Synthesis of Bismuth Film Assembly on Flexible Carbon Cloth for the Electrochemical Detection of Heavy Metal Ions

: The utilization of bismuth as a sensing material for the detection of heavy metal ions has gained significant attention due to its exceptional interfacial activity and selective absorption properties. However, it also poses challenges in terms of agglomeration and its inferior electrical conductivity during the synthesis process. This paper employed a facile in situ synthesis and elec-trodeposition approach to uniformly grow a bismuth film on a conductive carbon cloth, designated as Bi/Ag@CC. The Bi/Ag@CC electrode material exhibited benign electrochemical properties, enabling its application for detecting Pb 2+ in tap water and lake water samples. Furthermore, this work investigated the impact of electrochemical parameters, including electrolyte pH, deposition potential and pre-enrichment time, on the detection performance. The results demonstrated the sensor’s wide linear range (from 20 to 400 ppb) and detection limits (0.15 ppb) for heavy metal ion detection, along with excellent anti-interference capabilities and satisfactory repeatability, with an RSD of less than 2.31% (n = 6). This paper offers a novel strategy for positioning the bismuth-based composite as a promising candidate for practical electrochemical sensing applications.


Introduction
The issue of global ecological pollution has garnered considerable attention, as water resources are intricately tied to the survival of both humans and other living organisms [1][2][3].Nevertheless, due to industrialization, heavy metal pollution in aquatic environments not only causes ecological devastation but also poses a significant threat to human habitats, potentially resulting in public health crises [4].Among these heavy metal ions, Pb 2+ emerges as a particularly toxic ion capable of inflicting substantial harm to the heart, brain, and other organs in living organisms when present in concentrated forms [5].Nevertheless, ensuring environmental safety and mitigating the biological harm caused by the accumulation and non-degradability of heavy metal ions remains a daunting task for the global community.
Traditional heavy metal detection strategies, such as inductively coupled plasma mass spectrometry (ICP-MS), high-performance liquid chromatography (HPLC) and atomic absorption spectrometry (AAS), are widely recognized and employed extensively due to the benefits of extensive linearity, remarkable sensitivity and low detection limits.However, these sensing technologies demand substantial operational expertise and a considerable testing time [6,7].In recent years, fluorescence and colorimetric methods have emerged as cutting-edge technologies for visually detecting heavy metal ions with specific targeted sites.However, one of the primary problems lies in the limited detecting range of targeted heavy metals [8][9][10][11].Alternatively, the electrochemical sensor addresses this challenge by depositing the targeted ions on the electrode surface and inducing an electrochemical reaction of dissolution in the electrolyte under an applied potential.This reaction generates a distinct peak redox current, enabling the precise detection of the target substance [3,12,13].Owing to its convenience, cost efficiency and remarkable precision, this detection strategy has garnered significant attention in the field of heavy metal detection [14].Furthermore, electroanalytical techniques offer adequate sensitivity, miniaturized and portable equipment and satisfactory accuracy and precise performance [15,16].By employing conventional techniques such as spin coating and droplet-dripping, it is feasible to achieve the desired modifications on the electrode surface.Viviana et al. [17] proposed a synthetic approach for constructing carbon nanodots derived from biomass-based carbon materials.The modified electrode exhibited high stability and adsorption properties, enabling the electrochemical detection of heavy metal ions such as lead and cadmium ions.The conventional electrode modification method results in the degradation of the optimal performance of the working electrode due to interfacial adhesion [18].Taking into account the robust, sensitive and selective characteristics of metal-organic frameworks (MOFs) for the targeted metal ions, a rapid electrochemical detection of diverse heavy metal ions has been reported using the MOFs as electrode materials [19,20].Nevertheless, MOF materials on the surface of the glass carbon electrode over time compromise detection performances.
To address these limitations, in situ growth on the electrode surface was carried out and directly applied to detect heavy metal lead ions without interfacial adhesion.Wang and colleagues constructed a flexible nickel-doped WO 3 /CC (carbon cloth) electrode for glucose detection based on in situ synthesis, and the hierarchical microsheets of WO 3 exhibited a substantial specific surface area, greatly enhancing the rate of electron transfer [21].Gao et al. [6] presented a cupric ion-sensing electrode, featuring the in situ growth of porous rod-like tungsten oxide assembled onto stainless steel mesh, which demonstrated impressive detection capabilities and promising practical applications.Shao et al. [22] illustrated a molybdenum oxide adsorbent with mixed valence, exhibiting selectivity for silver detection and recovery in wastewater.Therefore, the process of in situ synthesis can significantly enhance the stability and reproducibility for the electrochemical detection of heavy metal ions.
Metallic nanomaterials, thanks to their minute size, extensive specific surface area, and exceptional electrical conductivity, could significantly enhance the sensitivity and linearity of electrochemical detection.Bismuth nanoparticles, among various metal particles such as gold and silver nanoparticles, exhibit superior cost effectiveness, environmental friendliness and resistance to oxygen, as well as low toxicity, positioning them as a promising candidate for the electrochemical detection of highly toxic mercury [3].With the assistance of the electrochemical plating method, Jiang et al. designed and fabricated an integrated and wearable detecting platform by printing bismuth films, and this platform was successfully utilized for the real-time detection of heavy metal ions [23] Feng et al. [24] successfully achieved remarkable stability and sensitivity in measuring trace amounts of lead ions by employing nitrogen-doped carbon nanosheets encapsulating bismuth nanoparticles (Bi@NC).The porous carbon composite, co-doped with Bi/Bi 2 O 3 , was derived from a bismuth-based organic framework, offering a wide linear range for the electrochemical detection of lead ions.Notably, the sensor exhibited exceptional stability, reproducibility and satisfactory selectivity [25].
In this work, an electrochemical sensor based on Bi/Ag@CC electrode material was constructed and applied to the detection of Pb 2+ in tap water and lake water samples.The introduction of Ag nanoparticles significantly enhanced the conductivity of the sensor, which was achieved through a simple solution-based synthesis method.Additionally, a Bi layer was deposited on the surface of Ag@CC using an electrochemical deposition approach.The integration of Bi with Ag improved both the electrochemical activity and acid resistance of the sensor.Furthermore, the carbon film serving as a support skeleton not only ensured high electrical conductivity and rapid electrochemical kinetics but also effectively mitigated volume changes during the detection of heavy metal ions [26].Finally, the Bi/Ag@CC composite was employed as an electrochemical detecting electrode material for Pb 2+ sensing using the DPV mode, demonstrating excellent electrochemical performance and electrocatalytic behavior towards heavy metal ions.

