Search Results (92)

Direct Air Capture (DAC) is emerging as a critical climate change mitigation strategy, offering a pathway to actively remove atmospheric CO₂. This comprehensive review synthesizes advancements in DAC technologies, with a particular emphasis on the pivotal role of nanostructured solid sorbent materials. The work critically evaluates the characteristics, performance, and limitations of key nanomaterial classes, including metal–organic frameworks (MOFs), covalent organic frameworks (COFs), zeolites, amine-functionalized polymers, porous carbons, and layered double hydroxides (LDHs), alongside solid-supported ionic liquids, highlighting their varied CO₂ uptake capacities, regeneration energy requirements, and crucial water sensitivities. Beyond traditional temperature/pressure swing adsorption, the review delves into innovative DAC methodologies such as Moisture Swing Adsorption (MSA), Electro Swing Adsorption (ESA), Passive DAC, and CO₂-Binding Organic Liquids (CO₂ BOLs), detailing their unique mechanisms and potential for reduced energy footprints. Despite significant progress, the widespread deployment of DAC faces formidable challenges, notably high capital and operational costs (currently USD 300–USD 1000/tCO₂), substantial energy demands (1500–2400 kWh/tCO₂), water interference, scalability hurdles, and sorbent degradation. Furthermore, this review comprehensively examines the burgeoning global DAC market, its diverse applications, and the critical socio-economic barriers to adoption, particularly in developing countries. A comparative analysis of DAC within the broader carbon removal landscape (e.g., CCS, BECCS, afforestation) is also provided, alongside an address to the essential, often overlooked, environmental considerations for the sustainable production, regeneration, and disposal of spent nanomaterials, including insights from Life Cycle Assessments. The nuanced techno-economic landscape has been thoroughly summarized, highlighting that commercial viability is a multi-faceted challenge involving material performance, synthesis cost, regeneration energy, scalability, and long-term stability. It has been reiterated that no single ‘best’ material exists, but rather a portfolio of technologies will be necessary, with the ultimate success dependent on system-level integration and the availability of low-carbon energy. The review paper contributes to a holistic understanding of cutting-edge DAC technologies, bridging material science innovations with real-world implementation challenges and opportunities, thereby identifying critical knowledge gaps and pathways toward a net-zero carbon future. Full article

This study reported covalent organic frameworks (COFs) and their hybrid composites with two-dimensional materials, graphene oxide (GO), graphitic carbon nitride (g-C₃N₄), and boron nitride (BN), to examine their structural, textural, and gas adsorption properties. Material characterization confirmed the crystallinity of COF-1 and the preservation of framework integrity after integrating the 2D nanomaterials. FT-IR spectra exhibited pronounced vibrational fingerprints of imine linkages and validated the functional groups from the COF and the integrated nanomaterials. TEM images revealed the integration of the two components, porous, layered structures with indications of interfacial interactions between COF and 2D nanosheets. Nitrogen adsorption–desorption isotherms revealed the microporous characteristics of the COFs, with hysteresis loops evident, indicating the development of supplementary mesopores at the interface between COF-1 and the 2D materials. The BET surface area of pristine COF-1 was maximal at 437 m²/g, accompanied by significant micropore and Langmuir surface areas of 348 and 1290 m²/g, respectively, offering enhanced average pore widths and hierarchical porous strcuture. CO₂ adsorption tests were investigated showing maximum adsorption capacitiy of 1.47 mmol/g, for COF-1, closely followed by COF@BN at 1.40 mmol/g, underscoring the preserved sorption capabilities of these materials. These findings demonstrate the promise of designed COF-based hybrids for gas capture, separation, and environmental remediation applications. Full article

Carbon quantum dots (CQDs), with their excellent photoluminescence, tunable surface chemistry, and low toxicity, have emerged as versatile nanomaterials in sensing technologies. Meanwhile, metal–organic frameworks (MOFs) possess exceptionally porous architectures and extensive surface areas, and tunable functionalities ideal for molecular recognition and analyte enrichment. The synergistic integration of CQDs and MOFs has significantly expanded the potential of hybrid materials with enhanced selectivity, sensitivity, and multifunctionality. While several reviews have addressed QD/MOF systems broadly, this review offers a focused and updated perspective on CQDs@MOFs composites specifically tailored for food safety and environmental sensing applications. This review provides a comprehensive analysis of recent advances in the design, synthesis, and surface functionalization of these hybrids, emphasizing the mechanisms of interaction, photophysical behavior, and performance advantages over conventional sensors. Special attention is given to their use in detecting food contaminants such as heavy metals, pesticides, antibiotics, mycotoxins, pathogens, and aromatic compounds. Key strategies to enhance stability, selectivity, and detection limits are highlighted, and current challenges and future directions for practical deployment are critically discussed. Full article

