Prussian Blue Analogues Research Articles

Dual-mode colorimetric-fluorometric immunoassay for foodborne parasitic infection

Immunoassays are the primary method used for detection of foodborne parasitic infection. The nanomaterials used in these assays often present challenges such as complex preparation requirements and low stability during long-term storage and transport. Herein, based on cost-effective K3[Fe(CN)6]-mediated in-situ generated CuFe Prussian blue analogues (CuFe-PBA) and quinoxaline derivatives with high fluorescence, a dual-mode immunoassay was proposed for foodborne parasitic infection. This platform is relied on the restoration of K3[Fe(CN)6] by ascorbic acid (AA). In addition to this process, K4[Fe(CN)6]-triggered the generation of CuFe-PBA, and the enhanced fluorogenic reaction of dehydrogenated AA and o-phenylenediamine (OPD) occur sequentially. Without complex probes preparation, the assay enabled the rapid on-site detection of ALP and foodborne parasitic infection through a colorimetric mode accessible via smartphone and offered enhanced sensitivity through a fluorescent mode. The method was used for the detection of ALP, achieving detection limits of 0.38 U/L and 0.03 U/L for colorimetric and fluorescence modes, respectively. Subsequently, the dual-mode immunoassay was applied to Trichinella spiralis infection. The sensitivity and specificity of both the colorimetric and fluorescence modes were 100 % in 950 pig serum samples. This immunosensor provides a universal analysis tool for the accurate, cost-effective and highly sensitive detection of foodborne parasitic infection

Modified multi-metal Prussian blue analogues toward high-performance cathode for sodium-ion battery

Increasing demand for energy storage devices coupled with lithium precursor shortage opens up a new opportunity for sodium-ion batteries (SIBs) to be considered as a replacement of lithium-ion batteries to become a new generation of energy storage device for commercial application. Prussian blue analogue (PBA) demonstrates great advantages as the cathodes for SIB owing to its simple synthesis method, inexpensive raw materials, and high theoretical specific capacity. Single phase multi-metal based PBA of Na1.92(Mn0.3Fe0.23Co0.3Ni0.17)[Fe(CN)6]0.88⋅2.16H2O with low contents of crystal water and [Fe(CN)6]4–defects was obtained by controlling the nucleation reaction rate via using sodium citrate as a chelating agent, and the assistance of N2 as an antioxidant and a protective gas. The obtained PBA with high purity and high crystallinity delivers a specific capacity of 120 mAh g−1, excellent rate capability, and impressive cycling performance with 82 % capacity retention after 1000 cycles.

High-Entropy and Component Stoichiometry Tuning Strategies Boost the Sodium-Ion Storage Performance of Cobalt-Free Prussian Blue Analogues Cathode Materials.

Prussian blue analogs (PBAs) are appealing cathode materials for sodium-ion batteries because of their low material cost, facile synthesis methods, rigid open framework, and high theoretical capacity. However, the poor electrical conductivity, unavoidable presence of [Fe(CN)6] vacancies and crystalline water within the framework, and phase transition during charge-discharge result in inferior electrochemical performance, particularly in terms of rate capability and cycling stability. Here, cobalt-free PBAs are synthesized using a facile and economic co-precipitation method at room temperature, and their sodium-ion storage performance is boosted due to the reduced crystalline water content and improved electrical conductivity via the high-entropy and component stoichiometry tuning strategies, leading to enhanced initial Coulombic efficiency (ICE), specific capacity, cycling stability, and rate capability. The optimized HE-HCF of Fe0.60Mn0.10-hexacyanoferrate (referred to as Fe0.60Mn0.10-HCF), with the chemical formula Na1.156Fe0.599Mn0.095Ni0.092Cu0.109Zn0.105 [Fe(CN)6]0.724·3.11H2O, displays the most appealing electrochemical performance of an ICE of 100%, a specific capacity of around 115 and 90 mAh·g-1 at 0.1 and 1.0 A·g-1, with 66.7% capacity retention observed after 1000 cycles and around 61.4% capacity retention with a 40-fold increase in specific current. We expect that our findings could provide reference strategies for the design of SIB cathode materials with superior electrochemical performance.

