Synthesis Of Materials Research Articles

Advancements in MXene Composite Materials for Wearable Sensors: A Review.

In recent years, advancements in the Internet of Things (IoT), manufacturing processes, and material synthesis technologies have positioned flexible sensors as critical components in wearable devices. These developments are propelling wearable technologies based on flexible sensors towards higher intelligence, convenience, superior performance, and biocompatibility. Recently, two-dimensional nanomaterials known as MXenes have garnered extensive attention due to their excellent mechanical properties, outstanding electrical conductivity, large specific surface area, and abundant surface functional groups. These notable attributes confer significant potential on MXenes for applications in strain sensing, pressure measurement, gas detection, etc. Furthermore, polymer substrates such as polydimethylsiloxane (PDMS), polyurethane (PU), and thermoplastic polyurethane (TPU) are extensively utilized as support materials for MXene and its composites due to their light weight, flexibility, and ease of processing, thereby enhancing the overall performance and wearability of the sensors. This paper reviews the latest advancements in MXene and its composites within the domains of strain sensors, pressure sensors, and gas sensors. We present numerous recent case studies of MXene composite material-based wearable sensors and discuss the optimization of materials and structures for MXene composite material-based wearable sensors, offering strategies and methods to enhance the development of MXene composite material-based wearable sensors. Finally, we summarize the current progress of MXene wearable sensors and project future trends and analyses.

Host-Guest Metal-Organic Frameworks-Based Long-Afterglow Luminescence Materials.

Long-afterglow materials have a broad of applications in optoelectronic devices, sensors, medicine and other fields due to their excellent luminescent properties. The host-guest long-afterglow MOFs material combines the advantages of multi-component characteristics and the stability of MOFs, which improves its luminous performance and expands its other properties. This review introduces the classification, synthesis and application of host-guest MOFs materials with long afterglow. Due to their rigid frames and multi-channel characteristics, MOFs can load common guest materials including rare earth metals, organic dyes, carbon dots, etc. The synthesis methods of loading guest materials into MOFs include solvothermal synthesis, post-encapsulation, post-modification, etc. Those long-afterglow host-guest MOFs have a wide range of applications in the fields of sensors, information security and biological imaging.

Pd-intercalated black phosphorus: An efficient electrocatalyst for CO2 reduction.

Nanoconfined catalysts enhance stabilization of reaction intermediates, facilitate electron transfer, and safeguard active centers, leading to superior electrocatalytic activity, particularly in CO2 reduction reactions (CO2RR). Despite their effectiveness, crafting nanoconfined catalysts is challenging due to unclear formation mechanisms. In this study, we introduce an electrochemical method to grow Pd clusters within the interlayers of two-dimensional black phosphorus, creating Pd cluster-intercalated black phosphorus (Pd-i-BP) as an electrocatalyst. Using in situ electrochemical liquid phase transmission electron microscopy (EC-TEM), we revealed the synthesis mechanism of Pd-i-BP, involving electrochemically driven Pd ion intercalation followed by reduction within the BP layers. The Pd-i-BP electrocatalyst exhibits exemplary CO2-to-formate conversion, achieving 90% Faradaic efficiency for formate production, owing to its distinct nanoconfined structure that stabilizes intermediates and enhances electron transfer. Density functional theory (DFT) calculations underscore the structural benefits for enhancing intermediate adsorption and catalyzing the reaction. Our insights deepen understanding of nanoconfined material synthesis, promising advanced, high-efficiency catalysts.

Porous Crystalline Materials Based on Tetrathiafulvalene and Its Analogues: Assembly, Charge Transfer, and Applications.

