Active Material Research Articles

Layered high-entropy sulfides: boosting electrocatalytic performance for hydrogen evolution reaction by cocktail effects

Abstract This study explores high-entropy sulfides (HESs) as potential electrocatalysts for the hydrogen evolution reaction (HER). Novel Pa-3 and Pnma structured HESs containing Fe, Mn, Ni, Co and Mo, were synthesized via a facile mechanochemical method. Structural and chemical properties were extensively characterized using x-ray diffraction, transmission electron microscopy, energy-dispersive x-ray spectroscopy, and x-ray photoelectron spectroscopy. The electrocatalytic performance of four as-prepared HESs in alkaline electrolyte for HER reveals the remarkable outperformance compared to medium-entropy and conventional sulfides. Particularly, (Fe0.2Mn0.2Ni0.2Co0.2Mo0.2)S2 demonstrated outstanding activities, with minimal overpotentials (187 mV at 10 mA cm–2) and outstanding durability under harsh alkaline conditions (a mere polarization increase ΔE = 17 mV after 14 h via chronopotentiometry). The remarkable catalytic activities can be attributed to synergistic effects resulting from the cocktail effects within the high-entropy disulfide. The introduction of Mo contributes to the formation of a layered structure, which leads to an increased surface area and thus to a superior HER performance compared to other HES and conventional sulfides. This work demonstrates the promising potential of HES and underscores that further development for catalytic applications paves the way for innovative routes to new and more efficient active materials for HER catalysis.

Construction of Chiral Covalent Organic Frameworks Through a Linker Decomposition Chiral Induction Strategy for Circularly Polarized Light Detection

AbstractExploring new strategies for construction of chiral covalent organic frameworks (COFs) is of paramount importance yet remains a challenge. Herein, we report the rational design and construction of chiral COFs through a linker decomposition chiral induction (LDCI) strategy. Three pairs of azine‐linked chiral COFs are successfully synthesized by the condensation reactions of C3‐symmetric 4,4′,4′′‐(1,3,5‐triazine‐2,4,6‐triyl)tribenzaldehyde (Tz) with flexible chiral dihydrazide linkers derived from malic acid, aspartic acid and tartaric acid, respectively. Remarkably, upon complete or partial decomposition from flexible chiral dihydrazides to hydrazine during COF synthesis, the homochirality of these COFs, originating from the single‐handedness conformation of propeller‐like Tz cores, is well preserved. Such a stereoselective chiral memory realized via the LDCI strategy is confirmed by time‐dependent powder X‐ray diffraction (PXRD), Fourier transform infrared (FT‐IR) and diffuse reflectance circular dichroism (DRCD). Moreover, the resultant azine‐linked chiral COFs are used as the active materials to fabricate photodetectors to directly distinguish circularly polarized light (CPL), showing impressive recognition performances on the identification of left‐handed circularly (LHC) and right‐handed circularly (RHC) polarized lights. Notably, the residual undecomposed flexible chiral linkers within the COFs are found to be conducive to improving the polarization discrimination ratio. This work highlights LDCI as a new and effective strategy for constructing homochiral COFs with promising future in chiral optical application.

High‐Entropy Electrolyte Driven by Multi‐Solvation Structures for Long‐Lifespan Aqueous Zinc Metal Pouch Cells

Aqueous zinc metal batteries (AZMBs) are promising for grid‐scale energy storage due to their low cost and high safety. However, poor stability and an unfavorable freezing point hinder their actual application. Herein, a ternary salts‐based high‐entropy electrolyte (HEE) composed of Zn0.2Na0.4Li0.4(ClO4)1.2·7H2O is proposed to address the above issues. The addition of perchlorate salts with different cations reduces the size of ion clusters, significantly increases the solvation structure species, and promotes the anion‐rich Zn2+ solvation structures, resulting in an enlarged electrochemical stability window, favorable viscosity and ionic conductivity, and low freezing point. Furthermore, characterization and calculations confirm that multiple types of solvation structures effectively increase the electrolyte entropy. As a consequence, the Zn/Zn symmetric cells in HEE can sustainably cycle for at least 1000 hours and 1500 hours under room and subzero temperatures, respectively. The Na0.33V2O5/Zn and polyaniline/Zn full cells can even last for 30000 and 20000 cycles without capacity decay at −20 °C, respectively. The pouch cells employing HEE deliver promising capacity and stability, even at high mass loading of active materials. This strategy of introducing multiple salts with different cations to construct a high‐entropy environment provides a facile approach for high‐performance and long‐lifespan AZMBs across a wide temperature range.