Preparation
Carbon cloth as a substrate was firstly soaked and cleaned with acid solution, ethyl alcohol and deionized water, respectively.After drying, the carbon cloth was cut into the size of 20 mm × 10 mm × 1 mm.The carbon cloth was soaked in 0.1 mM AgNO 3 for 20 min and then dried.Next, the dried carbon cloth was added into the 0.2 mM ascorbic acid solution for 10 min, leading to the reduction of Ag nanoparticles, which was named Ag@CC.The Bi/Ag@CC electrode was synthesized via an electrochemical deposition process.The deposition potential and time were selected to be −0.9V and 480 s, respectively, and the concentration of Bi(NO 3 ) 3 was 0.2 g/L.Then, the dried samples were named Bi/Ag@CC electrodes.For the Bi@CC electrode materials, the preparation process remains identical to the aforementioned procedure, with the exception of the absence of the in situ reduction of silver nitrate solution.

Morphological Characteristics
The scanning electron microscopy (ZEISS, GeminiSEM 300, Jena, Germany) with an accelerating voltage of 3 kV was applied to observe the morphology of the prepared electrodes and EDS elemental mapping images.And, the crystal structure of samples was recorded by an X-ray diffractometer (XRD, Tongda, Hong Kong, China) with a scanning speed of 5 • min −1 .X-ray photoelectron spectroscopy (XPS, PHI QUANTERA-II SXM, Waltham, MA, USA) was used to analyze the elements and valence states of the catalysts.The electronic conductivity was measured by a digital multimeter (RIGIOL, Beijing, China).