ConspectusThe directed synthesis and functionalization of porous crystalline materials pose significant challenges for chemists. The synergistic integration of different functionalities within an ordered molecular material holds great significance for expanding its applications as functional materials. The presence of coordination bonds connected by inorganic and organic components in molecular materials can not only increase the structural diversity of materials but also modulate the electronic structure and band gap, which further regulates the physical and chemical properties of molecular materials. In fact, porous crystalline materials with coordination bonds, which inherit the merits of both organic and inorganic materials, already showcase their superior advantages in optical, electrical, and magnetic applications. In addition to the inorganic components that provide structural rigidity, organic ligands of various types serve as crucial connectors in the construction of functional porous crystalline materials. In addition, redox activity can endow organic linkers with electrochemical activity, thereby making them a perfect platform for the study of charge transfer with atom-resolved single-crystal structures, and they can additionally serve as stimuli-responsive sites in sensor devices and smart materials.In this Account, we introduce the synthesis, structural characteristics, and applications of porous crystalline materials based on the famous redox-active units, tetrathiafulvalene (TTF) and its analogues, by primarily focusing on metal-organic frameworks (MOFs) and covalent organic frameworks (COFs). TTF, a sulfur-rich conjugated molecule with two reversible and easily accessible oxidation states (i.e., radical TTF•+ cation and TTF2+ dication), and its analogues boast special electrical characteristics that enable them to display switchable redox activity and stimuli-responsive properties. These inherent properties contribute to the enhancement of the optical, electrical, and magnetic characteristics of the resultant porous crystalline materials. Moreover, delving into the charge transfer phenomena, which is key for the electrochemical process within these materials, uncovers a myriad of potential functional applications. The Account is organized into five main sections that correspond to the different properties and applications of these materials: optical, electrical, and magnetic functionalities; energy storage and conversion; and catalysis. Each section provides detailed discussions of synthetic methods, structural characteristics, the physical and chemical properties, and the functional performances of highlighted examples. The Account also discusses future directions by emphasizing the exploration of novel organic units, the transformation between radical cation TTF•+ and dication TTF2+, and the integration of multifunctionalities within these frameworks to foster the development of smart materials for enhanced performance across diverse applications. Through this Account, we aim to highlight the massive potential of TTF and its analogues-based porous crystals in chemistry and material science.

Designing pH-Responsive alizarin hybrids with easily tunable physicochemical properties via polymer grafting

This study focuses on the synthesis and characterization of novel pH-sensitive color materials based on alizarin, (1,2-dihydroxyanthraquinone), a natural pigment with versatile properties. The polymer-based indicators were prepared by grafting poly(methyl methacrylate) (PMMA) and poly(2-hydroxyethyl methacrylate) (PHEMA) from alizarin through an ester pH-liable bond, allowing for easy tunability of their physicochemical properties. The synthesis process involved the esterification of alizarin using 2-bromo-2-methylpropionyl bromide, facilitated by triethylamine as an acid scavenger. The resulting alizarin served as a difunctional initiator for atom transfer radical polymerization (ATRP) of methyl methacrylate and 2-hydroxyethyl methacrylate. The molecular structures of the synthesized hybrids were confirmed using 1H NMR and GPC analyses. The color characteristic, surface energy, thermal stability, and pH sensing activity of the alizarin-based hybrids were studied according to the type of grafted polymer nature as well as their degree of polymerization. PHEMA-grafted alizarin showed more rapid and more visible color changes under the influence of NH3 vapours compared to PMMA hybrids, due to their less hydrophobic nature. Furthermore, kinetic plots demonstrated various hydrolysis rates, with PMMA hydrolysis being slower than that of PHEMA due to its stronger hydrophobic character. UV–Vis spectra and GPC traces confirmed the occurrence of hydrolysis and successful cleavage of the ester bond links between the grafted polymers and alizarin with a decrease of the molar mass by a factor of two as expected. Such behavior offers opportunities for tailoring degradation profiles and achieving specific release profiles upon application of a wide range of polymers with varied character. The designed polymer-based pigments exhibited a high ability to monitor calorimetrically the pH changes, especially in alkaline conditions. Overall, this study contributes to the broadening of the application of alizarin-based materials, paving the way for further exploration and development in the field of functional materials.

Real-Time Direct Monitoring of Chirality Fixation and Recognition at the Single-Molecule Level.

Chirality, a fundamental attribute of nature, significantly influences a wide range of phenomena related to physical properties, chemical reactions, biological pharmacology, and so on. As a pivotal aspect of chirality research, chirality recognition contributes to the synthesis of complex chiral products from simple chiral compounds and exhibits intricate interplay between chiral materials. However, macroscopic detection technologies cannot unveil the dynamic process and intrinsic mechanisms of single-molecule chirality recognition. Herein, we present a single-molecule detection platform based on graphene-molecule-graphene single-molecule junctions to measure the chirality recognition involving interactions between amines and chiral alcohols. This approach leads to the realization of in situ and real-time direct observation of chirality recognition at the single-molecule level, demonstrating that chiral alcohols exhibit compelling potential to induce the formation of the corresponding chiral configuration of molecules. The amalgamation of theoretical analyses with experimental findings reveals a synergistic action between electrostatic interactions and steric hindrance effects in the chirality recognition process, thus substantiating the microscopic mechanism governing the chiral structure-activity relationship. These studies open up a pathway for exploring novel chiral phenomena from the fundamental limits of chemistry, such as chiral origin and chiral amplification, and offer important insights into the precise synthesis of chiral materials.

