Specific Area Research Articles

A nanoporous nickel–iron alloy seamlessly anchored into hierarchical porous nickel for efficient and extremely stable water splitting

The development of a robust, low-cost electrode for electrochemical water splitting is a challenging, but essential task for realizing hydrogen production under industrial conditions. Here, we seamlessly anchor nanoporous nickel–iron into a hierarchical porous nickel foam (npNi–Fe/HPNF) by a designed gaseous oxidation–reduction engineering for a commercial nickel foam. The three-dimensional hierarchical porous structure considerably enhances the specific surface area of the electrode, yielding abundant electrocatalytic sites that promote the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). Moreover, owing to its mechanically robust, seamlessly anchored architecture, and remarkable superhydrophilicity/superaerophobicity, the electrolyzer composed of self-standing npNi–Fe/HPNF and its electro-activation derivative displays a current density of 10 mA cm−2 at 1.54 V, ultralong durability of more than 2000 h at 500 mA cm−2 in a 1 M KOH electrolyte, and high performance of 2 V at 1 A cm−2 in a quasi-industrial environment (5 M KOH and 70 °C), outperforming most alkaline electrolyzers based on state-of-the-art electrodes. Exceptional electrochemical performance and the ability to be prepared at a large scale (2500 cm2) make npNi–Fe/HPNF a promising candidate for industrial water splitting applications.

Determination of seven phenoxy carboxylic acid herbicides in water using dispersive solid phase extraction coupled with ultra-high performance liquid chromatography-tandem mass spectrometry based on metal-organic framework composite aerogel

Phenoxy carboxylic acid herbicides (PCAs) are difficult to degrade and, thus, pose significant threats to the environment and human health. The limit for 2,4-dichlorophenoxyacetic acid is 30 μg/L in China's standards for drinking water quality, 70 μg/L in the United States' drinking water standards, and 30 μg/L in the World Health Organization's guidelines for drinking water quality. Therefore, the development of an effective detection method for trace PCAs in water is a crucial endeavor. Metal-organic frameworks (MOFs) are novel porous materials that possess advantages such as a large specific surface area, adjustable pore size, and abundant active sites. They exhibit excellent adsorption capability for various compounds. However, the applications of MOFs as adsorbents are limited. For example, the process of isolating powdered MOFs from aqueous solutions is laborious, and microporous MOFs exhibit limited surface affinity, which decreases their mass transfer efficiency in the liquid phase. MOF crystals can be embedded in a substrate to overcome these limitations. Aerogels are obtained by drying hydrogels, which are hydrophilic polymers with a three-dimensional crosslinked network structure. Spongy aerogel materials exhibit unique structural properties such as high porosity, large pore volume, ultralow density, and easy tailorability. When MOFs are combined with an aerogel, their efficient and selective adsorption properties are preserved. In addition, MOF aerogels exhibit a hierarchical porous structure, which enhances the affinity and mass transfer efficiency of the MOF for target molecules. At present, MOF aerogels are primarily prepared by freeze-drying or using supercritical carbon dioxide. These drying processes require significant amounts of energy and time. Hence, the development of greener and more efficient methods to prepare skeleton aerogels is urgently needed. In this study, we prepared an environment-friendly aerogel at ambient temperature and pressure without the use of specialized drying equipment. This ambient-dried MOF composite aerogel was then used for the dispersive solid phase extraction (DSPE) of seven PCAs from environmental water, followed by ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). The key parameters affecting the efficiency of DSPE, including the extraction conditions, ratio of MIL-101(Fe)-NH2 to sodium alginate, pH of the aqueous samples, extraction time, ionic strength (salinity), and elution conditions, such as the elution solvent ratio, elution time, and elution volume, were investigated to obtain optimal extraction efficiency. The adsorbent could adsorb the target contaminants within 12 min, and the analytes could be completely desorbed within 30 s by elution with 4 mL of 1.5% (v/v) formic acid in methanol solution. The water samples could be analyzed without pH adjustment. The main adsorption mechanisms were electrostatic interactions and π-π conjugation. Thus, a new method based on MOF aerogels coupled with UHPLC-MS/MS was developed for the determination of the seven PCA residues in water. The calibration curves for the seven PCAs showed good linearity (r2≥0.9986), with limits of detection (LODs) and quantification (LOQs) ranging from 0.30 to 1.52 ng/L and from 1.00 to 5.00 ng/L, respectively. Good intra- and inter-day precision values of 6.5%-17.1% and 7.4%-19.4%, respectively, were achieved under low (8 ng/L), medium (80 ng/L), and high (800 ng/L) spiking levels. The developed method was applied to the detection of PCAs in surface water, seawater, and waste leachate, and the detected mass concentrations ranged from 0.6 to 19.3 ng/L. Spiked recovery experiments were conducted at mass concentrations of 8, 80, and 800 ng/L, and the recoveries ranged from 61.7% to 120.3%. The proposed method demonstrates good sensitivity, precision, and accuracy, and has potential applications in the detection of trace PCAs in environmental water.

