Search Results (122)

MXenes, a family of two-dimensional carbide and nitride nanomaterials, have demonstrated significant promise across various technological domains, particularly in energy storage applications. This review critically examines scalable synthesis techniques for MXenes and their potential integration into next-generation rechargeable battery systems. We highlight both top-down and emerging bottom-up approaches, exploring their respective efficiencies, environmental impacts, and industrial feasibility. The paper further discusses the electrochemical behavior of MXenes in lithium-ion, sodium-ion, and aluminum-ion batteries, as well as their multifunctional roles in solid-state batteries—including as electrodes, additives, and solid electrolytes. Special emphasis is placed on surface functionalization, interlayer engineering, and ion transport properties. We also compare MXenes with conventional graphite anodes, analyzing their gravimetric and volumetric performance potential. Finally, challenges such as diffusion kinetics, power density limitations, and scalability are addressed, providing a comprehensive outlook on the future of MXenes in sustainable energy storage technologies. Full article

Germanium/tin-containing silicon oxide [SiO–(GeO/SnO)] nanoclusters have been designed with different Si/Ge/Sn particles and characterized as electrodes for magnesium-ion batteries (MIBs) due to forming MgBe [SiO–GeO], MgBe [SiO–SnO], MgCa [SiO–GeO], and MgCa [SiO–SnO] complexes. In this work, alkaline earth metals of magnesium (Mg), beryllium (Be), and calcium (Ca) have been studied in hybrid Mg-, Be-, and Ca-ion batteries. An expanded investigation on H capture by MgBe [SiO–(GeO/SnO)] or MgCa [SiO–(GeO/SnO)] complexes was probed using computational approaches due to density state analysis of charge density differences (CDD), total density of states (TDOS), and electron localization function (ELF) for hydrogenated hybrid clusters of MgBe [SiO–GeO], MgBe [SiO–SnO], MgCa [SiO–GeO], and MgCa [SiO–SnO]. Replacing Si by Ge/Sn content can increase battery capacity through MgBe [SiO–GeO], MgBe [SiO–SnO], MgCa [SiO–GeO], and MgCa [SiO–SnO] nanoclusters for hydrogen adsorption processes and could improve the rate performances by enhancing electrical conductivity. A small portion of Mg, Be, or Ca entering the Si–Ge or Si–Sn layer to replace the alkaline earth metal sites could improve the structural stability of the electrode material at high multiplicity, thereby improving the capacity retention rate. In fact, the MgBe [SiO–GeO] remarks a small enhancement in charge transfer before and after hydrogen adsorption, confirming the good structural stability. In addition, [SiO–(GeO/SnO)] anode material could augment the capacity owing to higher surface capacitive impacts. Full article

The transition toward sustainable and decentralized energy solutions necessitates the development of innovative bioelectronic systems capable of harvesting and converting renewable energy. Here, we present a novel photo-bioelectrochemical fuel cell architecture based on a biohybrid anode integrating laser-induced graphene (LIG), poly(3,4-ethylenedioxythiophene) (PEDOT), and isolated thylakoid membranes. LIG provided a porous, conductive scaffold, while PEDOT enhanced electrode compatibility, electrical conductivity, and operational stability. Compared to MXene-based systems that involve complex, multi-step synthesis, PEDOT offers a cost-effective and scalable alternative for bioelectrode fabrication. Thylakoid membranes were immobilized onto the PEDOT-modified LIG surface to enable light-driven electron generation. Electrochemical characterization revealed enhanced redox activity following PEDOT modification and stable photocurrent generation under light illumination, achieving a photocurrent density of approximately 18 µA cm⁻². The assembled photo-bioelectrochemical fuel cell employing a gas diffusion platinum cathode demonstrated an open-circuit voltage of 0.57 V and a peak power density of 36 µW cm⁻² in 0.1 M citrate buffer (pH 5.5) under light conditions. Furthermore, the integration of a charge pump circuit successfully boosted the harvested voltage to drive a low-power light-emitting diode, showcasing the practical viability of the system. This work highlights the potential of combining biological photosystems with conductive nanomaterials for the development of self-powered, light-driven bioelectronic devices. Full article