Phenyl-bridged N,N,N'N'-Tetrasubstituted bis(2-amino-5-thiazolyl) diamine: Synthesis and applications in electrochromism and photocatalytic nitrobenzene reduction

A novel type of triphenylamine derivatives, phenyl-bridged N,N,N′,N′-tetrasubstituted bis(2-amino-5-thiazolyl) diamine (4) and its cationic form (5) were synthesized via the Hantzsch reaction. The UV–Vis spectroscopy, cyclic voltammetry (CV) and density functional theory (DFT) calculation results showed that the diamine possesses excellent redox properties and a narrow optical energy gap (∼1.85 eV). As an electrochromic material, compound 4 exhibits a notable color change from colorless to blue. It maintains stable cycling performance for up to 175 cycles, even within a higher voltage range of −2.4 to 2.4 V. In addition, as a catalyst, compound 5 exhibits good substrate compatibility and an aniline conversion rate of up to 89 % during the photocatalytic reduction of nitrobenzene. These results would contribute to understand the synthesis of triphenylamine electrochromic materials and expand their applications in the field of photocatalysis.

Sodium iron sulfate cathodes with ultra-long cycle-life and high safety for sodium-ion batteries

The development of low-cost and high-safety cathode materials is critically important to sodium-ion battery (Na-ion) research. Here we report a carbon nanotube (CNT)-percolating Na2Fe(SO4)2 cathode (NFS-CNT) prepared via a rationally designed mechano-chemical method. The material synthesis mechanism is elucidated for the first time by in situ X-ray diffraction and thermogravimetric analysis. It is discovered that Na2Fe(SO4)·4H2O is formed as an intermediate phase during the mechano-chemical process, which is dehydrated to produce the Na2Fe(SO4)2 cathode material upon a mild thermal treatment. The NFS-CNT composite cathode achieves an ultra-long cycle-life of over 13,000 cycles at 10 C at room temperature and over 6000 cycles at 55 °C, demonstrating its exceptional durability. The superior cycling performance is attributed to the small lattice change during Na-ion extraction/insertion and the percolating CNT network. Furthermore, the NFS/CNT cathode exhibits stable cycle performance in Na-ion full cells (93.4 % retention after 700 cycles) and a significantly lower heat release (∼ 229.2 J g−1) at the fully charged state compared to a wide range of Na-ion and Li-ion cathodes. materials. demonstrating its high thermal stability and safety. This work provides a promising path towards developing low-cost, high-performance Na-ion batteries.

The Three-Dimensional Hierarchical Structure of Bi x -Sn1-x O2 Used for Ultrasensitive Detection of Butanone under UV Irradiation.

Recent studies have identified butanone as a promising biomarker in the breath of lung cancer patients, yet the understanding of its gas-sensing properties remains limited. A key challenge has been to enhance the gas-sensing performance of materials toward butanone, particularly under ultraviolet light exposure. Herein, we report the synthesis of a novel three-dimensional composite material composed of SnO2 incorporated with Bi2O3 using facile hydrothermal and impregnation precipitation methods. Detailed physical and chemical characterizations were performed to assess the properties of the developed material. Upon activation with ultraviolet light, our composite exhibited exceptionally high sensitivity to butanone. Remarkably, the butanone response was nearly 3 times greater for the Bi2O3-loaded SnO2 composite than for pristine SnO2, achieving a response value of 70. This substantial improvement is due to the synergistic effect of the material's distinctive three-dimensional architecture and the presence of Bi2O3, which significantly augmented the gas-sensing capability of butanone. To elucidate the underlying gas-sensing mechanism, we conducted first-principles calculations using density functional theory (DFT). The computational analysis revealed that the Bi2O3-containing system possesses superior adsorption energy for butanone. Ultimately, our findings suggest that the Bi-SnO2 composite holds great promise as an optimal sensing material for the detection of butanone under ultraviolet illumination.

Electromagnetic Interference Shields Based on Highly Crystalline Single-Walled Carbon Nanotubes.

