Detection Of Heavy Metal Ions Research Articles

Novel selective ionic liquid membrane-coupled microfluidic chip for heavy metal separation and analytical strategies

The development of new low-cost, highly selective and efficient methods for the separation and detection of heavy metal ions in aqueous environments is of great importance for water safety and biological health. In this study, a novel ion separation membrane was prepared for the separation of copper ions in cadmium ion detection solution. Compared with the commercial membrane, the ion mobility was increased by 64.02 %, and further separated by selective complexation of thiacalix[4]arene-p-tetrasulfonate (TCAS), and the separation factor for Cu/Cd reached 34.66. This allowed Cd to be detected preferentially, and reduced the interference of other ions in the detection. The joint electric field environment was regulated to separate the organics and reduce the interference to the detection. The sensing performance was enhanced by modifying the screen-printed electrodes. The proposed sensing platform allows for simultaneous pre-processing and detection and has a detection limit of 0.19 μg-L−1 (S/N = 3) for Cd2+.

Preparation of cellulose nanofiber/polyvinyl alcohol-based composite films for metal ion detection by starch/disodium calcium ethylenediaminetetraacetate synergistic complexation effect

Heavy metal pollution causes irreversible damage to plants, animals, and humans. Therefore, it is meaningful to develop facile, fast, and efficient strategies for heavy metal ion (HMI) detection. Here, a portable composite film (CPSE) was designed for HMI detection with high sensitivity and wide detection range. The CPSE was prepared by using cellulose nanofibers (CNF)/polyvinyl alcohol (PVA) as the matrix and utilizing modified starch (HPS) to assist disodium calcium ethylenediaminetetraacetate (EDTA-Ca) to form stable complexes with HMI. The R, G and B values (the three primary colors of light) were captured using an image acquisition system to produce an HMI standard color card successfully. Specifically, the composite film can effectively distinguish Cu2+, Pb2+ and Fe3+. The response time of the composite film to HMI was 2–4 s, and the detection ranges of Cu2+ and Fe3+ were 5–700 ppm and 10–1000 ppm, respectively. Additionally, the synergistic effect of HPS and EDTA-Ca led to the increase in tensile strength (1.59–1.71 times), tear strength (3.29–3.57 times), and glass transition temperature (~ 6 °C) compared to CNF/PVA/HPS and CNF/PVA/EDTA-Ca films. This study confirms the value of CPSE films as materials for HMI detection and suggests innovative ideas for designing similar biomass detection materials in the future.

Development of dihydropyrimidine based chemosensor for Hg2+ ions

The detection and monitoring of heavy metal ions in water media is critical due to their toxic effects on human health and the environment. In this study, we propose a green approach for synthesizing a dihydropyrimidine-based ligand by utilizing the concept of the Biginelli reaction and incorporating Ag nanoparticles as activators. This synthesized ligand demonstrates exceptional potential as a chemosensor for detecting poisonous Hg2+ ions using a simple spectrofluorometer tool. The ligand exhibits high selectivity and sensitivity towards Hg2+ over other transition metal ions in aqueous solution. This innovative method aligns with green chemistry principles, emphasizing the importance of using a straightforward and efficient sensing method of fluorescence. This is the first report where a dihydropyrimidine-based moiety detects toxic heavy metal ions, Hg+2(minimum detection level is 5X10−7 M).

Optical fiber SPR Pb2+sensor with tip-printed Fabry-Perot interferometer for temperature compensation

Due to the serious biological toxicity and environmental refractory of heavy metal ions, the detection of heavy metal ions in liquids has attracted great attention. A novel fiber optic surface plasmon resonance (SPR) sensor is presented for detecting lead ions (Pb2+) with temperature compensation. The sensitivity of SPR channel to Pb2+ is up to -41.55 nm/μM and the detection limit is 7.05 nM after three parallel experiments by synthesizing Schiff base and fixing it on the sensor surface. Using femtosecond laser-induced two-photon polymerization (TPP) technology, a compact fiber-tip miniature Fabry-Perot interferometer (FPI) was printed at the end of the fiber-optic SPR sensor, thus realizing the temperature measurement in the process of detecting Pb2+. The FPI channel exhibits a linear response to temperature and remains unaffected by Pb2+ concentration, thus facilitating temperature correction. The experimental results also show that the proposed sensor has the advantages of compact structure, easy to prepare, good stability, specificity and repeatability. Therefore, this kind of sensor has great potential in various biochemical test applications, and opens up a new way to prepare compact and flexible optical sensors.

