Search Results (356)

The development of efficient and biocompatible sorbent nanomaterials for cesium removal is critical for environmental and biomedical decontamination. Here, hybrid composites based on ultra-small Prussian blue or Zn Prussian blue-type nanoparticles confined within porous chitosan beads are proposed for Cs⁺ extraction. Nanoparticle confinement ensures homogeneous dispersion and improved accessibility of ion-exchange sites, while preserving the porous polymeric network, as confirmed by physicochemical characterization. Cs⁺ adsorption was investigated under neutral and acidic conditions (pH 7.2 and 1.2), at concentrations of 0–9 mmol/L and contact times of 0–50 h, showing efficient uptake and favorable kinetics, with confirmed stability in simulated gastric fluid. In vivo performance was assessed in a mouse model of cesium contamination (70 mg Cs⁺/kg). Treatment with nanocomposites (225 mg/kg) was compared to bulk Prussian blue (75 mg/kg), revealing enhanced detoxification efficiency. Histological analysis of liver, spleen, and kidney tissues showed no detectable structural damage, consistent with unchanged systemic biomarkers. Overall, the proposed chitosan-confined Prussian blue-type nanocomposites combine high Cs⁺ removal efficiency, kinetic accessibility, and in vivo safety, highlighting their potential for decorporation applications. Full article

Herein, we describe a versatile synthetic strategy for constructing Prussian Blue (PB)-coated polymeric nanocapsules (PB@nanocapsules) with tunable sizes and controlled PB loading. A soft template was first formed from a miniemulsion composed of water/chloroform/hexadecane (94.55:5:0.2, w/w/w), using P4VP₈₂-b-PDMAA₁₈₀ as a stabilizer and varying amounts of P4VP homopolymer as a hydrophobe and additional reactive site provider. Crosslinked nanocapsules were obtained by adding 1,2-bis-(2-iodoethoxy)ethane (BIEE) as a crosslinker. The resulting nanocapsules exhibited average hydrodynamic diameters ranging from approximately 282 nm (without P4VP homopolymer) down to 58 nm (with 0.01 g P4VP homopolymer), as determined by DLS and TEM. Subsequently, sequential coordination with sodium pentacyanoammine -ferroate(II) hydrate (Na₃ [Fe(CN)₅NH₃]), followed by the addition of FeCl₃, yielded a uniform PB coating, as confirmed by the appearance of a characteristic absorption peak at 780 nm in the UV–Vis spectra and a CN stretching shift from 2060 to 2070 cm⁻¹ in FT-IR. TEM and HAADF-STEM with EDX mapping revealed the homogeneous distribution of Fe across the nanocapsule shells. The PB loading could be further controlled by varying the Fe³⁺ addition (5.0 × 10⁻³–4.5 × 10⁻² mmol), with higher loading improving thermal stability. This rational design provides a robust and generalizable platform for engineering polymer–inorganic hybrid nanostructures with tailored functionalities. Full article

Solid-contact ion-selective electrodes (SC-ISEs) are typically constructed using ion-selective membrane (ISM)-based configurations. However, such structures often suffer from water-layer formation and the weak mechanical stability of the ISM. Herein, we report an ISM-free K⁺-SC-ISE based on a Prussian blue analogue transducer, KMnFe(CN)₆, eliminating the need for a conventional ionophore-based ISM layer. KMnFe(CN)₆ was synthesized via a one-step citrate-assisted co-precipitation method. The material functions as a bifunctional transducer, in which the open framework structure with ion-transport channels enables selective K⁺ recognition, while the redox-active Mn centers facilitate ion-to-electron transduction. The fabricated KMnFe(CN)₆-based K⁺ sensor exhibits a near-Nernstian response with a sensitivity of 52.3 ± 1.0 mV dec⁻¹ and a rapid response time of 25 s. The linear range and limit of detection were determined to 10⁻⁴ to 10⁻¹ M and 5.8 × 10⁻⁵ M, respectively. The sensor also demonstrates selectivity to representative interfering ions, with log K_ij of −2.39 ± 0.12 (Na⁺), −2.86 ± 0.09 (Li⁺), −3.06 ± 0.09 (Ca²⁺), −2.74 ± 0.12 (Mg²⁺) and −0.95 ± 0.08 (NH₄⁺). By eliminating the ISM layer, the water-layer effect is effectively avoided, resulting in excellent long-term stability with a potential drift of 57.2 ± 6.1 μV h⁻¹ over 7 days. The sensor was further applied to the analysis of K⁺ in real lake water samples, where the measured concentration showed good agreement with ion chromatography results. This work provides an ISM-free SC-ISE strategy for ion analysis in water environments. Full article