Longevous Protic Hybrid Supercapacitors Using Bimetallic Prussian Blue Analogue/rGO-Based Nanocomposite Against MXene Anode.

MXenes exhibit a unique combination of properties-2D structure, high conductivity, exceptional capacity, and chemical resistance-making them promising candidates for hybrid supercapacitors (HSCs). However, the development of MXene-based HSCs is often hindered by the limited availability of cathode materials that deliver comparable electrochemical performance, especially in protic electrolytes. In this study, this challenge is addressed by introducing a durable protic HSC utilizing a bimetallic Prussian Blue Analogue (PBA) decorated on reduced graphene oxide (rGO) as a nanocomposite cathode paired with a single-layered Ti3C2Tx MXene (SL-MXene) anode. The bimetallic PBA, specifically nickel hexacyanocobaltate (NiHCC), is utilized by virtue of its open and stable structure that facilitates efficient charge storage, leading to enhanced stability and energy storage capabilities. The resulting NiHCC/rGO//SL-MXene cell demonstrates impressive performance, achieving a maximum specific energy of 38.03Wh kg-1 and a power density of 20666.67W kg-1. Remarkably, the NiHCC/rGO//SL-MXene HSC cell also exhibits excellent cycling stability without any loss even after 15000 cycles while retaining ≈100% coulombic efficiency. This work underscores the potential of bimetallic PBA materials with conductive rGO backbone for overcoming the limitations of current MXene-based protic HSCs, highlighting the significance of this work.

Determination of deoxynivalenol (DON) by a label-free electrochemical immunosensor based on Ni[sbnd]Fe PBA nanozymes

Deoxynivalenol (DON) contamination in food products significantly threatens human health, necessitating a reliable and sensitive detection method. This study aims to develop a simple, low-cost, and effective electrochemical immunoassay method for detecting DON based on the nickel‑iron bimetallic Prussian blue analog (NiFe PBA). The NiFe PBA nanozymes with high peroxidase-like activity were synthesized using an environmentally friendly chemical precipitation method. In the presence of hydrogen peroxide (H2O2), the current change of thionine oxidation initiated by NiFe PBA nanozymes can be exploited to diagnose DON. Under optimal conditions, the proposed method achieved quantitative detection of DON in the range of 10–107 pg mL−1 with a detection limit of 4.5 pg mL−1 (S/N = 3), demonstrating excellent selectivity, reproducibility, and stability. In addition, the DON immunosensor provides satisfactory results for the detection in real samples, demonstrating the feasibility of the proposed sensor in detecting of DON in such products.

Strong Electron Coupling Effect of Prussian Blue Analogs Derived Ultrathin Nitrogen‐Doped Carbon Wrapped Fe‐CoP for Enhanced Wide Spectrum Photocatalytic H2 Evolution

AbstractWith the advantages of large specific surface area and high porosity of general metal‐organic frame materials, russian blue analogs have broad application prospects in catalysis. In this work, a series of ultra‐thin N‐doped carbon coated Fe‐CoP (Fe‐CoP@NC) are prepared by phosphating Fe‐Co‐Co Prussian blue analogs (Fe‐Co‐Co PBA) in different degrees for the broad‐spectrum photocatalytic hydrogen evolution. The results show that Fe‐CoP@NC‐3 has the highest photocatalytic hydrogen production rate of 16.6 mmol h−1 g−1, which is 83 times greater than that of Fe‐Co‐Co PBA. The excellent stability of Fe‐CoP@NC‐3 is proved by cyclic experiments. The outstanding photocatalytic H2 production activity of Fe‐CoP@NC‐3 can be ascribed to the strong electron coupling effect between Fe‐CoP and N‐doped carbon layer. The photogenerated electrons of Fe‐CoP are transferred to the N‐doped carbon layer, which is electron transport mediator accelerating the electron transfer and synergetic improving the hydrogen evolution efficiency. This work provides an effective strategy for designing an ultra‐thin N‐doped carbon layer coated phosphide photocatalyst with strong electron coupling effect.