Electrochemical Characteristics
The electrochemical performances were measured via the electrochemical workstation (CHI-760E, CHI Instruments, Shanghai, China) with a conventional three-electrode system.The counter electrode, reference electrode and the working electrode were the graphite rod, Ag/AgCl electrode and the prepared electrodes, respectively.To mitigate the impact of extraneous ions on the accuracy of measurement results, the electrolyte solution employed in this study is a standardized lead nitrate solution.And, the pH of the electrolyte was adjusted by the acidic and basic solutions.Differential pulse voltammetry (DPV) was used by scanning from −1.0 V to −0.2 V, and the pulse height was set as 50 mV.The pulse amplitude and pulse time were set by the instrument without change.And, the scanning rate was adjusted during the experimental measurements.The deposition voltage and time were −1.2 V and 360 s for the preconcentration of heavy metal ions, respectively.The cyclic voltammetry (CV) with a measurement range of −0.6 V~0.6 V and the electrochemical impedance spectroscopy (EIS) at the frequency range of 0.01 Hz to 100 kHz were tested.All the tests were conducted at room temperature.

Morphological and Structural Characteristics
Scheme 1 demonstrated the synthesis of Bi/Ag@CC electrode materials via a combination of solution immersion and electrochemical deposition reactions.Firstly, the pristine carbon cloth was immersed in an acidic solution to remove the impurity and soaked into the AgNO 3 solution to yield silver nanoparticles on the carbon cloth surface, which was named Ag@CC.Subsequently, a Bi film was formed by employing electrodeposition on top of the Ag@CC to synthesize Bi/Ag@CC electrode material.Figure 1a depicts the SEM images of the untreated carbon cloth, which exhibit a dense fiber structure with an overall smooth appearance.The SEM images of Ag@CC are presented in Figure 1b, revealing silver nanoparticles attached to the surface of the fibers.Due to the specificity of nucleation sites, the silver particles exhibit a non-uniform distribution across the fiber surface.Ascorbic acid functions as a reducing agent, efficiently converting silver ions into silver monomers [27].Figure 1c,d depicts the SEM images of the fibers following bismuth electrodeposition.The bismuth film completely covered the fiber surfaces, providing an ample contact area for the subsequent adsorption of heavy metal ions.Additionally, Figure S1 illustrates the effect of varying silver plating concentrations on conductivity.The concentration of silver plating on the carbon cloth surface was adjusted by varying the soaking time in silver nitrate solution, and the soaking duration of 10 min yielded the most significant reduction in resistance on the CC surface, leading to an enhancement in the conductivity of the electrode.Therefore, the immersion duration for Ag@CC in the solution was standardized at 10 min for all subsequent experiments.To deposit a Bi film, an electrodeposition potential of −0.9 V and a pre-enrichment time of 480 s were selected, as depicted in Figure S2.The crystallographic structures of the prepared samples were determined t XRD analysis, with the diffraction peaks of Bi/Ag@CC, Ag@CC and CC presen Figure 2a.All samples exhibited broad and weak diffraction peaks at 2θ = 25.5° an corresponding to the (002) and (001) planes of graphite (PDF#41-1487) [28].Spec the XRD spectra of Bi/Ag@CC exhibited two primary peaks at 27.2° and 39.7°, a with the crystal facets of bismuth ( 012) and (110), respectively.And, the absence o impurity peaks suggested the exclusive deposition of metal Bi on the CC su 10 min yielded the most significant reduction in resistance on the CC surface, lea an enhancement in the conductivity of the electrode.Therefore, the immersion d for Ag@CC in the solution was standardized at 10 min for all subsequent experime deposit a Bi film, an electrodeposition potential of −0.9 V and a pre-enrichment 480 s were selected, as depicted in Figure S2.The crystallographic structures of the prepared samples were determined through XRD analysis, with the diffraction peaks of Bi/Ag@CC, Ag@CC and CC presented in Figure 2a.All samples exhibited broad and weak diffraction peaks at 2θ = 25.5 • and 43.4 • , corresponding to the (002) and (001) planes of graphite (PDF#41-1487) [28].Specifically, the XRD spectra of Bi/Ag@CC exhibited two primary peaks at 27.2 • and 39.7 • , aligned with the crystal facets of bismuth ( 012) and (110), respectively.And, the absence of other impurity peaks suggested the exclusive deposition of metal Bi on the CC substrate [29,30].The additional analysis of Bi@CC in Figure S3 reveals the absence of the diffraction peaks of Bi, indicating that the bismuth film cannot be effectively deposited on the carbon cloth surface without the silver nanoparticle pre-treatment.These findings suggested that silver nanoparticles on the carbon cloth not only enhance the electronic conductivity of the electrode materials but also facilitate the strong adhesion of bismuth film.Furthermore, the elemental composition and chemical states of the prepared samples were characterized using X-ray photoelectron spectroscopy (XPS).The XPS survey spectra confirmed the presence of Bi, Ag and C elements in the Bi/Ag@CC electrode material (Figure 2b).As depicted in Figure 2c, the high-solution XPS spectra of Bi 4f exhibited distinct peaks at binding energies of 164.5 eV and 159.4 eV, which can be unambiguously assigned to the 4f 5/2 and 4f 7/2 states of Bi 0 , respectively, in accordance with previous reports [31,32].This observation provided direct evidence for the successful in situ synthesis of bismuth film on CC surfaces.Furthermore, Figure 2d presents the XPS spectra of Ag, revealing fitted peaks at binding energies of 368.1 eV and 374.3 eV, which correspond to the 3d 5/2 and 3d 3/2 stated of Ag 0 , respectively.

