Search Results (57)

MXenes, a rapidly emerging family of two-dimensional transition metal carbides and nitrides, have attracted considerable attention in recent years for their potential in next-generation energy storage technologies. In solid-state batteries (SSBs), they combine metallic-level conductivity (>10³ S cm⁻¹), adjustable surface terminations, and mechanical resilience, which makes them suitable for diverse functions within the cell architecture. Current studies have shown that MXene-based anodes can deliver reversible lithium storage with Coulombic efficiencies approaching ~98% over 500 cycles, while their use as conductive additives in cathodes significantly improves electron transport and rate capability. As interfacial layers or structural scaffolds, MXenes effectively buffer volume fluctuations and suppress lithium dendrite growth, contributing to extended cycle life. In solid polymer and composite electrolytes, MXene fillers have been reported to increase Li⁺ conductivity to the 10⁻³–10⁻² S cm⁻¹ range and enhance Li⁺ transference numbers (up to ~0.76), thereby improving both ionic transport and mechanical stability. Beyond established Ti-based systems, double transition metal MXenes (e.g., Mo₂TiC₂, Mo₂Ti₂C₃) and hybrid heterostructures offer expanded opportunities for tailoring interfacial chemistry and optimizing energy density. Despite these advances, large-scale deployment remains constrained by high synthesis costs (often exceeding USD 200–400 kg⁻¹ for Ti₃C₂T_x at lab scale), restacking effects, and stability concerns, highlighting the need for greener etching processes, robust quality control, and integration with existing gigafactory production lines. Addressing these challenges will be crucial for enabling MXene-based SSBs to transition from laboratory prototypes to commercially viable, safe, and high-performance energy storage systems. Beyond summarizing performance, this review elucidates the mechanistic roles of MXenes in SSBs—linking lithiophilicity, field homogenization, and interphase formation to dendrite suppression at Li|SSE interfaces, and termination-assisted salt dissociation, segmental-motion facilitation, and MWS polarization to enhanced electrolyte conductivity—thereby providing a clear design rationale for practical implementation. Full article

Tomato waste (TW) was employed as a sustainable source for the synthesis of fluorescent carbon dots (CDs) via a microwave-assisted hydrothermal carbonization (Mw-HTC) method, aiming at its valorization. Several amines were used as nitrogen additives to enhance the fluorescence quantum yield (QY) of CDs, and a set of reaction conditions, including additive/TW mass ratio (0.04–0.32), dwell time (15–60 min), and temperature (200–230 °C) of the HTC process, were scrutinized. The structural analysis of the tomato waste carbon dots (TWCDs) was undertaken by FTIR and ¹H NMR techniques, revealing their most relevant features. In solid state, transmission electron microscopy (TEM) analysis showed the presence of nearly spherical nanoparticles with an average lateral size of 8.1 nm. Likewise, the topographical assessment by atomic force microscopy (AFM) also indicated particles’ heights between 3 and 10 nm. Their photophysical properties, revealed by UV–Vis, steady-state, and time-resolved fluorescence spectroscopies, are fully discussed. Higher photoluminescent quantum yields (up to 0.08) were attained when the biomass residues were mixed with organic aliphatic amines during the Mw-HTC process. Emission tunability is a characteristic feature of these CDs, which display an intensity average fluorescence lifetime of 8 ns. The new TWCDs demonstrated good antioxidant properties by the ABTS radical cation method (75% inhibition at TWCDs’ concentration of 5 mg/mL), which proved to be related to the dwell time used in the CDs synthesis. Moreover, the synthesized TWCDs suppressed the growth of Escherichia coli and Staphylococcus aureus at concentrations higher than 2000 μg/mL, encouraging future antibacterial applications. Full article