High-Entropy Electrolyte Driven by Multi-Solvation Structures for Long-Lifespan Aqueous Zinc Metal Pouch Cells.

Aqueous zinc metal batteries (AZMBs) are promising for grid-scale energy storage due to their low cost and high safety. However, poor stability and an unfavorable freezing point hinder their actual application. Herein, a ternary salts-based high-entropy electrolyte (HEE) composed of Zn0.2Na0.4Li0.4(ClO4)1.2·7H2O is proposed to address the above issues. The addition of perchlorate salts with different cations reduces the size of ion clusters, significantly increases the solvation structure species, and promotes the anion-rich Zn2+ solvation structures, resulting in an enlarged electrochemical stability window, favorable viscosity and ionic conductivity, and low freezing point. Furthermore, characterization and calculations confirm that multiple types of solvation structures effectively increase the electrolyte entropy. As a consequence, the Zn/Zn symmetric cells in HEE can sustainably cycle for at least 1000 hours and 1500 hours under room and subzero temperatures, respectively. The Na0.33V2O5/Zn and polyaniline/Zn full cells can even last for 30000 and 20000 cycles without capacity decay at -20 °C, respectively. The pouch cells employing HEE deliver promising capacity and stability, even at high mass loading of active materials. This strategy of introducing multiple salts with different cations to construct a high-entropy environment provides a facile approach for high-performance and long-lifespan AZMBs across a wide temperature range.

Construction of Chiral Covalent Organic Frameworks Through a Linker Decomposition Chiral Induction Strategy for Circularly Polarized Light Detection

AbstractExploring new strategies for construction of chiral covalent organic frameworks (COFs) is of paramount importance yet remains a challenge. Herein, we report the rational design and construction of chiral COFs through a linker decomposition chiral induction (LDCI) strategy. Three pairs of azine‐linked chiral COFs are successfully synthesized by the condensation reactions of C3‐symmetric 4,4′,4′′‐(1,3,5‐triazine‐2,4,6‐triyl)tribenzaldehyde (Tz) with flexible chiral dihydrazide linkers derived from malic acid, aspartic acid and tartaric acid, respectively. Remarkably, upon complete or partial decomposition from flexible chiral dihydrazides to hydrazine during COF synthesis, the homochirality of these COFs, originating from the single‐handedness conformation of propeller‐like Tz cores, is well preserved. Such a stereoselective chiral memory realized via the LDCI strategy is confirmed by time‐dependent powder X‐ray diffraction (PXRD), Fourier transform infrared (FT‐IR) and diffuse reflectance circular dichroism (DRCD). Moreover, the resultant azine‐linked chiral COFs are used as the active materials to fabricate photodetectors to directly distinguish circularly polarized light (CPL), showing impressive recognition performances on the identification of left‐handed circularly (LHC) and right‐handed circularly (RHC) polarized lights. Notably, the residual undecomposed flexible chiral linkers within the COFs are found to be conducive to improving the polarization discrimination ratio. This work highlights LDCI as a new and effective strategy for constructing homochiral COFs with promising future in chiral optical application.

