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This study investigates the impact of the uranium electrodeposition process on a boron-doped diamond electrode (BDD) surface at varying potentials as a means of environmental uranium remediation. The chronoamperometry technique was employed for the electrodeposition process, applying potentials ranging from − 0.60 to − 2.00 V vs. the reversible hydrogen electrode (RHE). A 2-mM uranyl acetate dihydrate (UO2(C2H3O2)2·2H2O) solution in 0.1-M KClO4 served as a model uranyl ion (UO22+) source. Analysis using scanning electron microscopy, energy-dispersive X-ray fluorescence spectroscopy, and atomic force microscopy (AFM) confirmed the presence of uranium and the formation of a thin layer on the electrode surface. Roughness measurements obtained through AFM analysis at different applied potentials vs. RHE were compared before and after uranium electrodeposition at BDD electrodes. Additionally, the identification of various uranium oxides resulting from the electrodeposition procedures was conducted using X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy. These analyses revealed the presence of UO2, UO3, and U3O8 on the BDD electrode surface due to the electrochemical deposition process, with a notable proportion of U3O8 observed. Ultimately, the optimal potential for efficient U6+ remediation from aqueous media and the formation of a homogenous thin layer conducive to nuclear technology development was determined to be − 1.75 V vs. RHE. [ABSTRACT FROM AUTHOR]

Through the utilization of a singular annealing procedure to merge CoFe, CoFe 2 C, and BDD, a novel BDD-based OER catalyst exhibiting remarkable long-lasting stability has been developed. This catalyst surpasses the performance of conventional RuO 2 catalysts and previously documented carbon-based FeCo catalysts. The exceptional performance of this catalyst is primarily attributed to the coherent interface and enduring BDD substrate. [Display omitted] The urgent need to develop efficient, durable, and cost-effective oxygen evolution reaction (OER) catalysts for energy conversion and storage has prompted extensive research. Currently available commercial noble metal-based OER catalysts are expensive and exhibit limited long-term stability. In this study, boron-doped diamond composites (BDDCs) consisting of CoFe and CoFe 2 C nanoparticles supported by boron-doped diamond (BDD) particles have been prepared. The BDDC catalyst, prepared through a straightforward annealing process, exhibits exceptional durability (up to 72 h at 10 mA cm−2), a low overpotential (306 mV at 10 mA cm−2), and modest Tafel slope (58 mV dec-1). The coherent interfaces between CoFe/CoFe 2 C nanoparticles and the BDD substrate are essential for enhancing the OER performance. The fabrication method and composite structures presented in this study may facilitate the design and production of promising catalysts. [ABSTRACT FROM AUTHOR]

We developed a sensing strategy that mimics the bead-based electrogenerated chemiluminescence immunoassay. However, instead of the most common metal complexes, such as Ru or Ir, the luminophore is luminol. The electrogenerated chemiluminescence of luminol was promoted by in situ electrochemical generation of hydrogen peroxide at a boron-doped diamond electrode. The electrochemical production of hydrogen peroxide was achieved in a carbonate solution by an oxidation reaction, while at the same time, microbeads labelled with luminol were deposited on the electrode surface. For the first time, we proved that was possible to obtain light emission from luminol without its direct oxidation at the electrode. This new emission mechanism is obtained at higher potentials than the usual luminol electrogenerated chemiluminescence at 0.3–0.5 V, in conjunction with hydrogen peroxide production on boron-doped diamond at around 2–2.5 V (vs Ag/AgCl). [ABSTRACT FROM AUTHOR]

In this study, the purification of caffeine by electrochemical oxidation, one of the advanced oxidation processes, was systematically investigated. A boron-doped diamond electrode was used as the anode, which has a high potential for the production of large amounts of hydroxyl radicals. The effects of applied current density, initial pH, supporting electrolyte concentration, cathode type, anode-cathode distance, and initial caffeine concentration were evaluated. The results showed that the electrochemical degradation rates of caffeine follow pseudo-first-order kinetics, with rate constants ranging from 0.0154 to 0.0496 min-1 depending on the operating parameters. The applied current density and the electrolysis time proved to be the most important parameters influencing both caffeine degradation and energy consumption. However, varying the initial caffeine concentration and the concentration of the supporting electrolyte also influenced the caffeine degradation rates. Changing the anode-cathode distance and the type of cathode has no effect on the rate of caffeine degradation, but it does have an effect on energy consumption. A current density of 20 mA cm-2, a supporting electrolyte concentration of 50 mM K2SO4, an anode-cathode distance of 2 mm, a cathode type of stainless steel, and an initial solution pH of 3 were found to be optimal values for the degradation of a solution containing 25 mg L-1 caffeine in 45 minutes using a boron-doped diamond anode. Finally, it was found that the pH value of the solution tended to increase during electrolysis. [ABSTRACT FROM AUTHOR]

We investigated the use of boron-doped diamond (BDD) with different surface morphologies for the enhanced detection of nine different peptides by matrix-assisted laser desorption/ionisation mass spectrometry (MALDI-MS). For the first time, we compared three different nanostructured BDD film morphologies (Continuous, Nanograss, and Nanotips) with differently terminated surfaces (-H, -O, and -F) to commercially available Ground Steel plates. All these surfaces were evaluated for their effectiveness in detecting the nine different peptides by MALDI-MS. Our results demonstrated that certain nanostructured BDD surfaces exhibited superior performance for the detection of especially hydrophobic peptides (e.g., bradykinin 1–7, substance P, and the renin substrate), with a limit of detection of down to 2.3 pM. Further investigation showed that hydrophobic peptides (e.g., bradykinin 1–7, substance P, and the renin substrate) were effectively detected on hydrogen-terminated BDD surfaces. On the other hand, the highly acidic negatively charged peptide adrenocorticotropic hormone fragment 18–39 was effectively identified on oxygen-/fluorine-terminated BDD surfaces. Furthermore, BDD surfaces reduced sodium adduct contamination significantly. [ABSTRACT FROM AUTHOR]