Electrochemical Characteristics
The electrochemical properties of the Bi/Ag@CC electrode materials were examined using the [Fe(CN)6] 3−/4− redox probe through cyclic voltammetry conducted at a scanning rate of 50 mV/s (Figure 3a).Additionally, Figure 3b illustrates the evolution of the redox peak current in cyclic voltammetry curves as the scanning rate increased in [Fe(CN)6] 3−/4− solution.Notably, the anodic current associated with the oxidation of Fe 2+ /Fe 3+ on the Bi/Ag@CC electrode increased proportionally with the scan rate.Figure 3b shows that the CV curve recorded at 150 mV/s exhibited the highest redox peak current, which demonstrated that as the scanning rate rose, the peak redox current was also augmented.Figure 3c presents the EIS curves of Bi/Ag@CC, Ag@CC and CC, which were measured over a frequency range of 0.01-100 kHz.These curves revealed that the electron-transfer resistance (Rct), a metric reflecting the interfacial properties of the electrode materials, was 5.6 Ω, 6.1 Ω and 46.3 Ω for Bi/Ag@CC, Ag@CC and bare CC, respectively.Based on the measurement results, the findings revealed that the Rct value of Bi/Ag@CC was lower compared to both Ag@CC and CC electrodes, indicating that the Bi/Ag@CC electrode material possessed superior electrochemical properties compared to other electrode materials, and the deposition of bismuth did not produce a significant alteration in the conductivity of the substrate [33].

Electrochemical Characteristics
The electrochemical properties of the Bi/Ag@CC electrode materials were examined using the [Fe(CN) 6 ] 3−/4− redox probe through cyclic voltammetry conducted at a scanning rate of 50 mV/s (Figure 3a).Additionally, Figure 3b illustrates the evolution of the redox peak current in cyclic voltammetry curves as the scanning rate increased in [Fe(CN) 6 ] 3−/4− solution.Notably, the anodic current associated with the oxidation of Fe 2+ /Fe 3+ on the Bi/Ag@CC electrode increased proportionally with the scan rate.Figure 3b shows that the CV curve recorded at 150 mV/s exhibited the highest redox peak current, which demonstrated that as the scanning rate rose, the peak redox current was also augmented.Figure 3c presents the EIS curves of Bi/Ag@CC, Ag@CC and CC, which were measured over a frequency range of 0.01-100 kHz.These curves revealed that the electron-transfer resistance (Rct), a metric reflecting the interfacial properties of the electrode materials, was 5.6 Ω, 6.1 Ω and 46.3 Ω for Bi/Ag@CC, Ag@CC and bare CC, respectively.Based on the measurement results, the findings revealed that the Rct value of Bi/Ag@CC was lower compared to both Ag@CC and CC electrodes, indicating that the Bi/Ag@CC electrode material possessed superior electrochemical properties compared to other electrode materials, and the deposition of bismuth did not produce a significant alteration in the conductivity of the substrate [33].The electrochemical performances of the prepared samples in a 100 ppb Pb 2+ solution are depicted through the DPV curves shown in Figure 3d.The Bi/Ag@CC electrode demonstrated a pronounced electrochemical response, manifesting that the preconcentration process enhances the reduction of heavy metal.Moreover, the activated The electrochemical performances of the prepared samples in a 100 ppb Pb 2+ solution are depicted through the DPV curves shown in Figure 3d.The Bi/Ag@CC electrode demonstrated a pronounced electrochemical response, manifesting that the preconcentration process enhances the reduction of heavy metal.Moreover, the activated Bi/Ag@CC electrode material treated with enriched lead exhibited a significantly more prominent peak current, with an increase of 8.53%, suggesting that the process necessitates pre-enrichment treatment rather than direct detection [34].And, the DPV measurements of the Bi@CC electrode material revealed the minimal peak current, suggesting that the pure bismuth film deposited on the carbon cloth did not exhibit a significant interfacial reaction with heavy metal ions.Similarly, the Ag@CC and carbon cloth electrode displayed limited current peaks, illustrating that the Ag nanoparticle and carbon substrate primarily facilitated the electronic path and did not significantly contribute to the electrochemical detection of heavy metal ions.

