Search Results (144)

The advancement of artificial intelligence and information technologies has presented higher demands on neuromorphic computing information devices, entailing the emergence of next-generation devices. Polyoxometalates (POMs) are emerging as promising molecular nanomaterials for next-generation neuromorphic computing, providing distinct advantages over conventional metal oxides. In contrast to bulk oxides that suffer from stochastic filament formation and device-to-device variability, POMs possess atomically precise structures with discrete, multi-electron redox states that enable highly reproducible and deterministic resistive switching. Their molecular nature allows for stable, multi-level data representation through stepwise reduction in metal centers (e.g., V, W, Mo) and the emulation of essential synaptic plasticity functions. Furthermore, the exceptional structural and chemical tunability of POMs favors covalent or supramolecular functionalization, enabling precise engineering of the POM-electrode interface and controlled self-assembly on surfaces. This molecular precision not only addresses the scalability challenges of traditional memristors but also unlocks unique functionalities, such as multimodal switching coupled with visible chromic response for state visualization. Taking the advantages of intermolecular crosstalk and countercation dynamics, POM-based networks offer a pathway toward constructing three-dimensional neuronal architectures, effectively connecting molecular redox chemistry to advanced high-density neuromorphic computing paradigms. Full article

The efficient oxidation of glucose to formic acid (FA) has emerged as a sustainable method for biomass utilization. Herein, we developed a new approach to fulfill oxidation of glucose to formic acid using a polyoxometalate (POM) K₁₀SiW₉Mn₃^IIO₃₇/O₃ system, and its high efficiency was presented with 79.3% yield of FA at 82.1% conversion at room temperature for 3 h. As evidenced by experiments, the components in Mn-POMs significantly influenced glucose conversion due to their effect on generating reactive oxygen species (ROSs) from O₃, which was essential for FA production. Full article

Polyoxometalates (POMs) exhibit significant potential for application in Alzheimer’s disease (AD) therapeutics owing to their inherent chemical and physical properties and structural tunability. Through transition metal substitution, functional modification, and the construction of POMs-based nanocomposites, POMs can precisely recognize and effectively modulate various key pathogenic proteins involved in Alzheimer’s disease. They can also intervene in disease progression through multiple mechanisms, including inhibition of Aβ aggregation, disaggregation of amyloid-β (Aβ), scavenging of reactive oxygen species (ROS), hydrolytic activity, and modulation of enzyme function. In addition, due to their outstanding physicochemical properties, the application of POMs in phototherapy has emerged as a significant direction in AD treatment research. This review systematically summarizes recent advances from 2011 to 2025 in POMs targeting key pathogenic proteins in AD, comprehensively analyzes their specific mechanisms of action across different therapeutic contexts, highlights their significant advantages and broad potential in AD treatment, and provides new insights for the future structural design, functional optimization, and clinical translation of POMs. Full article

Alzheimer’s disease (AD) signifies a devastating impact on the quality of life of patients and their families. At a biomolecular level, AD is characterized by the deposition of extracellular plaques of β-amyloid (Aβ), affecting language, spatial navigation, recognition abilities and memory. Among the selected 30 articles about polyoxometalates (POMs) and AD published from 2011 to 2025, pure POMs, hybrid POMs and POM nanoparticles can be found. The majority of POMs are polyoxotungstates (62%), the Keggin-type SiW₁₁O₃₉ being the most studied in AD. The main effect described is the inhibition of Aβ aggregates. Other effects include reversing the neurotoxicity induced by Aβ aggregates, decreasing ROS production and neuroinflammation, restoring memory and sequestering Zn²⁺ and Cu²⁺, among others, features that are well known to be associated with the pathology of AD. POMs have also shown the ability to induce the disaggregation of Aβ fibrils, particularly after irradiation, and to inhibit acetylcholinesterase activity at an nM range. Putting it all together, this review highlights a predominant trend in the exploration of POMs to act directly at the level of the formation and/or disaggregation of Aβ aggregates in the treatment of AD. Full article