Target Signal Communication Detection of Black Flying UAVs Based on Deep Learning Algorithm

Background: Unmanned aerial vehicles (UAVs) are being widely used in many fields, such as national economy, social development, national defense, and security. Currently, the number of registered UAVs in China is far less than that of flying UAVs-the frequent occurrence of unsafe incidents. Objective: The phenomenon of UAVs flying undeclared and unapproved has caused more serious troubles to social public order and people's production and life. Methods: In this paper, to assist the public security department in detecting the phenomenon of UAV black flying, our team conducts a series of research based on the deep learning YOLOv5 (You Only Look Once) algorithm. Results: Firstly, the Vision Transformer mechanism is integrated to enhance the robustness of the model. Secondly, depth-separable convolution is introduced to reduce parameter redundancy. Finally, the SimAM attention-free mechanism and CBAM attention-free mechanism are combined to enhance the attention of small target UAVs. Conclusion: Through the analysis of UAV targets in video surveillance, the rapid identification of black-flying UAVs can be realized, the monitoring and early warning ability of UAVs in a specific area can be improved, and the loss of life and property of people can be reduced or saved as much as possible.

Deep insight into the effect of smithsonite particle size on surface heterogeneity and adsorption behavior: A case of fatty acid system

The studies for microfine mineral flotation have focused on the two main directions of increasing the apparent mineral particle size and reducing the bubble size, while little research has been reported on the special surface properties and adsorption mechanisms of mineral particles of different sizes. In this study, sodium oleate was chosen as a typical surfactant. The mechanism of the effect of smithsonite particle size on the heterogeneity and adsorption behavior of the mineral surface was explored in depth. Through microflotation experiments, BET area tests, Washburn contact angle tests, particle agglomeration tests, adsorption tests and inorganic carbon analysis, it was pointed out that the smaller the size of the particles, the greater the surface wettability, and the smaller the density and thickness of adsorbed oleate on the surface. The difficulty of encapsulating the mineral surface with a hydrophobic layer of oleate hydrocarbon chains, as well as suboptimal particle aggregation sizes, are key reasons for the poor flotation behavior of fine smithsonite. Furthermore, the inhomogeneity of active sites and charge distribution of surface components of smithsonite with different sizes was revealed from a microscopic point of view by DRIFT spectroscopic analysis, XPS analysis and zeta potential measurements. As the particle size of smithsonite decreases, the positive charge density on the surface is higher and the hydration tendency is more intense, hindering the adsorption of oleate. This work is expected to guide the full particle size recovery of minerals in the flotation from a novel microscopic point of view.

Investigation on the Hydrothermal Condition in Synthesis of Active Matrix from Metakaolin: Physicochemical Properties and Intrinsic Cracking Activities

The current trends in research and development of FCC catalyst is focused on the formulation of active matrices that serve as pre-crackers, with the objective of reducing the diffusional resistance of the longer chain hydrocarbon molecule in the feed. In this study, an aluminosilicate active matrix was synthesised from metakaolin using hydrothermal method. The experimental variables that were varied were hydrothermal temperature, in the range of 80 to 110 °C, and hydrothermal time, in the range of 12 to 72 hours, to investigate the best conditions for synthesising the active matrix. Subsequently, the active matrix was subjected to a series of analyses, including X-ray fluorescence, X-ray diffraction, N2 physisorption, NH3-temperature programmed desorption, Fourier transform infrared spectroscopy, scanning electron microscopy and thermogravimetry, with the objective of determining its composition, crystal characteristics, surface characteristics, acidity, functional groups, material structure, and thermal characteristics. Additionally, the active matrix was tested for its intrinsic cracking activity using the micro activity test (MAT). The results indicate that the best temperature for hydrothermal synthesis of the active matrix is 80 °C. The active matrix synthesised with a heating time of 24 hours demonstrated the highest light cycle oil yield, reaching 38.9 wt%. Meanwhile, the active matrix synthesised at 48 hours exhibited the most favourable characteristics, with a specific surface area of 144.23 m2/g and a pore volume of 0.9933 cm3/g, as well as the highest cracking conversion of 70.0 wt%. Copyright © 2024 by Authors, Published by BCREC Publishing Group. This is an open access article under the CC BY-SA License (https://creativecommons.org/licenses/by-sa/4.0).

