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Aluminum air batteries (AABs) are a desirable option for portable electronic devices and electric vehicles (EVs) due to their high theoretical energy density (8100â Wh K-1 ), low cost, and high safety compared to state-of-the-art lithium-ion batteries (LIBs). However, numerous unresolved technological and scientific issues are preventing AABs from expanding further. One of the key issues is the catalytic reaction kinetics of the air cathode as the fuel (oxygen) for AAB is reduced there. Additionally, the performance and price of an AAB are directly influenced by an air electrode integrated with an oxygen electrocatalyst, which is thought to be the most crucial element. In this study, we covered the oxygen chemistry of the air cathode as well as a brief discussion of the mechanistic insights of active catalysts and how they catalyze and enhance oxygen chemistry reactions. There is also extensive discussion of research into electrocatalytic materials that outperform Pt/C such as nonprecious metal catalysts, metal oxide, perovskites, metal-organic framework, carbonaceous materials, and their composites. Finally, we provide an overview of the present state, and possible future direction for air cathodes in AABs.
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Aluminum-air batteries (AABs) are regarded as attractive candidates for usage as an electric vehicle power source due to their high theoretical energy density (8100â Wh kg-1 ), which is considerably higher than that of lithium-ion batteries. However, AABs have several issues with commercial applications. In this review, we outline the difficulties and most recent developments in AABs technology, including electrolytes and aluminum anodes, as well as their mechanistic understanding. First, the impact of the Al anode and alloying on battery performance is discussed. Then we focus on the impact of electrolytes on battery performances. The possibility of enhancing electrochemical performances by adding inhibitors to electrolytes is also investigated. Additionally, the use of aqueous and non-aqueous electrolytes in AABs is also discussed. Finally, the challenges and potential future research areas for the advancement of AABs are suggested.
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Aqueous Zn-ion battery systems (AZIBs) have emerged as the most dependable solution, as demonstrated by successful systematic growth over the past few years. Cost effectivity, high performance and power density with prolonged life cycle are some major reason of the recent progress in AZIBs. Development of vanadium-based cathodic materials for AZIBs has appeared widely. This review contains a brief display of the basic facts and history of AZIBs. An insight section on zinc storage mechanism ramifications is given. A detailed discussion is conducted on features of high-performance and long life-time cathodes. Such features include design, modifications, electrochemical and cyclic performance, along with stability and zinc storage pathway of vanadium based cathodes from 2018 to 2022. Finally, this review outlines obstacles and opportunities with encouragement for gathering a strong conviction for future advancement in vanadium-based cathodes for AZIBs.
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In recent years, the rapid growth in renewable energy applications has created a significant demand for efficient energy storage solutions on a large scale. Among the various options, rechargeable zinc-air batteries (ZABs) have emerged as an appealing choice in green energy storage technology due to their higher energy density, sustainability, and cost-effectiveness. Regarding this fact, a spotlight is shaded on air electrode for constructing high-performance ZABs. Cobalt oxide-based electrocatalysts on the air electrode have gained significant attention due to their extraordinary features. Particularly, exploration and integration of bifunctional behavior for energy storage has remarkably promoted both ORR and OER to facilitate the overall performance of the battery. The plot of this review is forwarded towards in-depth analysis of the latest advancements in electrocatalysts that are based on cobalt oxide and possess bifunctional properties along with an introduction of the fundamental aspects of ZABs, Additionally, the topic entails an examination of the morphological variations and mechanistic details mentioning about the synthesis processes. Finally, a direction is provided for future research endeavors through addressing the challenges and prospects in the advancement of next-generation bifunctional electrocatalysts to empower high-performing ZABs with bifunctional cobalt oxide.
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Polyaniline (PANI) has piqued the interest of nanotechnology researchers due to its potential as an electrode material for supercapacitors. Despite its ease of synthesis and ability to be doped with a wide range of materials, PANI's poor mechanical properties have limited its use in practical applications. To address this issue, researchers investigated using PANI composites with materials with highly specific surface areas, active sites, porous architectures, and high conductivity. The resulting composite materials have improved energy storage performance, making them promising electrode materials for supercapacitors. Here, we provide an overview of recent developments in PANI-based supercapacitors, focusing on using electrochemically active carbon and redox-active materials as composites. We discuss challenges and opportunities of synthesizing PANI-based composites for supercapacitor applications. Furthermore, we provide theoretical insights into the electrical properties of PANI composites and their potential as active electrode materials. The need for this review stems from the growing interest in PANI-based composites to improve supercapacitor performance. By examining recent progress in this field, we provide a comprehensive overview of the current state-of-the-art and potential of PANI-based composites for supercapacitor applications. This review adds value by highlighting challenges and opportunities associated with synthesizing and utilizing PANI-based composites, thereby guiding future research directions.
