Search Results (64)

Metallo-phthalocyanines (MPcs) are versatile materials with applications in electroanalysis because of their superior catalytic properties. This review presents the electrochemical methods based on MPc-modified electrodes and reports some of their remarkable properties and applications in the electroanalysis of monoamine neurotransmitters and biomolecules that play a crucial role in vital functions of the human body. The development of electrocatalytic chemically modified electrodes is based on their ability to provide a selective and rapid response toward a specific analyte in complex media without the need for sample pretreatment. The explanation of several phenomena occurring at the MPc-modified electrode surface (e.g., MPc-mediated electrocatalysis), the advantages of promoting different electron transfer reactions, and the detection mechanism are also presented. The types of MPcs and different materials, such as carbon nanotubes and graphene, used as substrates for modified working electrodes are discussed. Modifying the properties of MPcs through various interactions, or combining MPcs with carbonaceous materials, creates a synergistic effect. Such hybrid materials present both extraordinary catalytic and increased conductivity properties. We conducted a compilation study based on recent works to demonstrate the efficacy of the developed sensors and methods in sensing monoamine neurotransmitters. We emphasize the analyte type, optimized experimental parameters, working range, limits of detection and quantification, and application to real samples. MPc–carbon hybrids have led to the development of sensors with superior sensitivity and improved selectivity, enabling the detection of analytes at lower concentrations. We highlight the main advantages and drawbacks of the discussed methods. This review summarizes recent progress in the development and application of metallo-phthalocyanine-modified electrodes in the electroanalysis of monoamine neurotransmitters. Some possible future trends are highlighted. Full article

With increasing energy demands, fuel cells are a popular avenue for portability and low waste emissions. Hydrogen fuel cells are popular due to their potential output power and clean waste. However, due to storage and transport concerns, hydrogen peroxide fuel cells are a promising alternative. Although they have a lower output potential compared to hydrogen fuel cells, peroxide can act as both the oxidizing and reducing agent, simplifying the structure of the cell. In addition to reducing the complexity, hydrogen peroxide is stable in liquid form and can be stored in less demanding methods. This paper investigates chelated metals as electrode material for hydrogen peroxide fuel cells. Chelated metal complexes are ring-like structures that form from binding organic or inorganic compounds with metal ions. They are used in medical imaging, water treatment, and as catalysts for reactions. Copper(II) phthalocyanine, phthalocyanine green, poly(copper phthalocyanine), bis(ethylenediamine)copper(II) hydroxide, iron(III) ferrocyanine, graphene oxide decorated with Fe₃O₄, zinc phthalocyanine, magnesium phthalocyanine, manganese(II) phthalocyanine, cobalt(II) phthalocyanine are investigated as electrode materials for peroxide fuel cells. In this study, the performance of these materials is evaluated using cyclic voltammetry. The voltammograms are compared, as well as observations are made during the materials’ use to measure their effectiveness as electrode material. There has been limited research comparing the use of these chelated metals in the context of hydrogen peroxide fuel cells. Through this research, the goal is to further the viability of hydrogen peroxide fuel cells. Poly(copper phthalocyanine) and graphene oxide doped with iron oxides had strong redox catalytic activity for use in acidic peroxide single-compartment fuel cells, where the poly(copper phthalocyanine) electrode compound generated the highest peak power density of 7.92 mW/cm² and cell output potential of 0.634 V. Full article