Partially Fluorinated Alumina With Enhanced Stability: Application To Catalysis Under Aggressive Conditions

AbstractHere, we report the design of new aluminum hydroxyfluoride, mainly composed of amorphous phase, with enhanced stability under HF gas in term of textural properties, especially the specific surface area and the acidity. The material has been synthesized through an EISA (evaporation‐induced self‐assembly) route using liquid crystals as templates. Thanks to this stability, the catalyst designed by the dispersion of the active phase on this support shows a higher accessibility and activity of the active sites than the ones obtained by other methods

Advances in the Application of Graphene in Lithium-ion Batteries

The search for effective energy storage options has escalated due to the rising global energy demands and environmental concerns. Lithium-ion batteries (LIBs) emerge as a key technology. However, the performance of traditional LIBs still needs to be improved. Therefore, choosing new nanomaterials for the modification of LIBs has become an effective solution. Graphene, as a nanomaterial, is an excellent candidate material for modification. This paper delves into the application of graphene in enhancing the performance of LIBs. Graphene, with its superior electrical conductivity and substantial specific surface area, offers the potential to enhance the performance of both anode and cathode materials in LIBs. This can lead to significant improvements in the overall cycle life, energy density, and power density of these batteries. This work emphasizes the application of graphene in cathode and anode materials. In cathode materials, the layered structure of graphene enables lithium-ion with high theoretical capacity. Meanwhile, graphene helps improve the electron and lithium ion mobility of anode materials. Despite the promising developments, challenges such as lithium loading capacity and coulombic efficiency still remain. The continued exploration of graphene applications is expected to drive LIBs to unprecedented performance metrics. This is in line with the global quest for sustainable and efficient energy storage technologies.

In Situ Deprotection-Free Synthesis of Silver/Graphdiyne with a High Raman Sensing Effect for Detection of Polychlorophenols and Microplastics.

Since the first synthesis of graphdiyne (GDY), it has been widely receiving a lot of attention and has great application prospects in many fields, such as energy storage, catalysis, and sensing. However, the complex deprotection treatment and long reaction time limit its mass production and applications. Here, we present a strategy for the silver-catalyzed deprotection-free rapid synthesis of GDY. Crystalline GDY was synthesized in 8 h at room temperature and atmospheric pressure, and after the reaction, Ag nanoparticles with an ultrathin diameter of 2-3 nm were formed in situ inside and on the surface of GDY. This Ag/GDY composite exhibits a high specific surface area of 672.3 m2 g-1 and strong surface plasmon resonance behavior, showing a strong surface-enhanced Raman scattering effect. The enhancement factor and the lowest detection limit for rhodamine 6G are 3.54 × 108 and 1 × 10-14 M, respectively. The Ag/GDY achieves the simultaneous enrichment and detection of polychlorophenols and ultrafine nanoplastics.

A review of the progress of metal-organic frameworks in perovskite solar cells

Organic-inorganic hybrid perovskite solar cells (PSCs) have emerged as substantial challenges for future generations of photovoltaic apparatus, largely attributed to their power conversion efficiency (PCE) drastically elevated from below 10% to a staggering 25.7% over the past decade. Owing to characteristics distinct to them like substantial specific surface areas, copious binding locations, adjustable nanostructures, and mutual reinforcement, metal-organic frameworks (MOFs) are commonly utilized as either supplementary components or operational layers for augmenting both the efficiency and durability of PSCs. This paper primarily underlines the recent advancements in implementing MOFs across various operational strata of a PSC. The focal points of this study encompass an examination of the photovoltaic yields, the repercussions, and the advantages of fusing MOF materials into constituents like perovskite absorbers, electron transport, and hole transport layers, in addition to interface layers. The study also extends to an exploration of how MOFs effectively inhibit leakages of Pb2+ within halide perovskites and their associated apparatus. This paper concludes by discerning and shedding light on potential research prospects for the deployment of MOFs in PSCs.

