Innovative Synthesis Methods Research Articles

Designing Supported Nanoparticles via Synergistic Ex-Solution and Phosphorization for Tailored Active Site Generation.

Supported nanoparticles incorporating catalytically attractive nonmetal elements have gained significant attention as a promising strategy for enhancing catalytic activity in various industrial applications. This study presents an innovative one-pot synthesis method for fabricating hybrid catalysts, which simultaneously modifies surface properties through the precipitation of nanoparticles with the concurrent incorporation of nonmetal elements. The underlying concept is to synchronize the temperature required for particle formation with that of nonmetal incorporation by adjusting the oxygen chemical potential of the host oxide. As a case study, Ir- and Ru-doped WO3 are selected as the starting material, with phosphorus (P) as the representative nonmetal for surface functionalization. Notably, the hybrid catalyst, composed of amorphous (Ir,Ru)Px particles dispersed on P-rich WO2.9 sheets, is synthesized through a single heat treatment at 500°C, avoiding undesirable sintering of the host material. When used as a hydrogen evolution catalyst, this material exhibits outstanding mass activity, durability, compared to state-of-the-art Pt/C catalysts. Density functional theory calculations further reveal that the superior performance of the hybrid catalysts attributes to improved water dissociation and favorable adsorption and desorption of key reaction intermediates. This novel synthesis strategy offers considerable potential for advancing diverse areas of heterogeneous catalysis.

Onsite ammonia synthesis from water vapor and nitrogen in the air.

An innovative method for onsite ammonia synthesis under ambient conditions has been developed using a catalyst mesh composed of magnetite (Fe3O4) and Nafion polymer. We pass air through the catalyst, which condenses microdroplets from atmospheric water vapor and uses nitrogen from the air, resulting in ammonia concentrations ranging from 25 to 120 μM in 1 hour, depending on local relative humidity. Operated at room temperature and atmospheric pressure, this technique eliminates the need for additional electricity or radiation, thereby substantially reducing carbon dioxide emissions compared to the traditional Haber-Bosch process. In laboratory experiments, we further optimized the reaction conditions and scaled up the process. After 2 hours of spraying, the ammonia concentration increased to 270.2 ± 25.1 μM. In addition, we present a portable device designed for onsite ammonia production which consistently produces an ammonia concentration that is adequate for some agricultural irrigation purposes.

One-Pot Synthesis of Highly Dispersed VO2 on g-C3N4 Nanomeshes for Advanced Oxidation

Advanced oxidation catalyzed by metal oxides is a promising approach for degrading organic pollutants in wastewater. A critical strategy to enhance the performance of these catalysts is optimizing the dispersion of their active components through innovative synthesis methods. In this study, we report a one-pot synthesis of g-C3N4 nanomeshes supported with highly dispersed VO2 catalysts (V-g-C3N4) for the advanced oxidation of methylene blue (MB). The characterization results reveal that the involvement of VCl3 in the pyrolysis of melamine facilitates the formation of g-C3N4 nanomeshes with abundant amino groups (NH/NH2). The strong interaction between vanadia species and amino groups prevents VO2 particles from agglomerating, resulting in a significantly higher vanadia dispersion than V-g-C3N4-im synthesized via the traditional impregnation method. V-g-C3N4 exhibits a sophisticated microstructure and surface structure, which leads to a rate constant 2.3-fold higher than V-g-C3N4-im in the catalytic degradation of methylene blue using H2O2 as the oxidant. X-ray photoelectron spectroscopy, trapping experiments, and electron paramagnetic resonance measurements reveal that the rapid adsorption and fast diffusion of MB over g-C3N4 nanomeshes, together with the efficient H2O2 activation into ·OH radicals via the V4+/V5+ redox cycle, synergistically contribute to the superior MB removal efficiency of V-g-C3N4. Moreover, V-g-C3N4 demonstrates no significant decrease in activity even after the fourth cycle, indicating its excellent stability during the pollutant removal process.

Lignocellulose-Mediated Functionalization of Liquid Metals toward the Frontiers of Multifunctional Materials.

