Nanoscale Materials Research Articles

Eco-friendly nanocomposite particles CuO/Fe2O3 and CuFeO2 as corrosion inhibitors of reinforced steel for concrete

Abstract In the last period of scientific research, the application of nanoscale materials had a huge interest in enhancing sustainability and improving the performance of concrete. This paper discusses lots of experimental truths about nanoparticles (CuO, Fe2O3) and nanocomposite particles (CuFeO2 and CuO/Fe2O3), which are manufactured by green chemistry and their effect on concrete. Because of their advanced properties due to containing the two heavy transition metals iron and copper, these particles can It is possible to bring about a wide development in the field of building and construction, and they may finalize more than one function at the same time. The dispersion of nanoparticles (Nps) in concrete mixtures is a key strategy to achieve the tailoring process, which is used to design new materials with specific properties to perform desired functions or applications. In this paper, resistance against chemical corrosion is achieved. These nanocomposites (Ncps)can improve the microstructure, function, and strength. The SEM, physical, mechanical characterization, workability and electrochemical measurements of the concrete based on those Nps. The results discovered that those Nps are corrosion resistant, contributing to decreased failure corrosion problems, which may lead to continuing to work at the same level throughout the years of service. This communication aims to provide a deep comprehension of the role of (Ncps) admixtures in concrete composites. They provide possible methods to enhance their overall characteristics and establish the basis for a more sustainable and long-lasting future in the building field.

Exploring the atomic-scale dynamics of Fe3O4(001) at catalytically relevant temperatures using FastSTM

Surfaces and interfaces of functional nanoscale materials are typically highly dynamic when employed at elevated temperatures. Both, lateral surface and vertical bulk exchange diffusion processes set in, which can be relevant for applications such as heterogeneous catalysis. Time-resolved scanning tunneling microscopy (STM) is being pushed to ever faster measurement modes to follow such dynamic phenomena in situ. Here, we present FastSTM movies monitoring a range of atomic-scale dynamics of a prototypical reducible oxide catalyst support, Fe3O4(001), at elevated temperatures. Antiphase domain boundaries between two domains of the reconstructed surface exhibit local mobility from around 350 K, while Fe-rich point defects, in a stable equilibrium with the bulk, appear to diffuse in a peculiar zigzag pattern above 500 K. Finally, exploiting the diffusivity of Fe interstitials, we follow the propagation of step edges in the topmost atomic layer of the Fe3O4(001) surface in an oxygen atmosphere.

Nanostructured materials as hazardous wastewater micropullutants: Sources, behavior, and impact on functional bacterial community of activated sludge

Unique properties of nanoscale materials make them attractive for industrial, medical, agricultural, and environmental applications. Nevertheless, the release of nanoparticles into the environment is a major concern due to the lack of knowledge about their behavior in the environment and potential widespread environmental impacts. On the one hand, nanomaterials are perceived as pollutants that may affect activated sludge microorganisms and, consequently, the efficiency of wastewater treatment processes. On the other hand, some nanomaterials can be intentionally added to activated sludge systems to improve their performance in terms of, e.g., sludge settling and removing heavy metals or organic pollutants. As a result, nanoparticles are frequently accumulated in wastewater, which is considered to be a major source of nanoparticle release to the surrounding environment. Processes that involve the action of activated sludge are used worldwide in wastewater treatment plants due to their excellent capacity of removing nutrients, degrading toxins, and retaining biomass. High concentrations of nanoparticles entering activated sludge systems can affect their growth and metabolism. The research studies, which are reviewed in the present article, show that nanoparticles significantly reduce the relative abundance of the activated sludge microbial community associated with nitrification, denitrification, and phosphorus removal. The knowledge about the structure of the activated sludge microbial community with an assessment of nanomaterial toxicity can contribute to optimizing the sludge population and improving the performance of wastewater treatment plants.