Bilayer Boost to UV Assisted Supercapacitors: Enhanced Performance with Transparent TiO2/MoO3 Heterojunction Electrode

Photo‐assisted supercapacitor is a promising smart device component for achieving both energy conversion and storage. The photo‐assisted functionality in a supercapacitor is realized through the choice of photo responsive electrode material under suitable illumination conditions. The well‐known electrochemically active electrode materials are wide band gap semiconductors which absorb strongly in UV light. However, most of the prior studies on photo‐assisted supercapacitors used visible light. Herein, we present a transparent TiO2/MoO3 bi‐layer heterojunction made by simple solution process as an efficient electrode for photo‐assisted supercapacitors under UV light illumination. The electrochemical performance of the electrode is significantly enhanced even with a less intense (0.05mW/cm2) UV light, compared to dark as well as the single layer electrode under same illumination condition. The highest areal capacitance of 63.25 mF/cm2 at 0.1 mA/cm2 is achieved, that surpasses most of the recent relevant reports. The synergetic effect of UV illumination and the built‐in potential at the type II heterojunction interface encourages ion insertion and better collection of the photo‐generated carriers. The unique bi‐layer design also leads to better rate capability features. Thus, the work presents a new prospect for the development of transparent energy storage devices to be used in future smart technologies.

2D Graphene‐Like Carbon Coated Solid Electrolyte for Reducing Inhomogeneous Reactions of All‐Solid‐State Batteries

AbstractRecent studies have identified an imbalance between the electronic and ionic conductivities as the drivers of inhomogeneous reactions in composite cathodes, which cause the rapid degradation of all‐solid‐state battery (ASSB). To mitigate localized overcharge and utilize isolated active materials, the study proposes the coating of an argyrodite‐type Li6PS5Cl solid electrolyte (SE) with graphene‐like carbon (GLC@LPSCl), a 2D conductive material, to offer a continuous three‐dimensionally connected electron pathway within the composite cathode to facilitate ion mobility and promote homogeneous reactions. Despite reducing the content of the conducting agent, it is observed that the GLC@LPSCl cell exhibits high initial Coulombic efficiency and discharge capacity, reducing the inhomogeneous reactivity after 200 cycles compared with when ordinary conductive agents are deployed. Additionally, the presence of GLC@LPSCI surface suppresses the interfacial reaction between SE–cathode material, thus imparting the cell with excellent capacity retention (≈90%) after 200 cycles. Furthermore, the cell performance improves even after a fourfold increase in the cathode loading amount, demonstrating the criticality of a well‐developed continuous electron pathway to cell performance and highlighting the key role of ensuring a balance between the electron and ion conductivities in the development of high‐energy‐density and high‐power ASSBs.

In-Situ Constructing N,S-Codoped Carbon Heterointerface for High-Rate Cathode of Sodium-Ion Batteries.

Na3V2(PO4)3 (NVP) is considered one of the promising choices for cathodes of sodium-ion batteries, but the poor conductivity resulted inferior rate performance limited the practical development of NVP cathodes. In this study, we successfully synthesized N/S dual-atom doped carbon coatings in situ through a simple one-step solid-state sintering method. The uniformly coated carbon layer can inhibit the agglomeration and growth of active materials during the sintering process, shorten the Na+ migration path, and increase the contact area with the electrolyte, thus facilitating rapid Na+ migration. Notably, the doping of N elements can alter the electron distribution of carbon coating, enhancing electron conductivity. Furthermore, the introduction of S elements in the carbon layer can induce the formation of stable C-S-C bonds in the molecular layer, expanding the interlayer spacing, which is beneficial for Na+ transport and storage. Therefore, the modified NVP@NSC composite provides a high specific capacity of 90.3 mAh g-1 at a rate of 20 C, with a capacity retention rate of 94.4% after 8000 cycles, demonstrating excellent stability at high current densities. Moreover, the full cell exhibits remarkable electrochemical performance at 5 C. This research contributes to the practical development of NVP cathodes.