Lignocellulose-mediated liquid metal (LM) composites, as emerging functional materials, show tremendous potential for a variety of applications. The abundant hydroxyl, carboxyl, and other polar groups in lignocellulose facilitate the formation of strong chemical bonds with LM surfaces, enhancing wettability and adhesion for improved interface compatibility. Beyond serving as a supportive matrix, lignocellulose can be tailored to optimize the microstructure of the composites, adapting them for diverse applications. This review comprehensively summarizes the fundamental principles and recent advancements in lignocellulose-mediated LM composites, highlighting the advantages of lignocellulose in composite fabrication, including facile synthesis, versatile interactions, and inherent functionalities. Key modulation strategies for LMs and innovative synthesis methods for functionalized lignocellulose composites are discussed. Furthermore, the roles and structure-performance relationships of these composites in electromagnetic shielding, flexible sensors, and energy storage devices are systematically summarized. Finally, the obstacles and prospective advancements pertaining to lignocellulose-mediated LM composites are thoroughly scrutinized and deliberated upon. This review is expected to provide basic guidance for researchers to boost the popularity of LMs in diverse applications and provide useful references for design strategies of state-of-the-art LMs.

Innovative multiphase ultrasonic-assisted method for high-purity, stable, and cost-effective copper nanowire synthesis

The synthesis of copper nanowires (CuNWs) using modified polyols with hexadecylamine or octadecylamine as capping agents, known for their ease of operation, rapid reaction, and suitability for mass production, often encounters challenges such as the presence of copper particles, numerous copper nanorods, difficulty in purifying organic compounds, and air instability as by-products. In addressing these issues, this study introduces an innovative multiphase ultrasonic-assisted separation method. By utilizing ultrasound to accelerate the dissolution of hexadecylamine and facilitate the separation movement of CuNWs and by-products in hydrophilic and hydrophobic phases, the aim of achieving high purification of CuNWs is realized. Through the introduction of an ultra-thin hexadecylamine layer (~ 3.5 nm) on the surface of CuNWs and leveraging the active adsorption of silver seed crystals, combined with the control CuNWs reaction concentration, silver-coated CuNWs with a dense and uniform surface thickness of 12–15 nm are obtained. By enhancing purity, stability, and cost-effectiveness, this research represents a significant advancement in the field of one-dimensional nanowires and their devices.

Engineering intervention to disrupt the evolution of ZIF-67: Ultra-fast synthesis of arrayed Co(OH)2@ZIF-L in dozens of seconds for high-energy charge storage

Designing rational heterostructures of high-performance electroactive materials on conductive substrates with hierarchical structures is critical for advancing electrochemical energy storage technologies. In this study, a unique spatial structure is fabricated by vertically aligning two-dimensional (2D) structures of Co-ZIF-L on conductive nickel foam (NF) substrate through interruption of ZIF-67 formation. This is followed by an innovative electrochemical synthesis method that disrupts unstable surface coordination bonds in Co-ZIF-L, enabling the in-situ generation of Co(OH)2. The resulting Co(OH)2@ZIF-L/NF binder-free electrodes feature a hierarchical spatial structure and are synthesized in approximately 30 s. These electrodes showcase exceptional area capacity of 3.1 C cm−2 at 1 mA cm−2, attributed to their high specific surface area and layered architecture that promotes electrolyte penetration. Density Functional Theory (DFT) calculations reveal that the Co(OH)2@ZIF-L nanostructures have superior electrical conductivity compared to the individual components. Furthermore, a hybrid supercapacitor (HSC) based on Co(OH)2@ZIF-L/NF//AC exhibits an impressive energy density of 42 Wh kg−1 at a power density of 184.7 W kg−1. This research provides new insights into the efficient synthesis of high-performance electroactive materials with unique spatial structures and expands the potential applications of ZIF materials.