Although the convenience provided by electromagnetic waves used for information exchange is increasing, the energy of unwanted electromagnetic waves unintentionally emitted from devices is increasing as the devices work with higher frequency. In view of this vulnerability, thin films as lightweight electromagnetic wave shields against noise will be necessary for information protection. We propose the fabrication of lightweight electromagnetic wave shields using highly crystalline single-walled carbon nanotubes (HC-SWCNTs), which can be made large and flexible using a method based on a wet process, utilizing the optical and conductive properties of HC-SWCNTs. Electromagnetic wave shields are mainly classified into conductive, dielectric, and magnetic absorbers. We have developed a material synthesis technology for HC-SWCNTs and attempted to form an aqueous composite film using HC-SWCNTs and an organic binder. As a result, we found that the high crystallinity of CNTs suppresses the contact resistance between CNTs and we succeeded in constructing a flexible electromagnetic wave shielding film that can absorb electromagnetic waves in a wide bandwidth equivalent or superior to that of metal foil. This thin film can be applied to curved surfaces as desired because of its wet process, and it is expected to be a lightweight shield that can be used ubiquitously.

Synergy of carboxymethyl cellulose stabilized nanoscale zero-valent iron and Penicillium oxalicum SL2 to remediate Cr(VI) contaminated site soil

Nano zero-valent iron (nZVI) acting as a high-cost disposable material in soil Cr(VI) remediation faces significant challenges due to its easily oxidizable nature and biological toxicity. In addressing this issue, the present study undertook the synthesis of a series of modified nZVI and combined the selected material with Cr(VI)-resistant filamentous fungus Penicillium oxalicum SL2 for real-site chromium pollution remediation. Adsorption experiments demonstrated that the inclusion of carboxymethyl cellulose (CMC) significantly enhanced the adsorption capacity of nZVI for Cr(VI) by 19.3% (from 73.25 to 87.4 mg/L), surpassing both biochar (37.42 mg/L) and bentonite modified nZVI (48.03 mg/L). Characterization results validated the successful synthesis of the nano composite material. Besides, oxidative stress analysis explained the unique detoxification effects of CMC on SL2, acting as a free radical scavenger and isolating layer. In real-sites soil remediation experiments, a low dosage (0.4% w/w) of nZVI/CMC@SL2 (CMC modified nZVI combined with SL2) exhibited an impressive reduction of over 99.5% in TCLP-Cr(VI) and completely transformed 18% of unstable Cr to stable forms. Notably, nZVI/CMC demonstrated its capability to facilitate SL2 colonization in highly contaminated soil and modulate the microbial community structure, enriching chromium-removing microorganisms. In summary, the synergistic system of nZVI/CMC@SL2 merges as a cost-effective and efficient approach for Cr(VI) reduction, providing meaningful insights for its application in the remediating contaminated site soils.

Pressure generation under deformation in a large-volume press

Abstract Deformation can change the transition pathway of materials under high pressure, thus significantly affects physical and chemical properties of matters. However, accurate pressure calibration under deformation is challenging and thereby causes relatively large pressure uncertainties in deformation experiments, resulting in the synthesis of complex multiphase materials. Here, pressure generations of three types of deformation assemblies were well calibrated in a Walker-type large-volume press (LVP) by electrical resistance measurements combined with finite element simulations (FESs). Hard Al2O3 or diamond pistons in shear and uniaxial deformation assemblies significantly increases the efficiency of pressure generation compared with the conventional quasi-hydrostatic assembly. The uniaxial deformation assembly using flat diamond pistons possess the highest efficiency in these deformation assemblies. This finding is further confirmed by stress distribution analysis based on FESs. With this deformation assembly, we found shear can effectively promote the transformation of C60 into diamond under high pressure and realized the synthesis of pure-phase diamond at relatively moderate pressure and temperature conditions. The present developed techniques will help improve pressure efficiencies in LVP and explore the new physical and chemical properties of materials under deformation in both science and technology.