This paper investigated the preparation of NiSb/NiSe nanomaterials using a microwave method and explored their electrochemical properties and potential applications in supercapacitors. The NiSb/NiSe nanomaterials were synthesized on nickel foam using microwave radiation, resulting in uniformly distributed flower-like nanostructures. This structure not only provided abundant electrochemical reaction sites, but also improved the electrical conductivity and ion diffusion, contributing to the overall performance of supercapacitors. Electrochemical tests showed that the NiSb/NiSe material exhibited a high specific capacity of 525 mAh g⁻¹ at 1 A g⁻¹ and maintained 65% capacity after 8000 cycles, demonstrating excellent cycling stability and battery-type charge storage capability. In addition, a hybrid supercapacitor assembled using NiSb/NiSe as the anode material and activated carbon (AC) as the cathode material achieved an energy density of 100.34 Wh kg⁻¹ at a power density of 774.9 W kg⁻¹, significantly enhancing energy storage efficiency. The effect of different microwave powers and reaction times on the morphology and electrochemical properties of the materials were further investigated, with the optimal preparation conditions found to be 800 W and 150 s. The NiSb/NiSe materials synthesized under this condition not only have the best electrochemical properties, but also exhibit low charge transfer impedance and excellent electrical conductivity. In summary, NiSb/NiSe flower-like nanomaterials as supercapacitor electrode materials demonstrate great potential for energy storage applications due to their high specific capacity, good cycling stability and high energy density. Full article

Amperometric biosensors (ABSs) and enzymatic biofuel cells (BFCs) share several fundamental principles in their functionality, despite serving different primary purposes. Both devices rely on biorecognition, redox reactions, electron transfer (ET), and advanced electrode materials, including innovative nanomaterials (NMs). ABSs and BFCs, utilizing microbial oxidoreductases in combination with electroactive NMs, are both efficient and cost-effective. In the current study, several laboratory prototypes of BFCs have been developed with bioanodes based on yeast flavocytochrome b₂ (Fcb₂) and alcohol oxidase (AO), and a cathode based on fungal laccase. For the first time, BFCs have been developed featuring anodes based on Fcb₂ co-immobilized with redox NMs on a glassy carbon electrode (GCE), and cathode-utilizing laccase combined with gold–cerium–platinum nanoparticles (nAuCePt). The most effective lactate BFC, which contains gold–hexacyanoferrate (AuHCF), exhibited a specific power density of 1.8 µW/cm². A series of BFCs were developed with an AO-containing anode and a laccase/nAuCePt/GCE cathode. The optimal configuration featured a bioanode architecture of AO/nCoPtCu/GCE, achieving a specific power density of 3.2 µW/cm². The constructed BFCs were tested using lactate-containing food product samples as fuels. Full article

Anodic aluminum oxide (AAO) is a promising material for sensor applications due to its unique nanoporous structure and high surface area. This study investigates enhancing AAO’s sensing capabilities by incorporating carbyne-enriched nanomaterials. This research aimed to create a novel surface acoustic wave (SAW) sensor with improved performance characteristics. AAO films were fabricated using a two-step anodization process, followed by carbyne-enriched coating deposition via ion-assisted pulse-plasma deposition. The dielectric properties of the resulting composite material were characterized using impedance spectroscopy, while the sensing performance was evaluated by exposing the sensor to various ethanol concentrations. The results showed a significant increase in capacitance and dielectric permittivity for the carbyne-filled AAO compared to pristine AAO, along with a 5-fold improvement in sensitivity to ethanol vapor. The increased sensitivity is attributed to the synergistic combination of the AAO’s high surface area and the carbyne’s unique electrical properties. This work demonstrates the successful fabrication and characterization of a novel high-sensitivity gas sensor, highlighting the potential of carbyne-enriched AAO for advanced sensor applications. Full article

This review paper explores the emerging field of conversion cathode materials, which hold significant promises for advancing the performance of lithium-ion (LIBs) and lithium–sulfur batteries (LSBs). Traditional cathode materials of LIBs, such as lithium cobalt oxide, have reached their limits in terms of energy density and capacity, driving the search for alternatives that can meet the increasing demands of modern technology, including electric vehicles and renewable energy systems. Conversion cathodes operate through a mechanism involving complete redox reactions, transforming into different phases, which enables the storage of more lithium ions and results in higher theoretical capacities compared to conventional intercalation materials. This study examines various conversion materials, including metal oxides, sulfides, and fluorides, highlighting their potential to significantly enhance energy density. Despite their advantages, conversion cathodes face numerous challenges, such as poor conductivity, significant volume changes during cycling, and issues with reversibility and stability. This review discusses current nanoengineering strategies employed to address these challenges, including nano structuring, composite formulation, and electrolyte optimization. By assessing recent research and developments in conversion cathode technology, this paper aims to provide a comprehensive overview of their potential to revolutionize lithium-ion batteries and contribute to the future of energy storage solutions. Full article

