Search Results (69)

Carbon quantum dots (CQDs) are inherently photochemically active nanomaterials, exhibiting excitation-dependent emission, proton-responsive surface states, and modifiable redox properties, enabling various sensing applications across fluorescence, electrochemistry, and electrochemiluminescence (ECL) modalities. This comprehensive review elucidates their methodologies, including PET-driven “turn-off/on” fluorescence, ratiometric pH sensing, electrocatalytic currents, and co-reactant-amplified ECL, achieving low detection limits for metal ions, biomolecules, and environmental analytes. Surface-mediated responsiveness is essential to CQD performance, offering exceptional sensitivity while also conferring inherent cross-reactivity. Meta-analysis was conducted using data extracted from previously published studies on CQDs for the detection property, in which the failure ratio was computed as the number of unsuccessful detections divided by the total number of tests reported in each study. Additionally, critical examination reveals inconsistencies in the limit of detection (LOD) metrics and mechanistic uncertainties, as well as strategies for enhancing selectivity through rational doping and molecular recognition hybrids. Full article

Developing an ultrasensitive electrochemiluminescence (ECL) detection platform remains challenging due to the limited enrichment efficiency of ECL emitters and co-reactants at the electrode interface, as well as the insufficient catalytic enhancement of co-reactant conversion. Moreover, simultaneous in situ analyte enrichment and efficient anti-interference capability are often difficult to achieve in a single sensing interface. Herein, a new ECL platform was developed based on nanocatalyst-supported nanochannel-confined surfactant micelle (SM) system, which integrates an enhanced luminol-dissolved oxygen (DO) ECL response for the ultrasensitive detection of antibiotic rifampicin (RIF). A nanocomposite comprising nitrogen-doped graphene quantum dots and a molybdenum disulfide nanosheet (NGQDs@MoS₂) was modified on an indium tin oxide (ITO) electrode. This nanocomposite layer catalyzed the oxygen reduction reaction (ORR), boosting the co-reactant efficiency of DO. Vertically ordered mesoporous silica film filled with surfactant micelles (SM@VMSF) was subsequently grown in situ on the NGQDs@MoS₂ surface. The hydrophobic micelles enable the simultaneous enrichment of luminol, DO, and RIF. Integrating the triple-enrichment effect of surfactant micelles with the high electrocatalytic effect of NGQDs@MoS₂ nanocomposite results in significant ECL enhancement of the luminol–DO. SM@VMSF also provides an excellent molecular sieving effect, endowing the sensor with high anti-interference capability and stability. RIF quenches the ECL signal by consuming superoxide anion radicals, enabling sensitive detection. Detection of RIF was established with a high sensitivity (2927 a.u. per nM) wide linear range (10 pM to 10 μM) and a low limit of detection (LOD, 2.5 pM). The fabricated sensor exhibits good selectivity and high fabrication reproducibility (relative standard deviation, RSD, of 1.9%). Additionally, the determination of RIF in eye drops and seawater samples was realized. This work offers new insights for the design of high-performance ECL sensing interfaces and sensitive detection of RIF. Full article

Quantitative detection of alkaline phosphatase (ALP) activity is crucial in clinical diagnosis and bioanalysis. Herein, we have developed a highly sensitive electrochemiluminescence (ECL) biosensor that employs a biomimetic zirconia interface as its core sensing platform. The interface was constructed by immobilizing o-phosphorylethanolamine (PEA) onto zirconium oxide nanofilms (ZrO₂NFs), forming a surface rich in Zr-O-P bonds. This design mimics phosphate recognition and enzyme-triggered dephosphorylation processes, where ALP catalyzes the hydrolysis of these bonds, triggering a direct switch in the ECL signal from Ru(bpy)₃²⁺-loaded gold nanocage (Ru-AuNCs) emitters. This sensor achieves a wide linear range of 0.100–100 U/L and a low detection limit down to 0.0899 U/L. Its practical utility was validated through the accurate detection of ALP in fetal bovine serum samples, confirming high recovery and reliability. This strategy highlights the potential of biomimetic zirconia interfaces in developing robust biosensors for early disease diagnosis. Full article