In this work, we report on the fabrication of a novel Organic Double-Layer Supercapacitor (ODLSC) using recycled palm as the substrate and electrodes based on halogenated indium and copper phthalocyanines. The electrodes were characterized using Reflectance, the Kulbeka–Munk function, and Fluorescence. Finally, their electrical behavior was evaluated, and the results were compared with those obtained for a more conventional supercapacitor fabricated on polyethylene terephthalate substrate and using indium tin oxide film for electrodes. Based on the experimental measurements of the fabricated ODLSC, the parameter identification of the classical equivalent circuit model was carried out using the Least Squares of Orthogonal Distances (LSOD) algorithm. The results indicated that the palm supercapacitor exhibited behavior more like that of traditional supercapacitors, as the root square mean error (RMSE) values in the model approximation of the experimental data were in the order of ${10}^{-7}$. Furthermore, the models obtained allowed a determination of the device’s Electrical Impedance Spectroscopy (EIS), revealing that the Palm SC-T1 exhibited capacitive behavior. In contrast, the manufactured Palm SC-T2, PET SC-T1, and PET SC-T2 devices exhibited inductive behavior. All the materials used in this work, such as the substrates, electrodes, separator membranes, and electrolytes, have a high potential to be used in organic supercapacitors. Full article

In the quest for more sensitive gas sensors, researchers have studied how heating the sensors, using UV light, and thermally annealing sensors improve performance. During thermal annealing, the heating process can improve the crystallinity of the material while also increasing the electrode and sensing material interactions to create more available active sites and thus improve sensor performance. Hexadecafluorinated iron (II) phthalocyanine (FePcF₁₆) nanowires have high sensitivity towards NH₃ selectively, and thermally annealing the NWs after the deposition can further improve the sensing response and recovery. For this reason, the effect of annealing FePcF₁₆ NWs at different temperatures was studied to optimize these systems. In this work, FePcF₁₆ NWs were synthesized using physical vapor deposition (PVD) to deposit on interdigitated electrodes. The NWs were characterized by SEM, EDS, PXRD, FTIR, and Raman spectroscopy to confirm their purity. The sensors were annealed at different temperatures, inserted into a gas sensing chamber, and exposed to 1 ppm NH₃ in air, and the electrical current was measured. The results show that the optimized FePcF₁₆ NWs have excellent sensing properties, with a 58% increase in response towards NH₃ after a stepwise annealing at 300 °C confirming these systems are good prospective candidates for sensing NH₃ at room temperature. Full article

Phototransistors are three-terminal photodetectors that usually have a higher photocurrent gain than photodiodes due to the amplification of the gate electrode. In this work, a broad spectral phototransistor based on copper phthalocyanine (CuPc) and a Cs₃Bi₂I₉ (CBI) heterojunction is fabricated by the full vacuum evaporation method. Due to the complementary UV–visible absorption of CuPc and CBI, the device exhibits superior performance under three different types of visible light illumination. The experimental results show that the structure of the organic/perovskite heterojunction active layer has the characteristics of good compatibility and a simple process. Meanwhile, by utilizing the superior light-absorption characteristics of perovskite materials and the strong exciton dissociation efficiency of a hetero-type heterojunction interface, the CuPc/CBI-PT exhibits a higher photoresponsivity, photosensitivity, specific detection rate, and lower operating voltage than the CuPc reference device. The stability test shows that the CuPc/CBI-PT can still obtain a 0.73 A/W photoresponsivity under 660 nm light illumination after being stored in the air for 360 h without any packaging. This indicates that the organic/perovskite heterojunction PT may be a good choice for the preparation of high-performance photodetectors. Full article

Microbial fuel cells (MFCs) are sustainable energy recovery systems because they use organic waste as biofuel. Using critical raw materials (CRMs), like platinum-group metals, at the cathode side threatens MFC technology’s sustainability and raises costs. By developing an efficient electrode design for MFC performance enhancement, CRM-based cathodic catalysts should be replaced with CRM-free materials. This work proposes developing and optimizing iron-based air cathodes for enhancing oxygen reduction in MFCs. By subjecting iron phthalocyanine and carbon black pearls to controlled thermal treatments, we obtained Fe-based electrocatalysts combining high surface area (628 m² g⁻¹) and catalytic activity for O₂ reduction at near-neutral pH. The electrocatalysts were integrated on carbon cloth and carbon paper to obtain gas diffusion electrodes whose architecture was optimized to maximize MFC performance. Excellent cell performance was achieved with the carbon-paper-based cathode modified with the Fe-based electrocatalysts (maximum power density-PD_max = 1028 mWm⁻²) compared to a traditional electrode design based on carbon cloth (619 mWm⁻²), indicating the optimized cathodes as promising electrodes for energy recovery in an MFC application. Full article