Microwave-Assisted Synthesis of N, S Co-Doped Carbon Quantum Dots for Fluorescent Sensing of Fe(III) and Hydroquinone in Water and Cell Imaging.

The detection of heavy metal ions and organic pollutants from water sources remains critical challenges due to their detrimental effects on human health and the environment. Herein, a nitrogen and sulfur co-doped carbon quantum dot (NS-CQDs) fluorescent sensor was developed using a microwave-assisted carbonization method for the detection of Fe3+ ions and hydroquinone (HQ) in aqueous solutions. NS-CQDs exhibit excellent optical properties, enabling sensitive detection of Fe3+ and HQ, with detection limits as low as 3.40 and 0.96 μM. Notably, with the alternating introduction of Fe3+ and HQ, NS-CQDs exhibit significant fluorescence (FL) quenching and recovery properties. Based on this property, a reliable "on-off-on" detection mechanism was established, enabling continuous and reversible detection of Fe3+ and HQ. Furthermore, the low cytotoxicity of NS-CQDs was confirmed through successful imaging of HeLa cells, indicating their potential for real-time intracellular detection of Fe3+ and HQ. This work not only provides a green and rapid synthesis strategy for CQDs but also highlights their versatility as fluorescent probes for environmental monitoring and bioimaging applications.

Real-Time Wireless Detection of Heavy Metal Ions Using a Self-Powered Triboelectric Nanosensor Integrated with an Autonomous Thermoelectric Generator-Powered Robotic System.

The integration of the Internet of Things (IoT) with advanced sensing technologies is transforming environmental monitoring and public health protection. In this study, a fully self-powered and automated chemical sensing system is developed and integrated with a robotic hand for "touch and sense" detection of toxic heavy metal ions (Pb2⁺, Cr⁶⁺, As3⁺) in aquatic environments. The system combines a self-powered solid-liquid triboelectric nanosensor (SL-TENS) with a thermoelectric generator (TEG), which harnesses ambient heat to power the robotic hand, eliminating the need for external power sources. The robotic hand is controlled wirelessly via an exo-hand, minimizing the risk of exposure during remote monitoring. The sensing component uses copper oxide nanowires (CuO NWs) coated with ion-selective membranes (ISMs) to enhance triboelectric output and enable highly selective ion detection. The system demonstrates effective real-time, on-site detection in lake water and data transmitted wirelessly to the user. This innovative approach provides a highly safe and efficient method for detecting hazardous pollutants in difficult-to-access areas, offering significant potential for wireless and real-time environmental monitoring and hazard prevention, thus contributing to the safeguarding of human health. This study presents a novel advancement in the field of IoT-enabled environmental monitoring systems.

Plasma Tailoring of NH2-MIL-53 with Enhanced Fluorescence Emission for Simultaneous Detection of Multiple Heavy Metals in Water.

Indium, copper, and mercury are important raw materials in the electronics industry and often coexist in factory wastewater. Therefore, the development of a highly sensitive and selective method for the simultaneous detection of these heavy metal ions is of great significance for water quality monitoring and environmental protection. Herein, we report a NH2-MIL-53 fluorescent probe for the simultaneous detection of trace In3+, Cu2+, and Hg2+ in water. After a low-temperature NH3 plasma tailoring treatment for grafting electron-donor amine groups, the obtained NH2-MIL-53-M exhibited enhanced fluorescence emission intensity (∼6 times) coupled with selective adsorption of In3+, Cu2+, and Hg2+. This quenched the NH2-MIL-53-M fluorescence and allowed to significantly increase the selectivity and sensitivity for detection of In3+, Cu2+, and Hg2+. The fluorescence quenching constant (Ksv) values were 2.23 × 105, 1.00 × 105, and 2.74 × 104 M-1, while the limit of detection (LODs) values were 0.06, 0.14, and 0.53 μM, for In3+, Cu2+, and Hg2+, respectively. The concentrations of In3+, Cu2+, and Hg2+ in real environmental samples could be determined by addition of appropriate masking agents, and the recoveries were within the range of 94-110%. This study not only supplied a strategy for constructing a highly sensitive and selective fluorescent probe but also established a platform for simultaneous detection of multiple heavy metal ions in water.