In-Situ Construction of Fe-Doped NiOOH on the 3D Ni(OH)2 Hierarchical Nanosheet Array for Efficient Electrocatalytic Oxygen Evolution Reaction.

Accessible and superior electrocatalysts to overcome the sluggish oxygen evolution reaction (OER) are pivotal for sustainable and low-cost hydrogen production through electrocatalytic water splitting. The iron and nickel oxohydroxide complexes are regarded as the most promising OER electrocatalyst attributed to their inexpensive costs, easy preparation, and robust stability. In particular, the Fe-doped NiOOH is widely deemed to be superior constituents for OER in an alkaline environment. However, the facile construction of robust Fe-doped NiOOH electrocatalysts is still a great challenge. Herein, we report the facile construction of Fe-doped NiOOH on Ni(OH)2 hierarchical nanosheet arrays grown on nickel foam (FeNi@NiA) as efficient OER electrocatalysts through a facile in-situ electrochemical activation of FeNi-based Prussian blue analogues (PBA) derived from Ni(OH)2. The resultant FeNi@NiA heterostructure shows high intrinsic activity for OER due to the modulation of the overall electronic energy state and the electrical conductivity. Importantly, the electrochemical measurement revealed that FeNi@NiA exhibits a low overpotential of 240 mV at 10 mA/cm2 with a small Tafel slope of 62 mV dec-1 in 1.0 M KOH, outperforming the commercial RuO2 electrocatalysts for OER.

Hollow Prussian blue analogue–derived (CoFe)Se2 composites: Structural designing for preparing flexible, high-performance solid-state supercapacitors

Selenides show higher corrosion and oxidation resistance than conventional materials. Moreover, bimetallic selenide materials typically show higher electrical conductivity than monometallic materials, which accelerates their electron transfer kinetics during charge–discharge cycling. The combination of two different metals in bimetallic selenides improves the energy-storage capacity and provides a stable electrochemical environment resulting from their unique electronic structure and interaction with the electrolyte. Among various bimetallic selenides, cobalt–iron selenides are especially noted for their excellent electrocatalytic properties. In this study, we synthesised co-doped hollow Prussian blue (PB) analogue nanocubes with large sizes, high specific surface areas and many active sites. When employed as the positive electrode in a flexible solid-state supercapacitor, bimetallic (CoFe)Se2 nanocomposites obtained at 500°C in nitrogen showed high supercapacitor performance, with a capacitance of 1710 F g−1 at 1 A g−1; extended cycle life (maintaining 98.5 % of their initial capacitance after 3000 cycles at 5 A g−1) and near 100 % Coulombic efficiency. Further, a flexible asymmetric supercapacitor ((CoFe)Se2//activated carbon (AC)) was developed using AC and (CoFe)Se2 as the negative and positive electrodes, respectively. (CoFe)Se2//AC achieved a Coulombic efficiency of 90 % and outstanding cycling stability, maintaining 93.5 % of its original capacity after 10,000 cycles at 5 A g−1. The specific capacitance and energy density were 40 F g−1 at 1 A g−1 and 750 W kg−1 (10.41 W kg−1), respectively. This research paves the way for rational and environmentally friendly synthesis of bimetallic selenides with distinct sizes and topologies. By varying the metal dopant, our method can potentially produce bimetallic selenides for diverse applications.