Hollow core-shell Si-PEI@ZIF-67 with cross-linking effect for high-performance Li-ion batteries

Owing to its extremely high theoretical capacity (4200 mAh g−1), silicon (Si) has emerged as a promising candidate for lithium-ion batteries (LIBs) anodes. However, challenges such as a volumetric expansion of up to 300 % and poor electrical conductivity have impeded its application. Here, hollow core-shell Si-PEI@ZIF-67 synthesized via a simple one-pot method utilizing the unique properties of ZIF-67, including its porous nature, high surface area, and well-ordered structure, ZIF-67 coating effectively mitigates the volume expansion of nano-Si during cycles. Hollow core-shell structure can accelerate ion transfer and alleviate volume expansion. Moreover, Co2+ enrichment in the coating promotes the formation of a strong cross-linking network with the binder sodium alginate. This interaction not only enhances the adhesion between active material and current collector but also accelerates ion transport. Si-PEI@ZIF-67 composites demonstrate outstanding lithium storage performance in LIBs, achieving a stable capacity of 1134.4 mAh g−1 after 500 cycles at 1000 mA g−1. In addition, the discharge capacity of 828.7 mAh g−1 is maintained after 200 cycles at the high current density of 5000 mA g−1. The innovative synthesis method, utilizing ZIF-67 as a coating for nano-Si and establishing an interconnected network with the binder, offers a novel approach for other anodes.

A high-speed method to obtain Ni-Zn ferrite nanoparticles by microwave hydrotalcite decomposition for magnetic applications

Nanoparticles of Zn0.375Ni0.625Fe2O4 ferrite were successfully synthesized using an innovative, rapid, and efficient synthesis method based on microwave-assisted hydrotalcite decomposition, enabling nanoparticle crystallization in less than 15 minutes. A single composition was studied to better assess the impact of the synthesis method on structural, morphological, and magnetic properties. This new synthesis route was compared with the traditional ceramic method. The prepared hydrotalcite was analyzed by high-resolution transmission electron microscopy (HRTEM), identifying hydrotalcite diffraction planes consistent with selected area electron diffraction (SAED) and X-ray diffraction (XRD) patterns. The decomposition phases of the hydrotalcite were identified by simultaneous thermogravimetric and differential thermal analysis (DTA/TG). After hydrotalcite decomposition, the ferrite obtained was analyzed by XRD, confirming a single-phase cubic structure. Scanning electron microscopy (SEM) micrographs revealed nanoparticles less than 100 nm in size with the new method and larger than 2 µm with the traditional route. At a temperature of 5 K, the M-H graph obtained with a superconducting quantum interference device (SQUID) indicated that the spinel-type ferrite exhibited a smooth ferrimagnetic behavior, which was also corroborated by electron paramagnetic resonance (EPR). Magnetic saturation values of 105.73 emu/g were obtained in the synthesis microwave-assisted hydrotalcite decomposition and 51.49 emu/g in the traditional synthesis, representing an increase of over 100 %. The two synthesis methods were also compared using density functional theory (DFT) calculations, confirming the influence of morphology on magnetic properties, obtained thanks to different synthesis methods. These results indicate that the synthesized Ni-Zn spinel ferrite nanoparticles can be used in high-frequency applications, such as ceramic induction plates.

Experimental and theoretical study of multiple active site-functionalized Spirulina residue-based porous carbon as an economical adsorbent for NH3 and SO2 adsorption: Micro- and macro-mechanistic investigations