Quantum dots (QDs) are emerging as a new class of zero-dimensional nanomaterials with semiconducting properties. Among many applications, QDs find useful employment in high-capacity electrodes in secondary batteries by virtue of their nanodimension. The recent advancements of QDs and their application as QD-based nanocomposites in electrodes are published in numerous accounts. Well-dispersed QDs in conductive carbonaceous materials can lead to the formation of nanocomposites with excellent cyclic stabilities and large reversible capacities, which are suitable for applications in many batteries. Inorganic QDs are also being investigated as potential candidates to fabricate nanocomposites in different secondary batteries. However, there are not many review articles available detailing the synthetic methodologies used to fabricate such QD-based nanocomposites along with their electrochemical properties. In this article, we are documenting a comprehensive review of a variety of QD nanocomposites with their manufacturing processes and successful utilization in battery applications. We will be highlighting the application of QD-based nanocomposites as anode and cathode materials for applications in different secondary batteries and discussing the enhancement of the electrochemical performances of such batteries in terms of energy density and cyclability. Full article

Aqueous zinc batteries, mainly including Zn-ion batteries (ZIBs) and Zn–air batteries (ZABs), are promising energy storage systems, but challenges exist at their current stage. For instance, the zinc anode in aqueous electrolyte is impacted by anodic dendrites, hydrogen and oxygen precipitation, and some other harmful side reactions, which severely affect the battery’s lifespan. As for traditional cathode materials in ZIBs, low electrical conductivity, slow Zn²⁺ ion migration, and easy collapse of the crystal structure during ion embedding and migration bring challenges. Also, the slower critical oxygen reduction reaction (ORR), for example, in ZABs shows unsatisfactory results. All these issues greatly hindered the development of zinc batteries. Aerogel materials, characterized by their high specific surface area, unique open-pore structure formed by nanoporous structures, and excellent physicochemical properties, have a positive role in cathode modification, electrode protection, and catalytic reactions in zinc batteries. This manuscript provides a systematic review of aerogel materials, highlighting advancements in their preparation and application for zinc batteries, aiming to promote the future progress and development of aerogel nanomaterials and zinc batteries. Full article

Heavy metal pollution has become an increasingly serious environmental issue, making the detection of heavy metals essential for safeguarding public health and the environment. This review aims to highlight the commonly used methods for detecting heavy metals (such as atomic absorption spectroscopy (AAS), atomic emission spectroscopy (AES), inductively coupled plasma–mass spectrometry (ICP-MS), square-wave anodic stripping voltammetry (SWASV), etc.), with a particular focus on electrochemical detection and electrode modification materials. Metal nanomaterials (such as titanium dioxide (TiO₂), copper oxide (CuO), ZIF-8, MXene, etc.) are emphasized as promising candidates for enhancing the performance of sensors due to their high surface area and excellent catalytic properties. However, challenges such as interference from non-target heavy metal ions and the formation of organometallic complexes with organic compounds can complicate the detection process. To address these issues, two potential solutions have been proposed: the development of advanced algorithms (such as machine learning (ML), back-propagation neural network (BPNN), support vector machines (SVM), random forests (RF), etc.) for signal processing and the use of pretreatment methods (such as Fenton oxidation (FO), ozone oxidation, and photochemical oxidation) to suppress such interferences. This paper aims to review commonly used methods for detecting heavy metals, with a particular emphasis on electrochemical techniques. It will also highlight the challenges faced in these methods, such as interference and sensitivity limitations, and propose innovative solutions, including the use of metal nanomaterials for improved sensor performance and the integration of advanced algorithms and pretreatment techniques to address interference and enhance detection accuracy. Full article

