wire electrode (HNONE) was fabricated and AC heating circuit was used to heat the electrode. Furthermore, the improved electrocatalytic activity of the HNONE for methanol oxidation at elevated electrode temperature was demonstrated. A detection limit of 2.1×10^?4 M (S/N=3) could be obtained with an electrode temperature of 80 °C, about one magnitude lower than that at room temperature 20°. And the sensitivity was also enhanced about 10 times.     

A sensitive DNA biosensor based on the distance dependent quenching of Silica@Ru(bpy)32+-chitosan-GO electrochemiluminescence by Ferrocene@Gold nanoparticles

A sensitive electrochemiluminescence (ECL) biosensor for the specific DNA sequence of hepatitis C virus (HCV) was developed based on the efficient quenching effect of the ferrocene cluster functionalized gold nanoparticles (Fc@AuNPs) on the ECL of electrodeposited silica@Ru(bpy)₃²⁺-chitosan-graphene oxide nanocomposite (SiO₂@Ru−CS−GO). Graphene oxide (GO) can accelerate electron transfer rate, thus improving the ECL of Ru(bpy)₃²⁺ on electrode surface. The molecular beacons (MB) was fixed to SiO₂@Ru−CS−GO by glutaraldehyde (GA) using the Schiff reaction between amino groups of chitosan (CS) and MB. The ECL of SiO₂@Ru−CS−GO was depressed greatly by the Fc@AuNPs labelled at the end of MB, then, a stronger ECL was observed when the distance between Fc@AuNPs and SiO₂@Ru−CS−GO increased after the hybridization of target DNA with MB. Under optimum conditions, the restored ECL intensity increased linearly with the target DNA concentration in the range of 1.0×10⁻¹⁶∼1.0×10⁻¹⁰ mol ⋅ L⁻¹, and the limit of detection (LOD) is 1.4×10⁻¹⁷ mol ⋅ L⁻¹. The proposed method exhibits acceptable stability and reproducibility. In general, the constructed HCV biosensor can be used for the sensitive detection of HCV in human serum, suggesting potential application prospects in bioanalysis.     

Enhanced Anodic Electrochemiluminescence of Dissolved Oxygen with 2‐(Dibutylamino) ethanol at TiO2 Nanoparticles Modified Platinum Electrode for Dopamine Detection

The anodic electrochemiluminescence (ECL) of dissolved oxygen with 2‐(dibutylamino) ethanol (DBAE) on platinum electrode has been reported previously by our group. Interestingly, the ECL intensity can be greatly amplified at TiO₂ nanoparticles modified platinum electrode (TiO₂/Pt), which is due to the catalytic effect of TiO₂ nanoparticles to electrochemical oxidation of DBAE. It is the first case to obtain the enhanced ECL from luminophor by electrochemical catalysis of co‐reactant. The enhanced anodic ECL intensity can be quenched by dopamine sensitively. And the ECL intensity versus the logarithm of concentration of dopamine was linear over the 4.0×10^?12–1.8×10^?8 M (R²=0.9957), with the limit of detection of 2.7×10^?12 M (S/N=3).     

A reagentless DNA biosensor based on cathodic electrochemiluminescence at a C/CxO1−x electrode

A reagentless signal-on electrochemiluminescence (ECL) biosensor for DNA hybridization detection was developed based on the quenching effect of ferrocene (Fc) on intrinsic cathodic ECL at thin oxide covered glassy carbon (C/C_xO_1−x) electrodes. To construct the DNA biosensor, molecular beacon (MB) modified with ferrocene (3′-Fc) was attached to a C/C_xO_1−x electrode via the covalent bound between labeled amino (5′-NH₂) and surface functional groups. It was found that the immobilization of the probe on the electrode surface mainly depended on the fraction of surface carbonyl moiety. When a complementary target DNA (cDNA) was present, the stem-loop of MB on the electrode was converted into a linear double-helix configuration due to hybridization, resulting in the moving away of Fc from the electrode surface, and the restoring of the cathodic ECL signal. The restoration of the ECL intensity was linearly changed with the logarithm of cDNA concentration in the range of 1.0 × 10⁻¹¹ to 7.0 × 10⁻⁸ M, and the detection limit was ca. 5.0 pM (S/N = 3). Additionally, single-base mismatched DNA can be effectively discriminated from the cDNA. The great advantage of the biosensor lies in its simplicity and cost-effective with ECL generated from the electrode itself, and no adscititious luminophore is required.     