Here, we successfully synthesized a cost-effective (7.88 USD/kg) multi-active site (CuCl2, CuO and KCl) functionalized Spirulina residue-based porous carbon (MMBC). This innovative synthesis method utilizes Spirulina residue, a sustainable and low-cost biomass source, making the production of MMBC economically viable and environmentally friendly. Under ambient conditions, MMBC exhibits competitive adsorption capacities for NH3 and SO2 compared to other adsorbents, reaching 3.01 mmol/g (i.e., 51.26 mg/g) and 0.70 mmol/g (i.e., 44.85 mg/g), respectively, and tolerable recoverability. These values are significant improvements over many existing adsorbents, highlighting MMBC's efficiency in removing toxic industrial chemicals (TICs). Additionally, even at low molar fractions of NH3 or SO2, such as 0.001, MMBC demonstrates significant ideal adsorption solution theory (IAST) selectivity for NH3/N2 and SO2/N2, with values of 12.02 and 4.19, respectively. This high selectivity at low concentrations underscores MMBC's potential for applications in environments with trace amounts of pollutants. Furthermore, extensive research has been conducted in this study to elucidate the microscopic and macroscopic adsorption mechanisms of NH3 and SO2 on MMBC. Specifically, investigations in statistical physics models and statistical thermodynamics reveal that the adsorption of NH3 and SO2 on MMBC adhere to a non-aggregative, multilayer, multi-anchorage, and spontaneous exothermic physicochemical behavior. And the adsorption orientation occurs either horizontally or both horizontally and non-horizontally, contingent upon the system and temperature. These findings provide a deeper understanding of the adsorption processes and provide innovative insights into the adsorption mechanisms at the molecular level and at the macroscopic scale. Besides, the material characterization results reveal that the above adsorption process involves both physical interactions (pore diffusion and van der Waals forces) and chemical interactions (CuCl2 with NH3, CuO and KCl with SO2), indicating a physicochemical adsorption mechanism. This dual mechanism of adsorption offers a comprehensive explanation of the high performance of MMBC. In summary, this study developed a cost-effective Spirulina residue-based adsorbent, exhibiting high removal efficiency and selectivity for TICs, and providing deep insights into adsorption mechanisms. The innovative use of Spirulina residue addresses waste management issues and promotes the development of sustainable materials in the field of environmental remediation, contributing to cleaner production.

Green synthesis of potent anticancer and antibacterial xanthene and chromene derivatives using agar as a catalyst: Molecular docking and in silico ADMET insights

This study presents an innovative green synthesis method for xanthene, benzoxanthene, and chromene derivatives using agar as a natural catalyst. Our method achieves high yields (up to 95%) with short reaction times (less than 1 hour) under environmentally friendly conditions and simple work-up procedures. The docking analysis conducted provides insights into the complex binding energies, molecular interactions, and hydrogen bond energies and distances. Molecular docking studies reveal strong chemical interactions with human serum albumin (HSA) and DNA gyrase, suggesting strong anticancer and antibacterial potential with binding energies ranging from -8.5 to -9.8 kcal/mol. In silico ADMET analysis and drug-likeness analysis confirm favorable pharmacokinetic properties, including high oral bioavailability and low toxicity. This work offers a sustainable and effective approach to developing new therapeutic agents.

Shape-Preserved CoFeNi-MOF/NF Exhibiting Superior Performance for Overall Water Splitting across Alkaline and Neutral Conditions.

This study reported a multi-functional Co0.45Fe0.45Ni0.9-MOF/NF catalyst for oxygen evolution reaction (OER), hydrogen evolution reaction (HER), and overall water splitting, which was synthesized via a novel shape-preserving two-step hydrothermal method. The resulting bowknot flake structure on NF enhanced the exposure of active sites, fostering a superior electrocatalytic surface, and the synergistic effect between Co, Fe, and Ni enhanced the catalytic activity of the active site. In an alkaline environment, the catalyst exhibited impressive overpotentials of 244 mV and 287 mV at current densities of 50 mA cm-2 and 100 mA cm-2, respectively. Transitioning to a neutral environment, an overpotential of 505 mV at a current density of 10 mA cm-2 was achieved with the same catalyst, showing a superior property compared to similar catalysts. Furthermore, it was demonstrated that Co0.45Fe0.45Ni0.9-MOF/NF shows versatility as a bifunctional catalyst, excelling in both OER and HER, as well as overall water splitting. The innovative shape-preserving synthesis method presented in this study offers a facile method to develop an efficient electrocatalyst for OER under both alkaline and neutral conditions, which makes it a promising catalyst for hydrogen production by water splitting.