Chemical and Physical Properties of Selected Biochar Types and a Few Application Methods in Agriculture

Biochar, a carbon-rich by-product of organic matter pyrolysis, has a variety of physiochemical properties beside a variety of applications. This review highlights some physical and chemical characteristics of herbaceous, woody, and sewage waste biochar under different pyrolysis conditions, as well as soil and foliar applications of biochar. The controlling role of pyrolysis temperature was the reason for selecting the discussed biochar types in the study. This review concludes that increasing pyrolysis temperature mainly raised the values of some chemical properties of the biochar, such as pH, electrical conductivity (EC), ash content, total phosphorus (TP), and a few values of physical properties like porosity and specific surface area (SSA). On the other hand, yield and total nitrogen (TN) decreased with rising pyrolysis temperature. Among biochar application methods to soil, mixing biochar with soil before planting is one of the best methods of application, and in most cases, biochar reapplication improved soil properties, while foliar application of biochar has positive effects on plant growth and yield parameters, ranging from low rates to the highest ones.

Study of the Activator Effects on the Specific Surface Area of Porous Carbon and its Performance as Lithium-Sulfur Battery Cathode

A study was conducted to investigate the effect of activator types KOH, ZnCl2, and H3PO4 on the specific surface area of porous carbon and its performance as a Li-S battery. Porous carbon was synthesized from candlenut shells through a carbonization process at 700 °C using three types of activator solutions with a concentration of 0.36 M. The porous carbon activated with KOH achieved the best results, with a specific surface area of 681 m²g-1. The porous carbon candlenut shell-sulfur (PCCS-S) composite was obtained by the solid-state reaction method in a ratio of 1:2.5 w% and heat-treated at 155 °C to form the PCCS-S composite. The PCCS-S composite was then made into a slurry and coated onto Al-foil to obtain a layer of electrodes with a thickness of 200 µm. The PCCS-S cathode was then assembled into a coin battery with lithium metal as the anode and an electrolyte of 1.0 M LiTFSi solution dissolved in 1,3-dioxolane (DOL) and 1,2-dimethoxyethane (DME) (v/v, 1:1). Charge-discharge characterization was carried out at a charge rate of 1 C for 50 cycles. Characterization shows that the performance of the PCCS-S KOH composite cathode Li-S battery is stable at a specific capacity of 324 mAhg-1 after the first 10 cycles, with an average Coulombic efficiency of around 86.8 %.

MoS2/porous carbon nanofiber heterostructures for efficient evaporation-driven generators.

Evaporation power generators (EPGs) based on natural water evaporation can directly convert heat energy from the surrounding environment into electrical energy. However, EPGs are difficult to commercialize due to the low charge generation and transport efficiency of single material systems, resulting in unsatisfactory open-circuit voltages and short-circuit currents. Here, we step by step prepared MoS2/porous carbon nanofiber (PCNF) heterogeneous systems by electrospinning and hydrothermal methods. Electron microscope measurements proven the uniform coating of high-crystalline quality MoS2 nanosheets on PCNF fabrics, and the uneven concave-convex surface increased the specific surface area. MoS2 covered PCNF fabrics retained good hydrophilicity, which was suitable for absorbing water and keeping the surface wet during long-term evaporation. Moreover, layered MoS2 with rich surface charge improved the charge transfer of the MoS2/PCNF fabrics. As a result, the open-circuit voltage and short-circuit current of the EPGs prepared with MoS2/PCNF fabrics were improved to 0.25 V and 75 μA, respectively, compared with those based on PCNF fabrics, which demonstrated that the MoS2 coatings improved the interaction area with water and the charge transfer effect of the EPGs. This heterogeneous combination strategy provides ideas for the preparation of high-performance EPG materials.&#xD.

Achievements and Challenges in Surfactants-Assisted Synthesis of MOFs-Derived Transition Metal-Nitrogen-Carbon as a Highly Efficient Electrocatalyst for ORR, OER, and HER.