Progressive hollow engineering induced raspberry-like magnetoelectric microspheres via synergistic etching-assembly strategy toward boosted microwave attenuation

Optimizing the electromagnetic (EM) properties of composites through elaborate tailoring of their microstructures has become an attractive research branch, but determining the correlations between morphology, composition, and performance remains challenging. Herein, a novel progressive hollow engineering strategy is proposed for the construction of hollow CuFe Prussian blue analog (CuFePBA, CF) precursors with asymptotic variations of cavities and PBA units based on a synergistic etching-assembly approach, subsequently combined with a polydopamine (PDA) coating and carbothermal process to acquire raspberry-like hollow Cu/Fe/Fe3C@NC (CFC) composites. The proposed approach addresses the drawbacks caused by organic ligand depletion or corrosive agent usage. We then present a systematic investigation of the mechanism by which the progressive hollow engineering-induced concurrent evolution of hollow cavities, phases, defects, and inhomogeneous interfaces contributes to the improvement of the dielectric properties of the CFC samples. An optimal reflection loss (RLmin) of − 65.17 dB at 3.29 mm was realized for the CFC-2 sample and the CFC-3 sample achieved an effective absorption bandwidth (EAB) of 4.4 GHz at an ultra-thin thickness of 1.29 mm. This work reveals the synergistic effects of compositional, interfacial, and defect variations on the EM wave attenuation properties of the composites, and will provide new design inspiration for novel absorbers with modulatable hollow architectures.

Engineering of N doped carbon@FeCo alloy hollow spheres: Remarkable mid-frequency electromagnetic wave absorption performance exhibited by unique porous and wrinkled surface structure

The modulation of the shape and design of microstructures plays a crucial role in enhancing the efficient absorption of electromagnetic waves in absorbers. The electromagnetic parameters and scattering effects of these materials are directly influenced by their morphological characteristics. In this study, polystyrene microspheres were used as templates for a two-step in-situ growth process: Initially, Fe₃O₄ was coated onto the surfaces of these microspheres, followed by the in-situ growth of Fe-Co Prussian blue analogs. The rational design of electrical parameters during the conversion process was calculated and analyzed using Density Functional Theory. The precursor was calcined at various temperatures to generate a unique porous wrinkled surface hollow nanostructure. This nanostructure not only facilitates multiple reflections and scattering of incident electromagnetic waves but also promotes the occurrence of multiple interface polarizations. Doping with nitrogen and oxygen elements introduced abundant dipole polarization, thereby enhancing the electromagnetic wave attenuation capability of the composite material. The Fe3O4@PBA composite material synthesized at 600°C achieved a minimum reflection loss of −57.01 dB and a maximum effective absorption bandwidth of 4.58 GHz (7.52–12.1 GHz) at a thickness of 4 mm, covering nearly the entire X-band. This method provides a means to enhance magnetic loss by temperature adjustment to control the magnetic components in composite materials, providing a systematic approach to designing the microstructure of materials used for absorbing electromagnetic waves.

Fe-doped phosphide nanosheet array derived from prussian blue analogues for high-efficient electrocatalytic water splitting

Doping heterogeneous atoms can modulate electronic structure, which matters for creating efficient bifunctional electrocatalysts in realizing conversion of hydrogen and electricity. This study demonstrates that Fe-doped Ni5P4 nanosheet arrays on nickel foam (Fe–Ni5P4/NF) using Prussian blue analogues as precursors are successfully synthesized by straightforward hydrothermal reactions and phosphating. Fe–Ni5P4/NF exhibits great efficiency in creating hydrogen from water under alkaline conditions. The Fe–Ni5P4/NF dual electrode just need a minimal cell voltage of 1.54 V at 10 mA cm−2 and maintain operational stability for a minimum of 50 h, demonstrating outstanding bifunctional properties. The introduction of Fe modifies the electronic configuration for Ni5P4, substantially boosting the activity of the electrocatalyst. This study offers a framework for designing splendid bifunctional electrocatalysts through synergistic doping strategies in electrochemical applications.