The rapid detoxification and mineralization of Cr(VI) in aqueous environments hold critical importance for emergency response and resource recovery yet remain technically challenging. Herein, we report the synthesis of FeS₂/ZVI composites through ethanol-assisted wet ball-milling and their application in Cr(VI) removal under microwave (MW) irradiation. This study systematically investigates the effects of MW irradiation on the removal efficiency of Cr(VI) using FeS₂/ZVI composites, with particular focus on key parameters including composite dosage, initial pH, MW temperature, and Cr(VI) concentration. Notably, 1 g/L FeS₂/ZVI composites achieved near-complete removal (>99%) of 50 mg/L Cr(VI) within 7 min at a MW irradiation temperature of 333 K, which exhibited 5.9-fold and 13.1-fold superior performance compared to pure pyrite and ZVI, respectively. Additionally, there is a 96.1% reduction in reaction time in comparison to non-MW irradiation system. In real electroplating wastewater samples, Cr(VI) concentration was reduced from 38.93 to 0.42 mg L⁻¹ by MW irradiation-assisted treatment, validating its potential for practical applications in industrial Cr(VI) pollution control. The activation energy determined by fitting the Arrhenius equation showed a 39.7% reduction for the MW-assisted FeS₂/ZVI system (16.0 kJ mol⁻¹) compared to conventional thermal heating (from 25.6 kJ mol⁻¹), indicating that MW irradiation induced catalytic enhancement of FeS₂/ZVI, thereby lowering the energy barrier for Cr(VI) reduction. Moreover, MW irradiation-assisted processes facilitated the mineralization of reduced Cr(III) to stable spinel FeCr₂O₄. These findings collectively establish a synergistic mechanism between MW activation and FeS₂/ZVI composites, offering innovative pathways for efficient Cr(VI) detoxification and resource recovery from high-strength industrial wastewaters. Full article

Green chemistry seeks to find alternative synthesis routes that are less harsh to living organisms and the environment. In this communication, a microwave-assisted hydrothermal technique and a thermal annealing method were used in the reduction of graphene oxide (GO) to make reduced GO (rGO). Graphite powder was oxidised using the Improved Hummers’ method, exfoliated, and freeze-dried. Thereafter, an aqueous suspension of GO was reduced under microwave (MW) irradiation for 10 min at 600 W with and without the help of a reducing agent (hydrazine hydrate). Thermal annealing reduction was also conducted under a nitrogen atmosphere at 300 °C for 1 h. Prepared samples were analysed using Raman laser spectroscopy, X-ray diffraction (XRD), transmission electron microscopy (TEM), the Brunauer–Emmett–Teller (BET) method, and X-ray photoelectron spectroscopy (XPS). A successful reduction in the GO functional groups between the sheets was established using XRD. In the Raman analysis, the ratio of the intensity of the D and G band (I_D/I_G) in graphene sheets assisted in assessing the quality of the graphene films. An estimation of the number of structural defects was calculated using the I_D/I_G ratio. The Raman analysis showed an increase in the I_D/I_G ratio after both oxidation and reduction processes. The defect densities of both MW-treated samples were comparable while an increased defect density was evident in the thermally annealed sample. TEM micrographs confirmed the sheet-like morphology of the samples. The rGO sheets obtained from the MW-treated method appeared to be smaller when compared to the rGO ones obtained by thermal treatment. It was also evident from XRD analysis that thermal treatment promoted the coalition of graphitic layers, such that the estimated number of layers was larger than that of GO. The elemental analysis showed that the C/O ratio of GO increased from 2 to 7.8 after MW hydrazine reduction. Full article

Bis-heterocyclic compounds containing imidazo[1,2-a]pyridines (IMPs) are privileged heterocyclic drug scaffolds due to their potential applications. The Groebke–Blackburn–Bienaymé reaction (GBBR) is a greener alternative to synthesizing IMPs. On the other hand, 1,2,3-triazole scaffolds are biososteres of the trans amide, and their incorporation in bioactive molecules provides advantages such as resistance to cleavage mediated by proteases and improved stability. In this context, the CuAAC reaction is the most efficient approach to synthesizing 1,4-disustituted-1,2,3-triazoles. Herein, we describe a novel one-pot synthesis of IMPs by the GBBR-CuAAC strategy assisted by microwave irradiation. Full article