Carbon nanomaterials that include different forms such as graphene, carbon nanotubes, fullerenes, graphite, nanodiamonds, carbon nanocones, amorphous carbon, as well as porous carbon, are quite distinguished by their unique structural, electrical, and mechanical properties. This plays a major role in making them pivotal in various medical applications. The synthesis methods used for such nanomaterials, including techniques such as chemical vapor deposition (CVD), arc discharge, laser ablation, and plasma-enhanced chemical vapor deposition (PECVD), are able to offer very precise control over material purity, particle size, and scalability, enabling for nanomaterials catered for different specific applications. These materials have been explored in a range of different systems, which include drug-delivery systems, biosensors, tissue engineering, as well as advanced imaging techniques such as MRI and fluorescence imaging. Recent advancements, including green synthesis strategies and novel innovative approaches like ultrasonic cavitation, have improved both the precision as well as the scalability of carbon nanomaterial production. Despite challenges like biocompatibility and environmental concerns, these nanomaterials hold immense promise in revolutionizing personalized medicine, diagnostics, and regenerative therapies. Many of these applications are currently positioned at Technology Readiness Levels (TRLs) 3–4, with some systems advancing toward preclinical validation, highlighting their emerging translational potential in clinical settings. This review is specific in evaluating synthesis techniques of different carbon nanomaterials and establishing their modified properties for use in biomedicine. It focuses on how these techniques establish biocompatibility, scalability, and performance for use in medicines such as drug delivery, imaging, and tissue engineering. The implications of nanostructure behavior in biological environments are further discussed, with emphasis on applications in imaging, drug delivery, and biosensing. Full article

Waste nanomaterials pose environmental and human health concerns and they need to be urgently and efficiently managed. In this study, a fungal biotemplate was used to accumulate and recover nano-Fe₂O₃ materials from an aqueous solution. Then, recovered nano-Fe₂O₃ materials were activated to form a high-performance magnetic porous carbon composite (FePC) for energy storage and organic pollutant removal. The results indicate that high concentrations (500 mg/L) of 50 nm Fe₂O₃ particles can be completely recovered using a cross-linked Neurospora crassa fungus (NC), primarily because of its encapsulation function. In addition, the surface area, degree of graphitization, and heteroatom content of the FePC materials can be boosted by the catalytic effects of the incorporated Fe atoms. The developed FePC materials exhibit potential as high electrical double-layer capacitors as well as strong retention capabilities, excellent stability, and efficient adsorption of triclosan (TCS, ~526 mg/g). Additionally, these FePC materials exhibit superior capacities for energy storage and pollutant reduction compared to commercial and reported carbon materials. These results reveal a sustainable route for the recovery and reutilization of nanomaterials. Full article

The excessive utilization and emission of waste plastics have caused serious damage to the environment, and it is of great significance to explore high-value utilization methods for these waste plastics. To address this challenge, functional nano cobalt-loaded porous carbon materials (CoPC) with excellent antibiotic wastewater removal properties were prepared by one-step pyrolysis using waste PET plastics as a carbon source, a process described in this paper. Characterization revealed that the obtained CoPC-2 catalysts had a high degree of defects, a large specific surface area (343.41 m²/g), and an abundant pore structure. Degradation results displayed that CoPC-2 removed 87.93% of 20 mg/L tetracycline with a reaction rate constant of 0.0668 min⁻¹. Moreover, CoPC-2 exhibited excellent degradation performance for tetracycline over a wide range of pH levels (4–10) and in coexistence with multiple inorganic anions. Electron paramagnetic resonance and radical quenching experiments revealed that radicals (·OH, and SO₄·⁻) and non-radicals (¹O₂) pathway participated in tetracycline degradation, with the non-radical pathway being dominant. This study not only offers promising prospects for resource utilization of waste plastics, but also provides novel approaches for the design of functional nanomaterials for antibiotic wastewater treatment. Full article