MXene@PBA heterostructures via end-group-directed self-assembly strategy for effective inhibition of shuttle effect in lithium–sulfur batteries

The commercialization of lithium-sulfur batteries (LSBs) has been hindered by the shuttle effect and slow sluggish conversion kinetics. This study developed MXene and Prussian blue analogue (PBA) heterostructures using an end-group-directed self-assembly strategy. MXene@PBA heterostructures were synthesized through layer-by-layer stacking and in situ growth of Mn-PBA, driven by the electrostatic interactions between Mn2+ and the polar terminal groups of MXene. The dual-metal synergistic adsorption of Mn2+ and Fe3+ within PBA framework significantly enhances both the adsorption capacity and cycling stability of the composite. Furthermore, the in-situ growth of PBA not only reinforces the structural integrity but also increases the number of active sites, mitigates the collapse of the accordion-like layered structure, alleviates volume expansion, and accelerates rapid ion diffusion. Theoretical calculations confirm the composite's superior adsorption capacity for Li polysulfides (LiPSs). As a S host, MXene@PBA facilitates the solid-liquid phase transformation of polysulfides, improving reaction kinetics and delivering exceptional electrochemical performance. MXene@PBA composite exhibited an initial discharge capacity of 1220 mAh g−1 at 0.1 C. Its cycle stability is equally remarkable, with a minimal decay rate of 0.062 % per cycle after 500 cycles at 0.5 C. The construction of these layered heterostructures as S hosts presents an effective strategy to mitigate the shuttle effect and enhance the reaction kinetics of LSBs.

Copper and nickel hexacyanoferrates/carbon nanotube nanocomposites thin films as high-performance light cathode materials for aqueous sodium-ion batteries

Aqueous rechargeable Na-ion batteries are gaining popularity as an attractive alternative for energy storage systems due to their low cost, wide range of raw material sources, non-flammability, and ultrahigh ionic conductivity. Currently, Because of their three-dimensional open structure, high specific capacity, and inexpensive cost, Prussian blue analogues are being investigated as electrode materials for electrochemistry. In this work, we present an innovative strategy to create novel two-component nanoarchitected thin films that exhibit exceptional performance as cathodes in aqueous sodium-ion batteries (SIBs). By leveraging the versatility of the liquid-liquid interfacial method, we have prepared two distinct transparent nanocomposite films composed of carbon nanotubes and either copper or nickel hexacyanoferrate nanoparticles. The results show that the NiHCF/CNT and CuHCF/CNT deliver a high specific capacity of 152 mA h g−1 and 135 mA h g−1, respectively, at a high current density of 1 A g−1. Moreover, the cells (rGO//NiHCF and rGO//CuHCF) show that the energy density of the battery can reach up to 7.75 Wh kg−1 at a power density of 27.92 W kg−1 for rGO//NiHCF/CNT, while rGO//CuHCF/CNT showed an energy density of 3.67 Wh kg−1 at a power density of 13.21 W kg−1. The results demonstrate that NiHCF/CNT and CuHCF/CNT nanocomposite films provide new insight into the design of high-performance PBA cathodes.

Ultra-strong adsorption of ammonia nitrogen from low-temperature and complex systems by Prussian blue analogue

The aquatic ecosystem is threatened globally by eutrophication due to ammonia nitrogen inputs from wastewater. Developing high-performance adsorbents with high removal efficiency and selectivity for ammonia nitrogen is pivotal to ecological equilibrium. Here, the removal of ammonia nitrogen by a combined process of Co-based Prussian blue (NaCo-PBA) and coagulants was studied for the first time. The maximum adsorptive capacity of ammonia nitrogen by NaCo-PBA was 52.72 mg/g, and the removal reached 99 %. Compared with traditional adsorbents, NaCo-PBA showed high adsorption amounts (9–42 times). Most importantly, NaCo-PBA exhibited selectivity in complex systems and its adsorption quantity reached 42.6 mg/g in real domestic wastewater, compared to 4.7 mg/g for commercial adsorbent. NaCo-PBA was used in the coagulation and co-adsorption process to facilitate the separation of multiple contaminants in water. It is reasonable to believe that the collaboration between NaCo-PBA with special structure and coagulation will bring a new perspective to nitrogen removal in complex systems.