Electrochemical Detection of Pb 2+
To further elucidate the electrochemical properties of the Bi/Ag@CC electrode materials in detecting heavy metal ions, a comprehensive analysis of critical parameters, including electrolyte pH, deposition voltage and enrichment time, were conducted.Figure 4a displays the current peak response of the Bi/Ag@CC electrode with a pH range of 3.0 to 9.0, with a Pb 2+ concentration of 100 ppb.The acidity-alkalinity of the electrolyte was adjusted by nitric acid and sodium hydroxide solution.The testing results demonstrated that the peak current of Pb 2+ on the Bi/Ag@CC electrode increased under acidic conditions.However, as the acidity increased, bubbles were observed on the electrode surface when pH of the electrolyte was 3.0, potentially due to the interference from the hydrogen evolution reaction with the dissolution of Pb 2+ ions.For weak acid solution, the current signal decreased sharply.In alkaline environment, the sample electrode was damaged, resulting in a reduced peak current.Therefore, the optimized electrolyte pH of 4.5 was chosen for the subsequent experiments.Figure 4b displays the variation in peak currents with respect to various deposition potentials, ranging from −1.3 to −0.8 V.The maximum peak current value was observed at −1.2 V, leading to the selection of −1.2 V as the optimal deposition voltage for depositing Pb 2+ on the Bi/Ag@CC electrode surface.Furthermore, Figure 4c explores the relationship between the peak current and pre-enrichment time (pH = 3, −1.2 V), with the experimental results illustrating that the current peak is at 360 s.Consequently, 360 s was deemed as the optimal deposition time for the subsequent measurements.