Polymer modification has been established as a cost-effective, simple, in situ method for overcoming some of the inherent disadvantages of boron-doped diamond (BDD) electrodes, and its application has been extended to reliable, low-cost environmental monitoring solutions. The present review focuses on modifying BDD electrodes with semi-conductive polymers acting as redox mediators. This article reports on the development of a 3-methyl thiophene-modified boron-doped diamond (BDD/P3MT) sensor for the electrochemical determination of total phenolic compounds (TPCs) in tea samples, using gallic acid (GA) as a marker. GA is a significant polyphenol with various biological activities, making its quantification crucial. Thus, a simple, fast, and sensitive GA sensor was fabricated using the electroanalytical square wave voltammetry (SWV) technique. The sensor utilizes a semi-conductive polymer, 3-methyl thiophene, as a redox mediator to enhance BDD's sensitivity and selectivity. Electrochemical synthesis was used for polymer deposition, allowing for greater purity and avoiding solubility problems. The BDD/P3MT sensor exhibits good electrochemical properties, including rapid charge transfer and a large electrochemical area, enabling GA detection with a limit of detection of 11 mg/L. The sensor's response was correlated with TPCs measured by the Folin–Ciocalteu method. Square wave voltammetry (SWV) showed a good linear relationship between peak currents and GA concentrations in a wide linear range of 3–71 mg/L under optimal conditions. The BDD/P3MT sensor accurately measured TPCs in green tea, rooibos tea, and black tea samples, with green tea exhibiting the highest TPC levels. The results demonstrate the potential of the modified BDD electrode for the rapid and accurate detection of phenolic compounds in tea, with implications for quality control and antioxidant activity assessments. The prolific publications of the past decade have established BDD electrodes as robust BDD sensors for quantifying polyphenols. Fruits, vegetables, nuts, plant-derived beverages such as tea and wine, traditional Eastern remedies and various herbal nutritional supplements contain phenolic chemicals. The safety concerns of contaminated food intake are significant health concerns worldwide, as there exists a critical nexus between food safety, nutrition, and food security. It has been well established that green tea polyphenol consumption promotes positive health effects. Despite their potential benefits, consuming high amounts of these polyphenols has sparked debate due to concerns over potential negative consequences. [ABSTRACT FROM AUTHOR]

Overuse of levofloxacin (LEV) is often associated with bacterial resistance and serious health problems, underscoring the need for reliable sensing and monitoring of LEV molecules. Therefore, this study aimed to investigate LEV using boron-doped diamond (BDD) and boron-doped diamond modified with MXene (Ti3C2TX) (BDD-MXene) electrode. The successful deposition of MXene on the BDD surface was confirmed using scanning electron microscope (SEM). Cyclic voltammetry (CV) and square wave voltammetry (SWV) methods were also applied to evaluate the electrochemical behavior. The results showed that both electrodes had a linear response in the range of 30-100 µM. The limit of detection (LOD) and limit of quantitation (LOQ) were found to be 1.0 X 10-6 M and 3.37 x 10-6 M for bare-BDD, while on BDD-MXene, the values were 3.90 x 10-7 M and 1.30 x 10-6 M, respectively. Furthermore, both electrodes showed good responses on selectivity tests with glucose and another fluoroquinolone antibiotic such as ciprofloxacin. The results also indicated good precision with %RSD less than 5%. In real sample applications using wastewater, bare-BDD and BDD-MXene produced excellent %recovery of 92.96% and 101.29%, respectively. [ABSTRACT FROM AUTHOR]

Fast-scan cyclic voltammetry (FSCV) is an electrochemical sensing technique that can be used for neurochemical sensing with high spatiotemporal resolution. Carbon fiber microelectrodes (CFMEs) are traditionally used as FSCV sensors. However, CFMEs are prone to electrochemical fouling caused by oxidative byproducts of repeated serotonin (5-HT) exposure, which makes them less suitable as chronic 5-HT sensors. Our team is developing a boron-doped diamond microelectrode (BDDME) that has previously been shown to be relatively resistant to fouling caused by protein adsorption (biofouling). We sought to determine if this BDDME exhibits resistance to electrochemical fouling, which we explored on electrodes fabricated with either femtosecond laser cutting or physical cleaving. We recorded the oxidation current response after 25 repeated injections of 5-HT in a flow-injection cell and compared the current drop from the first with the last injection. The 5-HT responses were compared with dopamine (DA), a neurochemical that is known to produce minimal fouling oxidative byproducts and has a stable repeated response. Physical cleaving of the BDDME yielded a reduction in fouling due to 5-HT compared with the CFME and the femtosecond laser cut BDDME. However, the femtosecond laser cut BDDME exhibited a large increase in sensitivity over the cleaved BDDME. An extended stability analysis was conducted for all device types following 5-HT fouling tests. This analysis demonstrated an improvement in the long-term stability of boron-doped diamond over CFMEs, as well as a diminishing sensitivity of the laser-cut BDDME over time. This work reports the electrochemical fouling performance of the BDDME when it is repeatedly exposed to DA or 5-HT, which informs the development of a chronic, diamond-based electrochemical sensor for long-term neurotransmitter measurements in vivo. [ABSTRACT FROM AUTHOR]

Boron‐doped diamond is a wide‐bandgap semiconductor with excellent semiconductor properties, which is widely utilized in various applications. Till now, the thermodynamic rules governing the carrier transitions in this material have not been fully understood. In this research, the different luminescence behaviors of boron‐doped diamond under 193 nm pulse laser with high‐ and low‐ power density excitation are analyzed. Under high‐power density excitation (@≈63 kW cm−2), the emission intensity of excitons is nearly ten times higher than that of defect luminescence. Conversely, under low‐power density excitation (@≈1.4 kW cm−2, different emission peaks exhibit similar intensities, indicating a competitive relationship among them. Based on experimental and theoretical analyses, the difference is attributed to the thermodynamic distribution of carriers at varying excitation powers. Specifically, high excitation power brings an independent behavior of each emission peak, and the exciton emission is described by a phonon‐assisted radiation model; different from that, the competition among different emission centers under the condition of low excitation power cannot be neglected, and now the thermodynamic evolution of each emission peak is described by a carrier trapping‐dissociation model. [ABSTRACT FROM AUTHOR]