An Experimental Study on Algae Biodiesel with Nano-additives for Engine Performance and Emission Reduction

Introducing nano-additives like aluminum oxide and cerium oxide into the B20 blend biodiesel exhibited encouraging outcomes of combustion efficiency and emission reduction. These additives likely catalyzed combustion, leading to more complete fuel burn and lower emissions. Additionally, the presence of nano-additives might have facilitated better fuel atomization and distribution within the combustion chamber, resulting in enhanced engine performance. The results indicate that adding nano-additives to biodiesel blends has significant potential for reducing environmental impact and enhancing engine longevity and efficiency. Moreover, the utilization of nano-additives represents a promising avenue for addressing the dual challenges of energy sustainability and environmental preservation. By harnessing the synergistic effects of nano-scale materials, such as aluminum oxide and cerium oxide, in biodiesel formulations, engineers and researchers can strive towards developing cleaner and more efficient propulsion systems. This holistic approach underscores the importance of cooperation across disciplines between materials science, engineering, and environmental studies to advance the frontiers of sustainable energy technologies. The study attempted to improve combustion efficiency and reduce emissions by introducing nano-additives like aluminum oxide and cerium oxide into B20 biodiesel. The outcome showed enhanced engine performance, more complete fuel burn, and significant potential for reducing environmental impact.

Agricultural nanotechnology for a safe and sustainable future: current status, challenges, and beyond.

Nanotechnology, which involves manipulating matter at the atomic and molecular scales to produce structures and devices ranging from 1 to 100 nm, is increasingly being applied in agriculture. Nanoscale materials possess distinct optical, electrochemical, and mechanical properties that enable the smart, targeted delivery of pesticides, fertilizers, and genetic materials to plants, as well as rapid sensing and on-site monitoring of plant health, soil fertility, and water quality in a digital format. This review explores the application of nanotechnology in agriculture, examining the challenges and benefits related to all aspects of crop production, with a particular focus on regulatory issues. Key findings indicate that nanotechnology can improve crop production and reduce the environmental footprint of agriculture through precise input management. However, several critical issues need to be addressed, including the limited knowledge of the long-term environmental impacts associated with agricultural nanotechnology and the ambiguity of current regulations. This underscores the need for further research to elucidate its impact on soil, water, and environmental and human health, to inform evidence-based regulations. © 2024 The Author(s). Journal of the Science of Food and Agriculture published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.

Overview on Nanomaterials for Nanocosmetics

One of the scientific areas with the highest growth right now is nanotechnology. The development of nanocosmetics through the use of nanoscale materials has become more popular in recent years. Due to distinct structures, chemical, physical, physiochemical, and functional properties - most of them are absent in their non-nanoscale forms - some nanomaterial types are extremely appealing for use in the cosmetics sector. Regardless of their kind, form, morphology, or content, nanomaterials have two primary purposes in cosmeceutical inventory [1]: nano-constructs as (UV) filters, and [2] nanostructures as biologically active components for topical applications and other treatments associated with cosmeceuticals, such as moisturizers, skincare, makeup, sunscreen, and hair care products. As Ultraviolet filters or Ultraviolet protectants, various types of nanoparticles, such as silver, gold, titanium, and zinc, have been employed in the former scenario to hinder or to Utilize UV radiation and shield the layer beneath the skin from damaging consequences. Nanoliposomes are the delivery systems used in the 2nd concept usage. Therefore, next-generation cosmeceutical solutions for blossoming beauty that offer enhanced skin hydration, bioavailability, agent stability, and regulated UV occlusion have been highlighted as potentially becoming nanomaterial-loaded nanocosmetics. In light of the criticisms mentioned earlier and the potentialities of nanomaterials, we first examined the benefits of using nanoliposomes and nanoparticles as UV filters and delivery systems. The work's second split discusses the safety and legal implications of nanoparticles employed in compositions. Concluding remarks and suggestions for further study round out the work and enable material scientists to securely utilize nanoparticles in large-scale commercial goods.

