NaOH Etching Research Articles

Effect of NaOH etching and oxygen plasma treatments on surface characteristics and their potential to activate micro-arc oxidized TiO2 coatings

Activation treatments such as NaOH etching or O2 plasma can play an essential role in surface conjugation of titanium with biomolecules, providing a better interaction at the bone-implant interface. However, their application on complex titanium dioxide (TiO2) surfaces is still not explored. In this contribution, bioactive and porous TiO2 coatings produced by micro-arc oxidation (MAO) were treated with NaOH etching or O2 plasma and then placed in contact with a reactive isocyanate test compound to evaluate the potential of molecule conjugation. Results suggested that O2 plasma treatment has only changed the surface chemistry of the coating through carbon contaminants removal, plasma-driven oxidation and generation of functional OH species, including reactive carboxyl groups. This chemical modification by plasma has made the surface superhydrophilic. After NaOH etching, the coating became rougher and also superhydrophilic, containing titanate structures doped with sodium and calcium on its surface and inside the inner pores. Upon reaction with butyl isocyanate, the O2 plasma-treated surfaces seem to better provide molecule conjugation, introducing characteristic conjugation bonds, and also making MAO coatings more hydrophobic due to the surface-terminated methyl chains from isocyanate. This proof-of-concept study has demonstrated the promising grafting potential given by O2 plasma on complex TiO2 surfaces.

Nanochannels in Fused Silica through NaOH Etching Assisted by Femtosecond Laser Irradiation

Sodium hydroxide (NaOH) is increasingly drawing attention as a highly selective etchant for femtosecond laser-modified fused silica. Unprecedented etching contrasts between the irradiated and pristine areas have enabled the fabrication of hollow, high-aspect-ratio structures in the bulk of the material, overcoming the micrometer threshold as the minimum feature size. In this work, we systematically study the effect of NaOH solutions under different etching conditions (etchant concentration, temperature, and etching time) on the tracks created by tightly focused femtosecond laser pulses to assess the best practices for the fabrication of hollow nanostructures in bulk fused silica.

Defect Engineered Bi2Te3 Nanosheets with Enhanced Haloperoxidase Activity for Marine Antibiofouling.

Defective bismuth telluride (Bi2Te3) nanosheets, an artificial nanozyme mimicking haloperoxidase activity (hPOD), show promise as eco-friendly, bactericidal, and antimicrofouling materials by enhancing cytotoxic hypohalous acid production from halides and H2O2. Microscopic and spectroscopic characterization reveals that controlled NaOH (upto X = 250µL) etching of the nearly inactive non-transition metal chalcogenide Bi2Te3 nanosheets creates controlled defects (d), such as Bi3+species, in d-Bi2Te3-X that induces enhanced hPOD activity. d-Bi2Te3-250 exhibits approximately eight-fold improved hPOD than the as-grown Bi2Te3 nanosheets. The antibacterial activity of d-Bi2Te3-250 nanozymes, studied by bacterial viability, show 1, and 45% viability for Staphylococcus aureus and Pseudomonas aeruginosa, respectively, prevalent in marine environments. The hPOD mechanism is confirmed using scavengers, implicating HOBr and singlet oxygen for the effect. The antimicrofouling property of the d-Bi2Te3-250 nanozyme has been studied on Pseudomonas aeruginosa biofilm in a lab setting by multiple assays, and also on titanium (Ti) plates coated with the nanozyme mixed commercial paint, exposed to seawater in a real setting. All studies, including direct microscopic evidence, exhibit inhibition of microfouling, up to ≈73%, in the presence of nanozymes. This approach showcases that defect engineering can induce antibacterial, and antimicrofouling activity in non-transition metal chalcogenides, offering an inexpensive alternative to noble metals.