Polyoxometalates (POMs) represent a broad class of anionic inorganic (V, Mo, W) clusters with versatile structures of chemical and physical properties. POMs are inhibitors of many enzymes, including P-type ATPases, well-known to be a target of several approved drugs. Herein, two new hybrid POMs with Mo and mixed V/W, namely (C₂H₈N₁)₆[V₂Mo₁₈O₆₂].3H₂O (1) and (C₄H₁₆N₃)₄[V₂W₄O₁₉]₃.12H₂O (2), were synthesized via wet chemical methods in aqueous solution, and their purity was confirmed and characterized by single X-ray diffraction and infrared spectroscopy. The cations are dimethylammonium ((C₂H₈N)⁺) and diethylenetriammonium ((C₄H₁₆N₃)³⁺), respectively. POMs biological activities were investigated, specifically their inhibitory potential against Ca²⁺-ATPase. The sarcoplasmic reticulum Ca²⁺-ATPase activities were measured spectrophotometrically using the coupled enzyme pyruvate kinase/lactate dehydrogenase assay. For the Ca²⁺-ATPase activity, Dawson (1) showed an IC₅₀ value of 3.4 μM, whereas Lindqvist (2) displayed a value of 45.1 μM. The Ca²⁺-ATPase inhibitory potential of these POMs can be correlated with the net charge (namely 6- and 4-) and the charge density (namely 0.33 and 0.67). A structure–activity-relationship was established for a series of 17 POMs Ca²⁺-ATPase inhibitors correlating IC₅₀ values and POMs net charge and POMs charge density. The described features make Dawson (1) and Lindqvist (2) attractive POMs in a wide range of chemistry fields as well as in biomedical applications. Full article

Polyoxometalates (POMs) are nanoscale anionic clusters constructed from transition-metal oxide units with well-defined architectures and tunable electronic structures, offering abundant reversible redox sites and adjustable energy levels. Their diverse valence states and compositional flexibility of molecular architectures render them promising candidates for electrochemical energy storage. Rational molecular design and nano-structural engineering can significantly enhance the electrical conductivity, structural stability, and ion transport kinetics of POM-based materials, thus improving device performance. In solar cells, the tunable energy levels and light-harvesting capabilities contribute to enhanced photoconversion efficiency. In secondary batteries, the dense redox centers provide additional capacity. For supercapacitors, the rapid electron transfer supports high power density storage. This review systematically summarizes recent advances in POM-based functional nanomaterials, with an emphasis on material design strategies, energy storage mechanisms, performance optimization approaches, and structure–property relationships. Fundamental structures and properties of POMs are outlined, followed by synthesis and functionalization approaches. Key challenges such as dissolution, poor conductivity, and interfacial instability are discussed, together with progress in batteries and hybrid capacitors. Finally, future challenges and development directions are outlined to inspire further advancement in POM-based energy storage materials. Full article

This research focuses on the synthesis, characterization, and photocatalytic performance of Cu-based polyoxometalate (Cu-POM) as an effective catalyst for the degradation of organic dyes, specifically Congo Red (CR) and Phenol Red (PR). The main goals are to synthesize Cu-POM using a controlled self-assembly technique, characterize its optical and structural characteristics using FTIR, XRD, SEM, TGA, and UV-Vis spectroscopy, and estimate its photocatalytic activity when exposed to UV light. The outcomes confirm the successful formation of Cu-POM with well-defined nanostructures and a crystalline polyoxometalate framework. The determined optical bandgap of 3.65 eV indicates its strong UV-light responsiveness. The photocatalytic degradation experiments demonstrated high removal efficiencies of 58.1% for CR and 64.6% for PR under UV irradiation, corresponding kinetic rate constants of 0.00484 min⁻¹ and 0.00579 min⁻¹, respectively. The superior photocatalytic activity is attributed to the efficient charge carrier separation and high surface area of Cu-POM. These findings highlight the potential of Cu-POM as a promising heterogeneous photocatalyst for sustainable wastewater treatment and environmental remediation. Full article