Preparation of hollow CoFe Prussian blue analogues and their derived CoP-FeP nanoboxes as efficient electrocatalysts as oxygen evolution reactions

Reasonably designing and constructing transition metal based compounds with controllable composition and structure is a promising option for obtaining economically efficient oxygen evolution reaction (OER) electrocatalysts. This paper presents a one-pot self-templated epitaxial growth, phase transition and self-dissolution strategy for constructing hollow nanoboxes/solid nanocubes of CoFe bimetallic Prussian blue analogues (PBAs). The CoFe mixed phosphide with a porous hollow nanoboxes structure obtained after subsequent phosphating heat treatment exhibite enhanced OER electrocatalytic activity in alkaline media, exhibiting a low overpotential of 230 mV and a Tafel slope of 35.5 dec−1 at 10 mA cm−2, as well as excellent stability for 48 h. The excellent OER activity of CoP-FeP nanoboxes (CoP-FeP NBs) can be attributed to the combination effect between their composition and structure. Structurally, the exquisite porous hollow nanoboxes structure greatly expands the surface area, reduces ion diffusion pathways, and reduces charge transfer resistance. Compositionally, the inner transition metal phosphide exhibits good conductivity and undergoes surface reconstruction during OER, forming high valence Co(Fe)OOH active substances in situ. The strong interface coupling effect of CoOOH/FeOOH optimizes the electronic structure. This work presents a facile and efficient strategy for the construction of PBAs hollow structural materials and the exploitation of low-cost and efficient electrocatalysts.

Structure Remodeling Strategy for Open-Cage NiFe@Fe-bis-PBA with Enhanced Peroxidase-like Activity To Monitor Tumor Markers.

The inherent metal elements and structures of Prussian blue analogue (PBA) nanozymes have restricted their enzyme-mimicking activity. Therefore, the rational regulation of PBA nanozymes to improve their catalytic activity is highly desirable for biosensing applications. Herein, we propose a structure remodeling strategy to construct an open-cage Fe PBA-anchored NiFePBA (NiFe@Fe bis-PBA) nanozyme with significantly enhanced enzyme-mimicking activity. The formation process and mechanism for this bis-PBA nanozyme were studied in detail. Specifically, a cubic NiFePBA precursor was first synthesized and modified with polyvinylpyrrolidone (PVP). With the aid of hydrochloric acid, the added potassium ferricyanide was reduced by PVP and re-coordinated on the surface of NiFePBA to form the NiFe@Fe bis-PBA nanozyme with a special open-cage core-shell structure. The resultant NiFe@Fe bis-PBA nanozyme was further exploited to immobilize secondary antibodies, serving as a novel signal probe for developing highly sensitive electrochemical immunosensors for monitoring tumor markers. The constructed electrochemical immunosensor possesses a very wide linear range of 0.005-100 ng/mL and a low detection limit of 0.89 pg/mL for alpha-fetoprotein with high specificity and acceptable reproducibility and stability. This work offers a general and promising strategy for remodeling PBA nanozymes with a very favorable structure and metal element distribution, which enhances their enzyme-mimicking properties for applications in different fields.

