Search Results (57)

Excessive copper ions in the human body can cause a variety of diseases, such as gastrointestinal disorders, cirrhosis, and Alzheimer’s disease. Techniques like Inductively Coupled Plasma–Mass Spectroscopy and Atomic Absorption Spectroscopy are available for copper detection, but the associated cost issues for sample preparation and labor limit their application for on-site detection. Herein, we are reporting a versatile method for detecting copper ions using a peptide-functionalized gold nanoparticle sensor in combination with various optical spectroscopic techniques. The peptide (CW) exhibited selective sensing ability for Cu(II) with visual colorimetric and optical spectroscopic changes compared to other metal ions tested. CW showed a visual colorimetric response from colorless to light brown color after interaction with Cu(II). Converting CW to a gold nanoparticle appended (CW-AuNPs) nanoplatform enabled a multimodal detection platform for Cu (II), which utilizes colorimetric and optical spectrum changes and surface-enhanced Raman spectroscopy (SERS) to enable highly sensitive sensing of Cu(II), even at extremely low concentrations (76 nms.). CW-AuNPs exhibit a controlled aggregation property in the presence of Cu(II), resulting in the creation of hot spots for SERS-based detection. Moreover, the peptide unit attached to the gold nanoparticles serves both as a binding motif for Cu(II) and as a Raman reporter for Cu(II) sensing. Our comprehensive analysis, including solution-state and dry-mapping Raman spectroscopic studies, demonstrates remarkable picomolar sensitivity of the peptide–gold nanoparticle system for Cu(II) detection. Moreover, we prepared a paper test strip from CW-AuNPs and used it as a visual colorimetric platform for sensitive detection of copper ions. Full article

We present a dual-mode optical sensing strategy for selective and sensitive detection of sulfide ions (S²⁻), employing copper-anchored nitrogen-doped graphene quantum dots (Cu@N-GQDs) as bifunctional nanozymes. The Cu@N-GQDs were synthesized via citric acid pyrolysis in the presence of ammonium hydroxide (serving as both nitrogen source and reductant) and copper chloride, leading to uniform incorporation of copper oxide species onto the N-GQD surface. The resulting nanohybrids exhibit two synergistic functionalities: intrinsic fluorescence comparable to pristine N-GQDs, and significantly enhanced peroxidase-like catalytic activity attributed to the anchored copper species. Upon interaction with sulfide ions, the system undergoes a dual-optical response: (i) fluorescence quenching via Cu-S complexation, and (ii) inhibition of peroxidase-like activity due to the deactivation of Cu catalytic centers via the interaction with S²⁻. This dual-signal strategy enables sensitive quantification of S²⁻, achieving detection limits of 0.5 µM (fluorescence) and 3.5 µM (colorimetry). The sensor demonstrates excellent selectivity over competing substances and high reliability and precision in real tap water samples. These findings highlight the potential of Cu@N-GQDs as robust, bifunctional, and field-deployable nanozyme probes for environmental and biomedical sulfide ion monitoring. Full article

This study reports the development of a highly sensitive electrochemical sensor for phosphate ion detection, utilizing silicon nanowires (SiNWs) as the transducing elements and a novel copper (II) phthalocyanine-acrylate polymer adduct (Cu (II) Pc-PAA) as the functional sensing layer. Silicon nanowires were fabricated via metal-assisted chemical etching (MACE) with etching durations of 15, 25, 35, 45, and 60 min. The SiNWs etched for 15 min exhibited the highest sensitivity, showing superior electrochemical performance. Functionalized SiNWs were systematically evaluated for phosphate ion (HPO₄²⁻) detection over a wide concentration range (10⁻¹⁰ to 10⁻⁶ M) using Mott–Schottky measurements. The surface morphology of the SiNWs was thoroughly characterized before and after Cu (II) Pc-PAA layer functionalization. The sensing material was analyzed using contact angle goniometry and scanning electron microscopy (SEM), confirming both its uniform distribution and effective immobilization. The sensor displayed a Nernstian behavior with a sensitivity of 28.25 mV/Decade and an exceptionally low limit of detection (LOD) of 1.5 nM. Furthermore, the capacitive sensor exhibited remarkable selectivity toward phosphate ions, even in the presence of potentially interfering anions such as Cl⁻, NO₃⁻, SO₄²⁻ and ClO₄⁻. These results confirm the sensor’s high sensitivity, selectivity, and fast response, underscoring its suitability for environmental phosphate ion monitoring. Full article