Polyoxovanadates are a subclass of polyoxometalates (POMs) known to interact with proteins and to present anticancer, antimicrobial, and antiviral activities. Herein, we aimed to pursue the study of the breast anticancer activity of a mixed-valence polyoxovanadate, [Cl@V^V₇V^IV₈O₃₆]⁶⁻ (V₁₅) against MCF-7 and MDA-MB-231 cancer cell lines and to analyze its Ca²⁺-ATPase inhibition potential. ⁵¹V NMR and UV-Vis/NIR studies of V₁₅ indicated its stability in HEPES and RPMI media. For the Ca²⁺-ATPase activity, V₁₅ showed an IC₅₀ value of 14.2 μM and a mixed type of inhibition. The electrostatic potential map of V₁₅ and other POMs were correlated with the enzyme activity inhibition. V₁₅ also exhibited cytotoxicity against MDA-MB-231 (IC₅₀ = 17.2 μM) and MCF-7 (IC₅₀ = 15.1 μM) breast cancer cell lines. Using V₁₅ concentrations equivalent to half and 1/4 of the IC_50, it was observed that MDA-MB-231 cell migration was reduced by 90 and 70%, after 24 h, respectively. Moreover, V₁₅ caused morphological changes from fusiform to an epithelial-like (amoeboid) shape. Finally, V₁₅ induced the increase in RIPK1, MLKL, and RIPK3 gene expression, up to 3, 10, and 15-fold, respectively, pointing out that the mechanisms of cell death in the triple-negative breast cancer cell line may occur by necroptosis. Full article

In this work, the synthesis and structural characterization of the smallest possible member of the family of bis-functionalized {MnMo₆O₂₄} Anderson–Evans polyoxometalates (POMs) is reported. The synthesis of the title compound TBA₃{[HC(CH₂O)₃]₂MnMo₆O₁₈} (1) was accomplished by using trimethylolmethane as the capping unit (TBA: tetra(n-butyl)ammonium, n-B_u4N⁺). The molecular structure of the organic–inorganic POM gave rise to yet undisclosed ¹H-NMR features, which are discussed thoroughly. Single-crystal X-ray diffraction (XRD) analysis revealed a highly regular 3D packing of the polyoxoanions within a matrix of TBA cations. The hybrid POM is of particular interest regarding potential applications in photocatalysis (i.e., hydrogen evolution) and energy storage. Thus, the electrochemical and thermal properties of 1 are also analyzed. Full article

Polyoxometalate (POM)-type supramolecular materials have unique structures and hold immense potential for development in the fields of biomedicine, information storage, and electrocatalysis. In this study, (NH₄)₃ [AlMo₆O₂₄H₆]·7H₂O was employed as a polyacid anion template, pentacyclic imidazole molecules served as organic ligands, and the moderate-temperature hydrothermal and natural evaporation methods were used in combination for the design and synthesis of two octamolybdenum-oxo cluster (homopolyacids containing molybdenum-oxygen structures as the main small-molecular structures)-based organic–inorganic hybrid compounds, [(C₃N₂H₅)(C₃N₂H₄)][(β-Mo₈O₂₆H₂)]_0.5 (1) and {Zn(C₃N₂H₄)₄}{[(γ-Mo₈O₂₆)(C₃N₂H₄)₂]_0.5}·2H₂O (2). Structural and property characterization revealed that both compounds crystallized in the P-1 space group with relatively stable three-dimensional structures under the action of hydrogen bonding. Upon temperature stimulation, the [Zn(C₃N₂H₄)₄]²⁺ cation and water molecules in 2 exhibited obvious oscillations, leading to significant dielectric anomalies at approximately 250 and 260 K when dielectric testing was conducted under heating conditions. Full article

Polyoxometalates (POMs) surrounded by organic cations and related systems composed of POMs immobilized on functionalized Merrifield resin (MR) were synthesized, characterized and tested as catalysts for the oxidation of two natural terpenes, β-myrcene and β-caryophyllene, using H₂O₂ and TBHP as green oxidants. The ionic immobilization enabled easy catalyst recovery and reuse. The results showed high conversion and selectivity, with some catalysts maintaining their efficiency for at least three runs without leaching. The catalytic performances of both homogeneous and heterogeneous systems, along with the necessary characterizations, are discussed. Full article