Determination of Reduced Nicotinamide Adenine Dinucleotide Based on Immobilization of Tris(2,2′‐bipyridyl) Ruthenium(II) in Multiwall Carbon Nanotubes/Nafion Composite Membrane

Abstract

An electrochemiluminescence (ECL) method for reduced nicotinamide adenine dinucleotide (NADH) was proposed by immobilizing tris(2,2′‐bipyridyl) ruthenium(II) (Ru(bpy)₃ ²⁺) in multiwall carbon nanotubes (MWCNTs)/Nafion composite membrane that was formed on glassy carbon electrode surface. The electrochemical and ECL behaviors of the immobilized Ru(bpy)₃ ²⁺ were investigated. The cyclic votammogram of the modified electrode in pH 7.0 phosphate buffer solution showed a couple of redox peaks at +1190 and +1060 mV at 100 mV/s. The composite film had a more open structure and a large surface area allowing faster diffusion of Ru(bpy)₃ ²⁺. The presence of MWCNTs resulted in the improved ECL sensitivity and longer‐term stability of the modified electrode. The modified electrode showed a linear response to NADH in the concentration range of 1.0×10^?6 to 1.6×10^?5 M with a detection limit of 8.2×10^?7 M.     

Clopyralid detection by using a molecularly imprinted electrochemical luminescence sensor based on the “gate-controlled” effect

A new strategy for trace analysis was proposed by preparing a molecularly imprinted polymer (MIP) sensor. The template molecules of clopyralid were determined based on “gate-controlled” electrochemiluminescence (ECL) measurement. A dense polymer film was electropolymerized on an electrode surface to fabricate the MIP–ECL sensor. The process of template elution and rebinding acted as a gate to control the flux of probes, which pass through the cavities and react on the electrode surface. ECL measurement was conducted in the luminol–H₂O₂ system. A linear relationship between ECL intensity and clopyralid concentrations in the range of 1?×?10^?9 mol/L to 8?×?10^?7 mol/L exists, and the detection limit was 3.7?×?10^?10 mol/L. The prepared sensor was used to detect clopyralid in vegetables. Recoveries of 97.9 % to 102.9 % were obtained. The sensor showed highly selective recognition, high sensitivity, good stability, and reproducibility for clopyralid detection.     

Enhanced electrochemiluminescence of luminol at the gold nanoparticle/carbon nanotube/electropolymerised molecular imprinting composite membrane interface for selective recognition of triazophos

This paper reports a surface molecular self-assembly strategy for imprinting triazophos in the electropolymerised poly(aminthiophenol) (PATP) membranes at the surface of gold nanoparticle (AuNP)/carbon nanotube (CNT) composites modified glassy (GC) electrode for electrochemiluminescent (ECL) detection of pesticide triazophos. The electrochemical and ECL behaviours of luminol at the imprinted PATP/AuNP/CNT/GC electrode were investigated before and after the rebinding of triazophos. It was also found that the ECL intensity was strikingly enhanced by the adsorbed triazophos molecules in the imprinted PATP/AuNP/CNT composite membranes, which was about 5.2-fold as compared with the blank ECL intensity. On this basis, the molecularly imprinted polymer (MIP)-ECL sensor is established for high sensitive and selective detection of triazophos residues in vegetable samples. The resulting MIP-ECL sensor shows wide linear ranges from 3.1 × 10^?8 to 3.1 × 10^?5 g L^?1 with lower detection limit of 3.1 × 10^?9 g L^?1 for triazophos. Moreover, the MIP-ECL sensor has the advantages of high sensitivity, speed, specificity, stability and can become a promising technique for organophosphate pesticide detection.     

Electrochemiluminescence (ECL) Detection of Ammonium Ion Based on a Novel Iridium Complex Modified Electrode

We report that ammonium ion, as its organic amine counterparts, can be sensitively detected as a coreactant in the electrochemiluminescence (ECL) reaction of a novel iridium complex (pq)₂Ir(N-phMA), where pq is 2-phenylquinoline anion and N-phMA is N-phenylmethacrylamide. The modified ECL electrode was fabricated by casting deposition of a homogeneous MWNTs/PVA/(pq)₂Ir(N-phMA) dispersion solution onto the surface of a glassy carbon electrode. The electrode responds sensitively to ammonium ion in a wide concentration range. Two regression equations were established: Y = 0.7016X + 46.8 (R² = 0.9985) and Y = 0.2565X + 174.2 (R² = 0.9991) for the concentration from 1–180 nM and 180–1800 nM, respectively. The limit of detection was as low as 0.13 nM (S/N = 3).     