Melatonin (MEL) is a hormone that can discharge into aquatic bodies and act as an endocrine disruptor; thus, its determination is important. In this study, a boron‐doped diamond electrode was used to develop an electroanalytical method based on square‐wave voltammetry to determine trace concentrations of MEL in river water. The electroanalytical method was developed and optimized in 0.1 mol L−1 sodium phosphate (pH=4.0) with parameters f=10 s−1, a=50 mV, and ΔES=2 mV. The validation study was carried out in the working range of 1.2–10.8 μmol L−1 using the parameters and statistical tools recommended by the validation guidelines of regulatory agencies. The matrix effect was significant; therefore, an analytical curve was directly constructed in the sample matrix by standard addition method. Results of linear regression indicated that the standard addition curve data presented a good adjust to linear model and have therefore a good linearity. Low limits of detection (0.29 μmol L−1) and quantification (0.86 μmol L−1) were observed. The estimates for precision (RSD (%)<15 %) and accuracy (mean recovery>99.5 %) were suitable according to the limits established in the literature; thus, the method was precise and accurate for the adopted working range. The study findings indicate that square‐wave voltammetry combined with a boron‐doped diamond electrode can be used for reliable and consistent determination of trace concentrations of MEL in river water. Furthermore, it presents interesting features such as lower environmental impact, speed, and low cost. [ABSTRACT FROM AUTHOR]

L-tryptophan is an amino acid that is essential to the metabolism of humans. Therefore, there is a high interest for its detection in biological fluids including blood, urine, and saliva for medical studies, but also in food products. Towards this goal, we report on a new electrochemiluminescence (ECL) method for L-tryptophan detection involving the in situ production of hydrogen peroxide at the surface of boron-doped diamond (BDD) electrodes. We demonstrate that the ECL response efficiency is directly related to H2O2 production at the electrode surface and propose a mechanism for the ECL emission of L-tryptophan. After optimizing the analytical conditions, we show that the ECL response to L-tryptophan is directly linear with concentration in the range of 0.005 to 1 µM. We achieved a limit of detection of 0.4 nM and limit of quantification of 1.4 nM in phosphate buffer saline (PBS, pH 7.4). Good selectivity against other indolic compounds (serotonin, 3-methylindole, tryptamine, indole) potentially found in biological fluids was observed, thus making this approach highly promising for quantifying L-tryptophan in a broad range of aqueous matrices of interest. [ABSTRACT FROM AUTHOR]

In this study, a boron-doped diamond nanowire array (BDD-NWA)-based electrode is prepared by using a microwave plasma chemical vapor deposition system and treated with inductively coupled plasma reactive ion etching. The BDD-NWA electrode is used for trace detection of methylene blue, which has a wide linear range of 0.04–10 μM and a low detection limit of 0.72 nM. Both the superhydrophilicity (contact angle ~0°) and the dense nanowire array's structure after the etching process improve the sensitivity of the electrochemical detection compared to the pristine BDD. In addition, the electrode shows great repeatability (peak current fluctuation range of −3.3% to 2.9% for five detection/cleaning cycles) and stability (peak current fluctuation range of −5.3% to 6.3% after boiling) due to the unique properties of diamonds (mechanical and chemical stability). Moreover, the BDD-NWA electrode achieves satisfactory recoveries (93.8%–107.5%) and real-time monitoring in tap water. [ABSTRACT FROM AUTHOR]

In this study, we prepared a novel three-dimensional boron-doped diamond (BDD) electrode. Subsequently, we systematically conducted an electrochemical oxidation reaction on sulfamethoxazole (SMX) using a BDD anode and a platinum plate (Pt) cathode. The effects of initial concentration, current density, initial pH, and carrier electrolyte on SMX degradation were investigated. The SMX was completely removed after 4 h of electrolysis at a current density of 30 mA/cm2, 0.1 mol sodium sulphate as the supporting electrolyte, and a pH of 7. Additionally, the COD removal rate was 65.6 %, while the energy consumption was 40.1 %. Compared with two-dimensional BDD electrode degradation, the energy saving was 54 %. Density functional theory (DFT) and high-performance liquid chromatography (HPLC) were used to analyse the SMX degradation mechanism. Three possible degradation pathways were proposed: ·OH substitution of the amino group in the aromatic ring, oxidation of the amino group to nitrogen dioxide, and addition of ·OH to the isoxazole ring. The active sites detected in the reaction corresponded closely with the calculated results using DFT. Moreover, ECOSAR toxicity analysis was applied to evaluate the toxicity of the intermediates produced during electrolysis. We discovered that the toxicity of SMX and its intermediates decreased significantly during electrolysis.