A Bulk versus Nanoscale Hydrogen Storage Paradox Revealed by Material‐System Co‐Design

AbstractMetal hydrides are serious contenders for materials‐based hydrogen storage to overcome constraints associated with compressed or liquefied H2. Their ultimate performance is usually evaluated using intrinsic material properties without considering a systems design perspective. An illustrative case with startling implications is (LiNH2+2LiH). Using models that simulate the storage system and associated fuel cell of a light‐duty vehicle (LDV), the performance of the bulk hydrides is compared with a nanoscaled version in porous carbon (PC), (LiNH2+2LiH)@(6‐nm PC). Using experimental material properties, the simulations show that (LiNH2+2LiH)@(6‐nm PC) counterintuitively has higher usable gravimetric and volumetric capacities than the bulk counterpart on a system basis despite having lower capacities on a materials‐only basis. Nanoscaling increases the thermal conductivity and lowers the desorption enthalpy, which consequently increases heat management efficiency. In a simulated drive cycle for fuel cell‐powered LDV, the fuel cell is inoperable using bulk (LiNH2+2LiH) as the storage material but completes the drive cycle using the nanoscale material. These results challenge the notion that nanoscaling incurs mass and volume penalties. Instead, the synergistic nanoporous host‐hydride interaction can favorably modulate chemical and heat transfer properties. Moreover, a co‐design approach considering application‐specific tradeoffs is essential to accurately assess a material's potential for real‐world hydrogen storage.

Coordinate-based simulation of pair distance distribution functions for small and large molecular assemblies: implementation and applications.

X-ray scattering has become a major tool in the structural characterization of nanoscale materials. Thanks to the widely available experimental and computational atomic models, coordinate-based X-ray scattering simulation has played a crucial role in data interpretation in the past two decades. However, simulation of real-space pair distance distribution functions (PDDFs) from small- and wide-angle X-ray scattering, SAXS/WAXS, has been relatively less exploited. This study presents a comparison of PDDF simulation methods, which are applied to molecular structures that range in size from β-cyclo-dextrin [1 kDa molecular weight (MW), 66 non-hydrogen atoms] to the satellite tobacco mosaic virus capsid (1.1 MDa MW, 81 960 non-hydrogen atoms). The results demonstrate the power of interpretation of experimental SAXS/WAXS from the real-space view, particularly by providing a more intuitive method for understanding of partial structure contributions. Furthermore, the computational efficiency of PDDF simulation algorithms makes them attractive as approaches for the analysis of large nanoscale materials and biological assemblies. The simulation methods demonstrated in this article have been implemented in stand-alone software, SolX 3.0, which is available to download from https://12idb.xray.aps.anl.gov/solx.html.

An integrated push-to-pull micromechanical device: Design, fabrication, and in-situ experiment

The rapid advancement of micro-nano machining technology has led to a decrease in the dimensions of microdevices and microchips, following the principles of Moore’s law. In addition to conventional semiconductor materials like silicon, emerging nanoscale materials such as nanowires, nanotubes, and two-dimensional materials are being considered as promising alternative constituent materials. The mechanical properties of these materials have a significant impact on the performance and service life of these microdevices and microchips. However, conventional mechanical testing methods have difficulty in accurately measuring the properties of these materials at the nanoscale due to limitations in displacement control and microforce sensing. Consequently, there is an urgent need to develop a micromechanical device capable of testing nanoscale solid materials. In this study, we propose a concept based on high-resolution image sequences for the design of an integrated micromechanical device capable of synchronously measuring the force and deformation of tested specimens. The device has been fabricated using ultrafast femtosecond laser etching technology, which offers an efficient and cost-effective approach for manufacturing microstructures and is suitable for processing various materials such as metals and nonmetals. The stiffness of the device plays a crucial role in the design of the micromechanical device, and a stiffness-matching criterion is introduced to ensure appropriate design parameters. The fabricated device is employed to conduct in-situ tension experiments on SiC nanowires and multilayer molybdenum disulfide nanosheet within a scanning electronic microscope, enabling accurate measurement of their strength, modulus, and fracture strain.

A comparison of conventional sodium fluoride varnish and nano-sodium fluoride varnish regarding enamel microhardness of deciduous teeth: an in-vitro study.