Determination of Hg2+ in Tap Water Based on the Electrochemiluminescence of Ru(phen)32+ and Thymine at Bare and Graphene Oxide‐Modified Glassy Carbon Electrodes

The electrochemiluminescence (ECL) of the Ru(phen)₃²⁺/thymine (T) system at bare and graphene oxide (GO)‐modified glassy carbon (GC) electrodes was utilized to determine Hg²⁺ in tap water. The ECL intensity of Ru(phen)₃²⁺ was considerably enhanced by the addition of thymine because of the occurrence of ECL reaction between them. Subsequently, the ECL intensity of Ru(phen)₃²⁺/T system rapidly decreased with the addition of Hg²⁺ because of the formation of a T‐Hg²⁺‐T complex. A linear response (R²=0.9914) was obtained over a Hg²⁺ concentration range of 1.0×10^?9 mol/L to 1.0×10^?5 mol/L with a detection limit of 3.4×10^?10 mol/L at a bare GC electrode in 0.1 mol/L phosphate buffer (pH=8.0). The detection limit can be further reduced to 4.2×10^?12 mol/L after modification of the GC electrode by GO. To verify its applicability, the proposed method was utilized to determine Hg²⁺ in tap water and simulated wastewater. The method exhibited good reproducibility and stability and thus reveals the possibility of developing a novel ECL detection method for Hg²⁺.     

Hot Electron Induced Cathodic Electrochemiluminescence at Disposable Screen Printed Carbon Electrodes

Hot electron induced cathodic electrochemiluminescence (ECL) was observed at screen printed carbon electrodes (SPCEs) during pulse polarization. The thin insulating film resulted from the printing inks was found to be suitable for generating hot electrons, which can further be converted to hydrated electrons and induce the subsequent luminescence. Compared with disposable Al/Al₂O₃ electrode, SPCEs show more stable and reproducible ECL in a wider pH range without background emission. A sensitive ECL method for determination of quercetin is proposed. The detection limit is 8.0×10^?10 mol L^?1(S/N=3), which is two magnitudes lower than that of common ECL method.     

High Sensitive Electrochemiluminescence Biosensor Based on Ru(phen)32+-loaded Double Strand DNA as Signal Tags use to Detect DNA Methyltransferase Activity

DNA methyltransferase (DNA MTase) can act as biomarker for many diseases and it is important to develop some new methods for sensitive detection of DNA MTase. In this work, a highly efficient electrochemiluminescence (ECL) sensor had been designed for detection of DNA MTase based on Ru(phen)₃²⁺ loaded double strand DNA (dsDNA- Ru(phen)₃²⁺) as signal tags. Ru(phen)₃²⁺ had been efficiently embed in the dsDNA produced through a simple hybridization chain reaction. First, a hairpin probe was designed, which can be specifically recognized by Dam MTase and modified with -SH at one end. It was modified on the surface of gold electrode by -SH as an immobilization probe (IP). This IP will be methylated in the present of Dam MTase and digested by DpnI following. Results in the release of capture probe (CP) which remains on the surface of gold electrode. The CP can hybridize with the single stand part of the dsDNA- Ru(phen)₃²⁺ and make the immobilization of ECL tags on the electrode surface, which results in a strong ECL signals detected. However, without the effect of Dam MTase, the hairpin structure of IP remains stable and cannot capture signal tags, and can only detecte weak ECL signals. The biosensor can detect the activity of Dam MTase in the concentration range of 0.01 U/mL to 20 U/mL with the ECL intensity and the logarithm of the concentration have a linear relationship, and the detection limit is calculated to be 7.6 mU/mL. The developed sensor has the ability to specifically detect Dam MTase, which can be differentiated from other types of DNA MTase. In addition, the designed method has good applicability to detect Dam MTase activity in serum samples and been applied to detect its inhibitor with high efficiency.     