Rapid and efficient mineralization of methylene blue dye (above 95 % in 20 min) catalyzed by ZnO nanoparticles under sunlight

This novel communication reports rapid mineralization of methylene blue dye, reaching above 95% in 20 min under cloudy sunlight catalyzed by ZnO nanoparticles, which were synthesized from N-Dipentene as a reducing agent, at different zinc acetate concentrations from 0.1 M to 0.4 M. The synthesized ZnO nanoparticles structural, morphological, compositional, and optical characterizations were done using X-ray diffraction (XRD), high resolution scanning microscopy (HRSEM), energy dispersive spectroscopy (EDS) and photoluminescence (PL) respectively. From these characterizations ZnO wurtzite crystalline structure, average crystallite size (18–25 nm) with heterogeneous elongated nanoparticles mixed to triangle like particles and low content of byproducts as well as the presence of oxygen Vacancies transitions at the red-orange bands, which contributes to the PL main emission related to the visible region at the electromagnetic spectrum were obtained, these results were correlated to the photocatalytic activity. Meanwhile direct sunlight photocatalyst using 17 mg of ZnO for 10 ppm of methylene blue dye (MB) degradation was performed, the efficiency was analyzed by Fourier transform infrared spectroscopy (FT-IR) and UV–Vis spectroscopy, obtaining the kinetic adsorption ratio fitted to the pseudo second order (PSO) and the pseudo first order (PFO) to determine the mechanism that governs this process. All those analyses were correlated to the material characteristics and synthesis concentration. A 95.38 % efficiency was reached at 20 min for the champion sample D3R followed by D4R, D2R and D1R reaching an 89.19, 80.40 and 66.86 % for the same time. The maximum mineralization efficiency for D3RA was 98.08 % at 30 min, albeit it was observed that the adsorption kinetics obeys the Pseudo second order (PSO) for D3R, D4R and D2R meanwhile for D1R is governed by the Pseudo First Order mechanism (PFO), mainly by the diffusive chemical mechanism.

Fast preparation and thermoelectric performance of AgSTe based materials via plasma activated sintering

AgSTe based materials have recently been identified as promising thermoelectric materials that have favorable properties at room temperature. They are usually obtained by conventional processes involving melting, annealing, and sintering, which incur significant energy and time expenditures. The present investigation involved the synthesis of Ag20S7Te3 compounds by a fast non-equilibrium methodology, i.e., plasma activated sintering from raw elemental powders. The monoclinic Ag20S7Te3 phase crystal was successfully formed at a temperature of 673 K, accompanied by the presence of a secondary monoclinic phase, Ag2S. The Ag20S7Te3 phase predominated in the monoclinic form, constituting a significant percentage at temperature of 873 K. Furthermore, the thermoelectric figure of merit (zT) of the AgSTe phase at 873 K was determined to be 0.42. The rapid sample synthesis described herein has the potential to significantly reduce the duration required for material synthesis, hence presenting a conspicuous advantage in the context of manufacturing on a wide scale.

Low‐temperature chemical vapor deposition growth of 2D materials

AbstractTwo‐dimensional (2D) materials have atomic thickness, and thickness‐dependent electronic transport, optical and thermal properties, highlighting great promise applications in future semiconductor devices. Chemical vapor deposition (CVD) is considered as an industry‐oriented method for macro‐synthesis of 2D materials. In conventional CVD, high temperatures are required for the synthesis of high‐quality large‐size 2D materials, which is incompatible with of back‐end‐of‐line of the complementary metal oxide semiconductor (CMOS) techniques. Therefore, low‐temperature synthesis of 2D materials is of critical importance for the advancement toward practical applications of 2D materials with the CMOS technologies. In this review, we focus on strategies for the low‐temperature growth of 2D materials, including the use of low‐melting‐point precursors, metal‐organic CVD, plasma‐enhanced CVD, van der Waals‐substrate vapor phase epitaxy, tellurium‐assisted CVD, salt‐assisted CVD, etc., with discussions of their reaction mechanisms, applications, associated advantages, and limitations. We also provide an outlook and perspectives of future low‐temperature chemical vapor deposition growth of 2D materials.