Growth of CsPbX3 nanocrystals using sol–gel SiO2 solid powders as reactors without capping agents towards anomalous stable emission membranes

To overcome the poor stability of metal halide perovskite nanocrystals (NCs) prepared in organic solvents, a solid reaction method at high temperature was developed using sol–gel porous SiO2 as a reactor. Sol-gel SiO2 powders were used to encapsulate CsPbX3 NCs at high temperatures (600–800 °C) in air to get SiO2/CsPbX3 glass by dispersing growth cites in advance and no ligands added. After NaOH etching, a thin dense SiO2 shell was remained on the surface of CsPbX3 NCs (named as CsPbX3@SiO2).The photoluminescence (PL) quantum yield of the CsPbX3@SiO2 was 86.7 %, in which their PL peak wavelengths were adjusted from 410-707 nm by changing halogen components. The dense SiO2 shell on CsPbX3 NCs blocked the connection of CsPbX3 cores with water and oxygen in the external environment, resulting in CsPbX3@SiO2 revealed extraordinary high stability. After immersing in water for half year, the PL intensity of CsPbX3@SiO2 composites was remained unchanged and the composites still revealed bright PL after heat-treating in boiling water for 14 h. These highly stable composites were used to fabricate a white light-emitting diode, in which the color coordinates are located at (0.36, 0.33), and the color temperature reaches 5169 K which belongs to the warm white light range.

Undiminished performance in simultaneous phosphorus and dye recovery via ring-opening Mg-assembled carbonitride

The multiple effects of eutrophication and refractory organic dye may pose serious environmental risks, whereas conventional adsorbents mostly suffer from the disadvantage of performance degradation in complex environments. Herein, we designed Mg-assembled carbonitride (MAC) that allowed for phosphorus (P) and selective dye recovery (methylene blue (MB) as model pollutants) simultaneously, and then successfully separated the two pollutants in a simple way to obtain pure dyes and phosphorus-containing compounds. The triazine ring conjugation framework and abundant functional groups of carbonitride facilitated the doping of Mg sites. The adsorption capacity of MAC for P (211.6 ± 2 vs 207.4 mg P·g−1) and MB (116.5 ± 3 vs 117.8 mg MB·g−1) in the binary-polluted system exhibited little difference from the individual, implying synchronous and undiminished adsorption on MAC. This was attributed to the ring-opening reaction triggered by NaOH etching and thermal decomposition, generating the two new active sites, where cyano groups (C N) interacted with P and Mg–N bonds responded with both target pollutants. Moreover, the favorable selective adsorption ability of MAC for different dyes was attributed to electrostatic attraction, surface complexation, hydrogen bonds and π-π interactions. This study provides a good reference for exploiting performance-stable multifunctional adsorbents for applications in wastewater resource recovery.

In-situ construction of Bi25VO40/BiVO4 heterojunctions with boosted photocatalytic activity

In this study, Bi25VO40/BiVO4 heterojunctions were in-situ constructed by NaOH etching of BiVO4. The resulting samples exhibit significantly enhanced photocatalytic activity in removal of rhodamine B (RhB) under visible light irradiation. Notably, the photocatalytic efficiency of BiVO4 etched by NaOH with a concentration of 3 mol/L is 3.17 times of that of the reference BiVO4. Furthermore, the photocatalysts demonstrate remarkable stability during five successive cycle experiments. The heightened photocatalytic activity of BiVO4 treated by sodium hydroxide can be definitely attributed to improved separation efficiency of photogenerated charges owing to construction of Bi25VO40/BiVO4 heterojunctions.

Study on NaOH improving the surface morphology of three-dimensional printed poly- L- lactic acid mesh scaffolds

To explore the effect of NaOH on the surface morphology of three-dimensional (3D) printed poly- L-lactic acid (PLLA) mesh scaffolds. The 3D printed PLLA mesh scaffolds were prepared by fused deposition molding technology, then the scaffold surfaces were etched with the NaOH solution. The concentrations of NaOH solution were 0.01, 0.1, 0.5, 1.0, and 3.0 mol/L, and the treatment time was 1, 3, 6, 9, and 12 hours, respectively. There were a total of 25 concentration and time combinations. After treatment, the microstructure, energy spectrum, roughness, hydrophilicity, compressive strength, as well as cell adhesion and proliferation of the scaffolds were observed. The untreated scaffolds were used as a normal control. 3D printed PLLA mesh scaffolds were successfully prepared by using fused deposition molding technology. After NaOH etching treatment, a rough or micro porous structure was constructed on the surface of the scaffold, and with the increase of NaOH concentration and treatment time, the size and density of the pores increased. The characterization of the scaffolds by energy dispersive spectroscopy showed that the crystal contains two elements, Na and O. The surface roughness of NaOH treated scaffolds significantly increased ( P<0.05) and the contact angle significantly decreased ( P<0.05) compared to untreated scaffolds. There was no significant difference in compressive strength between the untreated scaffolds and treated scaffolds under conditions of 0.1 mol/L/12 h and 1.0 mol/L/3 h ( P>0.05), while the compression strength of the other treated scaffolds were significantly lower than that of the untreated scaffolds ( P<0.05). After co-culturing the cells with the scaffold, NaOH treatment resulted in an increase in the number of cells on the surface of the scaffold and the spreading area of individual cells, and more synapses extending from adherent cells. NaOH treatment is beneficial for increasing the surface hydrophilicity and cell adhesion of 3D printed PLLA mesh scaffolds.