Novel Designing of Chemically Modified Electrode (CME) of the Bio-MOF-1 for the Detection of Dopamine Based on Inhibition of [Ru(bpy)3]2+/DBAE System

Metal organic frameworks (MOFs) have attracted extensive attention in electrochemical research fields due to their high surface area and controlled porosity. Current study is design to investigate the ECL performance of the chemically modified electrode (CME) based on the bio-MOF-1, a porous zinc-adenine framework, which loaded ruthenium complex and employed for the detection of dopamine (DA). The composite material [Ru(bpy)₃]²⁺@bio-MOF-1 (Ru-bMOF) modified carbon glassy electrode (Ru-bMOF/GCE) exhibited an excellent ECL performance having a linear co-efficient response (R²=0.9968) for 2-(dibutyl amino) ethanol (DBAE), a classical ECL co-reactant was obtained over a concentration range of 1.0×10⁻⁹ M to 1.0×10⁻⁴ M in 0.10 M pH=6.0 phosphate buffer solution (PBS). Furthermore, DA was detected based on its inhibition effect on [Ru(bpy)₃]²⁺/DBAE system. Compared to traditional analytical methods, this method has various advantages such as simple electrode preparation, quick response, high reproducibility (RSD<2.0 %), low limit of detection (LOD=1.0×10⁻¹⁰ mol/L). This chemical investigated modified electrode had exploited potential for detection of DA.     

Detection of DNA immobilized on bare gold electrodes and gold nanoparticle-modified electrodes via electrogenerated chemiluminescence using a ruthenium complex as a tag

Electrogenerated chemiluminescence (ECL) for DNA hybridization detection is demonstrated based on DNA that was self-assembled onto a bare gold electrode and onto a gold nanoparticles modified gold electrode. A ruthenium complex served as an ECL tag. Gold nanoparticles were self-assembled on a gold electrode associated with a 1,6-hexanedithiol monolayer. The surface density of single stranded DNA (ssDNA) on the gold nanoparticle modified gold electrode was 4.8?×?10¹⁴ molecules per square centimeter which was 12-fold higher than that on the bare gold electrode. Hybridization was induced by exposure of the target ssDNA gold electrode to the solution of ECL probe consisting of complementary ssDNA tagged with ruthenium complex. The detection limit of target ssDNA on a gold nanoparticle modified gold electrode (6.7?×?10^?12 mol L^?1) is much lower than that on a bare gold electrode (1.2?×?10^?10 mol L^?1). The method has been applied to the detection of the DNA sequence related to cystic fibrosis. This work demonstrates that employment of gold nanoparticles self-assembled on a gold electrode is a promising strategy for the enhancement of the sensitivity of ECL detection of DNA.     

Enhanced Electrochemiluminescence Performance of Ru(bpy)32+/CuO/TiO2 Nanotube Array Sensor for Detection of Amines

Tripropylamine (TPA) is a highly toxic and carcinogenic compound, therefore, TPA concentration in water must be monitored to protect health and the environment. In this paper, an electrochemiluminescent (ECL) sensor was fabricated by immobilising Ru(bpy)₃²⁺‐modified CuO nanoparticles (NPs) on a TiO₂ nanotube array (TN) electrode. Compared to an ECL sensor fabricated by immobilising Ru(bpy)₃²⁺ on a TN only electrode, the as‐prepared sensor displays a 30 % enhanced ECL signal and a detection limit of 9.6×10^?10 M at a signal‐to‐noise ratio=3 with the concentration of TPA in a range 1×10^?9 to 1×10^?5 M. The results from this study indicated a new approach for the enhancement of performance of ECL sensor in detecting TPA in water.     

Electrochemiluminescent Detection Method for Glyphosate in Soybean on Carbon Fiber-ionic Liquid Paste Electrode

A carbon fiber paste electrode using ionic liquid as the binder (CFILE) was fabricated. The electrochemical characteristics of the electrode was examined in ferro‐/ferricyanide solution and showed better conductivity and reversibility when compared with graphite paste‐ionic liquid electrode (GPILE) and a little better than that on the carbon nanotube paste‐ionic liquid electrode (CNTILE). Glyphosate (GLY), a pesticide, exhibited excellent catalysis to the oxidation of Ru(bpy)²⁺₃ on CFILE and brought an obvious enhancement to the electrochemiluminescence (ECL) intensity of Ru(bpy)²⁺₃. Based on the catalytic ability of GLY, a simple ECL method for GLY detection had been established. Under optimum conditions, the enhanced ECL intensities were found to had linearly respond to the GLY concentration between 3.0×10^?7 and 3.0×10^?5 mol/L, and the detection limit (S/N=3) was 2.0×10^?7 mol/L. The electrode also showed excellent sensitivity in detecting GLY‐spiked soybean samples. The linear range for GLY in soybean samples was 1.0×10^?6–4.0×10^?5 mol/L and the detection limit was 5.0×10^?7 mol/L, equal to 8.45 µg GLY in per gram of soybean. The detection limit in soybean sample was lower than the USA, EU regulation and so on. If the method is coupled with the separation technology, it can be applied to detect the GLY in the contaminated samples.