The development of protective coatings that integrate self-healing and environmental tolerance is vital for extending substrate lifespan. In this study, a multifunctional hydrogel composite coating is developed based on a waterborne polyacrylate dynamic covalent network containing oxime–carbamate bonds. The functional monomer MEOC, which contains an oxime–carbamate dynamic bond, was synthesized and incorporated into the waterborne polyacrylate matrix to form a hydrogel network (OC-PA) with intrinsic self-healing capability. Prussian blue (PB) and nano-SiO₂ were incorporated to form a photothermal functional layer, imparting hydrophobicity and converting light into heat for de-icing, while also activating dynamic bond rearrangement within the substrate. When the MEOC content was 7 wt% and the PB content was 2 wt%, the coating temperature rose to 110 °C within 2 min under 0.6 W/cm² irradiation, and the scratch healed within 5 min. After 1 h of fracture repair, the tensile strength reached 6.68 MPa, with a repair rate as high as 92.91%, and de-icing time was reduced from 343 s to 183 s. The coating achieved a water contact angle >100°. At −20 °C, the icing delay time increased by 215%. The hydrogel coating also exhibited excellent abrasion resistance, chemical stability, UV aging resistance, and anti-fouling properties, offering a durable solution for demanding environments. Full article

The development of high-performance electrochemical sensors requires precise integration of electrode active materials that provide both superior electrocatalytic activity and long-term structural stability. Herein, we report a systematically optimized, one-pot electrochemical deposition approach for the fabrication of nanographenide-based nanoarchitectures, incorporating either a conducting polymer (PEDOT-NG) or Prussian blue (PB-NG). Derived from optimization-driven structural refinement—including applied potential, electrodeposition time, and precursor concentration—the robust nanoarchitecture exhibits a hierarchical morphology that provides an expanded electroactive surface area, accelerating charge transfer and enhancing electrochemical catalytic activity. The optimized PEDOT-NG exhibits exceptional sensitivity for the simultaneous determination of ascorbic acid (AA), dopamine (DA), and uric acid (UA), achieving wide linear ranges with low detection limits of 4.1, 0.12, and 0.18 μM, respectively. The PB-NG achieves a limit of detection of 4.39 μM, driven by highly reversible and stable redox kinetics. This performance is underpinned by narrowed peak-to-peak separations (ΔE) and reduced redox potentials. These results underscore the pivotal role of precise parametric control in developing high-performance electrochemical sensors. Furthermore, this work establishes a comprehensive strategy for designing resilient electrode active materials, thereby paving the way for next-generation electrochemical platforms tailored for diverse and robust sensing environments. Full article

The efficiency of hydrogen production via water electrolysis is severely constrained by the sluggish reaction kinetics of the oxygen evolution reaction (OER). Herein, we constructed a nitrogen-doped CoFe Prussian blue analog (CoFePBA-N) electrocatalyst with a nanosheet-assembled cubic architecture by plasma. Plasma treatment induces morphological reconstruction and introduces nitrogen dopants and abundant vacancies, which not only increase the number of exposed active sites but also modulate the electronic structure of Co/Fe centers. Consequently, the optimized CoFePBA-N catalyst achieves a current density of 500 mA cm⁻² at low overpotentials of 322, 344, and 374 mV in alkaline freshwater, alkaline simulated seawater, and alkaline natural seawater, respectively. Furthermore, the catalyst maintains stable operation for over 300 h in alkaline freshwater and nearly 270 h in alkaline natural seawater, exhibiting exceptional durability. The enhanced catalytic performance is attributed to the synergistic effects of nitrogen doping, vacancies, and improved charge-transfer capability. This study provides an effective approach for modulating the electronic structure of Prussian blue analogs, thereby enabling efficient alkaline water and seawater electrolysis. Full article