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Figure 4c explores the relationship between the peak current and pre-enrichment time (pH = 3, −1.2 V), with the experimental results illustrating that the current peak is at 360 s.Consequently, 360 s was deemed as the optimal deposition time for the subsequent measurements.During the conventional DPV measurement for heavy metal ion detection, two distinct electrochemical reactions occur on the electrode surface.Firstly, a fixed duration of negative electrodeposition potential was applied to deposit the targeted metallic ions onto the electrode surface.Then, these deposited metallic ions were dissolved by oxidation to metal ions with a specified potential under the DPV measurement mode, resulting in a distinct current peak [35,36].Figure 5a describes the DPV response of the Bi/Ag@CC electrochemical detection of Pb 2+ across a concentration range of 20 ppb to 400 ppb.And, the current variation in lead ion with a concentration of 5 ppb could be observed by the During the conventional DPV measurement for heavy metal ion detection, two distinct electrochemical reactions occur on the electrode surface.Firstly, a fixed duration of negative electrodeposition potential was applied to deposit the targeted metallic ions onto the electrode surface.Then, these deposited metallic ions were dissolved by oxidation to metal ions with a specified potential under the DPV measurement mode, resulting in a distinct current peak [35,36].Figure 5a describes the DPV response of the Bi/Ag@CC electrochemical detection of Pb 2+ across a concentration range of 20 ppb to 400 ppb.And, the current variation in lead ion with a concentration of 5 ppb could be observed by the electrochemical sensor, as shown in Figure S4. Figure 5b showcases the peak current values at −0.47 V, demonstrating a linear relationship between the peak current and the Pb 2+ concentration.The linear equation was calculated as Ip (µA) = 312.6 × 0.97C (ppb) (R 2 = 0.995) for the concentration of Pb 2+ ranging from 20 to 300 ppb and Ip (µA)= 542.2 × 1.89C (ppb) (R 2 = 0.956) for the concentration of Pb 2+ ranging from 300 to 400 ppb.Moreover, the limit of detection (LOD) value for Pb 2+ was evaluated to be 0.15 ppb (LOD = 3σ/S).The low LOD may be attributed to the shape of the calibration curve and the variability in the blank signal [37,38].To investigate the electrochemical detection process between the sample electrodes and heavy metal ions, Figure S5 depicts the elemental mapping of Bi/Ag@CC following DPV measurements, revealing the presence of trace amounts of lead on the surface of the electrode material.
During the conventional DPV measurement for heavy metal ion detection, two distinct electrochemical reactions occur on the electrode surface.Firstly, a fixed duration of negative electrodeposition potential was applied to deposit the targeted metallic ions onto the electrode surface.Then, these deposited metallic ions were dissolved by oxidation to metal ions with a specified potential under the DPV measurement mode, resulting in a distinct current peak [35,36].Figure 5a describes the DPV response of the Bi/Ag@CC electrochemical detection of Pb 2+ across a concentration range of 20 ppb to 400 ppb.And, the current variation in lead ion with a concentration of 5 ppb could be observed by the electrochemical sensor, as shown in Figure S4. Figure 5b showcases the peak current values at −0.47 V, demonstrating a linear relationship between the peak current and the Pb 2+ concentration.The linear equation was calculated as Ip (μA) = 312.6 × 0.97C(ppb) (R 2 = 0.995) for the concentration of Pb 2+ ranging from 20 to 300 ppb and Ip (μA)= 542.2 × 1.89C(ppb) (R 2 = 0.956) for the concentration of Pb 2+ ranging from 300 to 400 ppb.Moreover, the limit of detection (LOD) value for Pb 2+ was evaluated to be 0.15 ppb (LOD = 3σ/S).The low LOD may be attributed to the shape of the calibration curve and the variability in the blank signal [37,38].To investigate the electrochemical detection process between the sample electrodes and heavy metal ions, Figure S5 depicts the elemental mapping of Bi/Ag@CC following DPV measurements, revealing the presence of trace amounts of lead on the surface of the electrode material.The practical application capabilities of the electrochemical sensor hinge crucially on its selectivity, stability and reproducibility.Considering that the presence of non-target ions in electrolytes may disturb the detection outcome of Bi/Ag@CC, a thorough exami- The practical application capabilities of the electrochemical sensor hinge crucially on its selectivity, stability and reproducibility.Considering that the presence of non-target ions in electrolytes may disturb the detection outcome of Bi/Ag@CC, a thorough examination of detection accuracy in the presence of various interfering ions such as Cl − , SO 4 2− , HCO 3 − , Zn 2+ and CO 3 2− was performed.As Figure 6a illustrates, the experimental results exhibit acceptable anti-interference performance for Pb 2+ detection.Figure 6b showcases the peak current during repeatable testing, which experienced a 2.94% reduction after four measurement cycles.This slight decline could be attributed to the weakening of the bismuth film's performance on the carbon cloth surface due to the enrichment process.Furthermore, to evaluate the repeatability feature, the DPV responses (Pb ions at 100 ppb) of six Bi/Ag@CC samples produced using the same fabrication process are illustrated in Figure 6c.The obtained data demonstrated a relative standard deviation (RSD) of 2.31% for the peak current, manifesting the acceptable reproducibility of Bi/Ag@CC electrode materials.When compared to other reported detection strategies, the sensor presented in this work offers an acceptable linear range and superior detection performance (Table 1).Furthermore, to assess the practical utility of Bi/Ag@CC, tap water and lake water samples were collected and analyzed.These samples were spiked with different concentrations of Pb 2+ and measured by DPV.The results, presented in Table 2, demonstrate that Bi/Ag@CC, as electrochemical electrode material, exhibited relatively high precision and was capable of detecting Pb 2+ in actual samples.mance (Table 1).Furthermore, to assess the practical utility of Bi/Ag@CC, tap water and lake water samples were collected and analyzed.These samples were spiked with different concentrations of Pb 2+ and measured by DPV.The results, presented in Table 2, demonstrate that Bi/Ag@CC, as electrochemical electrode material, exhibited relatively high precision and was capable of detecting Pb 2+ in actual samples.