Cyclodextrins (CDs) are macrocycles that are well suited for forming inclusion complexes for surface-enhanced Raman scattering (SERS) detection of analytes due to their low Raman activity, which minimizes background SERS signals and enhances the detection of target molecules without interference. In this paper, we systematically investigated the synthesis of both silver (Ag) and gold (Au) nanoparticles (NPs) using CDs as reducing and capping agents in a basic environment using microwave (MW), ultrasound (US), and room temperature (RT) synthesis. We found that replacing NaOH with K₂CO₃ as an alkaline environment almost doubles the size (from <10 nm to around 20 nm) of AgNPs in the MW-assisted synthesis. Synthesis using the US produces less stable particles due to the sample evolution after US irradiation. Ag (20 nm) and Au (11 nm) were successfully obtained at room temperature in the presence of CDs and K₂CO₃. All synthesized particles present SERS activity. CD capping allowed us to detect hydrophobic molecules like naphthalene and melamine. In the case of methylene blue, the CD capping prevents the changes induced in the SERS by a basic pH. We also demonstrate that the newly synthesized NPs can discriminate by SERS the propranolol enantiomers. Moreover, propranolol inclusion in CDs leads to a dramatic change in its SERS spectrum. Full article

This paper presents a wideband fractional-N all-digital phase-locked loop (WBPLL) architecture featuring a triple-loop configuration capable of tuning frequencies from 1.9 to 6.1 GHz. The first and second loops, automatic frequency control (AFC) and counter-assisted phase-locked loop (CAPLL), respectively, perform coarse locking, while the third loop employs a digital sub-sampling architecture without a frequency divider for fine locking. In this third loop, fractional-N frequency synthesis is achieved using a delta-sigma modulator (DSM) and digital-to-time converter (DTC). To minimize area, digital modules such as counters, comparators, and differentiators used in the AFC and CAPLL loops are reused. Furthermore, a moving average filter (MAF) is employed to reduce the frequency overlap ratio of the digitally controlled oscillator (DCO) between the second and third loops, ensuring stable loop switching. The total power consumption of the WBPLL varies with the frequency range, consuming between 8.8 mW at the WBPLL minimum output frequency of 1.9 GHz and 12.8 mW at the WBPLL maximum output frequency of 6.1 GHz, all at a 1.0 V supply. Implemented in a 28 nm CMOS process, the WBPLL occupies an area of 0.055 mm². Full article

In cancer diagnostics, magnetic resonance imaging (MRI) uses contrast agents to enhance the distinction between the target tissue and background. Several promising approaches have been developed to increase MRI sensitivity, one of which is Overhauser dynamic nuclear polarization (ODNP)-enhanced MRI (OMRI). In this study, a macromolecular construct based on human serum albumin and nitroxyl radicals (HSA-NIT) was developed using a new synthesis method that significantly increased the modification to 21 nitroxide residues per protein. This was confirmed by electron paramagnetic resonance (EPR) spectroscopy and matrix-assisted laser desorption/ionization time-of-flight (MALDI ToF) mass spectrometry. Gel electrophoresis and circular dichroism showed no significant changes in the structure of HSA-NITs, and no oligomers were formed during modification. The cytotoxicity of HSA-NITs was comparable to that of native albumin. HSA-NITs were evaluated as potential “metal-free” organic radical relaxation-based contrast agents for ¹H-MRI and as hyperpolarizing contrast agents for OMRI. Relaxivities (longitudinal and transversal relaxation rates r₁ and r₂) for HSA-NITs were measured at different magnetic field strengths (1.88, 3, 7, and 14 T). Phantoms were used to demonstrate the potential use of HSA-NIT as a T₁- and T₂-weighted relaxation-based contrast agent at 3 T and 14 T. The efficacy of ¹H Overhauser dynamic nuclear polarization (ODNP) in liquids at an ultralow magnetic field (ULF, B₀ = 92 ± 0.8 μT) was investigated for HSA-NIT conjugates. The HSA-NITs themselves did not show ODNP enhancement; however, under the proteolysis conditions simulating cancer tissue, HSA-NIT conjugates were cleaved into lower-molecular-weight (MW) protein fragments that activate ODNP capabilities, resulting in a maximum achievable enhancement |E_max| of 40–50 and a radiofrequency power required to achieve half of E_max, P_1/2, of 21–27 W. The HSA-NIT with a higher degree of modification released increased the number of spin probes upon biodegradation, which significantly enhanced the Overhauser effect. Thus, HSA-NITs may represent a new class of MRI relaxation-based contrast agents as well as novel cleavable conjugates for use as hyperpolarizing contrast agents (HCAs) in OMRI. Full article