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Metal-Organic Frameworks (MOFs), a novel class of porous extended crystalline structures, are favored in different fields of heterogeneous catalysis, CO2 separation and conversion, and energy storage (supercapacitors) due to their convenience of synthesis, structural tailor-ability, tunable pore size, high porosity, large specific surface area, devisable structures, and adjustable compositions. Nickel (Ni) is a ubiquitous element extensively applied in various fields of catalysis and energy storage due to its low cost, high abundance, thermal and chemical stability, and environmentally benign nature. Ni-based MOFs and their derivatives provide us with the opportunity to modify different properties of the Ni center to improve their potential as heterogeneous catalysts or energy storage materials. The recent achievements of Ni-MOFs and their derivatives as catalysts, membrane materials for CO2 separation and conversion, electrode materials and their respective performance have been discussed in this review.
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The rising energy crisis and environmental concerns caused by fossil fuels have accelerated the deployment of renewable and sustainable energy sources and storage systems. As a result of immense progress in the field, cost-effective, high-performance, and long-life rechargeable batteries are imperative to meet the current and future demands for sustainable energy sources. Currently, lithium-ion batteries are widely used, but limited lithium (Li) resources have caused price spikes, threatening progress toward cleaner energy sources. Therefore, post-Li, batteries that utilize highly abundant materials leading to cost-effective energy storage solutions while offering desirable performance characteristics are urgently needed. Aluminum-ion battery (AIB) is an attractive concept that uses highly abundant aluminum while offering a high theoretical gravimetric and volumetric capacity of 2980â mAh g-1 and 8046â mAh cm-3 , respectively. As a result, intensified efforts have been made in recent years to utilize numerous electrolytes, anodes, and cathode materials to improve the electrochemical performance of AIBs, and potentially create high-performance, low-cost, and safe energy storage devices. Herein, recent progress in the electrolyte, anode, and cathode active materials and their utilization in AIBs and their related characteristics are summarized. Finally, the main challenges facing AIBs along with future directions are highlighted.
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The high surface-to-volume ratio and desirable chemical, thermal, and catalytic properties of nanomaterials have made them promising electrode materials for sensing applications. As such, different nanomaterials and their nanocomposite-based individual and/or simultaneous detection of dihydroxybenzene (DHB) have been reported in recent years. Due to the low degradation rate and high toxicity of DHB isomers, the development of innovative and robust sensors for their simultaneous detection has received considerable attention. In this review, applications of different nanomaterials (with the exception of carbon nanotubes, graphene, and their derivatives) for individual and/or simultaneous detection of DHB are briefly discussed. The focal point is on the characteristic features of the modified electrodes that improve their electrocatalytic activities toward DHB. Real sample analysis and electrolyte media are also summarized. This review includes studies published from 2011 to 2020.
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Dihydroxybenzene is regarded as a serious environmental pollutant. Its detection through electrochemical methods is still challenging due to having a similar structure and overlapping signals with the conventional bare electrode. Thanks to the unique features and wide applicability of carbon nanotubes, graphene, and their derivatives, they can be used as modifiers to overcome the poor resolution ability of bare electrodes in the detection of dihydroxybenzene. This review focuses on the use of carbon nanotubes, graphene, and their derivatives and nanocomposites to enhance the electrocatalytic activity of conventional bare electrodes for dihydroxybenzene sensing. The reports from 2011-2020 on the simultaneous and/or individual detection of three different dihydroxybenzenes - hydroquinone, catechol, and resorcinol - are summarized. This review also highlights the challenges and prospects surrounding the sensitive and selective detection of dihydroxybenzene.
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The development of efficient supercapacitors hinges on the innovation of superior electrodes, which are pivotal in augmenting their energy storage capabilities. Supercapacitors, recognized for their high-power density and extended cycle life, play a crucial role as sustainable solutions in addressing energy storage challenges. A fundamental aspect of supercapacitor functionality involves the electrode material, which works in concert with other key components such as the current collector, separator, and electrolyte. This study focuses on evaluating the impact of the current collector material on the performance of symmetric supercapacitors. We investigated the electropolymerization of polyaniline on woven steel mesh current collectors of varying mesh sizes, ranging from 20 to 200â mesh per inch, using assorted deposition conditions. The electrochemically modified woven steel meshes were utilized to construct symmetric supercapacitors. The electrochemical performance of the assembled supercapacitors, configured in a two-electrode system, was investigated using a variety of electrochemical techniques to better understand the kinetics of electrolyte ion migration. Notably, the 20-mesh size, characterized by the fewest pores per inch, demonstrated superior performance with an optimum capacitance of 4730â mF/cm2, an energy density of 317.8â µWh/cm2, and a power density of 400â µW/cm2 at a current density of 1â mA/cm2.