A novel sensitive and selective electrochemiluminescence (ECL) sensor using nitrogen-doped graphyne as the platform was proposed for kanamycin (KAN) detection. First, nitrogen-doped graphyne nanomaterial (1N-GY) with high conductivity was synthesized using a high-energy ball milling method. Compared with ordinary graphyne, the addition of nitrogen atoms can improve the conductivity of the material and reduce the electronic migration energy barrier. Then it was used as a substrate material of the ECL sensor, not only increasing the conductivity of the biosensor but also improving the sensitivity of the ECL sensor by providing more immobilization space for the luminescent probe of Nafion-coated mesoporous silica adsorbed Ru(bpy)₃²⁺ (mSiO₂@Nafion@Ru(bpy)₃²⁺). On this basis, mSiO₂@Nafion@Ru(bpy)₃²⁺ functionalized DNA probes were used as luminescent and capture probes to specifically recognize different concentrations of KAN to produce ECL signals. Under optimal conditions, the proposed ECL sensor exhibited good linearity (10⁻¹²–10⁻⁶ M KAN) and a low detection limit of 1.08 pM. The prepared biosensor with good stability and selectivity successfully detected KAN in honey and milk samples, with spiked recovery rates ranging from 98% to 111.79%. This method not only expands the application of 1N-GY as a novel graphitic material in ECL biosensors but also provides an effective way to check antibiotics in dairy products. Full article

Cobalt–ruthenium bypiridine–oxalate metal–organic frameworks (MOFs) were synthesized via a solvothermal method with a custom-designed reactor that permits stirring, which can result in changes in the morphology of the structures. In this work, we performed a morphological and structural study of MOFs with varying tris(2,2,bipyridyl) and diclororuthenium(II) hexahydrate ${\left(Ru\right(bpy)}_3^{2+})$ concentrations, demonstrating changes in the size of the MOFs, and these MOFs were used as the luminescent materials in an electrochemiluminescent (ECL) system for glyphosate (Gly) detection, which acts as a coreactant in the light emission of ${Ru\left(bpy\right)}_3^{2+}$. Gly is the most commonly used herbicide worldwide, and our system has a calibration curve range of 10–70 ppm, with a detection limit of 7.6 ppm. Full article

Lycium barbarum L. is a widely used medicinal and edible Chinese medicinal material. However, with consumers’ heightened concern for health and food safety, pesticide residues have become one of the major challenges affecting its quality and safety. Cyhalothrin is a pyrethroid insecticide and a typical type of pesticide with excessive pesticide residues in Lycium barbarum L. Rapid detection of pesticide residues is an effective way to ensure the quality and safety of traditional Chinese medicinal materials. In this work, a molecularly imprinted polymer electrochemiluminescence (ECL) sensor based on gold nanoparticles (AuNPs)@Ru-ZIF-8 was constructed for rapid detection of cyhalothrin residues. The prepared cyhalothrin molecularly imprinted polymers (MIPs) were used as a recognition element and modified on the surface of a glassy carbon electrode (GCE) by an electrochemical polymerization method. AuNPs were utilized to promote the excitation of Ru(bpy)₃²⁺ and TPrA in the ECL system, which improved the observability of the light signal. The GCE modified with the metal–organic frameworks (MOFs) ZIF-8 was employed to increase the specific surface area and enhance the electron transfer capacity on the electrode, thereby improving the sensing sensitivity of the sensor. In addition, the luminescent reagent of Ru(bpy)₃²⁺ was introduced into the synthesis process of ZIF-8, which caused Ru(bpy)₃²⁺ to be tightly bound around it and enhanced the stability of the sensor. Under optimal conditions, the linear detection range of the sensor is 1 × 10⁻¹~1 × 10⁴ nM, with a limit of detection (LOD) of 10 pM. The accuracy of the ECL-MIP sensor has been verified through spiked recovery experiments and actual sample detection. This study has opened up a new approach to rapid detection of pesticide residues in traditional Chinese medicinal materials used for both food and medicine. Full article