This article describes the one-pot microwave synthesis of silver nanoparticles (AgNPs) assisted with natural polyelectrolytes—humic substances (HS). The humic polyelectrolytes served both as chemical reductants for silver ions and as end-capping agents for AgNPs. Three commercially available sodium humates extracted from lignites and leonardite and one sodium fulvate isolated from natural brown water seeped through peat deposits were used in this study. The dynamics of the growth rate of AgNPs was characterised by UV–VIS spectroscopy by measuring the intensity of surface plasmon resonance at 420 nm. Transmission electron microscopy was used to characterise the size and morphology of AgNPs. Dynamic light scattering was used to determine size distributions of the synthesised AgNPs in the solutions. It was established that both conventional and microwave syntheses assisted with the coal humates produced small-size AgNPs in the range from 4 to 14 nm, with the maximum share of particles with sizes of (6 ± 2) nm by TEM estimates. The peat fulvate yielded much larger NPs with sizes from 10 to 50 nm by TEM estimates. DLS measurements revealed multimodal distributions of AgNPs stabilised with HS, which included both single NPs with the sizes from 5 to 15 nm, as well as their dominating aggregates with sizes from 20 to 200 nm and a smaller portion of extra-large aggregates up to 1000 nm. The given aggregates were loosely bound by humic polyelectrolyte, which prevented the coalescence of AgNPs into larger particles, as can be seen in the TEM images. The significant acceleration in the reaction time—a factor of 60 to 70—was achieved with the use of MW irradiation: from 240 min down to 210–240 s. The coal humate stabilised AgNPs showed antimicrobial properties in relation to S. aureus. A conclusion was made regarding the substantial advantages of microwave synthesis in the context of time and scaling up for the large-scale production of AgNP-HS preparations with antimicrobial properties suitable for external wound-healing applications. Full article

In this review, we focus on a small section of the literature that deals with the materials containing pristine defective carbon nanostructures (CNs) and those incorporated into the larger systems containing carbon atoms, heteroatoms, and inorganic components.. Briefly, we discuss only those topics that focus on structural defects related to introducing perturbation into the surface topology of the ideal lattice structure. The disorder in the crystal structure may vary in character, size, and location, which significantly modifies the physical and chemical properties of CNs or their hybrid combination. We focus mainly on the method using microwave (MW) irradiation, which is a powerful tool for synthesizing and modifying carbon-based solid materials due to its simplicity, the possibility of conducting the reaction in solvents and solid phases, and the presence of components of different chemical natures. Herein, we will emphasize the advantages of synthesis using MW-assisted heating and indicate the influence of the structure of the obtained materials on their physical and chemical properties. It is the first review paper that comprehensively summarizes research in the context of using MW-assisted heating to modify the structure of CNs, paying attention to its remarkable universality and simplicity. In the final part, we emphasize the role of MW-assisted heating in creating defects in CNs and the implications in designing their properties and applications. The presented review is a valuable source summarizing the achievements of scientists in this area of research. Full article

For pathogens identification, the PCR test is a widely used method, which requires the isolation of nucleic acids from different samples. This extraction can be based on the principle of magnetic separation. In our work, amine-functionalized magnesium ferrite nanoparticles were synthesized for this application by the coprecipitation of ethanolamine in ethylene glycol from Mg(II) and Fe(II) precursors. The conventional synthesis method involves a reaction time of 12 h (MgFe₂O₄-H&R MNP); however, in our modified method, the reaction time could be significantly reduced to only 4 min by microwave-assisted synthesis (MgFe₂O₄-MW MNP). A comparison was made between the amine-functionalized MgFe₂O₄ samples prepared by two methods in terms of the DNA-binding capacity. The experimental results showed that the two types of amine-functionalized magnesium ferrite magnetic nanoparticles (MNPs) were equally effective in terms of their DNA extraction yield. Moreover, by using a few minutes-long microwave synthesis, we obtained the same quality magnesium ferrite particles as those made through the long and energy-intensive 12-h production method. This advancement has the potential to improve and expedite pathogen identification processes, helping to better prevent the spread of epidemics. Full article