AuNPs enhanced electrochemical and optical dual-mode fiber optic sensor for trace Hg2+ detection

Efficient and low-concentration detection of heavy metal ions is crucial for healthcare and environmental monitoring. Traditional fiber optic surface plasmon resonance (SPR) sensors face challenges in detecting trace heavy metal ions due to limited sensitivity and the need for complex specific modifications. To overcome these challenges, an innovative electrochemical and optical dual-mode fiber optic sensor for in situ, real-time detection of trace mercury ions is proposed in this paper. The sensor utilizes a reflection-type fiber optic probe coated with thin gold (Au)/indium tin oxide (ITO) film and gold nanoparticles (AuNPs), enabling simultaneous electrochemical and optical interrogation. The coupling effect between the SPR of thin film and the localized surface plasmon resonance (LSPR) of AuNPs significantly improves optical sensitivity, with AuNPs also offering additional active sites for the redox reaction of Hg2+. The ITO film not only facilitates the stripping of Hg2+, leading to sharper stripping peaks but also enhances the ability of the sensor to rapidly respond to anomalous potential changes. Experimental results show that the sensor has a wide dynamic detection range from 10−10 M to 10−5 M, with a limit of detection reaching the pM level. The dual-mode functionality allows the simultaneous collection of voltage, current, and optical information, enabling cross-validation of the detection results and improving the accuracy and reliability of detection.

Luminescent Multifunctional Nanomaterials: Capacitive Removal and Enhanced Detection Efficiency of Heavy Metals Ions for Advanced Water and Wastewater Treatment Application

AbstractIn recent years, heavy metal ions pollution in the industrialized environment of the societies threaten human health that flaunt ill‐sorted blueprints in freshwater resources obviously. The paradigm of designing luminescent multifunctional nanomaterials finds directions to the strategies of synthesizing cost‐effective, green, and versatile nanomaterials not only for detection, but also removal process of heavy metal ions in large scale applications. Among them, discovering the advances of luminescent multifunctional nanomaterials provides broad types of biomaterials, polymers and porous nanoparticles that grabs focal of investigations over the past several years due to their unique advantages such as enhanced detection efficiency with lowest limit of detection (LOD), minimum ions interference in versatile removal process, fast responsivity and selectivity as outstanding as unique physicochemical properties. This review paper tries to highlight the paradigm of principles for design, development, and utilization of luminescence nanomaterials for considering fundamental detection and removal mechanisms of heavy metal ions. In particular, these nanomaterials increase the remediation quality that are tackled in detail by focusing on opportunities and challenges in the field. Finally, design methods of these nanomaterials and concentrating on empowered detection and removal efficiency for heavy metals ions highlights novel prospective and strategies for largescale applications.

Nanoarchitectonics with cetrimonium bromide on metal nanoparticles for linker-free detection of toxic metal ions and catalytic degradation of 4-nitrophenol.

Heavy metal ions and organic pollutants, such as 4-nitrophenol (4-NP), pose significant environmental and human health threats. Addressing these challenges necessitates using advanced nanoparticle-based systems capable of efficient detection and degradation. However, conventional approaches utilizing strong capping agents like cetrimonium bromide (CTAB) on nanoparticles lead to limitations due to the rigid nature of CTAB. This restricts its utility in heavy metal detection and 4-NP degradation, requiring additional surface modifications using linker molecules, thereby increasing process complexity and cost. To overcome these limitations, there is a critical need for the development of an easy-to-use, dual-functional, linker-free nanosystem capable of simultaneous detection of heavy metals and efficient degradation of 4-NP. For enabling linker-free/ligand-free detection of heavy metal ions and catalytic degradation of 4-NP, CTAB was engineered as a versatile capping agent on gold and silver nanoparticles. Various factors, including nanoparticle characteristics such as shape, size, metal composition, centrifugation, and NaOH amount, were investigated for their impact on the performance of CTAB-capped nanoparticles in heavy metal detection and 4-NP degradation. CTAB-Au nanospheres demonstrated limited heavy metal ion detection capability but exhibited remarkable efficiency in degrading 94.37% of 4-NP within 1 min. In contrast, silver nanospheres effectively detected Hg2+, Cu2+, and Fe3+ at concentrations as low as 1 ppm and degraded 90.78% of 4-NP within 30 min. Moreover, anisotropic gold nanorods (CTAB-AuNR1 and CTAB-AuNR2) showed promising sensing capabilities towards Cu2+, Cr3+, and Hg2+ at 0.5 OD, while efficiently degrading 4-NP within 5 min at 1 OD. This study emphasizes the importance of tailoring parameters of CTAB-capped nanoparticles for specific sensing and catalytic applications, offering potential solutions for environmental remediation and human health protection.