Biosensors function as sophisticated devices, converting biochemical reactions into electrical signals. Contemporary emphasis on developing biosensor devices with refined sensitivity and selectivity is critical due to their extensive functional capabilities. However, a significant challenge lies in the binding affinity of biosensors to biomolecules, requiring adept conversion and amplification of interactions into various signal modalities like electrical, optical, gravimetric, and electrochemical outputs. Overcoming challenges associated with sensitivity, detection limits, response time, reproducibility, and stability is essential for efficient biosensor creation. The central aspect of the fabrication of any biosensor is focused towards forming an effective interface between the analyte electrode which significantly influences the overall biosensor quality. Polymers and macromolecular systems are favored for their distinct properties and versatile applications. Enhancing the properties and conductivity of these systems can be achieved through incorporating nanoparticles or carbonaceous moieties. Hybrid composite materials, possessing a unique combination of attributes like advanced sensitivity, selectivity, thermal stability, mechanical flexibility, biocompatibility, and tunable electrical properties, emerge as promising candidates for biosensor applications. In addition, this approach enhances the electrochemical response, signal amplification, and stability of fabricated biosensors, contributing to their effectiveness. This review predominantly explores recent advancements in utilizing macrocyclic and macromolecular conjugated systems, such as phthalocyanines, porphyrins, polymers, etc. and their hybrids, with a specific focus on signal amplification in biosensors. It comprehensively covers synthetic strategies, properties, working mechanisms, and the potential of these systems for detecting biomolecules like glucose, hydrogen peroxide, uric acid, ascorbic acid, dopamine, cholesterol, amino acids, and cancer cells. Furthermore, this review delves into the progress made, elucidating the mechanisms responsible for signal amplification. The Conclusion addresses the challenges and future directions of macromolecule-based hybrids in biosensor applications, providing a concise overview of this evolving field. The narrative emphasizes the importance of biosensor technology advancement, illustrating the role of smart design and material enhancement in improving performance across various domains. Full article

Palladium phthalocyanine (PdPc) nanowires (NWs) were developed to achieve the gas sensing of NO₂ in the sub-parts-per-million (ppm) range. Non-substituted metal phthalocyanine are well known for their p-type semiconducting behavior, which is responsible for its gas-sensing capabilities. Nanofabrication of the PdPc NWs was performed by physical vapor deposition (PVD) on an interdigitated gold electrode (IDE). The coordination of palladium in the structure was confirmed with UV–Vis spectroscopy. Gas-sensing experiments for NO₂ detection were undertaken at different sensed gas concentrations from 4 ppm to 0.5 ppm at room temperature. In this work, the responses at different gas concentrations are reported. In addition, structural studies of the PdPc NWs with scanning electron microscopy (SEM) and electron-dispersive X-ray diffraction (EDS) are shown. Full article

Lithium–air batteries (LABs) have a theoretically high energy density. However, LABs have some issues, such as low energy efficiency, short life cycle, and high overpotential in charge–discharge cycles. To solve these issues electrocatalytic materials were developed for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER), which significantly affect battery performance. In this study, we aimed to synthesize electrocatalytic N-doped carbon-based composite materials with solution plasma (SP) using Co or Ni as electrodes from organic solvents containing cup-stacked carbon nanotubes (CSCNTs), iron (II) phthalocyanine (FePc), and N-nethyl-2-pyrrolidinone (NMP). The synthesized N-doped carbon-based composite materials were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS). TEM observation and XPS measurements revealed that the synthesized carbon materials contained elemental N, Fe, and electrode-derived Co or Ni, leading to the successful synthesis of N-doped carbon-based composite materials. The electrocatalytic activity for ORR of the synthesized carbon-based composite materials was also evaluated using electrochemical measurements. The electrochemical measurements demonstrated that the electrocatalytic performance for ORR of N-doped carbon-based composite material including Fe and Co showed superiority to that of N-doped carbon-based composite material including Fe and Ni. The difference in the electrocatalytic performance for ORR is discussed regarding the difference in the specific surface area and the presence ratio of chemical bonding species. Full article