Tailoring the adhesion of electrophoretic chitosan/bioactive glass coatings by the combined surface pre-treatments of Ti substrates

Composite chitosan/bioactive glass coatings developed by electrophoretic deposition (EPD) attract researchers' attention owing to their advantageous effect on the biological and corrosion responses of commonly used biomedical materials. However, fabricating a uniform coating with satisfactory adhesion to the biomaterials substrate is challenging, because chitosan and bioglass particles having different mobilities during the EPD process. Typically, attempts are made to improve adhesion by manipulating the EPD parameters. This work presents an alternative approach that involves combined mechanical and chemical pre-treatments of the Ti substrate. The surface pre-treatment procedure included shot peening and the following variants of acid etching: (i) HF etching, (ii) NaOH etching, and (iii) HF and NaOH etching. Shot peening followed by etching in HF and NaOH significantly improved the adhesion of the EPD coating. It was found that this effect was due to the development of a highly hydrophilic surface with micro- and nano-scale roughness.

An enhanced surface treatment for effective bonding of 7075-T6 aluminium alloys

ABSTRACT This study research focuses on optimising adhesion through surface treatments on 7075-T6 aluminium alloy substrates using a chromium-free protocol. The treatment involves acetone degreasing, NaOH etching, and sulphuric acid-based solution etching. Wettability analysis and scanning electron microscopy were used to characterise the treated surfaces, highlighting the effectiveness of the proposed protocol. The proposed etching protocol was then applied to aluminium alloy substrates, and fracture surfaces corresponding to each treatment were compared. Mechanical testing, specifically double cantilever beam (DCB) experiments, assesses the fracture energy of bonded assemblies in mode I. The results demonstrate that the sulphuric acid-based treatment significantly improves the surface characteristics, leading to enhanced adhesion and optimal fracture energy in bonded aluminium assemblies.

Bi/BSO Heterojunctions via Vacancy Engineering for Efficient Photocatalytic Nitrogen Fixation

AbstractPhotocatalytic nitrogen reduction represents a viable technology for green ammonia synthesis under mild conditions. However, the performance of the photocatalysts is typically limited by high charge carrier recombination and low adsorption and activation of nitrogen molecules. Herein, Bi/Bi2Sn2O7 (Bi/BSO) heterojunction nanocomposites are prepared via a one‐step hydrothermal method, where NaOH etching of oxygen vacancies in the Bi─O bonds of Bi2Sn2O7 (BSO) is exploited for the in situ formation of metallic Bi and hence Schottky junctions with the semiconducting BSO. This leads to a high separation rate of photogenerated charge carriers. Consequently, compared to the pure‐phase BSO, the Bi/BSO heterostructures exhibit markedly enhanced ammonia production, reaching an optimum rate of 284.5 µmol g−1 h−1, where the rectifying contact between the semiconducting BSO and metallic Bi facilitates directional BSO to Bi electron transfer, leading to enrichment of photogenerated electrons at the active sites of metallic Bi. First‐principles calculations confirm the alteration of active sites and the guided electron flow by the Schottky junctions and surface oxygen vacancies. Results from this study offer an effective paradigm of structural engineering in manipulating the photocatalytic activity of bismuth‐based pyrochlore materials toward nitrogen fixation to ammonia.

Time-efficient etching of LR-115 SSNTD film for indoor radon, thoron quantification.