Sodium-ion batteries (SIBs) have emerged as one of the most promising alternatives to lithium-ion systems, driven by the abundance and low cost of sodium resources as well as the urgent demand for sustainable large-scale energy storage. In recent years, remarkable advances have been achieved in electrode materials, electrolytes, and interfacial engineering, which have significantly improved the electrochemical performance of SIBs. Hard carbons and alloy-type anodes have shown encouraging progress in balancing capacity and stability, while layered oxides, polyanionic compounds, and Prussian blue analogues are leading candidates for cathodes due to their structural diversity and tunable redox properties. Concurrently, the development of advanced liquid and solid electrolytes, together with strategies to control the solid–electrolyte interphase (SEI) and cathode–electrolyte interphase (CEI), is enhancing safety and long-term cycling. Despite these achievements, critical challenges remain, including limited energy density, volumetric expansion in alloying anodes, interfacial instability, and scalability issues. This review provides a comprehensive overview of the fundamental principles, recent material innovations, and failure mechanisms of SIBs, and highlights the current status of industrial progress led by companies such as Faradion, HiNa Battery, CATL, and Tiamat. Finally, future perspectives are discussed, emphasizing the role of sodium-ion technology in grid-scale storage, renewable energy integration, and sustainable battery recycling. By bridging academic advances and industrial development, this article outlines the roadmap toward the commercialization of sodium-ion batteries. Full article

Objective: To evaluate the utility of synovial iron quantification using Magnetic resonance imaging (MRI) in assessing structural joint damage in the knee of patients with rheumatoid arthritis (RA). Methods: This cross-sectional study employed a two-stage design. In the initial comparative stage, 6 patients with RA and 5 patients with osteoarthritis (OA) were recruited to compare synovial R2* values, a metric derived from iterative decomposition of water and fat with echo asymmetry and least-squares estimation quantitation (IDEAL-IQ) MRI sequences representing synovial iron content. Following this, the RA cohort was expanded to a total of 51 patients to investigate the association between R2* values and clinical parameters, including disease activity and bone erosion. Synovial fluid iron levels were measured with an Iron Assay Kit and synovial iron deposits were semi-quantified via Prussian blue staining. Associations between R2* and clinical and laboratory parameters, including inflammatory factors and joint damage indices, were analyzed using Spearman’s rank correlation. Univariate and multivariate ordered logistic regression models were employed to identify factors associated with bone erosion severity. An R2*-based nomogram was developed and validated using receiver operating characteristic (ROC) analysis and calibration curves. Results: Synovial R2* values were significantly higher in RA patients than those with osteoarthritis (53.66 S⁻¹ vs. 31.38 S⁻¹, p < 0.05), consistent with Prussian blue staining results. While synovial R2* values showed no significant correlation with systemic iron metabolic markers, inflammatory indicators, or the Disease Activity Score 28, they were positively correlated with bone erosion severity (ρ = 0.500, p < 0.001) and negatively associated with the joint space width (ρ = −0.307, p < 0.05). Multivariate analysis identified R2* as an independent indicator linked to bone erosion extent (OR = 2358.336, p < 0.001). The R2*-based nomogram demonstrated good discriminative performance. (AUC = 0.83). Conclusions: The R2* value derived from IDEAL-IQ MRI is a reliable tool for quantifying synovial iron and may represent a promising non-invasive imaging biomarker reflecting bone erosion in RA patients. Full article

Calcium-ion batteries (CIBs) offer several advantages. CIBs are viable alternatives to lithium-based battery systems owing to the natural abundance, low cost, and high volumetric capacity of calcium. However, their development has been severely constrained by electrolyte instability and water sensitivity. We conducted a systematic examination of Ca(ClO₄)₂ and Ca(PF₆)₂ electrolytes, focusing on low-cost salt production, solvent selection, and stringent dehydration procedures. Acetonitrile (ACN) was the ideal solvent for high salt solubility and reversible Ca²⁺ electrochemistry, while carbonate solvents failed rapidly. We found that even a small amount of moisture in the electrolyte significantly affected the electrochemical performance. This study improved the dehydration process by using 3 Å molecular sieve (MS3A) and vacuum drying to reduce moisture to ppm levels, stabilizing the electrolyte. Prussian blue (PB) half cells exhibited reversible capacities of up to ≈95 mAh g⁻¹, whereas PB-hard carbon full cells utilizing dried Ca(ClO₄)₂ showed stable cycling over 240 cycles with a Coulombic efficiency of ≈99% and capacity loss of only ≈17%. This study establishes a moisture-controlled electrolyte as a critical enabler for practical CIBs. Full article

