Search Results (7)

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

Recent advances in electrochemiluminescence (ECL) leveraging thermally activated delayed fluorescence (TADF) have highlighted its potential for near-unity exciton harvesting. However, there are still very limited examples of TADF-ECL emitters. We present a rigid diboron-embedded multiple-resonance TADF emitter, which exhibits blue–green emission at 493 nm with a remarkably narrow bandwidth (FWHM = 22 nm) and minimized singlet-triplet energy gap (ΔE_ST = 0.2 eV), achieving a 67% photoluminescence quantum yield. DFT calculations confirm the short-range charge transfer, enabling narrowband emission. Co-reactant-dependent ECL shows that tripropylamine (TPrA) improves the ECL efficiency from 11% (annihilation) to 51%, while benzoyl peroxide (BPO) yields 1% due to poor radical stabilization. ECL spectra align with photoluminescence, confirming the singlet-state dominance without exciplex interference. TPrA enhances stable radical formation and energy transfer, whereas BPO induces non-radiative losses. These findings establish molecular rigidity and co-reactant selection as pivotal factors in developing high-performance TADF-ECL systems, providing fundamental guidelines for designing organic electrochemiluminescent materials with optimized exciton harvesting efficiency. Full article

Dopamine (DA) is an important catecholamine neurotransmitter and its abnormal concentration is closely related to diseases such as hypertension, Parkinson’s disease and schizophrenia. Due to the advantages of high sensitivity and fast response for electrochemiluminescence (ECL), developing ECL sensors for detecting DA was very critical in clinical diagnosis. ECL resonance energy transfer (ECL-RET) was an effective signaling mechanism. However, the shortage of highly efficient ECL-RET pairs impeded the development of DA sensors. Herein, methyl-modified perylene diimide derivative (PDI-CH₃) self-assembly nanorod materials as luminophores and CuO nanomaterials as acceptors were integrated into nanocomposites. An obvious ECL-RET was found in PDI-CH₃/CuO nanocomposites. After PDI-CH₃/CuO nanocomposites were treated with DA, a large increase in ECL intensity was observed. Then, PDI-CH₃/CuO nanocomposites were taken as an ECL platform to detect DA. This ECL sensor exhibited a linear response to DA from 10⁻¹² M to 10⁻⁸ M with a limit of detection of 0.20 pM. Compared with other sensors for DA detection, the constructed ECL sensor exhibited higher sensitivity. In addition, the novel ECL sensor in this work showed good practicability in a human serum sample. Full article

In this study, an electrochemiluminescence (ECL) immunosensor based on nanobody heptamer and resonance energy transfer (RET) between g-C₃N₄ (g-CN) and NU-1000(Zr) was proposed for ultrasensitive ochratoxin A (OTA) detection. First, OTA heptamer fusion protein was prepared by fusing OTA-specific nanometric (Nb28) with a c-terminal fragment of C4 binding protein (C4bpα) (Nb28-C4bpα). Then, Nb28-C4bpα heptamer with the high affinity used as a molecular recognition probe, of which plenty of binding sites were provided for OTA-Apt-NU-1000(Zr) nanocomposites, thereby improving the immunosensors’ sensitivity. In addition, the quantitative analysis of OTA can be achieved by using the signal quenching effect of NU-1000(Zr) on g-CN. As the concentration of OTA increases, the amount of OTA-Apt-NU-1000(Zr) fixed on the electrode surface decreases. RET between g-CN and NU-1000(Zr) is weakened leading to the increase of ECL signal. Thus, OTA content is indirectly proportional to ECL intensity. Based on the above principle, an ultra-sensitive and specific ECL immunosensor for OTA detection was constructed by using heptamer technology and RET between two nanomaterials, with a range from 0.1 pg/mL to 500 ng/mL, and the detection limit of only 33 fg/mL. The prepared ECL-RET immunosensor showed good performance and can be successfully used for the determination of OTA content in real coffee samples, suggesting that the nanobody polymerization strategy and the RET effect between NU-1000(Zr) and g-CN can provide an alternative for improving the sensitivity of important mycotoxin detection. Full article

Electrochemiluminescence (ECL) analysis has become a powerful tool in recent biomarker detection and clinic diagnosis due to its high sensitivity and broad linear range. To improve the analytical performance of ECL biosensors, various advanced nanomaterials have been introduced to regulate the ECL signal such as graphene, gold nanomaterials, and quantum dots. Among these nanomaterials, some plasmonic nanostructures play important roles in the fabrication of ECL biosensors. The plasmon effect for the ECL signal includes ECL quenching by resonant energy transfer, ECL enhancement by surface plasmon resonance enhancement, and a change in the polarized angle of ECL emission. The influence can be regulated by the distance between ECL emitters and plasmonic materials, and the characteristics of polarization angle-dependent surface plasmon coupling. This paper outlines the recent advances of plasmonic based ECL biosensors involving various plasmonic materials including noble metals and semiconductor nanomaterials. The detection targets in these biosensors range from small molecules, proteins, nucleic acids, and cells thanks to the plasmonic effect. In addition to ECL biosensors, ECL microscopy analysis with plasmonic materials is also highlighted because of the enhanced ECL image quality by the plasmonic effect. Finally, the future opportunities and challenges are discussed if more plasmonic effects are introduced into the ECL realm. Full article

Electrochemiluminescence (ECL)-based sensing systems rely on light emissions from luminophores, which are generated by high-energy electron transfer reactions between electrogenerated species on an electrode. ECL systems have been widely used in the detection and monitoring of diverse, disease-related biomarkers due to their high selectivity and fast response times, as well as their spatial and temporal control of luminance, high controllability, and a wide detection range. This review focuses on the recent strategic and technological advances in ECL-based biomarker detection systems. We introduce several sensing systems for medical applications that are classified according to the reactions that drive ECL signal emissions. We also provide recent examples of sensing strategies and technologies based on factors that enhance sensitivity and multiplexing abilities as well as simplify sensing procedures. This review also discusses the potential strategies and technologies for the development of ECL systems with an enhanced detection ability. Full article

The well-dispersive and superparamagnetic Fe₃O₄-nanocrystals (Fe₃O₄-NCs) which could significantly enhance the anodic electrochemiluminescence (ECL) behavior of luminol, were synthesized in this study. Compared to ZnS, ZnSe, CdS and CdTe nanoparticles, the strongest anodic ECL signals were obtained at +1.6 V on the Fe₃O₄-NCs coated glassy carbon electrode. The ECL spectra revealed that the strong ECL resonance energy transfer occurred between luminol and Fe₃O₄-NCs. Furthermore, under the optimized ECL experimental conditions, such as the amount of Fe₃O₄-NCs, the concentration of luminol and the pH of supporting electrolyte, BPA exhibited a stronger distinct ECL quenching effect than its structural analogs and a highly selective and sensitive ECL sensor for the determination of bisphenol A (BPA) was developed based on the Fe₃O₄-NCs. A good linear relationship was found between the ECL intensity and the increased BPA concentration within 0.01–5.0 mg/L, with a correlation coefficient of 0.9972. The detection limit was 0.66 × 10⁻³ mg/L. Good recoveries between 96.0% and 105.0% with a relative standard deviation of less than 4.8% were obtained in real water samples. The proposed ECL sensor can be successfully employed to BPA detection in environmental aqueous samples. Full article