Electrospun Multiscale Structured Nanofibers for Lithium‐Based Batteries

Abstract Electrospun is a unique technique for the fabrication of multiscale structured nanofibers (MSNFs), which can be used as functional units for improving the performance of lithium‐based batteries. This review systematically examines how MSNFs, including core–shell, hollow porous, multichannel, wire‐in‐tube, tube‐in‐tube, and hierarchical nanofibers, effectively improve battery performance as components in lithium‐based batteries. The application of aforementioned MSNFs and their chemical modification contributes to the development of lithium‐based batteries with high energy density and enhanced safety when used as electrodes, separators, and electrolytes. Specifically, MSNFs are used to derive electrodes and electrolytes that improve electron/ion transfer rates, increase the utilization ratio of active materials, suppress dendrite growth, and mitigate volume expansion, enabling fast and stable electrochemical reactions at the electrodes. Additionally, MSNFs‐derived separators, which feature more ion transport channels, exceptional mechanical properties, and the capability to inhibit thermal runaway, are also discussed. Finally, the challenges and prospective pathways for electrospun technology in the application of lithium‐based batteries are reviewed.

High performance SERS boosting by Fabry- Pérot cavities of silica-gold-silicon multilayers

Surface-enhanced Raman scattering (SERS), an advanced technique for molecular spectroscopy, relies heavily on the preparation of SERS active materials that can significantly enhance the Raman scattering signals for highly sensitive detection of trace molecules. Traditionally, SERS measurements are performed on silicon or silica substrates, the SERS performance is determined by the structure of SERS materials. Here, we show that the SERS signal can be amplified and modulated using Fabry-Pérot (F-P) cavities made of silica-silicon (SiO2-Si) or silica-gold-silicon (SiO2-Au-Si) multilayers as substrates. Periodic SERS signal variations as SiO2 thickness increases are observed, exhibiting optimal enhancement with the SiO2 thickness of 250 nm due to the optical interference in the cavity. Although the signal enhancement by optical interference is weaker than that by plasmonic resonance, additional signal amplification is essential for highly sensitive SERS materials. Moreover, we applied this strategy to detect thiram in bean sprout extracts, demonstrating that the detection sensitivity is two orders of magnitude higher than that using Si substrates. The utilization of the pseudo-internal standard intensity calibration method facilitates the quantitative analysis of thiram concentrations. Our results provide a promising approach for further amplification of SERS signals with great potential for practical applications.

Optimized Tungsten Disulfide via Pyrolytic Deposition for Improved Zn‐Ion Batteries

AbstractThe selection and optimization of cathode materials are crucial for enhancing the performance of aqueous zinc‐ion batteries. In this work, different active materials were created by combining Sulfur powder and polydopamine in four different mass ratios. The novel N‐doped carbon/WS2 is obtained. Thanks to the optimization of the dopamine‐carrying tungsten ion precursor and Sulfur powder (1 : 2, 1 : 4, 1 : 6 and 1 : 8), the four samples exhibited different morphology. The N−C/WS2‐6‐based zinc ion batteries with the highest specific capacity, 120.0 mAh/g in the first discharge at 2.0 A/g, and 78.0 mAh/g after 2500 cycles, with a capacity retention of 65 %, had a relatively good overall performance, according to the results. The reaction kinetics characteristics of the N−C/WS2‐6 cathode reveal that diffusion has a significant impact on the processes in the aqueous zinc ionic material N−C/WS2‐6.

The Recycling of Lithium from LiFePO4 Batteries into Li2CO3 and Its Use as a CO2 Absorber in Hydrogen Purification

The growing adoption of lithium iron phosphate (LiFePO4) batteries in electric vehicles (EVs) and renewable energy systems has intensified the need for sustainable management at the end of their life cycle. This study introduces an innovative method for recycling lithium from spent LiFePO4 batteries and repurposing the recovered lithium carbonate (Li2CO3) as a carbon dioxide (CO2) absorber. The recycling process involves dismantling battery packs, separating active materials, and chemically treating the cathode to extract lithium ions, which produces Li2CO3. The efficiency of lithium recovery is influenced by factors such as leaching temperature, acid concentration, and reaction time. Once recovered, Li2CO3 can be utilized for CO2 capture in hydrogen purification processes, reacting with CO2 to form lithium bicarbonate (LiHCO3). This reaction, which is highly effective in aqueous solutions, can be applied in industrial settings to mitigate greenhouse gas emissions. The LiHCO3 can then be thermally decomposed to regenerate Li2CO3, creating a cyclic and sustainable use of the material. This dual-purpose process not only addresses the environmental impact of LiFePO4 battery disposal but also contributes to CO2 reduction, aligning with global climate goals. Utilizing recycled Li2CO3 decreases the demand for virgin lithium extraction, supporting a circular economy. Furthermore, integrating Li2CO3-based CO2 capture systems into existing industrial infrastructure provides a scalable and cost-effective solution for lowering carbon footprints while securing a continuous supply of lithium for future battery production. Future research should focus on optimizing lithium recovery methods, improving the efficiency of CO2 capture, and exploring synergies with other waste management and carbon capture technologies. This comprehensive strategy underscores the potential of lithium recycling to address both resource conservation and environmental protection challenges.