Advances in Functional Ceramics for Water Splitting: A Comprehensive Review

The global demand for sustainable energy sources has led to extensive research regarding (green) hydrogen production technologies, with water splitting emerging as a promising avenue. In the near future the calculated hydrogen demand is expected to be 2.3 Gt per year. For green hydrogen production, 1.5 ppm of Earth’s freshwater, or 30 ppb of saltwater, is required each year, which is less than that currently consumed by fossil fuel-based energy. Functional ceramics, known for their stability and tunable properties, have garnered attention in the field of water splitting. This review provides an in-depth analysis of recent advancements in functional ceramics for water splitting, addressing key mechanisms, challenges, and prospects. Theoretical aspects, including electronic structure and crystallography, are explored to understand the catalytic behavior of these materials. Hematite photoanodes, vital for solar-driven water splitting, are discussed alongside strategies to enhance their performance, such as heterojunction structures and cocatalyst integration. Compositionally complex perovskite oxides and high-entropy alloys/ceramics are investigated for their potential for use in solar thermochemical water splitting, highlighting innovative approaches and challenges. Further exploration encompasses inorganic materials like metal oxides, molybdates, and rare earth compounds, revealing their catalytic activity and potential for water-splitting applications. Despite progress, challenges persist, indicating the need for continued research in the fields of material design and synthesis to advance sustainable hydrogen production.

Using scalable computer vision to automate high-throughput semiconductor characterization

High-throughput materials synthesis methods, crucial for discovering novel functional materials, face a bottleneck in property characterization. These high-throughput synthesis tools produce 104 samples per hour using ink-based deposition while most characterization methods are either slow (conventional rates of 101 samples per hour) or rigid (e.g., designed for standard thin films), resulting in a bottleneck. To address this, we propose automated characterization (autocharacterization) tools that leverage adaptive computer vision for an 85x faster throughput compared to non-automated workflows. Our tools include a generalizable composition mapping tool and two scalable autocharacterization algorithms that: (1) autonomously compute the band gaps of 200 compositions in 6 minutes, and (2) autonomously compute the environmental stability of 200 compositions in 20 minutes, achieving 98.5% and 96.9% accuracy, respectively, when benchmarked against domain expert manual evaluation. These tools, demonstrated on the formamidinium (FA) and methylammonium (MA) mixed-cation perovskite system FA1−xMAxPbI3, 0 ≤ x ≤ 1, significantly accelerate the characterization process, synchronizing it closer to the rate of high-throughput synthesis.

Recovery of Lithium from Industrial Li-Containing Wastewater Using Fluidized-Bed Homogeneous Granulation Technology

In this study, a novel fluidized-bed homogeneous granulation (FBHo-G) process was developed to recover lithium (Li) from industrial Li-impacted wastewater. Five important operational variables (i.e., temperatures, pH, [P]0/[Li]0 molar ratios, surface loadings, and up-flow velocities (Umf)) were selected to optimize the Li recovery (TR%) and granulation ratio (GR%) efficiencies of the process. The optimal operational conditions were determined as the following: a temperature of 75 °C, pH of 11.5, [P]0/[Li]0 of 0.5, surface loading of 2.5 kg/m2·h, and Umf of 35.7 m/h). The TR% and GR% at optimal condition could be as much as 90%. The material characterization of the recovery pellet products showed that they were highly crystallized Li3PO4 (purity ~88.2%). The pellets had a round shape and smooth surface with an average size of 0.65 mm, so could easily be stored and transported. The high purity enables them to be further directly reused as raw materials for a wide range of industrial applications (e.g., in the synthesis of cathode materials). Our calculation shows that the FBHo-G process could recover up to 0.1845 kg of lithium per cubic meter of Li-containing wastewater, at a recovery rate of ~90%. A brief technoeconomic analysis shows that FBHG process had economic viability, with an estimate production cost of USD 26/kg Li removed, while the potential gained profit for selling lithium phosphate pellets could be up to USD 48 per the same volume of wastewater and the net profit up to USD 22/m3 Li treated. In all, fluidized-bed homogeneous granulation, a seedless one-step recovery process, opens a promising pathway toward a green and sustainable recycling industry for the recovery and application of the resource-limited lithium element from nonconventional water sources.

Application of catalytic technology based on the piezoelectric effect in wastewater purification

The demands of human life and industrial activities result in a significant influx of toxic contaminants into aquatic ecosystems. In particular, organic pollutants such as antibiotics and dye molecules, bacteria, and heavy metal ions are represented, posing a severe risk to the health and continued existence of living organisms. The method of removing pollutants from water bodies by utilizing the principle of the piezoelectric effect in combination with chemical catalytic processes is superior to other wastewater purification technologies because it can collect water energy, mechanical energy, etc. to achieve cleanliness and high removal efficiency. Herein, we briefly introduced the piezoelectric mechanisms and then reviewed the latest advances in the design and synthesis of piezoelectric materials, followed by a summary of applications based on the principle of piezoelectric effect to degrade pollutants in water for wastewater purification. Moreover, water purification technologies incorporating the piezoelectric effect, including piezoelectric effect-assisted membrane filtration, activation of persulfate, and battery electrocatalysis are elaborated. Finally, future challenges and research directions for the piezoelectric effect are proposed.