Efficient isomerization of glucose into fructose by MgO-doped lignin-derived ordered mesoporous carbon

The conversion of glucose into fructose can transform cellulose into high-value chemicals. This study introduces an innovative synthesis method for creating an MgO-based ordered mesoporous carbon (MgO@OMC) catalyst, aimed at the efficient isomerization of glucose into fructose. Throughout the synthesis process, lignin serves as the exclusive carbon precursor, while Mg2+ functions as both a crosslinking agent and a metallic active center. This enables a one-step synthesis of MgO@OMC via a solvent-induced evaporation self-assembly (EISA) method. The synthesized MgO@OMCs exhibit an impeccable 2D hexagonal ordered mesoporous structure, in addition to a substantial specific surface area (378.2 m2/g) and small MgO nanoparticles (1.52 nm). Furthermore, this catalyst was shown active, selective, and reusable in the isomerization of glucose to fructose. It yields 41 % fructose with a selectivity of up to 89.3 % at a significant glucose loading of 7 wt% in aqueous solution over MgO0.5@OMC-600. This performance closely rivals the current maximum glucose isomerization yield achieved with solid base catalysts. Additionally, the catalyst retains a fructose selectivity above 60 % even after 4 cycles, a feature attributable to its extended ordered mesoporous structure and the spatial confinement effect of the OMCs, bestowing it with high catalytic efficiency.

NeRF-VPT: Learning Novel View Representations with Neural Radiance Fields via View Prompt Tuning

Neural Radiance Fields (NeRF) have garnered remarkable success in novel view synthesis. Nonetheless, the task of generating high-quality images for novel views persists as a critical challenge. While the existing efforts have exhibited commendable progress, capturing intricate details, enhancing textures, and achieving superior Peak Signal-to-Noise Ratio (PSNR) metrics warrant further focused attention and advancement. In this work, we propose NeRF-VPT, an innovative method for novel view synthesis to address these challenges. Our proposed NeRF-VPT employs a cascading view prompt tuning paradigm, wherein RGB information gained from preceding rendering outcomes serves as instructive visual prompts for subsequent rendering stages, with the aspiration that the prior knowledge embedded in the prompts can facilitate the gradual enhancement of rendered image quality. NeRF-VPT only requires sampling RGB data from previous stage renderings as priors at each training stage, without relying on extra guidance or complex techniques. Thus, our NeRF-VPT is plug-and-play and can be readily integrated into existing methods. By conducting comparative analyses of our NeRF-VPT against several NeRF-based approaches on demanding real-scene benchmarks, such as Realistic Synthetic 360, Real Forward-Facing, Replica dataset, and a user-captured dataset, we substantiate that our NeRF-VPT significantly elevates baseline performance and proficiently generates more high-quality novel view images than all the compared state-of-the-art methods. Furthermore, the cascading learning of NeRF-VPT introduces adaptability to scenarios with sparse inputs, resulting in a significant enhancement of accuracy for sparse-view novel view synthesis. The source code and dataset are available at https://github.com/Freedomcls/NeRF-VPT.

Solar radiation powered biodiesel synthesis using C&D waste catalyst – a novel approach

A significant amount of construction and demolition waste is generated in India every year. The proper management of this waste has become a crucial concern due to fast urban growth, building projects, and increased construction work. The volume of this waste is substantial, which can harm the environment, deplete resources, and pose health risks if not handled well. This study presents an innovative method for biodiesel synthesis, addressing the challenges of construction and demolition (C&D) waste management and renewable energy integration. The research introduces a novel catalyst derived from C&D waste through a calcination process, offering an eco-friendly solution for waste repurposing. This catalyst demonstrates potential for sustainable biodiesel production, marking a significant advancement in waste management practices. Furthermore, a pioneering solar-powered reactor is utilized for biodiesel synthesis, achieving an impressive 92.2% conversion rate under specific conditions. The system's energy efficiency, calculated as [Formula: see text], surpasses conventional methods, highlighting its potential for reducing energy consumption and environmental impact. Moreover, the produced biodiesel meets ASTM D6751 standards, ensuring quality and compatibility with industry requirements.