From Structure to Sensing: Molecular Mechanistic Insights into Plant-Derived Carbon Dots for Heavy Metal Ion Detection.

Plant-derived carbon dots (P-CDs) are gaining attention in environmental remediation due to their cost-effectiveness, availability, and lower toxicity compared with chemically synthesized carbon dots. This review comprehensively examines the recent advancements in the synthesis and application of P-CDs, with a particular emphasis on their efficacy in the sensing of heavy metals, which are among the most pervasive environmental contaminants. A detailed comparative analysis is presented by evaluating the performance of P-CDs against their chemically synthesized counterparts based on key parameters, such as optimal operating conditions and detection limits. Furthermore, sensing the potential of P-CDs towards every heavy metal ion has been discussed with in-depth mechanistic insights. Additionally, this review explores the industrial applications and future directions of P-CDs. This review provides a comprehensive analysis of -P-CDs for heavy metal sensing, aiming to enhance their sensitivity and selectivity toward heavy metal ions.

An active-conductive layer stacked sensor platform for real-time detection of heavy metal ions

The development of electrochemical sensors with high sensitivity and accuracy is crucial for the detection of low-concentration heavy metal ions (HMIs) such as Pb(II) and Hg(II), which remains challenging. To address this issue, MgFe-layered double hydroxide (MgFe-LDH) is synthesized as an active layer on the conductive layer SnO2 loaded with nickel foam (NF) with the assistance of oxygen vacancies (OVs) to form an active-conductive layer stacked sensor. The results show that MgFe-LDH@SnO2/NF exhibits superior sensitivity (Pb(II): 417 μA/μM; Hg(II): 986 μA/μM), wider linear range (1.1–2.2 μM) and lower limits of detection (Pb(II): 1.21 nM; Hg(II): 3.7 nM). The high performance of our sensor is attributed to the improved ability to adsorb HMIs via OV reduced binding energy as well as the promoted rapid electron transport via SnO2 reduced charge transfer resistance, as evidenced by density functional theory and electrochemical measurements. Particularly, by combining the newly proposed tiny electrochemical detection network (ECDNet-tiny) and WeChat mini program, we have built a real-time detection platform for Pb(II) and Hg(II) pollution categories and concentrations, which shows high accuracy (0.98) and recovery rate (91.6 %-106.8 %) in the detection of actual water samples. The qualitative and quantitative calculations of electrochemistry is innovatively implemented by deep learning. Besides, smartphones could display detection results transmitted from cloud servers. Thus, this work provides a new sensor platform to improve the sensitivity, accuracy, and intelligence of detecting quintessential HMIs.

Detection of Heavy Metal Ions With Ion Imprinting Microfiber Sensor Arrays

Detection of Heavy Metal Ions With Ion Imprinting Microfiber Sensor Arrays

A three-components-based disposable electrochemical sensor for the detection of heavy metal ions in water

The development of an efficient sensor based on a novel three-components nanocomposite is presented for the detection of heavy metal ions (Cd2+ and Pb2+) in water. For the preparation of three-components nanocomposite surface, the polydopamine reduced graphene oxide (PyDA/RGO) composite was initially prepared by a one-step polymerization of dopamine (DA) on RGO followed by surface modification of the prepared composite with cysteine (Cys). The formation of three-components nanocomposite surface (i.e., Cys/PyDA/RGO) was initially confirmed through physical characterization techniques, including X-ray diffraction and infrared spectroscopy, whereas scanning electron microscopy revealed the surface morphology after each step of sensor fabrication. The electrochemical properties of the sensing platform were evaluated through electrochemical techniques, including cyclic voltammetry and electrochemical impedance spectroscopy with an external ferri‐−/ferrocyanide redox probe. The prepared three-components nanocomposite on disposable pencil graphite electrode (Cys/PyDA/RGO/PGE) showed an improved charge transfer rate as compared to PyDA/RGO/PGE and bare PGE electrode. Targeted heavy metal ions were detected on the sensor surface using differential pulse voltammetry with greater sensitivity, showing detection limits of 0.77 and 1.13 ppb for Cd+2 and Pb+2 ions in citrate buffer solution, respectively. The sensor demonstrated comparable performance in the tap water samples.

