Lead ions (Pb2+) are heavy metal environmental pollutants that can significantly impact biological health. In this study, the synthesis of a ternary nanocomposite, ErVO4/P@g-C3N4/SnS2, was achieved using a combination of hydrothermal synthesis and mechanical grinding. The as-fabricated photoelectrochemical (PEC) sensor was found to be an ideal substrate for Pb2+ detection with high sensitivity and reliability. The ErVO4/P@g-C3N4/SnS2/FTO was selected as the substrate because of its remarkable and reliable photocurrent response. The Pb2+ sensor exhibited a low detection limit of 0.1 pM and a broad linear range of 0.002 to 0.2 nM. Moreover, the sensor exhibited outstanding stability, selectivity, and reproducibility. In real-time applications, it exhibited stable recovery and a low relative standard deviation, ensuring reliable and accurate measurements. The as-prepared PEC sensor was highly stable for the detection of Pb2+ in different water samples. This promising characteristic highlights its significant potential for use in the detection of environmental pollutants.

Herein, two simple fluorescent signal-on sensing strategies for detecting lead ions (Pb2+) were established based on structure-switching aptamer probes and exonuclease-assisted signal amplification strategies. Two hairpin-structure fluorescent probes with blunt-ended stem arms were designed by extending the base sequence of Pb2+ aptamer (PS2.M) and labelling the probes with FAM (in probe 1) and 2-aminopurine (2-AP) (in probe 2), respectively. In method 1, graphene oxide (GO) was added to adsorb probe 1 and quench the fluorescence emission of FAM to achieve low fluorescent background. In method 2, fluorescent 2-AP molecule inserted into the double-stranded DNA of probe 2 was quenched as a result of base stacking interactions, leading to a simplified, quencher-free approach. The addition of Pb2+ can induce the probes to transform into G-quadruplex structures, exposing single DNA strands at the 3\' end (the extended sequences). This exposure enables the activation of exonuclease I (Exo I) on the probes, leading to the cleavage effect and subsequent release of free bases and fluorophores, thereby resulting in amplified fluorescence signals. The two proposed methods exhibit good specificity and sensitivity, with detection limits of 0.327 nM and 0.049 nM Pb2+ for method 1 and method 2, respectively, and have been successfully applied to detect Pb2+ in river water and fish samples. Both detection methods employ the structure-switching aptamer probes and can be completed in two or three steps without the need for complex analytical instruments. Therefore, they have a broad prospect in the sensitive and simple detection of lead ion contamination in food and environmental samples.

Lead pollution has remained a significant global concern for several decades due to its detrimental effects on the brain, heart, kidneys, lungs, and immune system across all age groups. Addressing the demand for detecting trace amounts of lead in food samples, we have developed a novel biosensor based on fluorescence resonance energy transfer (FRET) from fluorescein R6G to gold nanoclusters (AuNCs-CCY). By utilizing polypeptides as a template, we successfully synthesized AuNCs-CCY with an excitation spectrum that overlaps with the emission spectrum of R6G. Exploiting the fact that Pb2+ induces the aggregation of gold nanoclusters, leading to the separation of R6G from AuNCs-CCY and subsequent fluorescence recovery, we achieved the quantitative detection of Pb2+. Within the concentration range of 0.002-0.20 μM, a linear relationship was observed between the fluorescence enhancement value (F-F0) and Pb2+ concentration, characterized by the linear equation y = 2398.69x + 87.87 (R2 = 0.996). The limit of detection (LOD) for Pb2+ was determined to be 0.00079 μM (3σ/K). The recovery rate ranged from 96 % to 104 %, with a relative standard deviation (RSD) below 10 %. These findings demonstrate the potential application value of our biosensor, which offers a promising approach to address the urgent need for sensitive detection of heavy metal ions, specifically Pb2+, in food samples.

The detection and removal of Pb2+ is of utmost importance for environmental protection and human health due to its toxicity, persistent pollution, and bioaccumulation effects. To address the limitations associated with organic small molecule-based fluorescence probes such as poor water solubility and single functionality in detecting Pb2+, a fluorescence probe based on halloysite nanotubes was developed. This probe not only enables specific, rapid, and reliable detection of Pb2+ but also facilitates efficient removal of it from water. The development of this bifunctional fluorescent probe provides a valuable insight for designing more advanced probes targeting heavy metal ions.