We present a chemiresistor sensor for NO₂ leaks. The sensor uses the organometallic semiconductor copper(II)phthalocyanine (CuPc), and is more easily manufactured and characterised than previously described organic transistor gas sensors. Resistance R is high but within the range of modern voltage buffers. The chemiresistor weakly responds to several gases, with either a small increase (NH₃ and H₂S) or decrease (SO₂) in R. However, the response is low at environmental pollution levels. The response to NO₂ also is near-zero for permitted long-term exposure. Our sensor is, therefore, not suited for environmental monitoring, but acceptable environmental pollutant levels do not interfere with the sensor. Above a threshold of ~87 ppb, the response to NO₂ becomes very strong. This response is presumably due to the doping of CuPc by the strongly oxidising NO₂, and is far stronger than for previously reported CuPc chemiresistors. We relate this to differences in the film morphology. Under 1 ppm NO₂, R drops by a factor of 870 vs. non-polluted air. An amount of 1 ppm NO₂ is far above the ‘background’ environmental pollution, thereby avoiding false alarms, but far below immediately life-threatening levels, thus giving time to evacuate. Our sensor is destined for leak detection in the nitrogen fertiliser industry, where NO₂ is an important intermediate. Full article

Copper is widely used in both its metallic form and as oxide across numerous scientific and industrial domains. The primary copper oxides, cuprite (Cu₂O) and tenorite (CuO), naturally form on the copper surface and play a crucial role in advanced technologies, such as solar cells, lithium batteries, and sensors. Tenorite is appreciated for its optical properties, stability, low toxicity, and reactivity. While copper oxide thin films are traditionally synthesized through thermal treatments and oxidation in alkaline environments, these conventional high-temperature methods not only require significant energy consumption but can also compromise the metal–film interface. This study aims to develop a sustainable alternative approach for forming a homogeneous CuO layer on a copper substrate through environmentally friendly treatments based on low temperature, cost-effective, and time-saving procedures. Three different eco-conscious treatments were investigated: (i) immersion in NaOH basic solution, (ii) exposure to NaOH basic solution vapours, and (iii) a combined treatment involving both immersion and vapour exposure. This green synthesis approach significantly reduces energy consumption compared to traditional thermal methods while maintaining product quality. The surface oxide layer was investigated through an optical microscope (OM), scanning electron microscopy (SEM), spectrocolorimetric analysis, peel-off test, µ-Raman and X-ray photoelectron spectroscopy (XPS) analysis to investigate the surface oxidation state. Full article

Radar sensors are critical for obstacle detection and navigation, especially for automated driving. Using the use-case “printing of heating coils on the inside of the front housing (primary radome)” needed for de-icing in winter, it is demonstrated that additive manufacturing (AM) can provide economic and functional benefits for manufacturing of the sensors. AM will allow significant cost reduction by eliminating parts and simplifying the manufacturing process. Different AM technologies for the coils were investigated, first, by applying the conductive traces by fused deposition modeling (FDM), and, second, by printing copper particle-free inks and pastes. The metal layers were electrically and mechanically characterized using a profilometer to measure the trace dimension and a four-point probe to measure the resistance. It was revealed that low-cost conductive filaments with low resistivity and current carrying capacity are commercially still not available. The best option sourced was a copper–polyester-based filament with 6000 µΩcm after printing. Therefore, low-cost particle-free copper inks and commercial copper flake paste were selected to print the heating coil. The Cu particle-free inks were amine-based Cu (II) formate complexes, where the Cu exists in an ionic form. Using contactless printing processes such as ink-jet printing or pneumatic dispensing, the traces could be deposited onto the low-melting temperature (225 °C) polymeric radome structure. After printing, the material needed to be sintered to form the conductive copper traces. To avoid damaging the polymer radome during sintering, two different processes were investigated: low-temperature (<150 °C) sintering in an oven for 30 min or fast laser sintering. The sintered Cu layers achieved the following specific electric resistivities when slowly sintered in the oven: paste 4 µΩcm and ink 8.8 µΩcm. Using laser sintering, the ink achieved 3.2 µΩcm because the locally high temperature provides better sintering. Also, the adhesion was significantly increased to (5 B). Therefore, laser sintering is the preferred technology. In addition, it allows fast processing directly after printing. Commercial equipment is available where printing and laser sintering is integrated. The potential of low-cost copper material and the integration in additive manufacturing of electronic systems using radar sensors as an example are demonstrated in this paper. Full article