Metal-organic frameworks (MOFs) are excellent precursors for preparing transition metal and nitrogen co-doped carbon catalysts, which have been widely utilized in the field of electrocatalysis since their initial development. However, the original MOFs derived catalysts have been greatly limited in their development and application due to their disadvantages such as metal atom aggregation, structural collapse, and narrow pore channels. Recently, surfactants-assisted MOFs derived catalysts have attracted much attention from researchers due to their advantages such as hierarchical porous structure, increased specific surface area, and many exposed active sites. This review mainly focuses on the synthesis methods of surfactants-assisted MOFs derived catalysts and comprehensively introduces the action of surfactants in MOFs derived materials and the structure-activity relationship between the catalysts and the oxygen reduction reaction, oxygen evolution reaction, and hydrogen evolution reaction performance. Apparently, the aims of this review not only introduce the status of surfactants-assisted MOFs derived catalysts in the field of electrocatalysis but also contribute to the rational design and synthesis of MOFs derived catalysts for fuel cells, metal-air cells, and electrolysis of water toward hydrogen production.

Enhanced photocatalytic performance of magnetically reclaimable N-doped g-C3N4/Fe3O4 nanocomposites for efficient tetracycline degradation

The growing environmental challenge posed by the persistence of tetracycline (TC) antibiotics in natural waters is of increasing concern. To address this, there is an imperative need for advanced methods to mitigate TC residues. Herein, we demonstrate the preparation of nitrogen-doped graphitic carbon nitride integrated with magnetic Fe3O4 (N-g-CN/Fe3O4) composites, showcasing narrow band gaps optimized for TC degradation. These advanced materials, conceived through a thermal poly-condensation approach, utilize citric acid and melamine as precursors for nitrogen and g-CN, respectively. These composites exhibit a face-centered cubic architecture, with particle dimensions between 8 to 12 nm and encompassing both meso and microporous structure. The results of the Brunauer–Emmett–Teller analysis indicated specific surface areas of 6.73 m²/g for g-CN, 69.80 m²/g for N-g-CN, 62.55 m²/g for Fe3O4, and 148.32 m²/g for N-g-CN/Fe3O4. These values demonstrate an increase in surface area upon the incorporation of heteroatom of nitrogen and Fe3O4, into the g-CN matrix, thus influence the photocatalytic performance. Under solar light exposure, the synthesized photocatalysts demonstrated photocatalytic activity with a degradation efficiency of 94.16 % within 120 min. Specifically, the N-g-CN/Fe3O4 (22.5 %) composites exhibited remarkable photocatalytic efficiency due to the narrow band gap energy between N-g-CN and Fe3O4, enhanced light absorption in the visible range, and effective charge carrier separation and transportation to the pollutants. N-g-CN/Fe3O4 (22.5 %) composites demonstrated good recyclability (five cycles), magnetic sustainability, and stability for the degradation of TC and emerging pollutants from wastewater using photocatalysts. Similarly, FGCN composites exhibited good recyclability (five cycles), magnetic retrievability, and stability for degrading organic and emerging pollutants from wastewater through photocatalysis. This efficiency can be attributed to the harmonious combination of nitrogen doping, refined surface area, and the natural heterojunction between N-g-CN and Fe3O4.

Effect of Structural Configurations on Mechanical and Shape Recovery Properties of NiTi Triply Periodic Minimal Surface Porous Structures

Based on the advantages of triply periodic minimal surface (TPMS) porous structures, extensive research on NiTi shape memory alloy TPMS scaffolds has been conducted. However, the current reports about TPMS porous structures highly rely on the implicit equation, which limited the design flexibility. In this work, novel shell-based TPMS structures were designed and fabricated by laser powder bed fusion. The comparisons of manufacturability, mechanical properties, and shape recovery responses between traditional solid-based and novel shell-based TPMS structures were evaluated. Results indicated that the shell-based TPMS porous structures possessed larger Young’s moduli and higher compressive strengths. Specifically, Diamond shell structure possessed the highest Young’s moduli of 605.8±24.5 MPa, while Gyroid shell structure possessed the highest compressive strength of 43.90±3.32 MPa. In addition, because of the larger specific surface area, higher critical stress to induce martensite transformation, and lower austenite finish temperature, the Diamond shell porous structure exhibited much higher shape recovery performance (only 0.1% residual strain left at pre-strains of 6%) than other porous structures. These results substantially uncover the effects of structural topology on the mechanical properties and shape recovery responses of NiTi shape memory alloy scaffolds, and confirm the effectiveness of this novel structural design method. This research can provide guidance for the structural design application of NiTi porous scaffolds in bone implants.