Aqueous zinc-ion batteries (AZIBs) are promising for large-scale grid storage due to inherent safety, low cost, environmental compatibility, high theoretical capacity (820 mAhg⁻¹), and suitable redox potential (−0.763 V vs. SHE). However, practical deployment is hindered by coupled challenges at the zinc anode–hydrogen evolution, dendrite growth, and corrosion/passivation, which severely limit cycle life and coulombic efficiency. This review systematically summarizes key advances in AZIB research. It first elucidates working principles and four cathode energy storage mechanisms: Zn²⁺ insertion/extraction, H⁺/Zn²⁺ co-insertion, chemical conversion, and dissolution/deposition. Second, it examines four mainstream cathodes (manganese-based, vanadium-based, Prussian blue analogs, and organic compounds), analyzing performance bottlenecks and corresponding optimization via structural modification. Third, it explores functional mechanisms of advanced separators (polymer, inorganic/ceramic composite, MOF-based, and cellulose-based) in regulating uniform Zn²⁺ deposition and suppressing dendrites. Fourth, it summarizes anode optimization strategies: artificial protective layers for interface stabilization, electrolyte additives to modulate Zn²⁺ solvation/deposition, and 3D porous structures to reduce local current density and provide nucleation sites. Finally, key scientific challenges and future directions are discussed—multi-strategy synergy, in situ characterization, practical battery construction, and sustainable technological development, offering theoretical guidance for advancing AZIBs toward large-scale applications. This review aims to provide a comprehensive perspective spanning from materials to systems, and from mechanisms to applications. Its core objective is not merely to list the types of cathode materials, but to establish a logical bridge directly connecting “key challenges” to “optimization strategies,” with a particular emphasis on the issues and solutions related to the cathode side. Full article

Potassium-ion batteries hold great promise for large-scale energy storage, but their commercialization is hindered by the large ionic radius of potassium, which causes sluggish kinetics and severe volume expansion in anode materials. To address this, we present a scalable spray-drying strategy coupled with NaCl salt-templating to synthesize hierarchical porous carbon/vanadium sulfide microspheres (p-V₃S₄/C MS). In this structure, V₃S₄ nanoparticles are uniformly encapsulated within a dextrin-derived amorphous carbon matrix, and pores are formed via selective NaCl etching. This unique architecture accommodates volume fluctuations while providing rapid ion diffusion pathways. As a result, the p-V₃S₄/C MS anode exhibits outstanding electrochemical performance, maintaining a reversible capacity of 107 mA h g⁻¹ after 2000 cycles at 2.0 A g⁻¹, and achieves a high pseudocapacitive contribution of 93% at 2.0 mV s⁻¹. Furthermore, a full cell paired with a Prussian blue (PB) cathode demonstrates practical viability and robust reversibility. Our findings demonstrate that this structural engineering effectively mitigates internal resistance and structural degradation, offering a cost-effective route for mass-producing high-performance anodes for next-generation energy storage. Full article

Hepatic encephalopathy is a severe complication of liver failure, traditionally investigated through brain–liver interactions; however, the involvement of extrahepatic organs remains poorly understood. This study examined splenic histopathological changes in a mouse model of acute hepatic encephalopathy induced by ammonium acetate administration, focusing on iron metabolism and macrophage activation. Although conventional hematoxylin and eosin staining revealed no overt structural abnormalities, unstained spleen sections demonstrated abundant black deposits, predominantly in the red pulp. Prussian blue staining confirmed a significant increase in hemosiderin-positive cells; however, a subset of black deposits was iron-negative. Immunohistochemical analyses revealed that these iron-negative pigments were localized within F4/80-positive macrophages and colocalized with heme oxygenase-1 (HO-1), suggesting enhanced heme degradation. Ultrastructural observations further identified electron-dense granules consistent with hematin accumulation in splenic macrophages. Hematological analyses revealed significant reductions in red blood cell count and hemoglobin levels, indicating accelerated erythrocyte destruction. Collectively, these findings demonstrate that acute hepatic encephalopathy induces splenic macrophage activation, accompanied by disordered iron metabolism and hematin accumulation. This study highlights the spleen as a previously underappreciated extrahepatic organ involved in the pathophysiology of hepatic encephalopathy and suggests that splenic heme–iron handling may represent a novel therapeutic target. Full article