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In the realm of material science, carbon materials, especially olive-derived carbon (ODC), have become vital due to their sustainability and diverse properties. This review examines the sustainable extraction and use of ODC, a carbohydrate-rich by-product of olive biomass. We focus on innovative preparation techniques like pyrolysis, which are crucial forenhancing ODC's microstructure and surface properties. Variables such as activating agents, impregnation ratios, and pyrolysis conditions significantly influence these properties. ODC's high specific surface area renders it invaluable for applications in energy storage (batteries and supercapacitors) and environmental sectors (water purification, hydrogen storage). Its versatility and accessibility underscore its potential for broad industrial use, makingit as a key element in sustainable development. This review provides a detailed analysis of ODC preparation methodologies, its various applications, and its role in advancing sustainable energy solutions. We highlight the novelty of ODC research and its impact on future studies, establishing this review as a crucial resource for researchers and practitioners in sustainable carbon materials. As global focus shifts towards eco-friendly solutions, ODC emerges as a critical component in shaping a sustainable, innovation-driven future.
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To combat with energy crisis considering clean energy, oxygen evolution reaction (OER) is crucial to implement electrolytic hydrogen fuel production in real life. Here, straightforward chemical synthesis pathways are followed to prepare cobalt tetraoxide nanoparticles (Co3 O4 NPs) in an alkaline OER process using poly[(2-methacryloyloxy)ethyl]trimethylammonium chloride (Co3 O4 NPs@PMTC) as support to prevent aggregation. In material characterization, the X-ray diffraction (XRD) pattern confirms the crystallinity of the synthesized Co3 O4 NPs@PMTC, and Raman spectroscopy indicates that the Co3 O4 NPs contain cubic close-packed oxides. The morphological analysis reveals the wrinkle-like disruption which is distributed evenly owing to the folded nanosheet arrays. Energy-dispersive X-ray spectroscopy indicates the presence of a significant number of cobalt atoms in the Co3 O4 NPs, and elemental mapping analysis demonstrates the composition of the NPs. At a current density of 10â mA cm-2 , oxygen is emitted at 1.67â V delivering an overpotential of 440â mV. This unique structure of Co3 O4 NPs@PMTC provides beneficial functions that are responsible for a large number of active sites and the rapid release of oxygen gas with long-term stability. Through kinetic study, we found a Tafel slope of 48.9â mV dec-1 which proves the catalytic behavior of Co3 O4 NPs@PMTC is promising toward the OER process.
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Electrochemical capacitors, also known as supercapacitors (SCs), have lately played an important role in energy storage and conversion systems due to their specific characteristics such as high strength, durability, and environmental friendliness. A wide range of materials is used as electrodes for SC applications because the electrochemical efficiency is primarily determined by the electrode materials used. Carbonaceous materials with unique surface, chemical, electrochemical, and electronic characteristics have become attractive for energy storage research, but they cannot meet the rising need for high specific energy and specific power. Besides, heteroatom-doped carbon materials have shown pseudocapacitance characteristics and improved specific energy, specific power, and conductivity. This makes them more adaptable in SC application. Among different heteroatom doping of carbon, S-doped carbon has gained considerable attention in SC applications due to its unpaired electrons and easily polarizable nature. S-doped carbon materials-based SCs have demonstrated enhanced surface wettability, improved conductivity, and induced pseudocapacitance effect, thereby delivering improved specific energy and specific power. Many reports on S-doped carbon for SC applications have been published, but there is no specific Review on the preparation of S-doped carbon for SC applications. This Review focuses on recent developments in the field of SC electrodes made from S-doped carbon materials. Herein, the preparation methods and applications of S-doped carbon for SCs were summarized following a brief discussion of different electrochemical characterization techniques of SCs. Finally, the challenges of S-doped carbon materials and their potential prospects were discussed to give crucial insights into the favorable factors for future innovations of SC electrodes. This Review aims to provide insight for further research on the preparation of S-doped carbon for electrochemical energy storage applications.
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Nitrite is one of the abundant toxic components existing in the environment and is likely to have a great potential to affect human health badly. For that reason, it has become crucial to build a reliable nitrite detection method. In recent years, several nitrite monitoring systems have been proposed. Compared with traditional analytical strategies, the electrochemical approach has a bunch of advantages, including low cost, rapid response, easy operation, simplicity, etc. In this case, noble metal nanomaterials, especially Au-based nanomaterials, have attracted attention in electrode modification because of higher catalytic activity, facile mass transfer, and broad active area for determining nitrite. This review is based on the state-of-the-art, which includes a variety of nanomaterials that have been coupled with gold nanoparticles (AuNPs) for the creation of nanocomposites, and the construction as well as development of electrochemical sensors for nitrite detection over the last few years (2016-2022). A background study on synthesizing different morphological AuNPs and nanocomposites has also been introduced. The fabrication methods and sensing capabilities of modified electrodes are given special consideration.