Water, the source of life, is undeniably essential to all living beings in nature. However, the process of industrialization has led to the pollution of water resources. Photocatalytic water treatment technology can convert solar energy into environmentally friendly and renewable chemical energy, effectively degrading organic pollutants in water. This offers a promising solution for the purification of water environments. The development of high-performance photocatalysts is crucial for photocatalytic reactions. Polyoxometalates (POMs) are anionic metal oxide clusters that come in various sizes and shapes. Their unique electronic properties, tunable structures, and photocatalytic activity make them highly promising materials for the efficient degradation of organic pollutants in water. This review summarizes the recent advances in emerging POM-based photocatalytic materials for water treatment, elaborating on their mechanisms of action. Finally, the current development prospects and the future challenges of POM-based photocatalytic materials are envisioned. Full article

Polyoxometalates are a promising family of compounds for the development of new catalyst materials, although up to now they have mainly been applied in acid catalysis and oxidative processes. In this study, we present the synthesis and characterisation of two new Keggin-type phosphomolybdates, H₆[PRuMo₁₁O₄₀] and H₉[PRu₂Mo₁₀O₄₀]. The successful synthesis was confirmed with ICP-OES (elemental composition) and infrared spectroscopy (structure). Furthermore, the molecular structure of H₆[PRuMo₁₁O₄₀] was determined by electron diffraction. The new compounds were comprehensively characterised using ³¹P-NMR spectroscopy, UV-Vis spectroscopy, and electrochemical methods. Square-Wave-Voltammetry revealed an additional RedOx peak for the Ru-substituted POMs compared to the unsubstituted phosphomolybdate at around 825 mV. In a test reaction, the new compounds showed promising catalytic activity for the hydrogenation of lactic acid. Full article

Solid electrolytes, including polymer electrolytes, are a promising option for improving the performance of environmentally friendly batteries such as rechargeable lithium-ion batteries or fuel cells. Hydrogen–oxygen fuel cells producing only water under power generation are attracting widespread attention, and they need proton conductors as electrolytes. Fluoropolymer electrolytes such as Nafion^® have been utilized for hydrogen–oxygen fuel cells below 100 °C; however, they are not applicable over the working temperature. Therefore, other types of polymer electrolytes are demanded for hydrogen–oxygen fuel cells. Polyoxometalate (POM) inorganic clusters are known as proton conductors and are utilized to prepare POM–polymer composites for solid electrolyte application. In such POM–polymer composites, distinct compositions and structures are significant for improving the performance of proton conductivity. Recently, POM–polymer composites with distinct compositions and structures have been synthesized to obtain high proton conductivity. The key factor is to use single-crystalline compounds. Here, several examples are overviewed by classifying them into three categories: (i) single-crystalline POM–polymer composites, (ii) organically modified POM (org-POM) polymers, and (iii) POM hybrid polymers using polymerizable cations. The application of proton-conductive solid electrolytes is focused on. Full article

Redox Flow Batteries (RFBs) are promising large-scale Energy Storage Systems, which support the integration of renewable energies into the current electric grid. Emerging chemistries for electrolytes, such as Polyoxometalates (POMs), are being studied. POMs have attracted great interest because of their reversible multi-electron transfers and the possibility of tuning their electrochemical properties. Recently, the cobalt-containing Keggin-type species [CoW₁₂O₄₀]⁶⁻ (CoW₁₂) has been successfully implemented in a symmetric RFB, and its further implementation calls for new materials for the membrane to enhance its cell performance. In this work, different types of ion exchange membranes (Nafion™-NR212, FAPQ-330 and Amphion™) were tested. The electrolyte uptake, swelling, conductivity and permeability of the membranes in the CoW₁₂ electrolyte, as well as a detailed cell performance study, are reported herein. Better performance results ascribed to the robustness, efficiency and energy density of the system were found for Nafion™-NR212, with 88.5% energy efficiency, 98.9% capacity retention and 3.1 Wh L⁻¹ over 100 cycles at 20 mA cm⁻². FAPQ-330 and Amphion membranes showed large capacity fade (up to 0.2%/cycle). Crossover and the low conductivity of these membranes in the mild pH conditions of the electrolyte were revealed to be responsible for the reduced cell performance. Full article