The ultrasensitive detection of microRNA-17 (miRNA-107) is required for clinical diagnosis. In this work, an aggregation-induced electrochemiluminescence (AIECL) sensor was developed for the quantification of miRNA-107, in which AIECL-active polymer dots (Pdots) were characterized by transmission electron microscopy, ultraviolet–visible spectroscopy, and cyclic voltammetry and used as ECL emitters. Black hole quencher-labeled hairpin DNA (HP-BHQ) was modified on the Pdot surfaces, resulting in the ECL signal of the Pdots being in the “off” state due to the resonant energy transfer (RET) between the BHQ and Pdots. In the presence of miRNA-107, HP-BHQ opened through RNA-DNA hybridization. Subsequently, the introduced duplex-specific nuclease (DSN) facilitated the cleavage of DNA in the RNA–DNA hybrid chain and led to the detachment of HP-BHQ from the electrode surface. The ECL signal of the Pdots recovered, i.e., to the “on” state. The variation in the ECL signal was related to the concentration of the target miRNA-107. As a result, the AIECL biosensor exhibited a wide linear response to miRNA-107 concentrations ranging from 1.0 fM to 10.0 pM, and a low detection limit of 0.82 fM. This work provides a novel platform for the sensitive analysis of miRNA. Full article

The pervasive presence of foodborne contaminants in foods poses a significant global threat, contributing to various foodborne diseases and food safety issues. Therefore, developing rapid, sensitive, and universal detection methods for them is essential to ensure public health and food safety. Electrochemiluminescence (ECL) sensors, particularly those incorporating innovative nanoaggregates, have been widely used to detect related contaminant residues in foodstuffs owing to their superior sensitivity and low background signals. This review summarizes recent advances in nanoaggregate-based novel ECL sensors for detecting a wide range of contaminants, with emphasis on their fundamentals and representative applications. This area has not yet been comprehensively covered in the existing literature. The current challenges and emerging trends for next-generation ECL sensors based on nanoaggregates in food safety monitoring are also discussed. Full article

To address the challenges of nonspecific adsorption interference and low mass transfer efficiency encountered by electrochemiluminescence (ECL) sensors in complex biological matrices, this study developed a Mn@CeO₂ nanozyme-based sensing interface. The Mn-doped CeO₂ enhanced electron transfer efficiency, increased oxygen vacancy concentration, and stabilized the Mn-O-Ce structure, collectively enabling highly efficient peroxidase (POD)-like activity. The design significantly improved ECL reaction efficiency, which simultaneously conferred synergistic antifouling and mass transport enhancing properties. The mesoporous silica nanoparticle on the sensing interface accelerated mass transfer processes, thereby overcoming the limitations of traditional diffusion-controlled kinetics. The Mn@CeO₂ nanozyme and mesoporous silica nanoparticle synergistically improved electron transfer and reactant enrichment, thereby significantly enhancing the signal response. Concurrently, a biomimetic anti-fouling coating was introduced at the interface to effectively suppress nonspecific adsorption of interferents. The constructed nanozyme-enhanced ECL sensing platform was demonstrated through the detection of dopamine (DA) as a model neurotransmitter, exhibiting favorable detection performance while maintaining high-accuracy detection in complex biological samples. This strategy offers a novel approach to developing highly sensitive and interference-resistant ECL sensors, with promising applications in disease biomarker monitoring and live physiological sample analysis. Full article