Dental caries is the most common chronic disease worldwide, and various forms of fluoride are considered useful preventive tools. The production of nanoscale materials can significantly improve their mechanical and chemical properties. The present study compared the microhardness of primary tooth enamel after applying sodium fluoride varnish (conventional) and nano-sodium fluoride varnish. Sixty-eight sound canine teeth were selected in this experimental study. The teeth were mounted so that the buccal surface was exposed. A 3 × 3mm square was obtained on the buccal surface of the crown of each tooth. Enamel surfaces were polished using sandpaper in the presence of water as a coolant. The samples were randomly divided into four groups (n = 17): G1, conventional 5% NaF; G2, 1% nano-NaF; G3, 5% nano-NaF; G4, control. The initial microhardness was measured. Before surface treatment with different fluoride compounds, the samples were placed in a demineralizing solution for two days, and the microhardness of all the samples was re-measured. Then G1, G2, and G3 were treated with the fluoride type specified for each group, and G4 was treated as a control (without treatment). Finally, pH cycling was applied, and the microhardness was measured again. Data were analyzed with SPSS 20, using Repeated measure ANOVA and post-hoc Tukey tests. P < 0.05 was considered significant. Repeated measure ANOVA showed that microharness of G1, G2, G3, and G4 was statistically significant different. Tukey tests showed that the microhardness of G1, G2, and G3 were not significantly different. However, these three groups exhibited significantly more microhardness than the control group (P = 0.024, P = 0.027, and P = 0.010). There was no significant differences in enamel microhardness of deciduous teeth between conventional 5% NaF,1% nano-NaF and 5% nano-NaF.

Sculpting the Electronic Nano-Terrain on a Perovskite Film for Efficient Charge Transport.

Nanopatterned halide perovskites have emerged to improve the performance of optoelectronic devices by controlling the crystallographic and optical properties via morphological modification. However, the correlation between the photophysical property and morphology transformation in nanopatterned perovskite films remains elusive, which hinders the rational design of nanopatterned halide perovskites for optoelectronic devices. In this study, we employed nanoimprinting lithography on a perovskite film to exert a precise control over grain growth and manipulate electronic structures at the level of individual grains. Surface-selective fluorescence lifetime imaging microscopy (FLIM) analyzes the spatiotemporally disentangled geometrical variations in carrier recombination rate and band structure modulation according to different pattern morphologies. Consequently, the stereoscopic mechanism of confined grain growth was unveiled, highlighting the quantitative grain size-based parameters that are crucial for nanoscale material engineering. Notably, the pattern-induced reduction of effective charge mass enabled exclusive control over the subdiffusive carrier transport dynamics on perovskite surfaces, ultimately realizing the surface-selective perovskite photodetectors. The implications of this study are expected to provide valuable guidelines, inspiring innovative design protocols for advancing the next-generation optoelectronic technologies.

Preparation of two-dimensional assembled silver nanowires and the disturbances faced

At present, self-assembled materials are widely applied and have become one of the most important methods for the preparation of nanomaterials due to their scale effect and structural diversity. Nanoscale self-assembled materials can be used to prepare media with different pore sizes, morphologies and distributions, resulting in larger specific surface area and transparency. Moreover, they can be used to prepare nanoelectronic devices, nanosensors, and nanophotonic devices. Metal self-assembled materials are widely used in nanocatalytic reactions, where their high specific surface area can improve the reaction efficiency and catalytic activity. Silver nanowires, a branch of self-assembled material, are excellent materials for fabricating transparent flexible electrodes. However, the preparation process of silver nanowires faces many difficulties, and it is very challenging to make the final product with low resistivity. Therefore, the paper aims to explore the preparation of silver nanowires and the many interfering factors facing the preparation process. Through the review of related literature, this paper analyzes the basic principles of a series of self-assembled materials, improves further understanding of the concept and application of self-assembled materials, and thus indicates the preparation methods that can obtain silver nanowires with better performance.