Assessing the Influence of Illumination on Ion Conductivity in Perovskite Solar Cells.

Whether illumination influences the ion conductivity in lead-halide perovskite solar cells containing iodide halides has been an ongoing debate. Experiments to elucidate the presence of a photoconductive effect require special devices or measurement techniques and neglect possible influences of the enhanced electronic charge concentrations. Here, we assess the electronic-ionic charge transport using drift-diffusion simulations and show that the well-known increase in capacitance at low frequencies under illumination is caused by electronic currents that are amplified due to the screening of the alternating electric field by the ions. We propose a novel characterization technique to detect a potential photoinduced increase in ionic conductivity based on capacitance measurements on fully integrated devices. The method is applied to a range of perovskite solar cells with different active layer materials. Remarkably, all measured samples show a clear signature of photoenhanced ion conductivity, posing fundamental questions on the underlying nature of the photosensitive mechanism.

Stable Dendrite‐Free Room Temperature Sodium‐Sulfur Batteries Enabled by a Novel Sodium Thiotellurate Interface

AbstractThe practical application of room‐temperature sodium‐sulfur (RT Na−S) batteries is severely hindered by inhomogeneous sodium deposition and notorious sodium polysulfides (NaPSs) shuttling. Herein, novel sodium thiotellurate (Na2TeS3) interfaces are constructed both on the cathode and anode for Na−S batteries to simultaneously address the Na dendritic growth and polysulfides shuttling. On the cathode side, a heterostructural sodium sulfide/sodium telluride embedded in a carbon matrix (Na2S/Na2Te@C) is rationally designed through a facile carbothermal reaction, where the Na2TeS3 interface will be in situ chemically obtained. Such an interface provides abundant electron/ion diffusion channels and ensures rich catalytic surfaces toward Na−S redox, which could significantly improve the utilization of active material and alleviate polysulfides shuttling in the cathode. On the anode side, the inevitable formation of soluble polytellurosulfides species will migrate on Na anode surface, finally constructing a compact and smooth solid‐electrolyte Na2TeS3 interphase (SEI) layer. Such electrochemical formed Na2TeS3 interface can significantly enhance ionic transport and stabilize Na deposition, thus realizing dendrite‐free Na‐metal plating/stripping. Benefitting from these advantages, an anode‐free cell fabricated with the Na2S/Na2Te@C cathode exhibits an ultrahigh initial discharge capacity of 634 mAh g−1 at 0.1 C, which could pave a new path to design high‐performance cathodes for anode‐free RT Na−S batteries.

Enhanced SERS signal in the hybrid substrate through electronic modulation of CVD grown single-layer graphene