The surface modification of carbon electrodes is an area of great interest in both fundamental and applied electrochemistry. Herein we demonstrate a reliable route for the modification of sp3 boron‐doped diamond electrodes through a diazonium reduction and subsequent solid phase synthesis to produce a stable, immobilised layer of surface‐bound anthraquinone. The electron transfer kinetics, surface coverage, and pKa of the immobilised anthraquinone were investigated and compared to those of anthraquinone immobilised via an identical synthetic route onto a glassy carbon sp2 interface. The pKa of anthraquinone was found to be 9.1 on glassy carbon but 6.6 on boron‐doped diamond. Differences in pKa were observed despite the use of identical surface modification strategies and the achievement of comparable surface densities for both types of electrode, and are attributed to the differing dielectric properties of the surface‐modified layers atop either an sp2 or sp3 interface. These results highlight how the underlying substrate can greatly influence the fundamental chemical and electrochemical properties of immobilised molecules, as well as the need for caution when applying well‐established sp2 solid phase synthesis methodologies to sp3 substrates. [ABSTRACT FROM AUTHOR]

The electrochemical reaction of carbon dioxide (CO2) in aqueous electrolyte solutions is attracting increasing attention for sustainable chemical production. Boron‐doped diamond (BDD) electrodes have been previously shown to be very effective for the stable electrochemical production of formic acid from CO2. Typically, the electrochemical production of formic acid by CO2 reduction (CO2R) reaction is performed with a dual‐compartment flow reactor equipped with a membrane separator. The problems caused by the membrane separator, such as scaling‐up, complicated operational control and materials costs can be solved using a membrane free single‐compartment reactor. Here we demonstrate anode reaction control for a single‐compartment CO2R flow reactor using a surface‐activated BDD cathode and achieve a Faradaic efficiency for formic acid production of over 70 %. [ABSTRACT FROM AUTHOR]

Selecting the ideal anodic potential conditions and corresponding limiting current density to generate reactive oxygen species, especially the hydroxyl radical (*OH), becomes a major challenge when venturing into advanced electrochemical oxidation processes. In this work, a step-by-step guide for the electrochemical generation of "OH on boron-doped diamond (BDD) for beginners is shown, in which the following steps are discussed: i) BDD activation (assuming it is new), ii) the electrochemical response of BDD (in electrolyte and ferri/ferro-cyanide), iii) Tafel plots using sampled current voltammetry to evaluate the overpotential region where *OH is mainly generated, iv) a study of radical entrapment in the overpotential region where "OH generation is predominant according to the Tafel plots, and v) finally, the previously found ideal conditions are applied in the electrochemical degradation of amoxicillin, and the instantaneous current efficiency and relative cost of the process are reported. [ABSTRACT FROM AUTHOR]

Various anodic substitution reactions such as fluorination, methoxylation, acetoxylation, and cyanation of heteroatom compounds containing a sulfur or nitrogen atom were comparatively studied using boron‐doped diamond (BDD), Pt, and glassy carbon (GC) anodes. It was found that BDD anode is highly effective for these anodic substitution reactions similarly to Pt anode although both BDD and GC electrodes are carbon‐based materials. [ABSTRACT FROM AUTHOR]

In this study, boron-doped diamond nanoparticles modified on the surface of a screen-printed electrode (SPE) were prepared for the sensitive and selective determination of Sb3+ using square wave voltammetry. The effect of electrochemical parameters such as the type of supporting electrolyte, pH, signal per background, and scan rate on the sensitivity of the sensor for the detection of Sb3+ was investigated. Under optimized conditions with an amplitude of 0.05 V, a frequency of 50 Hz, and an E-step of 0.05 V, the square wave voltammogram between -1.0 and 1.0 V gave a limit of detection of 2.41 × 10-8 M for an Sb3+ concentration range from 0.19 to 0.59 µM. The method was used to determine Sb3+ ions in river water with satisfactory results. The modified electrode displayed benefits such as high sensitivity and selectivity, long-term stability, easy preparation, and wide linear range. [ABSTRACT FROM AUTHOR]

Polymer modification has been established as a cost-effective, simple, in situ method for overcoming some of the inherent disadvantages of boron-doped diamond (BDD) electrodes, and its application has been extended to reliable, low-cost environmental monitoring solutions. The present review focuses on modifying BDD electrodes with semi-conductive polymers acting as redox mediators. This article reports on the development of a 3-methyl thiophene-modified boron-doped diamond (BDD/P3MT) sensor for the electrochemical determination of total phenolic compounds (TPCs) in tea samples, using gallic acid (GA) as a marker. GA is a significant polyphenol with various biological activities, making its quantification crucial. Thus, a simple, fast, and sensitive GA sensor was fabricated using the electroanalytical square wave voltammetry (SWV) technique. The sensor utilizes a semi-conductive polymer, 3-methyl thiophene, as a redox mediator to enhance BDD’s sensitivity and selectivity. Electrochemical synthesis was used for polymer deposition, allowing for greater purity and avoiding solubility problems. The BDD/P3MT sensor exhibits good electrochemical properties, including rapid charge transfer and a large electrochemical area, enabling GA detection with a limit of detection of 11 mg/L. The sensor’s response was correlated with TPCs measured by the Folin–Ciocalteu method. Square wave voltammetry (SWV) showed a good linear relationship between peak currents and GA concentrations in a wide linear range of 3–71 mg/L under optimal conditions. The BDD/P3MT sensor accurately measured TPCs in green tea, rooibos tea, and black tea samples, with green tea exhibiting the highest TPC levels. The results demonstrate the potential of the modified BDD electrode for the rapid and accurate detection of phenolic compounds in tea, with implications for quality control and antioxidant activity assessments. The prolific publications of the past decade have established BDD electrodes as robust BDD sensors for quantifying polyphenols. Fruits, vegetables, nuts, plant-derived beverages such as tea and wine, traditional Eastern remedies and various herbal nutritional supplements contain phenolic chemicals. The safety concerns of contaminated food intake are significant health concerns worldwide, as there exists a critical nexus between food safety, nutrition, and food security. It has been well established that green tea polyphenol consumption promotes positive health effects. Despite their potential benefits, consuming high amounts of these polyphenols has sparked debate due to concerns over potential negative consequences.