Site heterogeneity and broad surface-binding isotherms in modern catalysis: Building intuition beyond the Sabatier principle

Learning the science of heterogeneous catalysis and electrocatalysis always starts with the simple case of a flat, uniform surface with an ideal adsorbate. It has of course been recognized for a century that real catalysts are more complicated. For the increasingly complex catalysts of the 21st century, this Perspective argues that surface heterogeneity and non-ideal binding isotherms are central features, and their implications need to be incorporated in current thinking. A variety of systems are described herein where catalyst complexity leads to broad, non-Langmuirian surface isotherms for the binding of hydrogen atoms – and this occurs even for ideal, flat Pt(111) surfaces. Modern catalysis employs nanoscale materials whose surfaces have substantial step, edge, corner, impurity, and other defect sites, and they increasingly have both metallic and non-metallic elements MnXm, including metal oxides, chalcogenides, pnictides, carbides, doped carbons, etc. The surfaces of such catalysts are often not crystal facets of the bulk phase underneath, and they typically have a variety of potential active sites. Catalytic surfaces in operando are often non-stoichiometric, amorphous, dynamic, and impure, and often vary from one part of the surface to another. Understanding of the issues that arise at such nanoscale, multi-element catalysts is just beginning to emerge. Yet these catalysts are widely discussed using Brønsted/Bell-Evans-Polanyi (BEP) relations, volcano plots, Tafel slopes, the Butler-Volmer equation, and other linear free energy relations (LFERs), which all depend on the implicit assumption that the active sites are “similar” and that surface adsorption is close to ideal. These assumptions underly the ubiquitous intuition based on the Sabatier Principle, that the fastest catalysis will occur when key intermediates have free energies of adsorption that are not too strong nor too weak. Current catalysis research often aims to minimize the complexity of non-ideal isotherms through experimental and computational design (e.g., the use of single crystal surfaces), and these studies are the foundation of the field. In contrast, this Perspective argues that the heterogeneity of binding sites and binding energies is an inherent strength of these catalysts. This diversity makes many nanoscale catalysts inherently a high-throughput screen wrapped in a tiny package. Only by making the heterogeneity part of the foundation of catalysis models, sorting the types of active sites and dissecting non-ideal binding isotherms, will modern catalysis learn to harness the inherent diversity of real catalysts. Controlling and exploiting diversity rather than avoiding it will help to optimize complex modern catalysts and catalytic conditions.

Novel Approaches and Applications of Nanotechnology in the Delivery of Topical Drugs for Psoriasis via Nanocarriers

Psoriasis is a non-contagious, continuing, auto-immune disease that mostly affects the skin, and about 2%-3% of the world's population suffers from it. In this review article, the primary focus is on the strategies involved in conventional therapies and the latest advances that have been recorded in metallic nano, polymer-based, and lipid-based formulations in the spectrum of anti-psoriatic drugs. Liposomes, ethosomes, solid lipid nanoparticles, micelles, and dendrimers are only some of the nanocarrier systems that have been extensively researched in relation to their potential use in nano formulations. This study incorporates patent applications that illustrate the nanoparticle's function in treating psoriasis. Hence, on the basis of an extensive literature survey, it is concluded that nano-formulations are a promising medium to treat a disease like psoriasis as they offer enhanced penetration, target-specific delivery, and improved efficacy. When applied to the study of biological systems and the development of novel medical technologies, nanobiotechnology offers potentially promising possibilities for the efficient use of nanoscale materials and processes. In this approach, nanotechnology and biotechnology are combined in order to develop nanoscale devices, materials, and systems that can be used for the diagnosis, treatment, and prevention of psoriasis. The future of the therapeutic effect of antipsoriatic drugs is dependent on both the benefits they have the ability to bring and the progress being made in the mass production of these carriers. Researching novel carrier systems or combination therapies is essential, but so is working to scale up existing technologies so they may be commercialised and used to benefit society at large.

Eco-friendly nanotechnology in rheumatoid arthritis: ANFIS-XGBoost enhanced layered nanomaterials