The transition to sustainable energy storage solutions has driven significant interest in supercapacitors, which offer high power density, rapid charge–discharge capabilities, and exceptional cycle stability. Biomass-derived carbon nanomaterials have emerged as compelling candidates for supercapacitor electrodes due to their renewable origins, environmental compatibility, and cost-effectiveness. This study explores recent advancements in tailoring structural properties, for example in preparation methods and activation, which are essential for efficient charge storage and rapid ion transport. Attention is given to the dimensional configurations—spanning 0D to 3D structures—and their impact on electrochemical behaviors. This review outlines the challenges faced in scaling up and optimizing these materials for practical applications, alongside an outlook on future research directions. By bridging the gap between material design and application demands, this work contributes to advancing sustainable supercapacitor technologies for a greener energy future. Full article

This review explores the advances in developing adsorbent materials for solid-phase microextraction (SPME), focusing on nanoparticles, nanocomposites, and nanoporous structures. Nanoparticles, including those of metals (e.g., gold, silver), metal oxides (e.g., TiO₂, ZnO), and carbon-based materials (e.g., carbon nanotubes, graphene), offer enhanced surface area, improved extraction efficiency, and increased selectivity compared to traditional coatings. Nanocomposites, such as those combining metal oxides with polymers or carbon-based materials, exhibit synergistic properties, further improving extraction performance. Nanoporous materials, including metal–organic frameworks (MOFs) and ordered mesoporous carbons, provide high surface area and tunable pore structures, enabling selective adsorption of analytes. These advanced materials have been successfully applied to various analytes, including volatile organic compounds (VOCs), polycyclic aromatic hydrocarbons (PAHs), pesticides, and heavy metals, demonstrating improved sensitivity, selectivity, and reproducibility compared to conventional SPME fibers. The incorporation of nanomaterials has significantly expanded the scope and applicability of SPME, enabling the analysis of trace-level analytes in complex matrices. This review highlights the significant potential of nanomaterials in revolutionizing SPME technology, offering new possibilities for sensitive and selective analysis in environmental monitoring, food safety, and other critical applications. Full article

In recent years, the development of high-performance electrocatalysts for energy conversion and environmental remediation has become a topic of great interest. Covalent organic frameworks (COFs), linked by covalent bonds, have emerged as promising materials in the field of electrocatalysis due to their well-defined structures, high specific surface areas, tunable pore structures, and excellent acid–base stability. However, the low conductivity of COF materials often limits their intrinsic electrocatalytic activity. To enhance the catalytic performance of COF-based catalysts, various nanomaterials are integrated into COFs to form composite catalysts. The stable and tunable porous structure of COFs provides an ideal platform for these nanomaterials, leading to improved electrocatalytic activity. Through rational design, COF-based composite electrocatalysts can achieve synergistic effects between nanomaterials and the COF carrier, enabling efficient targeted electrocatalysis. This review summarizes the applications of nanomaterial-incorporated COF-based catalysts in hydrogen evolution, oxygen evolution, oxygen reduction, carbon dioxide reduction, and nitrogen reduction. Additionally, it outlines design principles for COF-based composite electrocatalysis, focusing on structure–activity relationships and synergistic effects in COF composite nanomaterial electrocatalysts, as well as challenges and future perspectives for next-generation composite electrocatalysts. Full article

Phenolic antioxidants such as tert-butylhydroquinone (TBHQ) can prolong the shelf life of edible oils by delaying the oxidation process. The excessive use of TBHQ can damage food quality and public health, so it is necessary to develop an efficient TBHQ detection technique. In this work, nickel-aluminum double hydroxide (NiAl-LDH) was grown on glucose carbon spheres (GC), which formed porous carbon nanomaterials (named NiAl-LDH@GC-800) after pyrolysis at 800 °C. The successful synthesis of the material was verified by scanning electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. The obtained NiAl-LDH@GC-800 was dopped onto a glass carbon electrode to prepare an electrochemical sensor for TBHQ. The synergistic effect of porous carbon and Ni metal reduced from NiAl-LDH by high-temperature calcination accelerated the electron transfer rate and improved the sensitivity of the sensor. The prepared sensor showed a low limit of detection (LOD) of 8.2 nM, a high sensitivity (4.2 A·M⁻¹), and a good linear range (20~300 µM) in detecting TBHQ. The sensor was also successfully used for TBHQ detection in edible oils, including chili oil, peanut oil, and rapeseed oil. Full article