Copper, along with gold, was among the first metals that humans employed. Thus, the copper pollution of the world’s water resources is escalating, posing a significant threat to human health and aquatic ecosystems. It is crucial to develop detection technology that is both low-cost and feasible, as well as ultra-selective and sensitive. This study explored the use of the NH₂-Xxx-His motif-derived peptide from phage display technology for ultra-selective Cu²⁺ detection. Various Cu-binding M13 phage clones were isolated, and their affinity and cross-reactivity for different metal ions were determined. A detailed analysis of the amino acid sequence of the unique Cu-binding peptides was employed. For the development of an optical chemosensor, a peptide with an NH₂-Xxx-His motif was selected. The dansyl group was incorporated during solid-phase peptide synthesis, and fluorescence detection assays were employed. The efficacy of the Cu²⁺-binding peptide was verified through spectroscopic measurements. In summary, we developed a highly selective and sensitive fluorescent chemosensor for Cu²⁺ detection based on a peptide sequence from a phage display library that carries the N-terminal Xxx-His motif. Full article

Carbon dots (CDs) derived from mandarin peel biochar (MBC) at different pyrolysis temperatures (200, 400, 600, and 800 °C) have been synthesized and characterized. This high-value transformation of waste materials into fluorescent nanoprobes for environmental monitoring represents a step forward towards a circular economy. In this itinerary, CDs produced via one-pot hydrothermal synthesis were utilized for the detection of copper (II) ions. The study looked at the spectroscopic features of biochar-derived CDs. The selectivity of CDs obtained from biochar following carbonization at 400 °C (MBC400-CDs towards various heavy metal ions resulted in considerable fluorescence quenching with copper (II) ions, showcasing their potential as selective detectors. Transmission electron microscopic (TEM) analysis validated the MBC-CDs’ consistent spherical shape, with a particle size of <3 nm. The Plackett–Burman Design (PBD) was used to study three elements that influence the F₀/F ratio, with the best ratio obtained with a pH of 10, for 10 min, and an aqueous reaction medium. Cu (II) was detected over a dynamic range of 4.9–197.5 μM and limit of detection (LOD) of 0.01 μM. Validation testing proved the accuracy and precision for evaluating tap and mountain waters with great selectivity and no interference from coexisting metal ions. Full article

Much progress has been made in the determination of As (III), while numerous electrochemical sensors based on metal nanomaterials with significant sensitivity and precision have been developed. However, further research is still required to achieve rapid detection and avoid interference from other metal ions (especially copper ions). In this study, bimetallic AuPt nanoparticles are electrochemically modified with screen printing electrodes. What’s more, L-cysteine also self-assembles with AuNPs through Au-S bond to enhance the electrochemical performance. To overcome the interference of Cu (II) in the sensing process, the reduced iron powder was chosen to remove Cu (II) and other oxidizing organics in aqueous solutions. The lowest detectable amount is 0.139 ppb, a linear range of 1~50 ppb with superlative stability by differential pulse anodic stripping voltammetry. Fortunately, the reduced iron powder could eliminate the Cu (II) with no effect on the As (III) signal. Full article