We investigated the use of boron-doped diamond (BDD) with different surface morphologies for the enhanced detection of nine different peptides by matrix-assisted laser desorption/ionisation mass spectrometry (MALDI-MS). For the first time, we compared three different nanostructured BDD film morphologies (Continuous, Nanograss, and Nanotips) with differently terminated surfaces (-H, -O, and -F) to commercially available Ground Steel plates. All these surfaces were evaluated for their effectiveness in detecting the nine different peptides by MALDI-MS. Our results demonstrated that certain nanostructured BDD surfaces exhibited superior performance for the detection of especially hydrophobic peptides (e.g., bradykinin 1–7, substance P, and the renin substrate), with a limit of detection of down to 2.3 pM. Further investigation showed that hydrophobic peptides (e.g., bradykinin 1–7, substance P, and the renin substrate) were effectively detected on hydrogen-terminated BDD surfaces. On the other hand, the highly acidic negatively charged peptide adrenocorticotropic hormone fragment 18–39 was effectively identified on oxygen-/fluorine-terminated BDD surfaces. Furthermore, BDD surfaces reduced sodium adduct contamination significantly.

Fast-scan cyclic voltammetry (FSCV) is an electrochemical sensing technique that can be used for neurochemical sensing with high spatiotemporal resolution. Carbon fiber microelectrodes (CFMEs) are traditionally used as FSCV sensors. However, CFMEs are prone to electrochemical fouling caused by oxidative byproducts of repeated serotonin (5-HT) exposure, which makes them less suitable as chronic 5-HT sensors. Our team is developing a boron-doped diamond microelectrode (BDDME) that has previously been shown to be relatively resistant to fouling caused by protein adsorption (biofouling). We sought to determine if this BDDME exhibits resistance to electrochemical fouling, which we explored on electrodes fabricated with either femtosecond laser cutting or physical cleaving. We recorded the oxidation current response after 25 repeated injections of 5-HT in a flow-injection cell and compared the current drop from the first with the last injection. The 5-HT responses were compared with dopamine (DA), a neurochemical that is known to produce minimal fouling oxidative byproducts and has a stable repeated response. Physical cleaving of the BDDME yielded a reduction in fouling due to 5-HT compared with the CFME and the femtosecond laser cut BDDME. However, the femtosecond laser cut BDDME exhibited a large increase in sensitivity over the cleaved BDDME. An extended stability analysis was conducted for all device types following 5-HT fouling tests. This analysis demonstrated an improvement in the long-term stability of boron-doped diamond over CFMEs, as well as a diminishing sensitivity of the laser-cut BDDME over time. This work reports the electrochemical fouling performance of the BDDME when it is repeatedly exposed to DA or 5-HT, which informs the development of a chronic, diamond-based electrochemical sensor for long-term neurotransmitter measurements in vivo.

L-tryptophan is an amino acid that is essential to the metabolism of humans. Therefore, there is a high interest for its detection in biological fluids including blood, urine, and saliva for medical studies, but also in food products. Towards this goal, we report on a new electrochemiluminescence (ECL) method for L-tryptophan detection involving the in situ production of hydrogen peroxide at the surface of boron-doped diamond (BDD) electrodes. We demonstrate that the ECL response efficiency is directly related to H2O2 production at the electrode surface and propose a mechanism for the ECL emission of L-tryptophan. After optimizing the analytical conditions, we show that the ECL response to L-tryptophan is directly linear with concentration in the range of 0.005 to 1 µM. We achieved a limit of detection of 0.4 nM and limit of quantification of 1.4 nM in phosphate buffer saline (PBS, pH 7.4). Good selectivity against other indolic compounds (serotonin, 3-methylindole, tryptamine, indole) potentially found in biological fluids was observed, thus making this approach highly promising for quantifying L-tryptophan in a broad range of aqueous matrices of interest.

This study investigates the effects of boron concentration on boron-doped diamond (BDD) electrodes for electrochemical sensors of ciprofloxacin. The effects of boron concentration, scan rate, and pH of BDD electrodes with boron concentrations of 0.1, 0.5, and 1% were examined to determine the optimal conditions. Furthermore, square wave voltammetry (SWV) in phosphate buffer pH 7 was used to analyze the electrochemical behavior of ciprofloxacin. The results revealed a linear calibration curve in the concentration range of 30–100 μM with a recovery of 85–110%. Meanwhile, BDD electrode with the highest boron concentration in this experiment (1%) showed a very low limit of detection of 0.17 μM, meaning that 1% BDD gave a highly sensitive and significant measurement result for the electrochemical sensor of ciprofloxacin. With the results given, this study provides new insights for controlling boron concentrations in diamond electrodes for the electrochemical sensors of quinolone antibiotics.

Abstract The surface modification of carbon electrodes is an area of great interest in both fundamental and applied electrochemistry. Herein we demonstrate a reliable route for the modification of sp3 boron‐doped diamond electrodes through a diazonium reduction and subsequent solid phase synthesis to produce a stable, immobilised layer of surface‐bound anthraquinone. The electron transfer kinetics, surface coverage, and pKa of the immobilised anthraquinone were investigated and compared to those of anthraquinone immobilised via an identical synthetic route onto a glassy carbon sp2 interface. The pKa of anthraquinone was found to be 9.1 on glassy carbon but 6.6 on boron‐doped diamond. Differences in pKa were observed despite the use of identical surface modification strategies and the achievement of comparable surface densities for both types of electrode, and are attributed to the differing dielectric properties of the surface‐modified layers atop either an sp2 or sp3 interface. These results highlight how the underlying substrate can greatly influence the fundamental chemical and electrochemical properties of immobilised molecules, as well as the need for caution when applying well‐established sp2 solid phase synthesis methodologies to sp3 substrates.

To promote the electrocatalytic transformation from CO2 to value-added chemicals with boron doped diamond (BDD) electrode, it is critical to make clear that the relationship between the B doping state and the position of B atom in BDD materials and CO2 reduction performance. Here, a series of BDD electrodes with constant B dopant amount on the surface were prepared by the same process but based on different deposition time (3, 6, 12, and 24 h) using the heat filament chemical vapor deposition. The results demonstrated that the surface grain size, abundances of B–C relative to B–B bonds of the BDD films increased with increasing the deposition time. Moreover, the formic acid yield and faradaic efficiency also increased as well during electrochemical CO2 reduction due to more available B atoms doped in crystallinity (B–C bonds) rather than in grain boundary (B–B bonds) of BDD. Finally, electrochemical analysis revealed that the B–C bonds in the crystal of BDD films is the active sites for the reduction of CO2. This study provides a simple and convenient path to figure out what is the active site of the BDDs and its how to impact the CO2 reduction.