Acid-assisted synthesis of core-shell Prussian blue cathode for sodium-ion batteries

In recent years, core–shell structured Prussian Blue Analogues (PBAs) have been considered as highly promising cathode materials for sodium-ion batteries. Reducing production costs and simplifying the preparation method for core–shell PBAs have also become crucial considerations. This paper presents a novel approach for the first time: by acid-treating the as-synthesized solution from a simple coprecipitation reaction, a high-crystallinity, sodium-rich Mn2+-doped iron hexacyanoferrate (Fe/MnHCF) shell material is self-grown on the surface of manganese hexacyanoferrate (MnHCF). This method significantly improves the electrochemical properties of the MnHCF material. The core–shell structured PBA exhibits excellent cycling performance (with a capacity retention of 95.5 % for 400 cycles at 1 A/g) and high rate performance (134.2mAh/g@10 mA/g, 95.2mAh/g@1 A/g). In this article, we explore the growth mechanism of the high-sodium content, high-crystallinity shell structure and introduce a green chelating agent that is better suited for the crystallization of Mn and Fe-type PBA systems. Our study demonstrates that Mn2+ doping enhances the conductivity of the shell material. Meanwhile, the heterojunction structure of MnHCF@Fe/MnHCF conducive to charge separation and migration. This straightforward synthesis strategy offers a novel approach for fabricating high-performance core–shell structured Prussian Blue Analogue materials.

Reasonable design of PBA-derived interfacial modified ternary compounds and hollow structure materials in high-performance asymmetric supercapacitors

Prussian blue analogues (PBA), common metal-organic frameworks (MOFs), are typically binary metal compounds. In this study, chromium was incorporated during the preparation of nickel‑cobalt PBA, resulting in the adjustment of the micro-morphology of PBA and the synthesis of small-sized PBA (sPBA) electrode materials with diameters ranging from 20 to 30 nm. These materials underwent various interfacial modifications to yield ternary metal phosphide (sPBA-P) and hollow nanostructures (sPBA-C). Additionally, by integrating graphene oxide (GO) as the growth substrate, successful preparation of GO@sPBA-P and GO@sPBA-C electrode materials was achieved. Significantly, these materials showcase outstanding electrochemical properties and interesting interfacial reactions when employed as cathode and anode components. Through a comprehensive series of characterization analyses, the electrochemical properties and reaction mechanisms of these materials were thoroughly investigated. Ultimately, an asymmetric supercapacitor (ASC) was assembled using the synthesized GO@sPBA-P and GO@sPBA-C to explore the material's potential in energy materials applications.

Single, binary, and ternary nanocomposite electrodes of reduced graphene oxide@polyaniline@Co-Prussian analog for supercapacitors

The present work includes fabrication of a binary and ternary and composites of reduced graphene oxide (RGO), Polyaniline (Pani), and cobalt Prussian blue analog (Co-PA) for high performance supercapacitor. The materials were characterized using XRD, SEM, FT-IR, and BET techniques. The results confirm the formation of the desired nanocomposites. The electrochemical properties were evaluated in three electrode configuration using CV, CCD and EIS methods. The ternary composite of RGO@Pani@Co-PA showed better electrochemical properties than that obtained from the binary composites as well as their constituent components. The ternary-based sample had a specific capacitance of 490 Fg-1 at a current density of 1 A g-1 and a minimal capacitance loss of 93.9% after 3000 electric cycles. The ternary composites' remarkable electrochemical performance has been attributed to their well-thought-out, distinctive architecture, which offers a substantial surface area and promotes synergistic effects among the other ingredients. The ternary RGO@Pani@Co-PA composite was used as the anode electrode (positive) and activated carbon as the cathode (negative) materials in the assembly of the asymmetric supercapacitor (ASC) device. Over a wide potential window of 2 V, the fabricated ASC had a remarkable specific energy of 58.9 Wh kg-1 at a specific power of 9210 W kg-1 and 88.5% device capacitance stability after 5000 cycles of charge/discharge.

Synthesis of α,ω-Primary Hydroxyl-Terminated Polyether Polyols Using Prussian Blue Analogs as Catalysts

Synthesis of α,ω-Primary Hydroxyl-Terminated Polyether Polyols Using Prussian Blue Analogs as Catalysts