The ever-growing demand for sensitive and reliable detection of hazardous material in the food chain and trace detection of chemical entities in a variety field attracted advanced Surface Enhanced Raman Spectroscopy (SERS) active material such as graphene-based hybrid SERS. The graphene‑silver nanostructures (AgNS) based hybrid SERS substrates are explored to understand the critical role of pristine graphene grown by chemical vapor deposition (CVD) on SERS signal and its possible mechanism. A lithography-free fabrication process has been developed for growth of uniform array of AgNS with varying both particle sizes and inter-particle gaps. The optimal AgNS with feature size ~40 nm and inter-particle spacing of ~13 nm demonstrated the maximum SERS enhancement with Rhodamine 6G (R6G). The single-layer graphene (SLG) grown by CVD with the aid of controlling the reaction geometry with growth under a free molecular regime leads to the highest quality graphene with I2D/IG ratio of ~3.58 and ID/IG ratio of 0.1539. The flow regime-controlled CVD-grown SLG integrated with AgNS and its SERS enhancement mechanism is explored for trace detection of R6G. The graphene with its ability to modulate the electronic structure and tune it relative to the highest occupied molecular orbital-lowest occupied molecular orbital (HOMO-LUMO) levels of R6G molecules resulted in improved SERS signal by about an order for graphene-AgNS hybrid structure as compared to bare AgNS. The obtained findings paved the way for the futuristic and reliable hybrid SERS substrate for trace-level detection of a wide range of chemical entities.

Stabilizing zinc powder anodes via bifunctional MXene towards flexible zinc-ion batteries

Flexible zinc (Zn) batteries have gained considerable attention as wearable energy storage devices because of their inherent safety and high theoretical capacity. However, conventional Zn anodes suffer from dendrite growth, high rigidity, and poor cycling stability issues, hindering their practical application in flexible zinc-ion batteries. Herein, a dendrite-free and flexible Zn anode is designed using direct ink writing (DIW) printed MXene as a flexible and highly conductive current collector and MXene-wrapped Zn powder (ZnP) as the active material by carefully optimising the rheological properties of MXene-based dispersion. As a result, the synergistic effects of the MXene-based current collector and the MXene protective layer promoted dendrite-free Zn deposition and prevented side reactions, achieving an outstanding cycling performance that exceeded 130 h at a high depth of discharge of 30%. When paired with a Vanadium pentoxide (V2O5)-based cathode, the flexible full cell demonstrated stable electrochemical performance under mechanical deformation and can power electronic devices, presenting a promising pathway for the development of flexible zinc-ion batteries.

Facile synthesis and first principles calculations of Li-MoS2/rGO nanocomposite for high-performance supercapacitor applications

Two-dimensional (2D) nanostructured materials such as graphene oxide nanosheets and molybdenum disulfide (MoS2) are potential candidates for electrochemical energy storage applications. The layered structure of MoS2 makes it a promising active electrode material for supercapacitors. Lithium (Li) interacted with MoS2/reduced graphene oxide (Li-MoS2/rGO) nanocomposite has been synthesized in two steps using a sonochemical dispersion method, and a one-pot hydrothermal method resulting in few-layered MoS2/rGO nanosheets of 2D heterointerfaces. The Li-MoS2/rGO nanocomposite exhibits a high specific capacitance of 173.3 F g−1 at a current density of 1 A g−1. Furthermore, an asymmetric supercapacitor device fabricated with Li-MoS2/rGO achieves a good energy density of 10.6 Wh kg−1 at a power density of 686.3 W kg−1 and outstanding cycling stability with 81.2 % capacity retention over 10,000 cycles. The dispersion of 2D-MoS2 in water is due to the strong electrostatic interface. The structural and electronic properties are theoretically calculated for pristine and Li-interacted MoS2/rGO heterostructure using density functional theory. A comparison of the density of states plots of the two heterostructures and the difference charge density plot of Li-MoS2/rGO heterostructure clearly brings out the importance of the presence of Li. A value of 64 μF cm−2 for the quantum capacitance for pristine MoS2/graphene heterostructure increases to a value 99 μF cm−2 corroborating the experimental observations and we assign this change to the transfer of charge from the Li atom to the outer S atoms in the MoS2/graphene heterostructure. This comprehensive approach, combining experimental synthesis with computational modelling, significantly advances the development and optimization of high-performance supercapacitor materials in the energy storage field. The Li-MoS2/rGO nanocomposite has excellent electrochemical specific capacitance and long-term cyclic stability and has been effectively used for supercapacitor applications with high electrochemical performance.