In this work we studied the semiconductor behavior of titanyl phthalocyanine (TiOPc) and vanadyl phthalocyanine (VOPc), doped with anthraflavic acid and deposited on Tetrapak/graphite as flexible electrodes. The molecular structure was approached using the density functional theory and astonishingly, it was found that the structure and electronic behavior can change depending on the metal in the phthalocyanine. Experimentally, the Root Mean Square was found to be 124 and 151 nm for the VOPc-Anthraflavine and TiOPc-Anthraflavine films, respectively, and the maximum stress was 8.58 MPa for the film with VOPc. The TiOPc-Anthraflavine film presents the smallest fundamental gap of 1.81 eV and 1.98 eV for indirect and direct transitions, respectively. Finally, the solid-state devices were fabricated, and the electrical properties were examined. The tests showed that the current–voltage curves of the devices on Tetrapak and VOPc-Anthraflavine on a rigid substrate exhibit the same current saturation behavior at 10 mA, which is achieved for different voltage values. Since the current–voltage curves of the TiOPc-Anthraflavine on a rigid substrate presents a defined diode model behavior, it was approximated by nonlinear least squares, and it has been determined that the threshold voltage of the sample for the different lighting conditions is between 0.6 and 0.8 volts. Full article

A sensitive and robust electrochemical cholinesterase-based sensor was developed to detect the quaternary ammonium (QAs) biocides most frequently found in agri-food industry wash waters: benzalkonium chloride (BAC) and didecyldimethylammonium chloride (DDAC). To reach the maximum residue limit of 28 nM imposed by the European Union (EU), two types of cholinesterases were tested, acetylcholinesterase (AChE, from Drosophila melanogaster) and butyrylcholinesterase (BChE, from horse serum). The sensors were designed by entrapping AChE or BChE on cobalt phthalocyanine-modified screen-printed carbon electrodes. The limits of detection (LOD) of the resulting biosensors were 38 nM for DDAC and 320 nM for BAC, using, respectively, AChE and BChE. A simple solid-phase extraction step was used to concentrate the samples before biosensor analysis, allowing for the accurate determination of DDAC and BAC in tap water with limits of quantification (LOQ) as low as 2.7 nM and 5.3 nM, respectively. Additional assays demonstrated that the use of a phosphotriesterase enzyme allows for the total removal of interferences due to the possible presence of organophosphate insecticides in the sample. The developed biosensors were shown to be stable during 3 months storage at 4 °C. Full article

Understanding the metabolism of pharmaceutical compounds is a fundamental prerequisite for ensuring their safety and efficacy in clinical use. However, conventional methods for monitoring drug metabolism often come with the drawbacks of being time-consuming and costly. In an ongoing quest for innovative approaches, the application of electrochemistry in metabolism studies has gained prominence as a promising approach for the synthesis and analysis of drug transformation products. In this study, we investigated the hepatic metabolism of voriconazole, an antifungal medication, by utilizing human liver microsomes (HLM) assay coupled with LC-MS. Based on the obtained results, the electrochemical parameters were optimized to simulate the biotransformation reactions. Among the various electrodes tested, the chemometric analysis revealed that the iron(II) phthalocyanine electrode was the most effective in catalyzing the formation of all hepatic voriconazole metabolites. These findings exemplify the potential of phthalocyanine electrodes as an efficient and cost-effective tool for simulating the intricate metabolic processes involved in drug biotransformation, offering new possibilities in the field of pharmaceutical research. Additionally, in silico analysis showed that two detected metabolites may exhibit significantly higher acute toxicity and mutagenic potential than the parent compound. Full article