LR-115 Solid State Nuclear Track Detector (SSNTD) is commonly utilized for quantifying indoor radon-thoron levels, by tallying the tracks formed in the films by exposure to these gases. Conventionally, sodium hydroxide (NaOH) is used to etch LR-115 films for 90 min at 60°C. However, this study suggests a time-efficient alternative approach utilizing potassium hydroxide (KOH) as the etchant. In an initial investigation, the bulk etch rates of KOH were examined at different normalities and temperatures, revealing that KOH exhibited nearly double the bulk etch rates compared to NaOH. Subsequently, a specially designed controlled experiment was conducted to assess the efficacy of the technique by enumerating the tracks generated in the films. Both etchants demonstrated very similar track counts for identical controlled exposures, indicating the reliability of the method. A consistent behavior was observed in the real-case scenario of LR-115 films exposed indoors to alpha particles from radon and its decay products. In both experiments, the etching with KOH for 45 min gave track densities comparable to standard NaOH etching for 90 min, highlighting the time efficiency of this method. Investigations were carried out into track shape and size features, aspects crucial to the measurement technique, using microscopic imaging of samples treated with both etchants. Strikingly similar track shapes and sizes were observed, affirming the consistency in the track measurement technique. Collectively, these findings suggest that KOH etchant reduces the etching time, presenting itself as a time-efficient method for quantifying radon and thoron track density.

Construction of MoB@LDH heterojunction and its derivates through phase and interface engineering for advanced supercapacitor applications

Layered double hydroxide (LDH) has been attracted widespread attention in supercapacitor due to their unique layered structure and associated advantages. However, the inherent limitations of low electrical conductivity and reaction kinetics rate of LDH restrict its widespread application. Various modification techniques, such as heterojunction formation, phosphorization and introduction of phosphorus vacancies, are employed to modify LDH with the goal of improving the electrochemical performance. Preparation of composite materials using MoB MBene as conductive template and phosphorization are the effective ways for enhancing the electrical conductivity of electrode materials. MoB MBene is prepared using a modified method that combines NaOH etching and a high-temperature hydrothermal process. The presence of phosphorus vacancy is beneficial for enhancing the kinetics rate during electrode reactions. Through the synergistic effect of various modification methods, MP2 demonstrates an optimal electrochemical performance with a superior specific capacitance of 1731.19F/g (238.28 mAh g−1) at 1 A/g. It also demonstrates an impressive rate capacity of 81.28 % at 10 A/g and maintains a satisfactory capacitance retention of 88.14 % after 5000 cycles. In addition, a fabricated MP2//AC ASC device achieves an impressive energy density of 39.91 Wh kg−1 at the power density of 948.25 W kg−1 and demonstrates satisfactory cycling stability of 78.76 % after 5000 cycles. This work presents a comprehensive framework for analyzing the impact of material structure, components, and crystal phases on energy storage performance. It also examines the regulatory impact of different modification methods on energy storage mechanisms.

Effect of HF and NaOH Etching on Chemical and Structure Stability of Hollow SiOC Ceramics

Effect of HF and NaOH Etching on Chemical and Structure Stability of Hollow SiOC Ceramics

Fabricating Pt0-acid synergy in Pt/Beta phenol hydrodeoxygenation catalysts via a surface modification strategy of Beta molecular sieves

As for metal/zeolite supported phenol hydrodeoxygenation catalysts, it is important to improve the dispersion of metallic sites and build synergistic relationship between metallic and acid sites. The current research proposes a surface modification strategy by introducing CTAB in the NaOH etching of Beta. CTAB interacts with crystal defects to inhibit excessive crystal destruction. Aluminum atoms are protected from being removed and acid sites are reserved. Generated silicon hydroxyl groups anchor Pt0 particles. Pt0 particles are spatial resisted on the internal surface of catalysts to activate C–O bonds of phenol. Preserved acid sites provide reactive sites for dehydration reaction of cyclohexanol on the external surface of Pt/Beta-H. The high phenol conversion (i.e., 92.26 %) and cyclohexane yield (i.e., 7.18 %) were obtained at 80 °C due to the functional synergistic effect between acid and Pt0 sites. Proposed surface modification strategy proposes references for the structure design and development of efficient phenolics hydrodeoxygenation catalysts.