For the first time, composites of metal-organic framework MOF-5 and conjugated polymer polyaniline (PANI), (MOF-5/PANI), prepared using PANI in its conducting (emeraldine salt, ES) or nonconducting form (emeraldine base, EB) at various MOF-5 and PANI mass ratios, were evaluated as electrode materials for the electrochemical detection of cadmium (Cd2+) and lead (Pb2+) ions in aqueous solutions. Testing of individual components of composites, PANI-ES, PANI-EB, and MOF-5, was also performed for comparison. Materials are characterized by Raman spectroscopy, scanning electron microscopy (SEM) and dynamic light scattering (DLS), and their electrochemical behavior was discussed in terms of their zeta potential, structural, morphology, and textural properties. All examined composites showed high electrocatalytic activity for the oxidation of Cd and Pb to Cd2+ and Pb2+, respectively. The MOF/EB-1 composite (71.0 wt.% MOF-5) gave the highest oxidation currents during both individual and simultaneous detection of two heavy metal ions. Current densities recorded with MOF/EB-1 were also higher than those of its individual components, reflecting the synergistic effect where MOF-5 offers high surface area for two heavy metals adsorption and PANI offers a network for electron transfer during metals\' subsequent oxidation. Limits of detection using MOF/EB-1 electrode for Cd2+ and Pb2+ sensing were found to be as low as 0.077 ppm and 0.033 ppm, respectively. Moreover, the well-defined and intense peaks of Cd oxidation to Cd2+ and somewhat lower peaks of Pb oxidation to Pb2+ were observed at voltammograms obtained for the Danube River as a real sample with no pretreatment, which implies that herein tested MOF-5/PANI electrodes could be used as electrochemical sensors for the detection of heavy metal ions in the real water samples.

Pb2+ is a heavy metal ion pollutant that poses a serious threat to human health and ecosystems. The conventional methods for detecting Pb2+ have several limitations. In this study, we introduce a novel fluorescent probe that enables the detection of Pb2+ in the near-infrared region, free from interference from other common ions. A unique characteristic of this probe is its ability to rapidly and accurately identify Pb2+ through ratiometric measurements accompanied by a large Stokes shift of 201 nm. The limit of detection achieved by probe was remarkably low, surpassing the standards set by the World Health Organization, and outperforming previously reported probes. To the best of our knowledge, this is the first organic small-molecule fluorescent probe with both near-infrared emission and ratiometric properties for the detection of Pb2+. We present a triple-mode sensing platform constructed using a probe that allows for the sensitive and selective recognition of Pb2+ in common food items. Furthermore, we successfully conducted high-quality fluorescence imaging of Pb2+ in various samples from common edible plants, HeLa cells, Caenorhabditis elegans, and mice. Importantly, the probe-Pb2+ complex exhibited tumour-targeting capabilities. Overall, this study presents a novel approach for the development of fluorescent probes for Pb2+ detection.

To solve the problem of biochar lack of adsorption sites for heavy metal ions and the difficulty of recycling, CoFe2O4 magnetic nanoparticles confined in nitrogen, sulfur co-doped 3D network biochar matrix (C-CoFe2O4/N,S-BC) was designed and fabricated successfully. The obtained C-CoFe2O4/N,S-BC displays remarkable adsorption performance for both Pb2+ and ciprofloxacin (CIP) removal at the single or binary system due to the role of N,S as metal ion anchoring compared to the N,S-free sample (CoFe2O4/BC). N,S co-doped BC not only participates in adsorption reaction but also effectively inhibites the agglomeration of CoFe2O4 nanoparticles and increases the active sites as a carrier at the same time. In the single system, CoFe2O4/N,S-BC demonstrates a fast adsorption rate (equilibrium time: 30 min) and high adsorption capacity (224.77 mg g-1 for Pb2+, 400.11 mg g-1 for CIP) towards Pb2+ and CIP. The adsorption process is befitted pseudo-second-order model, and the equilibrium data are in great pertinence with Langmuir model. In the binary system, the maximum adsorption capacity of CoFe2O4/N,S-BC for Pb2+ and CIP is 244.80 mg g-1 (CIP: 10.00 mg L-1) and 418.42 mg g-1 (Pb2+: 10.00 mg L-1), respectively. The adsorption mechanism is discussed based on the experimental results. Moreover, C-CoFe2O4/N,S-BC shows good practical water treatment capacity, anti-interference ability and stable reusability (the removal efficiency＞80% after eight cycles). The rapid, multifunctional, reusable, and easily separable adsorption properties make C-CoFe2O4/N,S-BC promising for efficient environmental remediation. This study also offers a viable method for the construction of adsorption material for complex wastewater treatment.