Indium oxide (In₂O₃) is a promising anode material for next-generation lithium-ion batteries and is prized for its high electrical conductivity, environmental friendliness, and high theoretical capacity. However, its practical application is significantly limited by severe volume expansion and contraction during the lithium insertion/extraction process. This volume change disrupts the solid electrolyte interphase (SEI) and degrades contact with the current collector, undermining battery performance. Although the nano-structured design of In₂O₃ can mitigate the volume effect to some extent, pure In₂O₃ nanomaterials are prone to agglomeration during frequent charging and discharging. The pure In₂O₃-based electrode shows a sustained and rapid capacity degradation. In this study, we embed ultrafine In₂O₃ particles in a carbon nanofiber framework using electrospinning and thermal annealing. The 1D carbon nanofiber structure provides an effective electronic conductive network and reduces the length of lithium-iondiffusion, which enhances the reactivity of the nanocomposite and improves electrode kinetics. Additionally, the carbon nanofiber framework isolates ultrafine In₂O₃ particles, preventing their aggregation. The small volume changes due to the ultrafine size of the In₂O₃ are buffered by the carbon materials, allowing the overall structure of the In₂O₃/C composite nanofiber to remain largely intact without crushing during charging and discharging cycles. This stability helps avoid electrode fracture and excessive SEI growth, resulting in superior cycle and rate performance compared with the pure In₂O₃ nanofiber electrodes. Full article

Microbial fuel cells (MFCs) are a candidate for green energy sources due to microbes’ ability to generate charge in their metabolic processes. The main problem in MFCs is slow charge transfer between microorganisms and electrodes. Several methods to improve charge transfer have been used until now: modification of microorganisms by conductive polymers, use of lipophilic mediators, and conductive nanomaterials. We created an MFC with a graphite anode, covering it with 9,10-phenatrenequinone and polypyrrole-modified Saccharomyces cerevisiae with and without 10 nm sphere gold nanoparticles. The MFC was evaluated using cyclic voltammetry and power density measurements. The peak current from cyclic voltammetry measurements increased from 3.76 mA/cm² to 5.01 mA/cm² with bare and polypyrrole-modified yeast, respectively. The MFC with polypyrrole- and nanoparticle-modified yeast reached a maximum power density of 150 mW/m² in PBS with 20 mM Fe(III) and 20 mM glucose, using a load of 10 kΩ. The same MFC with the same load in wastewater reached 179.2 mW/m². These results suggest that this MFC configuration can be used to improve charge transfer. Full article

A Pb-containing PtAu nanoflower electrocatalyst was deposited on the cathode via galvanic replacement reaction in a double-cabin galvanic cell (DCGC) with a Cu plate as the anode, a multiwalled carbon nanotube (MWCNT) modified glassy carbon electrode (GCE) as the cathode, 0.1 M HClO₄ aqueous solution as the anolyte, and Pb²⁺-containing Pt⁴⁺ salt and Au³⁺ salt mixed aqueous solution as the catholyte, respectively, and the electrocatalytic performance of the modified electrode toward methanol oxidation in the alkaline medium was investigated. Electrochemical studies reveal that the stripping of bulk Cu can induce underpotential deposition (UPD) of Pb on Pt during the galvanic replacement reaction, which affects the morphology and composition of Pb-containing PtAu nanoparticles. Under the optimal experimental conditions, a Pb-Pt₃Au₁/MWCNTs/GCE shows the highest activity and the best stability toward electrocatalytic oxidation of methanol in the alkaline medium, and the Pt active area-normalized specific electrocatalytic activity of Pb-Pt₃Au₁/MWCNTs/GCE is as high as 59.8 mA cm_Pt⁻². We believe that the method presented here of depositing highly active noble metal nanostructures by galvanic replacement reaction in a DCGC device is expected to be widely applied in the preparation of nanomaterials for their study in fuel cells and electrocatalysis. Full article

In this study, we have synthesized a nanostructured core–shell framework of carbon-coated copper sulfide (C@CuS) through a one-step precipitation technique. The carbon sphere template facilitated the nucleation of CuS nanostructures. The synthesized nanocomposites have demonstrated remarkable lithium-ion storage capabilities when utilized as an anode in lithium-ion batteries. Notably, they exhibit an impressive rate capability of 314 mAh g⁻¹ at a high current density of 5000 mA g⁻¹, along with excellent long-term cycle stability, maintaining 463 mAh g⁻¹ at 1000 mA g⁻¹ after 800 cycles. This superior performance is due to the core–shell architecture of the composite, where the carbon core enhances the conductivity of CuS nanoparticles and mitigates volume expansion, thus preventing capacity loss. Our study not only elucidates the significance of carbon in the construction of nano-heterojunctions or composite electrodes but also presents a practical approach to significantly boost the electrochemical performance of CuS and other metal sulfides. 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