General Synthesis of Single-Crystalline Ta2O5 Nanorods Towards Enhanced Photocatalytic H2 Production Activity.

As a potential candidate for photocatalytic H2 production from water splitting, Ta2O5 catalyst presents suitable conduction and valence band positions, but suffers from poor charge transfer ability, which seriously limits its photocatalytic performance enhancement. Here, a facile and eco-friendly hydrothermal method was developed for the fabrication of one-dimensional (1D) Ta2O5 nanorods using the freshly precipitated tantalic acids as the precursors. An oriented attachment mechanism was proposed for the growth of Ta2O5 nanorods. Moreover, the present synthetic approach was further extended to direct synthesis of nine kinds of alkaline tantalates and alkaline-earth tantalates nanostructures, suggesting its general applicability. A significant increase in activity in photocatalytic H2 production was revealed on 1D Ta2O5 nanorods. The improved photocatalytic H2 production activity of Ta2O5 nanorods was mainly attributed to its 1D nanorods structure with high crystallization and large specific surface areas as well as excellent charge transfer efficiency.

Effects of pyrolysis temperatures on the structural properties of straw biochar and its adsorption of tris-(1-chloro-2-propyl) phosphate

To investigate the effect of pyrolysis temperature on the adsorption behavior of the emerging organic pollutant tris-(1-chloro-2-propyl) phosphate (TCIPP) on biochar, corn stover was used as raw materials to prepare biochars at different pyrolysis temperatures (250, 350, 500, 700 °C) through limited oxygen carbonization. Elemental analysis, Boehm titration, FTIR, XPS, and other analytical methods were used to reveal the effect of pyrolysis temperature on the physicochemical properties of biochar and its mechanism of TCIPP adsorption. The results showed that the pyrolysis temperature had a significant impact on the physicochemical properties of biochar. As the pyrolysis temperature increases, the specific surface area of biochar rises from 3.083 m2/g to 435.573 m2/g, the pH value increases from 6.60 to 10.66, the mass percentage of C increases from 63.10 to 80.58%, and the mass percentage of O decreases from 26.42 to 9.20%. Additionally, the hydrophobicity and aromaticity of biochar also increase with rising pyrolysis temperature, while its polarity decreases. Boehm titration, FTIR, and XPS analysis showed that the total amount of functional groups on the surface of biochar decreased relatively with increasing temperature. Functional groups such as -OH, C = C/C = O, and C-O-C participated in the adsorption of TCIPP on biochar, and ester groups were produced after adsorption. The adsorption process of TCIPP on biochar fits best with the pseudo-second-order equation, indicating that the adsorption process is mainly chemical adsorption, and the main rate-controlling stage is intraparticle diffusion. The isothermal adsorption results were more in line with the Temkin model, indicating that the adsorption process of TCIPP on biochar was mainly surface adsorption. As the pyrolysis temperature increases, the maximum adsorption capacity of biochar increases from 0.8837 mg/g to 2.2574 mg/g. The adsorption process of TCIPP on biochar mainly included pore filling, hydrogen bonding, P-π interaction, hydrophobic interaction, and electrostatic attraction. Among them, pore filling, P-π interaction, and hydrophobic interaction were significantly enhanced with increasing temperature, while hydrogen bonding was relatively weakened. This study will provide a theoretical basis and technical support for the removal of TCIPP from water using biochar adsorption.

Novel polystyrene‐based light diffusing materials: Introduction of magnesium hydroxide to enhance scattering range and thermal conductivity

AbstractIn high‐power lighting, large‐screen display, and other practical application scenarios, Light diffusing materials (LDMs) with favorable thermal conductivity are desired to assist in heat dissipation. In this paper, platy magnesium hydroxide (pMH) and mesoporous spherical magnesium hydroxide (sMH) were introduced as scattering particles for the first time to prepare polystyrene (PS)‐based LDMs. The limited refractive index mismatch allowed MH to be filled in large quantities with less sacrifice of light transmission performance. Owing to the complex surface morphology and large specific surface area, sMH possesses stronger scattering capability, and its combination addition with pMH could effectively increase scattering range. Meanwhile, an effective filler network was constructed with the combined use of pMH and sMH, and thus enhanced the thermal conductivity of the composites. Additionally, PS/pMH‐sMH composites exhibited higher thermal stability. This study expands the auxiliary thermal management capability of light diffusion materials and presents a new application possibility for MH as scattering particles.Highlights A new application possibility for Magnesium hydroxide as scattering particles. Light transmittance degradation of PS/MH at high filler loadings was mitigated by RI matching. Complex surface morphology endowed sMH with strong scattering capability. Optimal filling ratio of pMH to sMH was tested for better scattering performance. Extended scattering range, improved TC and thermal stability was achieved.