Nano-needle boron-doped diamond (NNBDD) films increase their performance when used as electrodes in the determination of Pb2+. We develop a simple and economical route to produce NNBDD based on the investigation of the diamond growth mode and the ratio of diamond to non-diamond carbon without involving any templates. An enhancement in surface area is achievable for NNBDD film. The NNBDD electrodes are characterized through scanning electron microscopy, Raman spectroscopy, X-ray diffraction, cyclic voltammetry, electrochemical impedance spectroscopy, and differential pulse anodic stripping voltammetry (DPASV). Furthermore, we use a finite-element numerical method to research the prospects of tip-enhanced electric fields for sensitive detection at low Pb2+ concentrations. The NNBDD exhibits significant advantages and great electrical conductivity and is applied to detect trace Pb2+ through DPASV. Under pre-deposition accumulation conditions, a wide linear range from 1 to 80 µgL-1 is achieved. A superior detection limit of 0.32 µgL-1 is achieved for Pb2+, which indicates great potential for the sensitive detection of heavy metal ions.

Isomerism is an essential and ubiquitous phenomenon in organic chemistry, yet it is rarely observed in covalent organic frameworks (COFs). Herein, we synthesized two framework-isomeric COFs (BATD-Dma-COF-K and BATD-Dma-COF-R) and found for the first time that the light scattering signal of the COFs can be used for the analytical detection of lead ion. By using solvothermal and room temperature solvent synthesis methods, controlling different synthesis conditions, and introducing regulators to increase the energy difference between different products, the product with the lowest energy could be synthesized under specific conditions. This method could control the morphology of the synthesized COF and realize the precise synthesis of framework-isomeric COF by changing the experimental conditions. The structures of the two framework-isomeric COFs were characterized and confirmed by a series of analytical methods. Based on the principle that lead ions coordinate with N and O on the surface of two skeletal isomers BATD-Dma-COFs to enhance the light scattering signal of the COFs, a light scattering probe was developed by BATD-Dma-COF for the detection of metal lead ion in water samples. Lead ion concentration in the range from 2.0 to 250.0 μM had a good linear relationship with the light scattering intensity increase of the COFs with detection limit as low as 0.8397 μM by BATD-Dma-COF-K and 0.9207 μM by BATD-Dma-COF-R.

As a highly toxic and refractory heavy metal contaminant, Pb2+ seriously endangers human health. The problems of low sensitivity and high cost of signal labeling widely exist in common electrochemical biosensors. Herein, a Pb2+ electrochemical biosensor was constructed using a DNAzyme-driven bipedal DNA Walker and catalytic hairpin assembly as the multistage signal amplification strategy. Compared with Zr-MOF, AuNPs@Zr-MOF has a larger porosity and specific surface area, which can effectively load MB to amplify the current signal. Pb2+ can trigger a dual signal amplification reaction to gradually accumulate the signal of methylene blue/gold nanoparticle @ zirconium-based metal organic frameworks (MB/AuNPs@Zr-MOF) on the electrode. The ingeniously designed sensing strategy realized the analysis of Pb2+ with a wide linear range from 0.05 to 1000 nmol/L and a lower limit of detection (LOD) of 4.65 pmol/L. In addition, the sensor has strong anti-interference ability and can accurately detect Pb2+ in various food samples.