Chlorpheniramine maleate (CPM) is a first-generation antihistamine that is frequently used to treat allergic reactions. However, excessive consumption presents potential health risks. Therefore, it is crucial to develop a quick and precise technique for identifying CPM levels. In this study, nickel cobalt phosphide (NiCoP), a binary metal phosphide, was successfully incorporated into carbon nanofibers. This involved creating a pore structure by adding polyvinylpyrrolidone (PVP) as a pore-forming template to a polyacrylonitrile (PAN) substrate via electrostatic spinning. An innovative electrochemiluminescent sensor for CPM detection was constructed using NiCoP/PVP/PAN carbon nanofibers (NiCoP/PVP/PAN/CNFs). Under optimal conditions, the electrochemical behavior of CPM was studied using NiCoP/PVP/PAN/CNF-modified working electrodes. These findings demonstrate that the three-dimensional porous network architecture of NiCoP/PVP/PAN/CNFs enhances the conductive properties of the material. Consequently, an electrochemical optical sensor fabricated using this structure exhibited remarkable performance. The linear detection range of the sensor was 1 × 10⁻⁸–7 × 10⁻⁵ mol/L, and the detection limit was 7.8 × 10⁻¹⁰ mol/L. When human urine and serum samples were examined, the sensor was found to have a high recovery rate (94.35–103.36%), which is promising for practical applications. Full article

Glucose (Glu) detection, as a fundamental analytical technique, has applications in medical diagnostics, clinical testing, bioanalysis and environmental monitoring. In this work, a solid-phase electrochemiluminescence (ECL) enzyme sensor was developed by immobilizing the ECL emitter in a stable manner within bipolar silica nanochannel array film (bp-SNA), enabling sensitive glucose detection. The sensor was constructed using an electrochemical-assisted self-assembly (EASA) method with various siloxane precursors to quickly modify the surface of indium tin oxide (ITO) electrodes with a bilayer SNA of different charge properties. The inner layer, including negatively charged SNA (n-SNA), attracted the positively charged ECL emitter tris(2,2′-bipyridyl)ruthenium(II) (Ru(bpy)₃²⁺) via electrostatic interaction, while the outer layer, including positively charged SNA (p-SNA), repelled it, forming a barrier that efficiently concentrated the Ru(bpy)₃²⁺ emitter in a stable manner. After modifying the amine groups on the p-SNA surface with aldehyde groups, glucose oxidase (GOx) was covalently immobilized, forming the enzyme electrode. In the presence of glucose, GOx catalyzed the conversion of glucose to hydrogen peroxide (H₂O₂), which acted as a quencher for the Ru(bpy)₃²⁺/triethanolamine (TPA) system, reducing the ECL signal and enabling quantitative glucose analysis. The sensor exhibited a wide linear range from 10 μM to 7.0 mM and a limit of detection (LOD) of 1 μM (S/N = 3). Glucose detection in fetal bovine serum was realized. By replacing the enzyme type on the electrode surface, this sensing strategy holds the potential to provide a universal platform for the detection of different metabolites. Full article

In this work, we developed a highly sensitive and reproducible electrochemiluminescent sensor based on a heterostructure of cadmium selenide quantum dots capped with 3-mercaptopropionic acid (MPA) + 3-morpholinoethanesulfonic acid (MES) (QDs CdSe) and carbon nitride nanosheets (g-C₃N₄) for the detection of H₂O₂ in lyophilized serum samples. To enhance the sensor sensitivity, g-C₃N₄ nanosheets were utilized as a platform to immobilize the QDs CdSe. An exhaustive characterization of the heterostructure was conducted, elucidating the interaction mechanism between QDs CdSe and g-C₃N₄. It was revealed that g-C₃N₄ acts as a hole (h⁺) donor, while QDs CdSe act as energy acceptors in a resonance energy transfer process, with the electrochemiluminescence emission originating from the QDs CdSe. The electrochemiluminescence intensity decreases in the presence of H₂O₂ due to the deactivation of the excited states of the QDs CdSe. This electrochemiluminescent sensor demonstrates exceptional performance for detecting H₂O₂ in aqueous systems, achieving a remarkably low limit of detection (LOD) of 1.81 nM, which is more sensitive than most reported sensors to detect H₂O₂. The applicability of the sensor was successfully tested where sub-µM levels of H₂O₂ were accurately quantified. These results highlight the potential of this electrochemiluminescent sensor as a reliable and pre-treatment-free tool for H₂O₂ detection in biochemical studies and human health applications. Full article