An effective strategy to prepare non-graphitic carbon with increased pseudo-graphitic content for sodium-ion battery anode with enhanced plateau capacity

The practical application of sodium-ion batteries is mainly hindered by relatively low energy density, which can be effectively overcome by increasing the pseudo-graphitic content in non-graphitic carbon (NGC) anodes. Herein, a simple and efficient strategy was reported to promote the growth of pseudo-graphitic domains in NGC thanks to the synergistic effect of pre-carbonization and NaOH etching using semi-coke as precursor. Based on pre-carbonization at 800 °C and NaOH etching with NaOH/carbon ratio of 0.5 at 600 °C, the resultant NGC (FC-800–0.5–600) exhibits a 13 % increase in percentage of pseudo-graphitic structure meanwhile 14 % decrease for graphite-like structure, but similar content of highly disordered structure compared with its counterpart. Notably, although similar in sloping capacity, FC-800–0.5–600 possesses much higher plateau capacity (<0.1 V) of 218.6 mAh g−1 than its counterpart (174.9 mAh g−1), which is attributed to the enhanced “interlayer intercalation” effect related with pseudo-graphitic structure. Thus, FC-800–0.5–600 can deliver an impressive reversible capacity of 326.8 mAh g−1 at 20 mA g−1, together with a considerable ICE of 84.7 %. This work proposed an effective strategy to increase pseudo-graphitic structure content in NGC, providing a rational guide for designing high-performance anodes in SIBs for practical use.

Ni/NiO/carbon derived from covalent organic frameworks for enzymatic-free electrochemical glucose sensor

An electrochemical enzyme-free glucose sensor based on a novel material with high catalytic performance was constructed. Specifically, a covalent-organic framework (COFBD) with abundant O,N,O′-metal chelating sites was firstly grown on the surface of SiO2 sacrificial template and then coordinated with Ni2+. Finally, Ni/NiO/cellular carbon foam (Ni/NiO/NC) nanocomposite was obtained by carbonizing the above material and removing the SiO2 template through NaOH etching. The electrocatalytic performance of Ni/NiO/NC could be adjusted by cavity size of NC and size of Ni/NiO nanoparticles. The enzyme-free glucose sensor based on Ni/NiO/NC showed a low detection limit of 0.2 μM, a wide detection range of 0.6 μM–8.6 mM and a high sensitivity of 76.03 μA mM−1 cm−2. Moreover, the paper-based wearable glucose sensor was also implemented and the results exhibited that the detection limit was 0.4 μM, the linear range was 1.1 μM–5.2 mM and the sensitivity was 42.38 μA mM−1 cm−2. The electrochemical enzyme-free glucose sensor also showed outstanding practical application performance for detection of glucose in real samples of juice, human serum and sweat. The works provided a method to construct novel material with good catalytic performance for sensitive glucose sensor.

Pharmacological evaluation and preclinical studies of hypochlorous acid solution

The article presents materials on the electrochemical synthesis of hypochlorous acid and its pharmacological and toxicological evaluation. In the market of veterinary drugs, special attention has been paid to long-known, potent detoxifying antimicrobial agents based on active oxygen obtained by the electrolysis method. In addition to a broad spectrum of antimicrobial action, such drugs have several other advantages, especially the biogenic nature, which causes the absence of allergic reactions. New electrocatalysts were proposed for the electrochemical synthesis of hypochlorous acid, which was produced according to the following method using a combined electrochemical-pyrolytic method. VT1-0 technical titanium was used as a current collector. The current collectors were subjected to several preliminary preparation steps, such as NaOH degreasing and etching in 6 M HCl. Initial nanotubes were obtained by anodizing Ti foil in ethylene glycol with 0.3 wt.% ammonium fluoride and 2 vol.% water for 4 hours. The electrochemical reduction was carried out in 1 M HClO4 by cathodic polarization for 1 hour. Later, a thin discontinuous layer of platinum or consecutive layers of platinum-palladium were applied to the base by electrodeposition. Nitrite electrolytes for platinization and phosphate-palladation were used for this purpose. Depending on the task, platinum, and palladium on the ground's surface varied from 0.1 to 2.0 mg/cm2. The obtained material was heat-treated in an air atmosphere. At this stage, the surface layers of composites were formed due to the oxidation of the base and encapsulation of platinum and palladium particles in titanium oxide. It was established that the solution of hypochlorous acid, obtained by the electrolysis method, is a low-hazard substance that belongs to the fourth class of toxicity. Its half-lethal dose (DL50) is not determined. The fact that, in nature, hypochlorite acid is formed by granulocytes of neutrophils involved in the last link of phagocytosis confirms that the resulting solution is low-toxic, environmentally safe, and incapable of causing side effects and distant consequences. The obtained results proved the perspective of using new technology for producing hypochlorite acid for veterinary medicine; its development is highly relevant, clinically expedient, and economically justified.