Redox-mediated dsDNA-dye photooxidase mimic enable catalytic oxidation of 3,3′,5,5′-tetramethylbenzidine by dissolved O2 at neutral pH for improved biosensing

Catalytic oxidation of 3,3′,5,5′-Tetramethylbenzidine (TMB, an excellent chromogenic substrate) at neutral pH is critically important for amplified bioanalysis. Although some nanozymes exhibited the peroxidase activity at neutral pH, it is difficult to modulate their activity for homogeneous detection of biomolecules. In this work, we developed a redox-mediated dsDNA-dye photooxidase mimic that enables catalytic oxidation of TMB by dissolved O2 at neutral pH for improved biosensing. During illumination, the double-stranded DNA-SYBR Green I (dsDNA-SG) photogenerated singlet oxygen (1O2) can oxidized Mn2+ to Mn3+ that can efficiently oxidize TMB to produce a distinct blue within 4 min under neutral conditions. The catalytic oxidation of TMB can be readily modulated by the formation or dissociation of dsDNA during the sensing. After investigating a series of redox mediators, we found that only the Mn3+/Mn2+ redox mediator can lead to the oxidation of TMB at neutral pH. The maximum reaction rate of Mn2+-mediated dsDNA-SG photooxidase mimic under neutral conditions (pH 7.0) was 1.7 × 10−4 mM/s, even higher than that of horseradish peroxidase (HRP, 8.0 × 10−5 mM/s). The redox-mediated dsDNA-SG photooxidase mimic was used for detection of APE1 at pH 7.0 with over 130-fold higher sensitivity than that at 4.0, owing to the high enzymatic activity of APE1 at neutral pH. Meanwhile, we further extended this photooxidase mimic for the sensitive detection of DNA (LOD, 8 pM) and heavy metal ions at neutral pH. The redox-mediated dsDNA-dye photooxidase mimic with the ease of modulating its enzymatic activity and working at neutral pH is quite appealing for biosensing.

Nafion/graphite-bismuth nanoplate with a vibration unit for portable heavy metal ion detection

Contamination of natural resources, particularly water sources, by heavy metal ions, even at low concentrations, poses a significant threat to ecosystems and human health, underscoring the importance of developing sensors with point-of-use (POU) applications. To that end, a vibration-unit-equipped portable electrochemical system (vPES) capable of extremely sensitive detection of Pb2+ and Cd2+ in water is reported herein. The vibration unit enhances sensitivity by facilitating sample diffusion, and its compactness makes it suitable for point-of-use applications through mobile phone connectivity. The system also integrates Nafion and a graphite/bismuth-nanoplate-functionalized screen-printed carbon electrode to detect heavy metals efficiently. The approach implemented in this study and validated through experiments and simulations suggests that vibration-based mixing leads to 540 % and 511 % higher Pb2+ and Cd2+ detection efficiencies, respectively, than those in the absence of vibration. Additionally, the sensor exhibits the limits of detection of 0.98 and 1.65 nM for Pb2+ and Cd2+, respectively, in laboratory environments. Samples collected from the Nakdong River in Korea and real environmental specimens—freshwater, soil, and serum—validate the detection performance. Overall, this study highlights the potential of vPES as a rapid, sensitive POU sensor for heavy metal detection, thereby bolstering environmental and public health monitoring efforts.

Modulating NFO@N‐MWCNTs/CC Interfaces to Construct Multilevel Synergistic Sites (Ni/Fe‐O‐N‐C) for Multi‐Heavy Metal Ions Sensing

AbstractA hierarchical heterogeneous composite electrode of NiFe2O4@nitrogen‐doped multi‐walled carbon nanotubes/carbon cloth (NFO@N‐MWCNTs/CC) is prepared via a dip‐coating method, followed by a hydrothermal process. The flexible carbon cloth (CC) substrate provides robust support and the cross‐linked nitrogen‐doped multi‐walled carbon nanotubes (N‐MWCNTs) on the CC form a highly porous network with a large specific area that facilitates electron‐transfer. The stable support strengthens the framework and prevents pore structure disorder within the porous network, that could lead to the structural instability of the active sites. The decorated NiFe2O4 nanoparticles offer abundant active sites for enhanced electrocatalytic activity. Benefiting from the synergistic effect of the 3D hierarchical heterogeneous microstructure and multilevel bimetallic oxide active site (Ni/Fe‐O‐N‐C) constructs, the NFO@N‐MWCNTs/CC electrode achieves stable detection of multiple heavy metal ions (HMIs) with high reproducibility. The modified electrode allowed stable detection of multiple heavy metal ions with high reproducibility. The sensitivities of the electrode for Cd(II), Pb(II), Bi(III), and Hg(II) are 344.98, 441.02, 176.484, and 371.099 µA µm−1, respectively. The assay recoveries ranged from 95.3% to 106.8%, highlighting its practical applicability. This study provides innovative composites and theoretical insights to facilitate further advances in the simultaneous high‐performance detection of heavy metal ions.