The dual-signal output self-calibration mode reduces the false positive and negative signals of electrochemiluminescence (ECL) aptamer sensors. A competitive dual-signal ECL platform was designed for the ultrasensitive detection of kanamycin (KAN) using a zirconium metal–organic framework (Zr MOF) and Luminol as ECL emitters. To enhance the ECL efficiency, a co-reactant (polyethyleneimine, PEI) was covalently bound to the Zr MOF to achieve self-enhanced ECL. Based on the selective interaction between KAN and its aptamer, the Luminol/KAN/Zr MOF-PEI “sandwich” structure was immobilized on the electrode surface. The competition for PEI between emitters increased the Luminol ECL signal and decreased the Zr MOF’s ECL signal. The ratio in ECL signals between the two competitive emitters enabled the quantitative analysis of KAN, achieving a detection limit as low as 7.86 × 10⁻⁴ ng/mL. This study elucidated the synergistic mechanism between self-enhanced ECL and ECL competition, offering a novel approach for constructing dual-signal ECL sensors using a single co-reactant. Full article

Electrochemiluminescence (ECL)/electrochemistry (EC) dual-mode sensors have garnered significant interest for their enhanced analytical reliability through the cross-verification of dual-signal outputs. However, conventional approaches necessitate two potential scans to acquire ECL and EC signals independently, resulting in temporal and environmental discrepancies between the two detection modes. In this paper, we present a novel synchronous ECL/EC dual-mode sensing platform for lead ion (Pb²⁺) detection via a one-step potential scan (0.2 to −0.4 V vs. Ag/AgCl) utilizing a G-quadruplex (G4)–hemin DNAzyme complex. This complex synergistically catalyzed the electrochemical reduction of dissolved oxygen, concurrently generating a distinct cathodic ECL emission from Ru(bpy)₃²⁺ and a synchronous reduction current peak at −0.25 V. Pb²⁺ quantification was achieved through its dose-dependent suppression of DNAzyme activity by destabilizing the G4–hemin interaction, thereby proportionally attenuating both ECL intensity and EC signal (reduction current). The integrated sensor demonstrated high sensitivity (detection limits of 1.51 nM for ECL detection and 2.03 nM for EC detection), robust anti-interference capability, and satisfactory reproducibility, with recoveries ranging from 95.5 to 103.1% in environmental water analysis. This work established a paradigm for one-step dual-mode sensor design, offering new prospects for environmental monitoring. Full article

Ciprofloxacin (CIP), a widely used broad-spectrum antibiotic, poses a serious threat to human health and environmental safety due to its residues. The complementary monomers molecularly imprinted electrochemiluminescence sensor (MIECLS) based on a polyvinylpyrrolidone-functionalized copper nanowires (CuNWs@PVP) luminescent probe was constructed for the ultra-sensitive detection of CIP. CuNWs with low cost and high conductivity exhibited near-infrared electrochemiluminescence (NIR ECL) properties, yet their self-aggregation and oxidation led to a weakened emission phenomenon. PVP with solvent affinity and large skeleton was in situ attached to CuNWs surface to avoid CuNWs sedimentation and aggregation, and self-enhanced ECL signals were achieved. The bifunctional monomers molecularly imprinted polymer (MIP) possessed complementary active centers that increased their affinity with CIP, enhancing the accurate and sensitive detection of the target substances. The linear range of CIP using MIECLS was 5.00 × 10⁻⁹–5.00 × 10⁻⁵ mol L⁻¹ with a low limit of detection (LOD) of 2.59 × 10⁻⁹ mol L⁻¹, while the recovery rates of CIP in the spiking recovery experiment were 84.39% to 92.48%. The combination of bifunctional monomer MIP and NIR copper-based nano-luminescent probe provides a new method for the detection of CIP in food. Full article