Ru-core Ir-shell electrocatalysts deposited on a surface-modified Ti-based porous transport layer for polymer electrolyte membrane water electrolysis

Novel Ru-core Ir-shell catalyst-integrated porous transport electrodes (PTEs) for polymer electrolyte membrane water electrolysis (PEMWE) cells are prepared, in which Ru-core Ir-shell catalyst nanostructures are directly deposited onto a porous transport layer (PTL) via arc plasma deposition (APD). The PTL has a nanostructured TiO2 surface prepared via NaOH etching, acting as a catalyst support. The performance and durability of these Ru-core Ir-shell catalysts depend strongly on the ratio of Ir and Ru. The current-voltage (I–V) characteristics of PEMWE cells were improved by applying these core-shell catalysts with a low Ir loading of around 0.1 mg cm−2. The core-shell catalyst-integrated PTEs can operate at current densities of up to 10 A cm−2 without exhibiting limiting current behavior. This unique combination of the core-shell catalyst and the PTE structure enables PEMWE cell operation with low iridium loading and high current density, potentially reducing the cost of green hydrogen.

Introducing Hybrid Defects of Silicon Doping and Oxygen Vacancies into MOF-Derived TiO2-X @Carbon Nanotablets Toward High-Performance Sodium-Ion Storage.

Titanium dioxide (TiO2 ) is a promising anode material for sodium-ion batteries (SIBs), which suffer from the intrinsic sluggish ion transferability and poor conductivity. To overcome these drawbacks, a facile strategy is developed to synergistically engineer the lattice defects (i.e., heteroatom doping and oxygen vacancy generation) and the fine microstructure (i.e., carbon hybridization and porous structure) of TiO2 -based anode, which efficiently enhances the sodium storage performance. Herein, it is successfully realized that the Si-doping into the MIL-125 metal-organic framework structure, which can be easily converted to SiO2 /TiO2-x @C nanotablets by annealing under inert atmosphere. After NaOH etching SiO2 /TiO2-x @C which contains unbonded SiO2 and chemically bonded SiOTi, thus the lattice Si-doped TiO2-x @C (Si-TiO2-x @C) nanotablets with rich Ti3+ /oxygen vacancies and abundant inner pores are developed. When examined as an anode for SIB, the Si-TiO2-x @C exhibits a high sodium storage capacity (285mAhg-1 at 0.2Ag-1 ), excellent long-term cycling, and high-rate performances (190mAhg-1 at 2Ag-1 after 2500 cycles with 95.1% capacity retention). Theoretical calculations indicate that the rich Ti3+ /oxygen vacancies and Si-doping synergistically contribute to a narrowed bandgap and lower sodiation barrier, which thus lead to fast electron/ion transfer coefficients and the predominant pseudocapacitive sodium storage behavior.

A microdots array-based fluoremetric assay with superwettability profile for simultaneous and separate analysis of iron and copper in red wine.

A microdots array-based fluoremetric method with superwettability profile has been developed for the simultaneous and separate detection of Fe3+ and Cu2+ ions in red wine samples. A wettable micropores array was initially designed with high density by using polyacrylic acid (PAA) and hexadecyltrimethoxysilane (HDS), followed by the NaOH etching route. Zinc metal organic frameworks (Zn-MOFs) were fabricated as the fluorescent probes to be immobilized into the micropores array to obtain the fluoremetric microdots array platform. It was found that the fluorescence of Zn-MOFs probes could decrease significantly in the presence of Fe3+ and/or Cu2+ ions towards their simultaneous analysis. Yet, the specific responses to Fe3+ ions could be expected if using histidine to chelate Cu2+ ions. Moreover, the developed Zn-MOFs-based microdots array with superwettability profile can enable the accumulation of targeting ions from the complicated samples without any tedious pre-processing. Also, the cross-contamination of different samples droplets can be largely avoided so as to facilitate the analysis of multiple samples. Subsequently, the feasibility of simultaneous and separate detection of Fe3+ and Cu2+ ions in red wine samples was demonstrated. Such a design of microdots array-based detection platform may promise the wide applications in analyzing Fe3+ and/or Cu2+ ions in the fields of food safety, environmental monitoring, and medical diseases diagnostics.