Nicotine is the one of the major addictive substances; the overdose of nicotine (NIC) consumption causes increasing heart rate, blood pressure, stroke, lung cancer, and respiratory illnesses. In this study, we have developed a precise and sensitive electrochemical sensor for nicotine detection in saliva samples. It was built on a glassy carbon electrode (GCE) modified with graphene (Gr), iron (III) phthalocyanine-4,4′,4″,4′′′-tetrasulfonic acid (Fe(III)Pc), and gold nanoparticles (AuNPs/Fe(III)Pc/Gr/GCE). The AuNPs/Fe(III)Pc/Gr nanocomposite was prepared and characterized by using FE-SEM, EDX, and E-mapping techniques to confirm the composite formation as well as the even distribution of elements. Furthermore, the newly prepared AuNPs/Fe(III)Pc/Gr/GCE-nanocomposite-based sensor was used to detect the nicotine in phosphate-buffered solution (0.1 M PBS, pH 7.4). The AuNPs/Fe(III)Pc/Gr/GCE-based sensor offered a linear response against NIC from 0.5 to 27 µM with a limit of detection (LOD) of 17 nM using the amperometry (i–t curve) technique. This electrochemical sensor demonstrated astounding selectivity and sensitivity during NIC detection in the presence of common interfering molecules in 0.1 M PBS. Moreover, the effect of pH on NIC electro-oxidation was studied, which indicated that PBS with pH 7.4 was the best medium for NIC determination. Finally, the AuNPs/Fe(III)Pc/Gr/GCE sensor was used to accurately determine NIC concentration in human saliva samples, and the recovery percentages were also calculated. Full article

The development of materials for multiple applications is a challenge in the fields of technology and materials science. In this work, screen-printed carbon electrodes (SPCEs) were modified with an electropolymerized nickel tetrasulfonated phthalocyanine film (polymeric-NiTsPc = p-NiTsPc) decorated with gold nanoparticles (AuNP). The modified SPCEs were applied as a sensing platform for analysis via electrochemical and surface-enhanced Raman scattering (SERS) spectroscopy. The SPCEs modification was based on the potential cycling firstly in a NiTsPc solution and then in an AuHCl4 solution, with the fast formation of spherical AuNP through the p-NiTsPc film surface. The modified electrode based on SPCE/p-NiTsPc/AuNP showed a synergetic effect in voltammetric measurements in [Fe(CN)₆]³⁻/[Fe(CN)₆]⁴⁻ probe as well as an electrocatalytic effect in the presence of dopamine. The calibration curve towards dopamine detection presented a linear range from 1 to 10 μmol/L with a limit of detection of 0.73 μmol/L. The spectroelectrochemistry measurements combining SERS and the applied potential of −60 mV showed that the SPCE/p-NiTsPc/AuNP and SPCE/AuNP can be powerfully used as a dual sensing platform for dopamine detection. In the case of SPCE/p-NiTsPc/AuNP, p-NiTsPc plays an important role in facilitating electron transfer during the electrochemical reaction, while AuNP is crucial for obtaining SERS signals for dopamine detection. Full article

The goal of achieving the large-scale production of zero-emission vehicles by 2035 will create high expectations for electric vehicle (EV) development and availability. Currently, a major problem is the lack of suitable batteries and battery materials in large quantities. The rechargeable zinc–air battery (RZAB) is a promising energy-storage technology for EVs due to the environmental friendliness and low production cost. Herein, iron, cobalt, and nickel phthalocyanine tri-doped electrospun carbon nanofibre-based (FeCoNi-CNF) catalyst material is presented as an affordable and promising alternative to Pt-group metal (PGM)-based catalyst. The FeCoNi-CNF-coated glassy carbon electrode showed an oxygen reduction reaction/oxygen evolution reaction reversibility of 0.89 V in 0.1 M KOH solution. In RZAB, the maximum discharge power density (P_max) of 120 mW cm⁻² was obtained with FeCoNi-CNF, which is 86% of the P_max measured with the PGM-based catalyst. Furthermore, during the RZAB charge–discharge cycling, the FeCoNi-CNF air electrode was found to be superior to the commercial PGM electrocatalyst in terms of operational durability and at least two times higher total life-time. Full article