Selecting the ideal anodic potential conditions and corresponding limiting current density to generate reactive oxygen species, especially the hydroxyl radical (•OH), becomes a major challenge when venturing into advanced electrochemical oxidation processes. In this work, a step-by-step guide for the electrochemical generation of •OH on boron-doped diamond (BDD) for beginners is shown, in which the following steps are discussed: i) BDD activation (assuming it is new), ii) the electrochemical response of BDD (in electrolyte and ferri/ferro-cyanide), iii) Tafel plots using sampled current voltammetry to evaluate the overpotential region where •OH is mainly generated, iv) a study of radical entrapment in the overpotential region where •OH generation is predominant according to the Tafel plots, and v) finally, the previously found ideal conditions are applied in the electrochemical degradation of amoxicillin, and the instantaneous current efficiency and relative cost of the process are reported.

The engineering of porous boron-doped diamond (BDD) film has sparked significant interest in improving electric double-layer (EDL) capacitance. However, the presence of disordered and tortuous pores in the BDD film hinders the accessibility of the bottom pore surface area, leading to a decrease in specific EDL capacitance. Herein, a novel porous BDD film with vertically open pore channels is constructed through the overcoating of diamond nanoplatelet template with a BDD layer using chemical vapor deposition. Electrochemical investigations manifest that the specific areal EDL capacitance of the porous BDD is ∼428 times greater than that of the planar BDD film. More impressively, the porous BDD film demonstrates a higher specific volumetric EDL capacitance (39.30 F/cm3) and superior long-term stability (100% capacitance retention after 12,000 cycles), surpassing the performance of most developed porous BDD electrodes. The exceptional performance of the porous BDD film was attributed to the abundant vertically open pore channels, good hydrophilic property, maximized electrochemical available area, and good chemical/mechanical stability. This work benefits the development of the BDD film as an EDL micro-capacitor electrode, and the methodology proposed here shows great potentials to fabricate an ordered porous BDD nanostructure with large specific area for more electrochemical applications.

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. [ABSTRACT FROM AUTHOR]

Theophylline is a drug with a narrow therapeutic range. Electrochemical sensors are a potentially effective method for detecting theophylline concentration to prevent toxicity. In this work, a simple modification of a boron-doped diamond electrode using nickel nanoparticles was successfully performed for a theophylline electrochemical sensor. The modified electrode was characterized using a scanning electron microscope and X-ray photoelectron spectroscopy. Square wave voltammetry and cyclic voltammetry methods were used to study the electrochemical behavior of theophylline. The modified nickel nanoparticles on the boron-doped diamond electrode exhibited an electrochemically active surface area of 0.0081 cm2, which is larger than the unmodified boron-doped diamond's area of 0.0011 cm2. This modified electrode demonstrated a low limit of detection of 2.79 µM within the linear concentration range from 30 to 100 µM. Moreover, the modified boron-doped diamond electrode also showed selective properties against D-glucose, ammonium sulfate, and urea. In the real sample analysis using artificial urine, the boron-doped diamond electrode with nickel nanoparticle modifications achieved a %recovery of 105.10%, with a good precision of less than 5%. The results of this work indicate that the developed method using nickel nanoparticles on a boron-doped diamond electrode is promising for the determination of theophylline. [ABSTRACT FROM AUTHOR]

A boron-doped diamond electrode with a network structure of PdNi alloy nanowires, which is deposited onto its surface by laser ablation in superfluid helium, is considered as a possible sensor for formaldehyde. It is shown that the electrode is highly sensitive to trace amounts of formaldehyde. [ABSTRACT FROM AUTHOR]

This paper focuses on the development of a novel electrode based on boron-doped diamond nanosheet full-volume-enriched screen-printed carbon electrodes (BDDPE) for use as an impedimetric biosensor. Impedimetric biosensors offer high sensitivity and selectivity for virus detection, but their use as point-of-care devices is limited by the complexity of nanomaterials' architecture and the receptor immobilisation procedures. The study presents a two-step modification process involving the electroreduction of diazonium salt at the BDDPE and the immobilisation of antibodies using zero-length cross-linkers for a selective impedimetric biosensor of Haemophilus influenzae (Hi). The incorporation of diamond nanosheets into BDDPE leads to enhanced charge transfer and electrochemical behaviour, demonstrating greatly improved electrochemically active surface area compared with unmodified screen-printed electrodes (by 44% and 10% on average for [Ru(NH3)6]Cl2 and K3[Fe(CN)6], respectively). The presented sensing system shows high specificity towards protein D in Hi bacteria, as confirmed by negative controls against potential interference from other pathogens, with an estimated tolerance limit for interference under 12%. The Hi limit of detection by electrochemical impedance spectroscopy was 1 CFU/mL (measured at − 0.13 V vs BDDPE pseudo-reference), which was achieved in under 10 min, including 5 min sample incubation in the presence of the analyte. [ABSTRACT FROM AUTHOR]