Electrochemical and photoelectrochemical sensors are a rapidly developing field in analytical chemistry. However, commercial systems often lack versatility and affordability, hindering wider adoption. Additionally, the absence of integrated excitation light sources limits their application in photoelectrochemical sensing. Here, we present a highly precise, versatile, affordable measurement system for both electrochemical and photoelectrochemical sensing applications. The system incorporates a three-electrode potentiostat with a synchronized excitation light source. This design enables the system to perform conventional electrochemical measurements like cyclic voltammetry, chronoamperometry, and photoelectrochemical amperometric measurements with controlled light excitation. The developed measurement system operates within a voltage range suitable for a measurable current range of 1 nA to 18 mA, with a high precision of 99%. The excitation source is a monochromatic LED system offering seven distinct wavelengths with digitally controlled intensity via a digital-to-analog converter. Furthermore, an Android-based user interface allows wireless system control via Bluetooth Low Energy. The report also details the construction of a photoelectrochemical experiment using copper (II) oxide nanorods synthesized by the hydrothermal process as the photoactive material employed to test the experiment on a potassium ferricyanide/potassium ferrocyanide solution. This user-friendly system allows broader exploration of electrochemical and photoelectrochemical sensing applications. Full article

A novel copper(II) ion indicator based on polymer conformational change is designed and its chemo-response to the target analyte is tested in this paper. The word ‘telechelic’ in the title means that a polymer has two different fluorophores on either end. If one of them is a fluorescent donor and the other is a fluorescent acceptor, then the extent of Foerster resonance energy transfer (FRET) will depend on polymer conformation. The sensitivity of these sensors is tunable based on the chain length and the amount of the receptor on the polymer. This is revealed by the fluorescence response of 30mer, 50mer, and 100mer of poly(N-isopropyl)acrylamide with different amounts of metal chelation monomers. We also address the change in fluorescence over time due to the untangling of poly(N-isopropylacrylamide) in water. The fluorescent signal can maintain stability after metal binding. The photoluminescence results agree with the length calculation of polyelectrolytes. A fluorescent standard curve is created for the measurement of different concentrations of copper ions. The sensing limit can reach 10⁻¹⁰ M analytes, which is suitable for the measurement of chemicals in trace amounts in the environment. Full article

Knowing nutrient allocation dynamics in the tissues and the characteristics related to growth in different forest species is crucial to fertilization management and selecting better species for specific environments, ensuring greater fertilization efficiency and consequent sustainability in the forestry sector through the rational use of fertilizers. The objectives of this study were (i) to evaluate the content of macro- and micronutrients in different tissues of eucalyptus species and (ii) to relate them with their growth. The treatments were composed of six eucalyptus species (Eucalyptus camaldulensis Dehnh., Corymbia citriodora Hook., E. saligna Sm., E. grandis W. Hill ex Maiden, E. urograndis, and E. urophylla S. T. Blake). Macro- (nitrogen, phosphorus, potassium, calcium, magnesium, and sulfur) and micronutrient (boron, copper, iron, manganese, and zinc) contents were determined in the leaves, bark, and sapwood. To study the functional patterns in macro- and micronutrient contents, Canonical Variable Analysis (CVA) was performed. The first two canonical variables in nutrient content of leaves, bark, and sapwood and the growth variables of eucalyptus species accumulated values greater than 80% of variance. The species E. grandis and E. urograndis showed the highest means for volume and total height but showed no differences regarding the concentration of major elements in the tissues, except the iron content in the bark, which was higher compared to other species. CVA proved to be an excellent tool for understanding, identifying, and classifying the strategies of Eucalyptus sp. regarding the content of nutrients in the shoot biomass tissues and may support genetic improvement programs aiming at identifying potential species. Future research involving the use of remotely piloted aircraft and remote sensors could be a strategy to monitor nutrient contents in different parts of trees throughout the cycle of different eucalyptus species. Full article