Fe2O3 Review: Nanostructure, Synthesis Methods, and Applications

Iron sand, which contains magnetite iron ore, exhibits unique magnetic properties when exposed to magnetic fields. Iron ore content, including ?-Fe2O3, FeTiO3, Magnetite (Fe3O4), and others, provides potential uses in various industries such as electronics, energy, chemical, ferrofluids, catalysts, and biomedicine. The location of the discovery of iron sand can affect its mineral characteristics and geological conditions. This research aims to develop innovative synthesis methods to produce hematite nanomaterials from iron sand. Nano-size hematite nanoparticles exhibit unique characteristics, including an increase in specific surface area that is beneficial in applications such as gas sensors, catalysts, lithium-ion batteries, and the manufacture of permanent magnets. Through a literature review, this article presents comprehensive insights into the characteristics of iron sand, variations in synthesis methods, and the structure of hematite nanoparticles. Applications of hematite nanoparticles in water treatment, catalysis, and energy storage are also detailed. This article is expected to contribute to the development of innovative nanomaterial technologies as well as explore the potential of iron sand resources for wider industrial applications.

Synthesis of Periclase Phase (MgO) from Colloidal Cassava Starch Suspension, Dual Application: Cr(III) Removal and Pigment Reuse

Synthesis of Periclase Phase (MgO) from Colloidal Cassava Starch Suspension, Dual Application: Cr(III) Removal and Pigment Reuse

CO2 to solar fuel: design and reactivity of inorganic perovskites

Carbon dioxide release by human activity is the major cause of global warming. Decreasing the concentration of CO2 in the atmosphere is a challenge that needs to be addressed. In addition to their negative impact on the environment, the availability of petroleum-based fuel is decreasing. The photoconversion of CO2 into so-called green solar fuel is a possible alternative to reduce the quantity of carbon dioxide in the atmosphere aiming the limitation of greenhouse effect. Among the photocatalyst studied for these reactions, the perovskite-based appeared as one of the most promising class of materials. These materials possess unique optoelectronic properties and exhibit significant variability in terms of their dimensionality, structure, morphology, grain size, and tunable band gap, as well as the position of their valence band and conduction band. This review discusses both the classics and innovative perovskite synthesis methods such as solid-state reaction, hydrothermal and solvothermal synthesis, hot injection or chemical precipitation. Then, the use of these materials for the photoreduction of CO2 into fuel such as formic acid, methanol and methane is detailed.

Recent advances in gel coatings: from lab to industry

The review summarizes and categorizes innovative gel synthesis methods and coating fabrication techniques with robust interfacial adhesion, focusing on the strategies of user and eco-friendliness in versatile scenarios.

Mechanochemical Oxidative Coupling of Amine to Azo-based Polymers by Hypervalent Iodine Oxidant.

Among porous organic polymers (POPs), azo-linked POPs represent a crucial class of materials, making them the focus of numerous catalytic systems proposed for their synthesis. However, the synthetic process is limited to metal-catalyzed, high-temperature, and liquid-phase reactions. In this study, we employ mechanochemical oxidative metal-free systems to encompass various syntheses of azo-based polymers. Drawing inspiration from the "rule of six" principle (six or more carbons on an azide group render the organic compound relatively safe), an azo compound featuring significant steric hindrance is obtained using the hypervalent iodine oxidation strategy. Furthermore, during the polymerization process, steric hindrance is enhanced in monomers to effectively prevent explosions resulting from direct contact between hypervalent iodine oxidants and primary amines. Indeed, this approach provides a facile and innovative solid-phase synthesis method for synthesizing azo-based materials.

Facile and fast synthesis of highly ordered L10-FeNi nanoparticles

The chemically ordered L10-FeNi alloy is a promising candidate for next generation rare-earth-free permanent magnets, which can revolutionize the high-performance magnets market currently dominated by Nd-Fe-B. Despite many efforts, the experimental results fall short of theoretical predictions, and current approaches are not suitable for industrial implementation. In this work, we propose an innovative and efficient synthesis method that exploits the natural order of a crystalline Ni/Fe complex, which closely mimics the atomic organization in the L10 structure, to drive the formation of the ordered phase. By low-temperature reduction of the complex salt, carbon coated aggregates of FeNi alloy nanoparticles (20 – 120 nm) with a >55% of L10 phase, high coercivity (up to 65 mT) and large saturation magnetization (∼ 140 Am2/kg) were obtained. The results pave the way for the development of a novel and sustainable route to produce high-anisotropy FeNi nanoparticles of potential interest for next generation critical-element-free permanent magnets.