Rheumatoid arthritis (RA) is a chronic autoimmune disorder characterized by inflammation and pain in the joints, which can lead to joint damage and disability over time. Nanotechnology in RA treatment involves using nano-scale materials to improve drug delivery efficiency, specifically targeting inflamed tissues and minimizing side effects. The study aims to develop and optimize a new class of eco-friendly and highly effective layered nanomaterials for targeted drug delivery in the treatment of RA. The study's primary objective is to develop and optimize a new class of layered nanomaterials that are both eco-friendly and highly effective in the targeted delivery of medications for treating RA. Also, by employing a combination of Adaptive Neuron-Fuzzy Inference System (ANFIS) and Extreme Gradient Boosting (XGBoost) machine learning models, the study aims to precisely control nanomaterials synthesis, structural characteristics, and release mechanisms, ensuring delivery of anti-inflammatory drugs directly to the affected joints with minimal side effects. The in vitro evaluations demonstrated a sustained and controlled drug release, with an Encapsulation Efficiency (EE) of 85% and a Loading Capacity (LC) of 10%. In vivo studies in a murine arthritis model showed a 60% reduction in inflammation markers and a 50% improvement in mobility, with no significant toxicity observed in major organs. The machine learning models exhibited high predictive accuracy with a Root Mean Square Error (RMSE) of 0.667, a correlation coefficient (r) of 0.867, and an R2 value of 0.934. The nanomaterials also demonstrated a specificity rate of 87.443%, effectively targeting inflamed tissues with minimal off-target effects. These findings highlight the potential of this novel approach to significantly enhance RA treatment by improving drug delivery precision and minimizing systemic side effects.

Fabrication and characterization of polyvinyl alcohol-chitosan composite nanofibers for carboxylesterase immobilization to enhance the stability of the enzyme

Electrospinning stands out as a flexible and viable method, presenting designed nanoscale materials with customized properties. This research demonstrates the immobilization of carboxylesterase protein Ha006a, reported for its adequacy in pesticide bioremediation by utilizing the electrospinning strategy. This strategy was utilized to create nanofibers by incorporating variable mixtures of biodegradable and cost-effective polyvinyl alcohol (PVA)-chitosan (CS) nanofiber solution (PVA100, PVA96, PVA94, PVA92 and PVA90). All the mixtures were electrospun at a reliable voltage of 21 kV, maintaining a gap of 12 cm from the nozzle. The Ha006a, sourced from Helicoverpa armigera, was consolidated into the optimized PVA90 polymer mixture. The electrospun nanofibers experienced comprehensive characterization utilizing distinctive microscopy and spectroscopy procedures counting FESEM, TGA, XRD and FTIR. The comparative investigation of the esterase property, ideal parameters and stability of the unbound and bound/immobilized Ha006a was scrutinized. The results uncovered an essential elevation in the ideal conditions of enzyme activity post-immobilization. The PVA-CS control nanofiber and Ha006a-PVA-CS showed a smooth structure, including an average breadth of around 170.5 ± 44.2 and 222.5 ± 66.5 nm, respectively. The enzyme-immobilized nanofibers displayed upgraded stability and comprehensive characterization of the nanofiber, which guaranteed genuineness and reproducibility, contributing to its potential as a potent device for bioremediation applications. This investigation opens the way for the manufacture of pesticide-resistant insect enzyme-based nanofibers, unlocking their potential for assorted applications, counting pesticide remediation and ensuring environmental sustainability.

Development of Nanozymatic Characteristics in Metal-Doped Oxide Nanomaterials.

Nanozymes are nanoscale materials that exhibit enzymatic-like activity, combining the benefits of nanomaterials with biocatalytic effects. The addition of metals to nanomaterials can enhance their nanozyme activity by mimicking the active sites of enzymes, providing structural support and promoting redox activity. In this study, nanostructured oxide and silicate-phosphate nanomaterials with varying manganese and copper additions were characterized. The objective was to assess the influence of metal modifications (Mn and Cu) on the acquisition of the nanozymatic activity by selected nanomaterials. An increase in manganese content in each material enhanced proteolytic activity (from 20 to 40 mUnit/mg for BG-Mn), while higher copper addition in glassy materials increased activity by 40%. Glassy materials exhibited approximately twice the 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid radical activity (around 40 μmol/mL) compared to that of oxide materials. The proteolytic and antioxidant activities discussed in the study can be considered indicators for evaluating the enzymatic properties of the nanomaterials. Observations conducted on nanomaterials may aid in the development of materials with enhanced catalytic efficiency and a wide range of applications.