An active and Cr-tolerant high-entropy La0.7Sr0.3FeO3-δ based cathode for solid oxide fuel cells

The development of high active and stable cathode materials is one of the main challenges of intermediate temperature solid oxide fuel cells (SOFCs). Herein, a high-entropy Fe-based perovskite oxide La0.7Sr0.3Fe0.3Ni0.3Co0.3Mo0.1O3-δ (LSFNCM) is synthesized by self-propagation combustion based on La0.7Sr0.3FeO3-δ (LSF) and the electrochemical properties are systematically tested. The symmetric half-cell with the LSFNCM cathode has a high catalytic activity with a polarization impedance of 0.12 Ω·cm2 at 800 °C, and also shows outstanding CO2 resistance and chromium resistance owing to the entropy stabilization strategy. After 50h of treatment in a 10% CO2 environment, the polarization impedance of the LSF electrode increases by 8.89 Ω·cm2, while that of the LSFNCM electrode only increases by 1.81 Ω·cm2. Additionally, after being treated for 24h in a chromium vapor environment, the polarization impedance of the LSF electrode increases by 5.95 Ω·cm2, whereas that of the LSFNCM electrode only increases by 0.44 Ω·cm2. Moreover, the single cell with LSFNCM cathode exhibits the maximum power density of 932.82 mW/cm2 and the polarization impedance of 0.34 Ω·cm2 at 800 °C with humidify hydrogen as fuel. Our results indicate that high-entropy perovskite oxide LSFNCM is an active and Cr-tolerant promising cathode for SOFCs.

Activation of peroxymonosulfate by Fe based metal organic framework for selective degradation of phenol in water

Phenol is a common pollutant in various wastewater, which is required to be removed to a certain standard before the wastewater can be discharged. Persulfate-based advanced oxidation processes (PS-AOPs) are an effective technology for phenol removal, with efficacy contingent upon the activation methods and materials employed. In this study, Fe-based metal-organic frameworks (Fe-MOFs) constructed with carboxylic acid as a ligand were synthesized by a solvothermal method, which can form chelates with ferrous ions. Fe-MOFs showed the activity similar to the homogeneous catalyst thus improving their activation efficiency, and can be used to activate peroxymonosulfate (PMS) for phenol degradation in water. The effects of catalyst dosage, PMS and phenol concentration, temperature, and pH on the degradation efficiency were investigated. Under the optimum reaction conditions, the 96 % of phenol can be rapidly removed in 5 min. SO4·− was determined as the primary radical. Fe species on Fe-MOFs acted as the key active sites. Density functional theory (DFT) analysis suggested enhanced charge redistribution, fostering electron-rich sites that facilitate electron transfer in AOPs, thus boosting phenol degradation. The Fe-MOFs/PMS system enables iron recycling and efficient phenol degradation in water, indicating the potential for phenol-contaminated water treatment.

Functional composite films incorporating triphala-derived carbon dots for extending chicken preservation

Triphala-based carbon dots (T-CDs) were successfully prepared using a simple one-step hydrothermal method. T-CDs were characterized by absorbance, fluorescence, Fourier-transform infrared, X-ray photoelectron spectroscopy, and high-resolution transmission electron microscopy. T-CDs showed bright blue fluorescence at 434 nm upon excitation at 360 nm. Functional composite films were prepared using poly(vinyl alcohol) and gelatin mixture by incorporating T-CDs and applied as a packaging film to extend the shelf life of chicken. The antibacterial activity of T-CDs against Listeria monocytogenes and Staphylococcus aureus was evaluated using well diffusion and colony count methods. T-CDs were evenly dispersed throughout the PVA/Gel solution to form a dense and uninterrupted film. They also formed strong bonds with polymer chains, which improved the tensile strength of the film from 32.44 to 42.70 MPa. Furthermore, the presence of T-CDs significantly enhanced the UV-blocking ability of the PVA/Gel films, achieving 99.7 % for UV-B and 97.2 % for UV-A. In addition, the PVA/Gel/T-CDs composite films showed excellent antioxidant, antimicrobial and UV-barrier properties, extending the shelf life of chicken. Therefore, the PVA/Gel/T-CDs composite films showed great potential as an active food packaging material to extend the shelf life and preserve the visual quality of packaged meat.