Conclusions
In summary, this paper presents the development of a bismuth film composite supported by carbon cloth, serving as electrode materials for the electrochemical detection of heavy metal ions.Through the optimization of electrochemical parameters, the

Conclusions
In summary, this paper presents the development of a bismuth film composite supported by carbon cloth, serving as electrode materials for the electrochemical detection of heavy metal ions.Through the optimization of electrochemical parameters, the optimal deposition potential and preconcentration time for DPV measurements were identified as −1.2 V and 360 s, respectively.Furthermore, the impact of varying targeted ion concentrations (5-400 ppb) and pH values (3-9) on the detection performance was examined.The resulting sensor demonstrated an impressive linear range of 20-300 ppb, with detection limits reaching 0.15 ppb for Pb 2+ ions.Notably, it exhibited excellent anti-interference capabilities and satisfactory repeatability, with an RSD of less than 2.31% (n = 6).Additionally, the simplicity of the in situ electrodeposition synthesis strategy, cost-effective non-precious reactants and remarkable detection performance collectively position this bismuth-based composite as a promising candidate for practical electrochemical sensing applications.

Supplementary Materials:
The following supporting information can be downloaded at: https: //www.mdpi.com/article/10.3390/chemosensors12060103/s1, Figure S1: The resistance variation in Ag@CC with the soaking time.Figure S2: The electrodeposition parameters of bismuth film.(a) Deposition potential and (b) deposition time for the Bi film on the Ag@CC surface.Figure S3: XRD spectra of Bi@CC. Figure S4: The current variation in the electrochemical sensor for lead ions in concentration of 5 ppb. Figure S5: SEM images and elemental mapping of Bi/Ag@CC following DPV testing.

Scheme 1 .
Scheme 1. Schematic illustration of the synthesis of Bi/Ag@CC.The red dotted circle illustr Bi 3+ .Scheme 1. Schematic illustration of the synthesis of Bi/Ag@CC.The red dotted circle illustrated the Bi 3+ .

Figure 2 .
Figure 2. The characteristics of phase structure and elemental composites of Bi/Ag@CC.(a) XRD patterns of different treatment samples.(b-d) The XPS spectra of Bi/Ag@CC.

Figure 2 .
Figure 2. The characteristics of phase structure and elemental composites of Bi/Ag@CC.(a) XRD patterns of different treatment samples.(b-d) The XPS spectra of Bi/Ag@CC.

Figure 4 .
Figure 4. Influence of pH value (a), deposition potential (b) and pre-concentration time (c) on the DPV peak currents of Bi/Ag@CC in 100 ppb Pb 2+ solution.

Figure 4 .
Figure 4. Influence of pH value (a), deposition potential (b) and pre-concentration time (c) on the DPV peak currents of Bi/Ag@CC in 100 ppb Pb 2+ solution.

Figure 5 .
Figure 5. (a) DPV responses at Bi/Ag@CC electrode with various concentrations of Pb 2+ , and (b) the calibration curves of voltametric curves.

Figure 5 .
Figure 5. (a) DPV responses at Bi/Ag@CC electrode with various concentrations of Pb 2+ , and (b) the calibration curves of voltametric curves.

Figure 6 .
Figure 6.(a) The peak current values of Bi/Ag@CC with 100 ppb Pb 2+ containing various ions, (b) the peak current values of Bi/Ag@CC with 100 ppb Pb 2+ for four cycling testing and (c) the reproductivity testing.

Figure 6 .
Figure 6.(a) The peak current values of Bi/Ag@CC with 100 ppb Pb 2+ containing various ions, (b) the peak current values of Bi/Ag@CC with 100 ppb Pb 2+ for four cycling testing and (c) the reproductivity testing.

Table 1 .
Comparison of various Bi-based electrodes for determination of Pb 2+ .

Table 2 .
The determination of Pb 2+ in real samples.

Table 1 .
Comparison of various Bi-based electrodes for determination of Pb 2+ .

Table 2 .
The determination of Pb 2+ in real samples.