Hydrogen peroxide (H2O2) plays a role in many facets — a household item, an important industrial chemical, a biomarker in vivo, and several others. For this reason, its measurement and quantification in a variety of media are important. While spectroscopic detection is primarily used for H2O2, electrochemical methods offer advantages in versatility, cost, and sensitivity. In this work, we investigate a 2-step surface metal nanoparticle (NP) modification for platinum (Pt) and palladium (Pd) on boron-doped diamond (BDD) electrodes for the detection of H2O2. Several parameters such as the metal salt concentration and electrodeposition charge in the 2-step modification were varied to find an optimum. Using cyclic voltammetry (CV), the BDD-PdNP electrode types were found to yield a sharper, more well-resolved H2O2 oxidation peak compared to the BDD-PtNP electrodes. Both metal NP electrode types significantly improved the response compared to the bare BDD electrode; a 150–200× improvement in sensitivity was observed across all modified electrode types. Calibration experiments were completed at both low and high concentration ranges in stagnant and flow-based solutions. The lowest limit of detection (LOD) obtained was 50 nM (5E-08 M) on a BDD-PdNP electrode modified with 1.0 mM PdCl2 to 5.0 mC in the wet chemical seeding and electrodeposition steps. 0.25 mM PdCl2 to 3.23 mC and 0.25 mM HPtCl6− to 3.23 mC also yielded a sufficient response for low-level H2O2, with LODs around 100 nM (1E-07 M). Overall, this work exemplifies the wide applicability of BDD and achieves sub-μM H2O2 LODs with a non-enzymatic electrode material. [ABSTRACT FROM AUTHOR]

Boron-doped diamond (BDD) electrodes are well known for the in situ production of strong oxidants. These antimicrobial agents are produced directly from water without the need of storage or stabilization. An in situ production of reactive oxygen species (ROS) used as antimicrobial agents has also been used in recently developed medical applications. Although BDD electrodes also produce ROS during water electrolysis, only a few medical applications have appeared in the literature to date. This is probably due to the difficulties in the miniaturization of BDD electrodes, while maintaining a stable and efficient electrolytic process in order to obtain a clinical applicability. In this attempt, a cannula-based electrode design was achieved by insulating the anodic diamond layer from a cathodic cannula, using a second layer of non-conducting diamond. The undoped diamond (UDD) layer was successfully grown in a spotted pattern, resulting in a perfectly insulated yet still functional BDD layer, which can operate as a miniaturized flow reactor for medical applications. The spotted pattern was achieved by introducing a partial copper layer on top of the BDD layer, which was subsequently removed after growing the undoped diamond layer via etching. The initial analytical observations showed promising results for further chemical and microbial investigations. [ABSTRACT FROM AUTHOR]

This paper describes a new, simple, and highly selective analytical technique for the detection of sulfur dioxide in wine, as a real sample with a relatively complicated matrix. The detection of the above analyte was based on the electrogeneration of iodine from iodide on a boron-doped diamond electrode, without modifications, in the presence of 0.1 mol dm−3 HClO4 as a supporting electrolyte. The electrogenerated iodine reacted with sulfur dioxide, forming iodide ions and sulfuric acid (i.e., a Bunsen reaction). The product of this reaction, the iodide ion, diffused back to the surface of the boron-doped diamond electrode and oxidized itself again. This chemical redox cycling enhanced the voltammetric response of the boron-doped diamond electrode. The selectivity of the determination was assured using NaOH and formaldehyde during sample preparation, and a blank was also measured and taken into account. The detection limit was estimated to be 10−6–10−7 mol dm−3. However, the content of sulfur dioxide in wine is significantly higher, which can lead to more accurate and reliable results. [ABSTRACT FROM AUTHOR]

High-performance non-enzymatic glucose sensor composite electrodes were prepared by loading Ni onto a boron-doped diamond (BDD) film surface through a thermal catalytic etching method. A carbon precipitate with a desired thickness could be formed on the Ni/BDD composite electrode surface by tuning the processing conditions. A systematic study regarding the influence of the precipitated carbon layer thickness on the electrocatalytic oxidation of glucose was conducted. While an oxygen plasma was used to etch the precipitated carbon, Ni/BDD-based composite electrodes with the precipitated carbon layers of different thicknesses could be obtained by controlling the oxygen plasma power. These Ni/BDD electrodes were characterized by SEM microscopies, Raman and XPS spectroscopies, and electrochemical tests. The results showed that the carbon layer thickness exerted a significant impact on the resulting electrocatalytic performance. The electrode etched under 200 W power exhibited the best performance, followed by the untreated electrode and the electrode etched under 400 W power with the worst performance. Specifically, the electrode etched under 200 W was demonstrated to possess the highest sensitivity of 1443.75 μA cm−2 mM−1 and the lowest detection limit of 0.5 μM. [ABSTRACT FROM AUTHOR]

The treatment of emerging pollutants is challenging due to the very low concentration in which they are found in nature, along with their general recalcitrant characteristic. One way to overcome these limitations is combining a pre-concentration step followed by the degradation of the concentrated pollutant. This can be achieved in a first adsorption step, followed by a second electrochemical carbon regeneration/pollutant degradation. This study applies this principle to caffeine treatment by coupling adsorption on activated carbon (AC) with electrochemical regeneration/caffeine degradation onto a boron-doped diamond (BDD) anode. The AC is morphologically and structurally characterized by N2 adsorption/desorption experiment (surface area) and scanning electron microscopy (surface morphology). The isoelectric point of the AC is measured to identify the surface charge depending on the pH, and the equilibrium isotherms allow us to estimate the caffeine adsorption capacity. The concept of adsorption/electrochemical regeneration is applied to caffeine treatment, analyzing the influence of operating parameters such as the fluidization of the carbon, the electrolyte, and the applied current. Under AC fluidization, using NaCl as the electrolyte and a current density of 0.5 A, a regeneration efficiency of 87% can be achieved. Furthermore, after 5 adsorption/regeneration cycles, this parameter slightly drops to 80%, demonstrating its capacity to preserve the carbon capacity and effectiveness in recovering the AC. Finally, the intermediates formed during the electrochemical regeneration are also identified. [ABSTRACT FROM AUTHOR]