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Técnicas Biosensibles , Nanopartículas del Metal , Nanocompuestos , Humanos , Oro , Nitritos , Técnicas Electroquímicas/métodos , Límite de Detección , Electrodos , Técnicas Biosensibles/métodosRESUMEN
Direct attachment of gold nanoparticles to a green support without the use of an external reducing agent and using it for removing toxic pollutants from wastewater, i. e., reduction of nitroarene to amine, are described. A novel approach involving the reduction of gold by the jute plant (Corchorus genus) stem-based (JPS) support itself to form nanoparticles (AuNPs) to be used as a catalytic system ('dip-catalyst') and its catalytic activity for the hydrogenation of series of nitroarenes in aqueous media are presented. AuNPs/JPS catalyst was characterized using SEM, UV-Vis, FTIR, TEM, XPS, and ICP-OES. Confined area elemental mapping exhibits uniform and homogeneous distribution of AuNPs on the support surface. TEM shows multi-faceted AuNPs in the range of 20-30â nm. The reactivity of AuNPs/JPS for the transfer hydrogenation of nitroarene as well as hydrogenation of quinoline under molecular H2 pressure was evaluated. Sodium borohydride, when used as the hydrogen source, demonstrates a high catalytic efficiency in the transfer hydrogenation reduction of 4-nitrophenol (4-NP). Quinoline is quantitatively and chemoselectively hydrogenated to 1,2,3,4-tetrahydroquinoline (py-THQ) using molecular hydrogen. Reusability studies show that AuNPs are stable on the support surface and their selectivity is not affected.
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Nanopartículas del Metal/química , Nitrobencenos/química , Quinolinas/química , Compuestos de Anilina/síntesis química , Catálisis , Corchorus/química , Oro/química , Tecnología Química Verde/instrumentación , Hidrogenación , Modelos Químicos , Oxidación-Reducción , Tallos de la Planta/química , Quinolinas/síntesis químicaRESUMEN
Dopamine (DA) is an important neurotransmitter, which is created and released from the central nervous system. It plays a crucial role in human activities, like cognition, emotions, and response to anything. Maladjustment of DA in human blood serum results in different neural diseases, like Parkinson's and Schizophrenia. Consequently, researchers have started working on DA detection in blood serum, which is undoubtedly a hot research area. Electrochemical sensing techniques are more promising to detect DA in real samples. However, utilizing conventional electrodes for selective determination of DA encounters numerous problems due to the coexistence of other materials, such as uric acid and ascorbic acid, which have an oxidation potential close to DA. To overcome such problems, researchers have put their focus on the modification of bare electrodes. The aim of this review is to present recent advances in modifications of most used bare electrodes with carbonaceous materials, especially graphene, its derivatives, and carbon nanotubes, for electrochemical detection of DA. A brief discussion about the mechanistic phenomena at the electrode interface has also been included in this review.
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Dopamina/análisis , Técnicas Electroquímicas , Grafito/química , Nanotubos de Carbono/química , HumanosRESUMEN
Nano-Co3 O4 was used for electrocatalytic water oxidation due to its promising features of better performance and low cost. An enhanced electrochemical water oxidation performance of the nanoparticles can be achieved by mixing them with other types of highly conductive nano/micro-structured materials. Conductive polymers would be one of the candidates to achieve this goal. Here, we report our recently developed nano-Co3 O4 and polypyrrole composites for enhanced electrochemical water oxidation. We chose polypyrrole as a support of nano-Co3 O4 to obtain highly active sites of nano-Co3 O4 with high conductivity. Morphological and chemical characterization of the prepared materials were performed using scanning electron microscopy (SEM), energy-dispersive spectroscopy (EDS), and X-ray photoelectron spectroscopy (XPS). After immobilizing them individually on fluorine doped tin oxide (FTO) substrate, their electrocatalytic properties toward water oxidation were investigated. The optimum composite materials showed significantly higher electrocatalytic properties compared to that of pure nano-Co3 O4 and polypyrrole. Electrochemical impedance studies indicated that the composite materials possess significantly less electron transfer resistance toward water oxidation reaction compared to that of only polypyrrole or nano-Co3 O4 , while the higher double-layer capacitance and polarization resistance values obtained from fitting of the impedance data represent the faster electrode kinetics in the composite electrocatalyst. Due to the synergetic effect, the optimum nano-Co3 O4 and polypyrrole composites could be represent a novel and promising material for water oxidation.