Reductive amination is a powerful tool in sustainable organic synthesis that allows chemists to access a wide range of valuable amine products using renewable feedstocks and mild reaction conditions, with minimal waste generation. Practical applications can be found in various fields, including pharmaceuticals, contributing to greener and more sustainable chemical processes. In this work, we present a heterogeneous (Rh and Pt) catalyzed protocol for the fast and efficient synthesis of ractopamine hydrochloride (β-adrenergic drug) under microwave-assisted reductive amination protocol starting from raspberry ketone and octopamine. Microwave (MW) successfully accelerated the hydrogenation reaction and reduced the reaction time from 13 h to only 3 h under mild conditions (50 °C at 10 bar). The best catalysts were Pt/C and Rh/C, which led to high conversion and selectivity towards ractopamine:HCl. Different solvents and ketone substrates were also experimented. Acetophenone, cyclohexanone, and 2-butanone reacted at lower H₂ pressure (5 bar), and highest selectivity was observed with cyclohexanone (99%). These preliminary experiments may be useful for further process improvements in the synthesis of β-adrenergic agonists and related structures and underline the positive synergy between MW and heterogeneous catalysis. Full article

In the present research, we report on an innovative and quick procedure for the synthesis of metal oxides: a sol-gel procedure which is followed by two steps that are assisted by microwaves (MW) heating. First, MW heating promotes gel drying and successively permits the calcination of the xerogel in a few minutes, using a susceptor that rapidly reaches high temperatures. The procedure was employed for the synthesis of zirconium dioxide (ZrO₂), and MW-assisted calcination enables the collection of tetragonal ZrO₂, as confirmed by different experimental techniques (PXRD, HR-TEM and Raman spectroscopy). Using this MW-assisted sol-gel procedure, a promoted sulphated zirconia (SZ) has been obtained. Both the nature and strength of SZ surface acidity have been investigated with FTIR spectroscopy using CO and 2,6-dimethylpyridine (2,6-DMP) as probe molecules. The obtained materials were tested as catalysts in acid hydrolysis of glucose to give 5-(hydroxymethyl)furfural (5-HMF). One of the obtained catalysts exhibited a better selectivity towards 5-HMF with respect to SZ material prepared by a classical precipitation route, suggesting that this procedure could be employed to obtain a well-known catalyst with a less energy-consuming procedure. Catalytic results also suggest that good selectivity to 5-HMF can be achieved in aqueous media in the presence of weak Lewis and Brønsted sites. Full article

The use of alternative energy sources, such as microwaves (MW) or ultrasounds (US), and their mutual cross-combination have been widely described in the literature in the development of new synthetic methodologies in organic and medicinal chemistry. In this review, our attention is focused on representative examples, reported in the literature in the year range 2013–2023 of selected N-containing bicyclic heterocycles, with the aim to highlight the advantages of microwave- and ultrasound-assisted organic synthesis. Full article

Meropenem is currently the most common carbapenem in clinical applications. Industrially, the final synthetic step is characterized by a heterogeneous catalytic hydrogenation in batch mode with hydrogen and Pd/C. The required high-quality standard is very difficult to meet and specific conditions are required to remove both protecting groups [i.e., p-nitrobenzyl (pNB) and p-nitrobenzyloxycarbonyl (pNZ)] simultaneously. The three-phase gas–liquid–solid system makes this step difficult and unsafe. The introduction of new technologies for small-molecule synthesis in recent years has opened up new landscapes in process chemistry. In this context, we have investigated meropenem hydrogenolysis using microwave (MW)-assisted flow chemistry for use as a new technology with industrial prospects. The reaction parameters (catalyst amount, T, P, residence time, flow rate) in the move from the batch process to semi-continuous flow were investigated under mild conditions to determine their influence on the reaction rate. The optimization of the residence time (840 s) and the number of cycles (4) allowed us to develop a novel protocol that halves the reaction time compared to batch production (14 min vs. 30 min) while maintaining the same product quality. The increase in productivity using this semi-continuous flow technique compensates for the slightly lower yield (70% vs. 74%) obtained in batch mode. Full article