Transition metal oxides have been widely used in microwave-absorbing materials, but how to improve impedance matching is still an urgent problem. Therefore, we introduced urea as a polymer carbon source into a three-dimensional porous structure modified by Co₃O₄ nanoparticles and explored the influence of different heat treatment temperatures on the wave absorption properties of the composite. The nanomaterials, when calcined at a temperature of 450 °C, exhibited excellent microwave absorption capabilities. Specifically, at an optimized thickness of 9 mm, they achieved a minimum reflection loss (RL_min) of −97.3 dB, accompanied by an effective absorption bandwidth (EAB) of 9.83 GHz that comprehensively covered both the S and Ku frequency bands. On the other hand, with a thickness of 3 mm, the RL_min was recorded as −17.9 dB, with an EAB of 5.53 GHz. This excellent performance is attributed to the multi-facial polarization and multiple reflections induced by the magnetic loss capability of Co₃O₄ nanoparticles, the electrical conductivity of C, and the unique three-dimensional structure of diatomite. For the future development of bio-based microwave absorption, this work provides a methodology and strategy. Full article

The adsorption properties of microporous carbon materials modified with iron citrate were investigated. The carbon materials were produced based on resorcinol-formaldehyde resin, treated in a microwave assisted solvothermal reactor, and next carbonized in the tube furnace at a temperature of 700 °C under argon atmosphere. Iron citrate was applied as a modifier, added to the material precursor before the synthesis in the reactor, in the quantity enabling to obtain the nanocomposites with C:Fe mass ratio equal to 10:1. Some samples were additionally activated using potassium oxalate or potassium hydroxide. The phase composition of the produced nanocomposites was determined using the X-ray diffraction method. Scanning and transmission electron microscopy was applied to characterize the changes in samples’ morphology resulting from the activation process and/or the introduction of iron into the carbon matrix. The adsorption of nitrogen from gas phase and dyes (methylene blue and congo red) from water solution on the obtained materials was investigated. In the case of methylene blue, the adsorption equilibrium isotherms followed the Langmuir isotherm model. However, in the case of congo red, a linear dependency of adsorption and concentration in a broad equilibrium concentration range was found and well-described using the Henry equation. The most efficient adsorption of methylene blue was noticed for the sample activated with potassium hydroxide and modified with iron citrate, and a maximum adsorption capacity of 696 mg/g was achieved. The highest congo red adsorption was noticed for the non-activated sample modified with iron citrate, and the partition coefficient for this material equaled 171 dm³/g. Full article

Oxidized carbon nanohorn (CNHox) a carbon nanomaterial that has attracted attention due to its unique material properties. It is expected to be applied in various areas like cancer treatment, gene-expression technology, fluids with high thermal conductivity, lubricants, and so on. While the rheological measurements of suspensions provide information on the effective size and interactions of suspended particles, the rheological behaviors of aqueous suspensions of CNHox have never been systematically investigated. To clarify the rheological behaviors of aqueous suspensions of CNHox, their viscosity and dynamic viscoelasticity were measured with changing particle concentration and salt concentration. The viscosity of a CNHox suspension showed yield stress at low shear rates and showed shear-thinning behavior with increasing shear rates. The viscosity of 5 weight % CNHox suspensions was comparable to that of 60 weight % silica suspensions. This high viscosity at a low CNHox concentration is probably due to the porous structure and large effective volume of the CNHox particle. The estimated effective volume of CNHox calculated by the Krieger−Dougherty equation was 18.9 times larger than the actual volume calculated by the mass concentration and density. The dependence of rheological behavior of the CNHox suspension on salt concentration was weak compared to that of the colloidal silica suspension. This weak dependence on salt concentration may be due to the roughness of the particle surface, which would weaken the effect of electric double-layer interactions and/or van der Waals interactions between particles. These rheological behaviors of the aqueous suspension of CNHox shown in this research will be useful in efforts to improve the efficiency of its utilization for the various applications. Full article

Transition metal sulfides are widely used in supercapacitor electrode materials and exhibit excellent performance because of their rich variety, low price, and high theoretical specific capacity. At present, the main methods to prepare transition metal sulfides include the hydrothermal method and the electrochemical method. In order to further improve their electrochemical performance, two aspects can be addressed. Firstly, by controllable synthesis of nanomaterials, porous structures and large surface areas can be achieved, thereby improving ion transport efficiency. Secondly, by combining transition metal sulfides with other energy storage materials, such as carbon materials and metal oxides, the synergy between different materials can be fully utilized. However, future research still needs to address some challenges. In order to guide further in-depth research, it is necessary to combine the current research-derived knowledge and propose a direction for future development of transition metal sulfide electrode materials. Full article