Nanoparticle-based Biosensors for Detection of Heavy Metal Ions

Heavy metal pollution is one of the most serious environmental problems in the world. Many efforts have been made to develop biosensors for monitoring heavy metals in the environment. Development of nanoparticle-based biosensors is the most effective way to solve this problem. This review presents the latest technology of nanoparticle-based biosensors for environment monitoring to detect heavy metal ions, which are magnetic chitosan biosensor, colorimetric biosensor, and electrochemical biosensor. Magnetic chitosan biosensor acts as a nanoabsorbent, which can easily detect and extract poisonous heavy metal ions such as lead ions and copper ions. There are several methods to prepare the chitosan based on the nanoparticle, which are cross-linking, co-precipitation, multi-cyanoguanidine, and covalent binding method. In colorimetric biosensor, gold and silver nanoparticles are commonly used to detect the lead and mercury ions. In addition, this biosensor is very sensitive, fast and selective to detect metal ions based on the color change of the solution mixture. Meanwhile, electrochemical biosensor is widely used to detect heavy metal ions due to a simple and rapid process, easy, convenient and inexpensive. This biosensor is focused on the surface area, which leads to significant improvement in the performance of devices in terms of sensitivity. The wide surface area can affect the performance of the biosensor due to a limited space for operation of electrode. Therefore, reduced graphene oxide is a suitable material for making the electrochemical biosensor due to a wide surface area, good conductivity and high mechanical strength. In conclusion, these three technologies have their own advantages in making a very useful biosensor in the detection of heavy metal ions.

1D supramolecular assembly-induced emission and colorimetry toward precise onsite mercury(II) detection

Manipulation of the one-dimensional (1D) supramolecular assembly of platinum(II) terpyridyl complex is promising for achieving precise onsite mercury(II) detection in complex environments, but still challenging. Herein, by systematic molecular design of platinum(II) terpyridyl complex, chloride-mediated 1D supramolecular assembly has been successfully achieved, exhibiting not only improved recognition ability but also dual-visual signal, with turn-on red luminescence and high-contrast color change from pale-yellow to orange-red. The probe also shows excellent selectivity and anti-interference properties, fast response rate (< 1 s) and low detection limit, stretching to 20.6 fg when incorporated in a hydrogel matrix. Structure insight for the dual-visual response shows that this high detection performance derives from the ancillary ligand of -NCS, which endows the increase of ion-association ability between platinum(II) terpyridyl complex and [HgCl4]2−, leading that 1D packing mode with strengthened Pt-Pt interactions. In all, this work highlights a new strategy of 1D supramolecular assembly construction for high performance detection of heavy metal ions.

Novel Ternary System for Electrochemiluminescence Biosensor and Application toward Pb2+ Assay.

This study constructed an electrochemiluminescence (ECL) biosensor for ultrasensitive detection of Pb2+ in a ternary system by employing DNAzyme. The ternary system is composed of a potassium-neutralized perylene derivative (K4PTC) as the ECL emitter, K2S2O8 as the coreactant, and neodymium metal-organic frameworks (Nd-MOFs) as the coreaction accelerators. Nd-MOFs immobilize DNAzymes and enhance the luminescence intensity of the K4PTC/K2S2O8 system. As part of this system, K4PTC enhances the ECL signal in solution and supports Pb2+ detection. The sequence of ferrocene (Fc)-linked DNA (DNA-Fc) is catalytically cleaved by DNAzymes in the presence of Pb2+. This causes the removal of DNA1-Fc from the electrode surface to recover the ECL signal. As a result, the as-prepared ECL biosensor can quantify Pb2+ with a detection limit (LOD) of 4.1 fM in the range of 1 μM to 10 fM. The ECL biosensor displays high specificity, good stability, excellent reproducibility, and desirable practicality for Pb2+ detection in tap water. Moreover, by simply changing the sequence of the DNAzyme, new biosensors can be designed for ultrasensitive detection of different heavy metal ions, offering an excellent approach for monitoring water quality safety.