Optimization of Photocatalytic Degradation of Rhodamine B and Indigo Carmine Dyes Using Eco‐Friendly Kaolinite‐Silver Oxide Quantum Dots Nanocomposite Under Sunlight Irradiation

ABSTRACTIn this work, we present a simple method for the pyrofabrication of a new kaolinite‐ silver oxide quantum dots nanocomposite (Kao‐Ag2O/QDs) that is used for the degradation of rhodamine B (RhB) and indigo carmine (IC) dyes. A homogenous combination of kaolinite and silver nitrate was sintered up to 350 °C to create the extremely effective photocatalyst (Kao‐Ag2O/QDs). Various analytical techniques were employed to characterize the Kao‐Ag2O/QDs photocatalyst such as XRD, FTIR, XPS, SEM–EDX, TEM, DTA/TGA, ZP, BET, and UV–Vis DRS. The degradation of RhB and IC dyes through the photocatalyst was carried out in aqueous solutions utilizing several pH dye solutions and sustainable solar energy in atmosphere conditions. The nanocomposite that was prepared had shown an enhanced specific surface area of 53.3005 m2/g, a pore size of 8.1197 nm, and a total pore volume of 0.216 cm3/g. It also displayed an optical band gap energy of 2.9 eV. The study creates that employing the ideal dose of 2000 and 1500 mg/L of the Kao‐Ag2O/QDs photocatalyst at neutral conditions (pH = 7) resulted a maximum degradation effectiveness of RhB and IC of 91.06 and 93.46% after 90 min, respectively. RhB and IC dyes degradation followed Langmuir first‐order kinetics with a rate constant of 0.0217 and 0.0216 min−1 at pH = 7, respectively. The photocatalytic degradation activity for RhB dye is based on hydroxyl radicals (˙OH) and superoxide radicals (˙O2−), while the mechanism of IC removal is based on superoxide radicals (˙O2−), as revealed by scavenger‐based radical trapping studies. A triple reusability study found that the Kao‐Ag2O photocatalyst is highly stable with degradation efficiencies of RhB and IC dyes from the initial 91.09 to 90.04, 88.54, and 86.27% and from the initial 93.46 to 92.8, 91.4 and 89.32%, respectively. The optimal situations for the parameters were identified by the Box–Behnken design (BBD), which was well matched with photocatalytic degradation tests.

Functional metal-organic frameworks derived electrode materials for electrochemical energy storage: a review.

Pristine metal-organic frameworks (MOFs) are built through self-assembly of electron rich organic linkers and electron deficient metal nodes via coordinate bond. Due to the unique properties of MOFs like highly tunable frameworks, huge specific surface areas, flexible chemical composition, flexible structures and a large volume of pores, they are being used to design the electrode materials for electrochemical energy storage devices. As per the literature, MOFs (including manganese, nickel, copper, and cobalt-based zeolitic imidazolate frameworks (ZIFs), University of Oslo (UiO) MOFs, Hong Kong University of Science and Technology (HKUST) MOFs and isoreticular MOFs (IRMOFs)) have attracted much attention in the field of supercapacitors (SCs)/batteries. According to their dimensionality such as 1D, 2D and 3D, pristine MOFs are mainly used as SC materials. Highly porous materials and their composites are capable for intercalation of metal ions (Na+/Li+). Moreover, the supramolecular features (π⋯π, C-H⋯π, hydrogen bond interactions) of redox stable MOFs provide better insight for electrochemical stability. So, this review provides an in-depth analysis of pure MOFs and MOF derived composites (MOF composites and MOF derived porous carbon) as electrode materials and also discusses their metal ion charge storage mechanism. Finally, we provide our perspectives on the current issues and future opportunities for supercapacitor materials.