The Future of Protection: Unleashing the Power of Nanotech against Corrosion

Corrosion and nanomaterials application gives a complete understanding of corrosion, a pervasive and costly problem that affects a variety of industries worldwide. This study investigates the negative effects of corrosion on infrastructure, safety, and product durability by examining its natural processes and various forms. Regardless of their relative effectiveness, intrinsic restrictions typically limit conventional corrosion control techniques. This article aims to investigate the topic of nanomaterials, which are rapidly emerging and have the potential to significantly reduce corrosion. This abstract delves into the fascinating world of nanomaterials, which range in size from 1 to 100 nanometres, and explores their remarkable powers. Nanomaterials offer substantial advancements in corrosion management, such as better coatings, self-healing mechanisms, and even "smart" coatings with sensing capabilities. The article focuses on the potential benefits of employing nanoparticles for corrosion management, drawing on recent research and imaginative applications. Nanotechnology enables the creation of novel solutions like superior barriers, increased durability, self-repairing capabilities, and targeted corrosion avoidance. However, hurdles remain as the abstract investigates the complexities of manufacturing costs, uncertainty about long-term efficiency, potential environmental effects, and scalability problems associated with adding nanomaterials to corrosion control systems. Understanding corrosion and nanomaterial applications provides essential insights into the fundamental mechanics of corrosion, as well as the significant impact of nanotechnology. This abstract aims to encourage academics, engineers, and policymakers to use nanomaterials to address the ongoing problem of corrosion. Its goal is to promote the use of nanomaterials in diverse industries by giving interdisciplinary insights and forward-thinking ideas that improve durability, safety, and sustainability. Corrosion, a relentless degrader of infrastructure and industrial assets, necessitates novel approaches to mitigate its negative impacts. Nanotechnology has lately emerged as a promising frontier in corrosion mitigation, presenting unrivalled opportunities for improved protection and a longer service life. This paper examines the current state of nanotechnology-based corrosion protection, discusses key obstacles and prospects, and makes recommendations for future advances. Nanotechnology's ability to manipulate materials at the atomic and molecular level has transformed the field of corrosion protection. Nanomaterials, which include nanoparticles, nanocomposites, and nanocoatings, have distinct features that make them particularly effective in inhibiting corrosion start-up and propagation. Nanotech-based solutions outperform conventional coatings in terms of adhesion, barrier characteristics, and chemical resistance, thanks to precise engineering and surface modification approaches. Despite tremendous advancements, broad implementation of nanotechnology-based corrosion prevention confronts challenges. Standardisation and regulation are critical for ensuring the safety, reliability, and environmental sustainability of nanomaterials and coatings. Academics, industry, and regulating authorities must work together to provide comprehensive criteria for material synthesis, characterization, and application. Initiatives that promote education and awareness are critical for accelerating the use of nanotechnology in corrosion protection. Training programmes and knowledge-sharing platforms can provide engineers and industry experts with the necessary skills and competence to properly implement nanotech-based solutions. Public communication efforts emphasizing the benefits of nanotechnology in maintaining infrastructure integrity can garner support from stakeholders and governments. The future possibilities for nanotech-based corrosion prevention are very promising. Advances in nanomaterial production techniques provide unparalleled control over material properties, paving the way for the creation of tailored coatings with superior performance characteristics. Integration with other emerging technologies, like artificial intelligence and the Internet of Things (IoT), has the potential to improve corrosion monitoring and management approaches. Furthermore, the creation of self-healing nanoparticles constitutes a significant advancement in corrosion protection. Inspired by biological systems, self-healing nanocomposites can repair corrosion-induced damage on their own, prolonging the service life of infrastructure assets and lowering lifecycle costs. Continued investment in research and development is crucial to realising nanotechnology's full promise for corrosion protection and ushering in a new era of resilience and dependability. Nanotechnology provides transformative corrosion control solutions that have the potential to revolutionise a variety of industrial sectors. By addressing important obstacles and capitalising on emerging opportunities, we can use nanotechnology to protect infrastructure, conserve resources, and assure long-term growth for future generations.