Nanoscale mineral as a novel class enzyme mimic (mineralzyme) with total antioxidant capacity detection: Colorimetric and smartphone-based approaches

Nanozymes, synthetic nano-scale materials with enzyme-like behavior, have shown remarkable advancements and widespread utilization across various applications. However, the majority of nanozymes require precursor of synthetic-chemicals, which are sometimes expensive and undergo complicated preparations and tedious purification procedures. Therefore, it is of utmost significance to find an enzyme mimic that is affordable, abundant, highly efficient, and sustainable for various applications in biomedicine, environmental sciences, and the food industry. We prove the efficient peroxidase-like activities of the earthly available mineral, barunite-II. The braunite-II mineral micro-nanoparticles (NB) were prepared via physical milling. The enzyme mimetic activity of mineral nanoparticles, referred to as “mineralzyme,” could oxidize the chromogenic blue color of TMB (3,3′,5,5′-tetramethylbenzidine) to oxTMB (3,3′,5,5′-tetramethylbenzidine oxide). Michaelis-Menten constant (Km) and maximum velocity (Vmax) were 135 mM and 62.73 mM min−1 for TMB as a substrate, 139.2 mM, and 2.69 mM min−1 for H2O2 as a substrate. The Km values are much lower than those for HRP. We accurately quantified the total antioxidant capacity in seminal fluid samples from infertile patients using the peroxidase activity of the mineral nanoparticles. This investigation will open new avenues to explore the realm of mineralzyme, revealing its significant potential for a wide range of applications involving diverse enzymatic behaviors.

Nanozyme-Enabled Biomedical Diagnosis: Advances, Trends, and Challenges.

As nanoscale materials with the function of catalyzing substrates through enzymatic kinetics, nanozymes are regarded as potential alternatives to natural enzymes. Compared to protein-based enzymes, nanozymes exhibit attractive characteristics of low preparation cost, robust activity, flexible performance adjustment, and versatile functionalization. These advantages endow them with wide use from biochemical sensing and environmental remediation to medical theranostics. Especially in biomedical diagnosis, the feature of catalytic signal amplification provided by nanozymes makes them function as emerging labels for the detection of biomarkers and diseases, with rapid developments observed in recent years. To provide a comprehensive overview of recent progress made in this dynamic field, here an overview of biomedical diagnosis enabled by nanozymes is provided. This review first summarizes the synthesis of nanozyme materials and then discusses the main strategies applied to enhance their catalytic activity and specificity. Subsequently, representative utilization of nanozymes combined with biological elements in disease diagnosis is reviewed, including the detection of biomarkers related to metabolic, cardiovascular, nervous, and digestive diseases as well as cancers. Finally, some development trends in nanozyme-enabled biomedical diagnosis are highlighted, and corresponding challenges are also pointed out, aiming to inspire future efforts to further advance this promising field.

Achieving Non-Interfacial Blocking Zinc Ion Transport Based on MOF Derived Manganese Oxides and Amorphous Carbon Hybrid Materials.

How to coordinate electron and ion transport behavior across scales and interfaces within ion battery electrodes? The exponential increase in surface area observed in nanoscale electrode materials results in an incomprehensibly vast spatial interval. Herein, to address the problems of volume expansion, dissolution of cathode material, and the charge accumulation problem existing in manganiferous materials for zinc ion batteries, metal organic framework is utilized to form the architecture of non-interfacial blocking ~10 nm Mn2O3 nanoparticles and amorphous carbon hybrid electrode materials, demonstrating a high specific capacity of 361 mAh g-1 (0.1 A g-1), and excellent cycle stability of 105 mAh g-1 after 2000 cycles under 1 A g-1. The uniform and non-separated disposition of Mn and C atoms constitutes an interconnected network with high electronic and ionic conductivity, minimizing issues like structural collapse and volume expansion of the electrode material during cycling. The cooperative insert mechanism of H+ and Zn2+ are analyzed via ex-situ XRD and in-situ Raman tests. The model battery is assembled to present practical possibilities. The results indicate that MOF-derived carbonization provides an effective strategy for exploring Mn-based electrode materials with high ion and electron transport capacity.