YBa₂Cu₃O_6+x (YBCO) cuprates are semiconductive when oxygen depleted (x < 0.5). They can be used for uncooled thermal detection in the near-infrared: (i) low temperature deposition on silicon substrates, leading to an amorphous phase (a-YBCO); (ii) pyroelectric properties exploited in thermal detectors offering both low noise and fast response above 1 MHz. However, a-YBCO films exhibit a small direct current (DC) electrical conductivity, with strong non-linearity of current–voltage plots. Calcium doping is well known for improving the transport properties of oxygen-rich YBCO films (x > 0.7). In this paper, we consider the performances of pyroelectric detectors made from calcium-doped (10 at. %) and undoped a-YBCO films. First, the surface microstructure, composition, and DC electrical properties of a-Y_0.9Ca_0.1Ba₂Cu₃O_6+x films were investigated; then devices were tested at 850 nm wavelength and results were analyzed with an analytical model. A lower DC conductivity was measured for the calcium-doped material, which exhibited a slightly rougher surface, with copper-rich precipitates. The calcium-doped device exhibited a higher specific detectivity ($D^{*}=7.5\times {10}^7 \mathrm{c}\mathrm{m}·\sqrt{\mathrm{H}\mathrm{z}}/\mathrm{W}$ at 100 kHz) than the undoped device. Moreover, a shorter thermal time constant (<8 ns) was inferred as compared to the undoped device and commercially available pyroelectric sensors, thus paving the way to significant improvements for fast infrared imaging applications. Full article

This paper describes the synthesis and characterization of seven different copper(II) coordination compounds, as well as the formation of a protonated ligand involving all compounds from the same reaction. Their synthesis required hydrothermal conditions, causing the partial in situ transformation of 5-fluoro uracil-1-acetic acid (5-FUA) into an oxalate ion (ox), as well as the protonation of the 4,4′-bipyridine (bipy) ligand through a catalytic process resulting from the presence of Cu(II) within the reaction. These initial conditions allowed obtaining the new coordination compounds [Cu₂(5-FUA)₂(ox)(bipy)]_n·2n H₂O (CP2), [Cu(5-FUA)₂(H₂O)(bipy)]_n·2n H₂O (CP3), as well as the ionic pair [(H₂bipy)⁺² 2NO₃⁻] (1). The mother liquor evolved rapidly at room temperature and atmospheric pressure, due to the change in concentration of the initial reagents and the presence of the new chemical species generated in the reaction process, yielding CPs [Cu(5-FUA)₂(bipy)]_n·3.5n H₂O, [Cu₃(ox)₃(bipy)₄]_n and [Cu(ox)(bipy)]_n. The molecular compound [Cu(5-FUA)₂(H₂O)₄]·4H₂O (more thermodynamically stable) ended up in the mother liquor after filtration at longer reaction times at 25 °C and 1 atm., cohabiting in the medium with the other crystalline solids in different proportions. In addition, the evaporation of H₂O caused the single-crystal to single-crystal transformation (SCSC) of [Cu(5-FUA)₂(H₂O)(bipy)]_n·2n H₂O (CP3) into [Cu(5-FUA)₂(bipy)]_n·2n H₂O (CP4). A theoretical study was performed to analyze the thermodynamic stability of the phases. The observed SCSC transformation also involved a perceptible color change, highlighting this compound as a possible water sensor. Full article

A simple and rapid method for determining mercury (II) has been developed using L-cysteine-capped copper nanocluster (CuNCs) with o-phenylenediamine (OPD) as the sensor. The characteristic fluorescence peak of the synthesized CuNCs was observed at 460 nm. The fluorescence properties of CuNCs were strongly influenced by the addition of mercury (II). Upon addition, CuNCs were oxidized to form Cu²⁺. Then, the OPD were rapidly oxidized by Cu²⁺ to form o-phenylenediamine oxide (oxOPD), as evidenced by the strong fluorescence peak at 547 nm, resulting in a decrease in the fluorescence intensity at 460 nm and an increase in the fluorescence intensity at 547 nm. Under optimal conditions, a calibration curve between the fluorescence ratio (I547/I460) and mercury (II) concentration was constructed with a linearity of 0–1000 µg L⁻¹. The limit of detection (LOD) and limit of quantification (LOQ) were found at 18.0 µg L⁻¹ and 62.0 µg L⁻¹, respectively. The recovery percentage was in the range of 96.8–106.4%. The developed method was also compared with the standard ICP-OES method. The results were found to be not significantly different at a 95% confidence level (t_stat = 0.365 < t_crit = 2.262). This demonstrated that the developed method could be applied for detecting mercury (II) in natural water samples. Full article