Sodium-ion batteries (SIBs) are regarded as an important complementary technology to lithium-ion batteries due to their abundant resources and low cost, demonstrating broad application prospects, especially in large-scale energy storage. As a core component of SIBs, the cathode material directly determines key performance indicators such as energy density, cycling stability, and rate capability. Currently, the main cathode material systems under extensive research include transition metal oxides, polyanionic compounds, and Prussian blue analogues (PBAs), each exhibiting distinct characteristics in terms of crystal structure and electrochemical performance. Transition metal oxides have attracted significant research interest owing to their high specific capacity, while polyanionic compounds are known for their excellent structural stability and operating voltage. PBAs, on the other hand, have gained considerable attention due to their open framework structure and simple synthesis process. In recent years, modification strategies such as nanostructure engineering, surface coating, and elemental doping have significantly enhanced the electrochemical performance of these cathode materials. Future research should focus on addressing critical scientific challenges, including low intrinsic electronic conductivity and poor interfacial stability, while also exploring novel composite cathode material systems to facilitate the practical application of sodium-ion batteries. Full article

There is an increasing demand for multifunctional devices, that can operate simultaneously as energy storage and electrochromic display devices, widely known as electrochromic supercapacitors. For instance, Prussian blue (PB) exhibits outstanding electrochromic properties; however, it has not been well explored for energy storage applications. Moreover, the electrochemical properties can be enhanced by surface engineering the host material via compositing with conducting polymers. In this work, we studied the electrochromic supercapacitor properties of composites such as Prussian blue-polyaniline (PB-PANI). The PB-PANI 90 composite thin-film electrode exhibited the highest coloration efficiency of 461.39 cm²/C and demonstrated superior electrochemical performance, with an aerial capacitance of 50.80 mF/cm² and an optical modulation of 19.4%. All samples achieved rapid switching times of less than 3 s. These findings highlight the potential of optimizing conducting polymer coatings on Prussian blue to achieve a well-balanced composite structure with enhanced morphological properties, paving the way for advanced multifunctional electrochromic supercapacitor devices in next-generation smart systems. Full article

This study focuses on the synthesis and characterization of buckwheat husk-derived activated carbon, chemically activated with potassium hydroxide (KOH) and subsequently modified with urea and Prussian Blue (PB). The obtained carbons were evaluated in terms of particle-size distribution, surface morphology, structural features, and electrokinetic properties using scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM–EDS), Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, and electrophoresis, as well as N₂ adsorption–desorption (BET surface area and porosity analysis). The results confirmed that both pyrolysis conditions and the type of modifier significantly affect the physicochemical properties of the activated carbon and its behavior in electrolyte solutions. Colloidal stability and particle size were strongly dependent on pH and the type of anions present in solution, with sodium nitrate (NaNO₃) systems showing higher stability than sodium chloride (NaCl). Modification with KOH and urea imparted a more basic surface character, whereas PB introduced more acidic properties. All samples exhibited predominantly negative surface charges and mesoporous structures, which are favorable for adsorption processes and enhance affinity for heavy-metal cations. Among the tested materials, BH-KOH-Fe (Fe-modified KOH-activated carbon) showed the most favorable performance for the targeted application, while BH-KOH (KOH-activated buckwheat husk-derived carbon) exhibited high surface area and good colloidal stability. The prepared materials show promising applicability for water purification, including the removal of organic pollutants and radionuclides (e.g., ¹³⁷Cs and ⁹⁰Sr), as well as metal cations (K⁺, Na⁺, and Li⁺). Full article