The rising concentration of carbon dioxide (CO2) as one of the greenhouse gases in the atmosphere is a major source of worry. Electrochemical reduction of CO2 is one of many ways to convert CO2 gas into usable compounds. An electrochemical technique was applied in this study to reduce CO2 using a boron-doped diamond (BDD) working electrode modified with MXene (Ti3C2Tx) material to improve electrode performance. MXene concentrations of 0.5 mg/mL (MXene-BDD 0.5), 1.0 mg/mL (MXene-BDD 1.0), and 2.0 mg/mL (MXene-BDD 2.0) were drop-casted onto the BDD surface. MXene was effectively deposited on top of the BDD surface, with Ti weight loads of 0.12%, 4.06%, and 7.14% on MXene-BDD 0.5, MXene-BDD 1.0, and MXene-BDD 2.0, respectively. The modified working electrode was employed for CO2 electroreduction with optimal CO2 gas aeration. The existence of the MXene substance in BDD reduced the electroreduction overpotential of CO2. For the final result, we found that the MXene-BDD 2.0 electrode effectively generated the most formic acid product with a maximum reduction potential as low as −1.3 V (vs. Ag/AgCl). [ABSTRACT FROM AUTHOR]

In order to deposit arsenic residues from copper production in a stable way, the trivalent arsenic must first be xidized to arsenic(V). A well-known but quite expensive method for this is oxidation with hydrogen peroxide. In order to enable the oxidation of arsenic on a large scale in the future, a potentially cheaper method has to be found, which offers the possibility of oxidizing extremely high arsenic concentrations. As a novel alternative, electrochemical oxidation using a boron-doped diamond electrode is investigated. Based on previous work, this paper concentrates on the presence of interfering ions during oxidation. Furthermore, it is shown that the electrochemically xidized arsenic(V) can be precipitated as scorodite. Finally, an economic analysis shows the potential financial benefit of oxidation via BDD electrodes compared to hydrogen peroxide. [ABSTRACT FROM AUTHOR]

Neurotransmitter release is important to study in order to better understand neurological diseases and treatment approaches. Serotonin is a neurotransmitter known to play key roles in the etiology of neuropsychiatric disorders. Fast-scan cyclic voltammetry (FSCV) has enabled the detection of neurochemicals, including serotonin, on a sub-second timescale via the well-established carbon fiber microelectrode (CFME). However, poor chronic stability and biofouling, i.e., the adsorption of interferent proteins to the electrode surface upon implantation, pose challenges in the natural physiological environment. We have recently developed a uniquely designed, freestanding, all-diamond boron-doped diamond microelectrode (BDDME) for electrochemical measurements. Key potential advantages of the device include customizable electrode site layouts, a wider working potential window, improved stability, and resistance to biofouling. Here, we present a first report on the electrochemical behavior of the BDDME in comparison with CFME by investigating in vitro serotonin (5-HT) responses with varying FSCV waveform parameters and biofouling conditions. While the CFME delivered lower limits of detection, we also found that BDDMEs showed more sustained 5-HT responses to increasing or changing FSCV waveform-switching potential and frequency, as well as to higher analyte concentrations. Biofouling-induced current reductions were significantly less pronounced at the BDDME when using a "Jackson" waveform compared to CFMEs. These findings are important steps towards the development and optimization of the BDDME as a chronically implanted biosensor for in vivo neurotransmitter detection. [ABSTRACT FROM AUTHOR]

Ferri/ferro-cyanide ([Fe(CN)6]3−/4−) redox couple has been extensively used as a benchmark to assess electrocatalytic degradation capability of boron-doped diamond (BDD) electrodes. However, the [Fe(CN)6]3−/4− is far more sensitive to the surface terminal groups of BDD surface than the other factors (e.g. surface morphology and electrode configuration) that are closely related to electrocatalytic degradation properties. Thus, inconsistency exists while correlating the degradation properties of BDD with electrochemical properties determined from ferri/ferro-cyanide redox couple. Herein, an exemplar pollutant, reactive blue 19 (RB-19), was electrochemically degraded using various terminated BDD electrodes, including hydrogen-terminated (H-BDD), oxygen-terminated (O-BDD) and porous oxygen-terminated BDDs (OE-BDD), obtained via cathodic and anodic polarization as well as oxygen plasma etching, respectively. Surprisingly, OE-BDD with the lower heterogeneous electron transfer rate constant for [Fe(CN)6]3−/4− showed a better electrocatalytic degradation capability toward RB-19, indicating the inconsistency for qualitatively evaluating degradation properties according to the kinetic parameters extracted from [Fe(CN)6]3−/4− redox system.

Pesticide wastewater is difficult to treat, and it is necessary to develop a new anode material electrochemical oxidation to efficiently degrade pesticide wastewater. DIL-PbO2-Ti/BDD electrodes with better electrocatalytic oxidation performance were obtained by using dicationic ionic liquid (DIL) for assisted electrodeposition of PbO2 modified boron-doped diamond (BDD) electrodes. At a current density of 100 mA cm−2 and a temperature of 25 °C, the DIL-PbO2-Ti/BDD electrode was used as anode and titanium plate as cathode. The electrochemical window and oxygen evolution potential (OEP) of the DIL-PbO2-Ti/BDD electrode obtained by CV testing at a scan rate of 50 mV s−1 in 1 M H2SO4 were 4.12 and 3.29 V, respectively. Under the conditions of current density of 100 mA cm−2, 25 °C, pH 12, salt content of 8%, chemical oxygen demand (COD) of 24,280.98 mg L−1, and total nitrogen (TN) content of 5268 mg L−1, after electrification for 12 h, the removal efficiency of COD and TN reached 64.88 and 67.77%, respectively, indicating that the DIL-PbO2-Ti/BDD electrode has excellent electrocatalytic performance. In order to further understand the mechanism of electrochemical degradation of pesticide wastewater, HPLC-MS was used to detect the intermediates in the degradation process, and the possible degradation pathways were proposed in turn. HIGHLIGHTS Electrochemical oxidation degradation of pesticide wastewater by DIL-PbO2-Ti/BDD electrode for the first time.; The electrochemical window and OEP of the DIL-PbO2-Ti/BDD electrode are 4.12 and 3.29 V, respectively.; Putative degradation reaction of carbosulfan and thiodimethoxam by HPLC-MS.; Excellent performance in electrochemical catalytic oxidation of pesticide wastewater.;