Publications by authors named "Fei-Yan Yi"

It is especially essential to develop high-performance and low-cost nonprecious metal catalysts for large-scale hydrogen production. A large number of electrochemical catalysts composited by transition metal centers has been reported; however, it is still a great challenge to design and manipulate target electrocatalysts to realize high overall water-splitting activity at the atomic level. Herein, we develop totally new P-(Fe,V)-codoped metastable-phase β-NiMoO.

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Two-dimensional (2D) metal-organic framework (MOF) nanosheets with large surface area, ultrathin thickness, and highly accessible active sites have attracted great research attention. Developing efficient approaches to realize the controllable synthesis of well-defined 2D MOFs with a specific composition and morphology is critical. However, it is still a significant challenge to construct thin and uniform 2D MOF nanosheets and resolve the reagglomeration as well as poor stability of target 2D MOF products.

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Developing inexpensive electrocatalysts with high activity and stability is of great value for overall water splitting. In this work, we designed a series of 3d-4f (FeMnCe)-trimetallic MOF-74 with different ratios of 3d- and 4f-metal centers. Among them, FeMnCe-MOF-74/NF exhibited the best electrocatalytic performance for the oxygen evolution reaction (OER) and hydrogen evolution reaction (HER) in an alkaline solution.

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Prussian blue analogues (PBAs) are a family of classic coordination polymers. They have been widely applied in various fields including electrochemical sensors. Cubic nanoparticle structure is their common morphology.

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In this work, a highly efficient multifunctional non-enzymatic electrochemical sensor is successfully fabricated based on a facile two-step synthetic strategy. It resolves two important challenges of poor stability and low reproducibility compared to conventional electrochemical enzyme-based sensors. Herein, a metal-organic framework (UiO-66) is selected as a sacrificial template to construct the corresponding Prussian blue analogue (PBA) target to improve its stability and conductivity, namely, PBA/UiO-66/NF.

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Exploring non-precious metal-based electrocatalysts is still challenging in 21 century. In this work, a series of hexagonal bipyramidal Ce-based PBA materials as precursors with different Fe/Co metal ratios, namely as CeFe Co -PBA, are successfully constructed via co-precipitation method and converted into corresponding metal oxides (denoted as Fe Co CeO ) via thermal treatment. Then, they as electrocatalysts realize highly efficient oxygen evolution reaction (OER).

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Article Synopsis
  • - This study reveals a new application of the pore-space-partition (PSP) strategy in electrochemistry, leading to the development of highly efficient and stable metal-organic framework (MOF) electrocatalysts for water splitting.
  • - The vanadium-based trimetallic building cluster (MV) is integrated into these MOFs, resulting in impressive electrocatalytic activity for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), with notably low overpotentials.
  • - The FeV-MOF demonstrates superior performance compared to commercial counterparts, achieving a current density of 10 mA/cm² at a potential of just 1.6 V, while maintaining structural integrity in alkaline conditions, highlighting the
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Metal-organic frameworks (MOFs) as classic crystalline porous materials have attracted great interest in the catalytic field. However, how to realize molecular regulation of the MOF structure to achieve a remarkable oxygen evolution reaction (OER) electrocatalyst is still a challenge. Herein, we designed several series of special MOF materials to explore the relationship between the structure and properties as well as the related reactive mechanism.

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In this work, an indium-based metal-organic framework was successfully constructed, namely, as In-MOF, by elaborately selecting an In center with unique properties and a functional tetracarboxylic acid with unsaturated and open-coordinated nodes. Interestingly, the In center was connected to a single-metal-node-based porous three-dimensional pts net. Its structure was dentified by single-crystal and powder X-ray diffraction, Fourier transform infrared, thermogravimetric analysis, etc.

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Prussian blue (PB) and its analogue (PBA) are a kind of representative cyanide-based coordination polymer. They have received enormous research interest and have shown promising applications in the electrochemical sensing field due to their excellent electrochemical activity and unique structural characteristics including open framework structure, high specific surface area, and adjustable metal active sites. In this review, we summarize the latest research progress of PB/PBA as an electrochemical sensor in detail from three aspects: fabrication strategy, synthesis method and electrochemical sensor application.

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The fabrication of two-dimensional (2D) metal-organic frameworks (MOFs) and Prussian blue analogues (PBAs) combines the advantages of 2D materials, MOFs and PBAs, resolving the poor electronic conductivity and slow diffusion of MOF materials for electrochemical applications. In this work, 2D leaflike zeolitic imidazolate frameworks (Co-ZIF and Fe-ZIF) as sacrificial templates are in situ converted into PBAs, realizing the successful fabrication of PBA/ZIF nanocomposites on nickel foam (NF), namely, CoCo-PBA/Co-ZIF/NF, FeFe-PBA/Fe-ZIF/NF, CoFe-PBA/Co-ZIF/NF, and Fe/CoCo-PBA/Co-ZIF/NF. Such fabrication can effectively reduce transfer resistance and greatly enhance electron- and mass-transfer efficiency due to the electrochemically active PBA particles and NF substrate.

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Article Synopsis
  • Researchers developed efficient and sustainable electrocatalysts for the hydrogen evolution and oxygen evolution reactions using metal-organic frameworks (MOFs).
  • The FeM-MOF system, where iron is replaced by other metals, significantly improves performance, with the FeCo-MOF showing a low overpotential of 339 mV for OER and the FeZn-MOF achieving 221 mV for HER.
  • This work presents a simple method for creating multifunctional catalysts that excel in energy conversion with long-term stability and enhanced performance mechanisms.
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Article Synopsis
  • The study focuses on creating a new nanocomposite electrode material, combining Prussian blue analogue (PBA) with Ni-Co layered double hydroxides (NiCo-LDH), aimed at enhancing supercapacitor performance.
  • Researchers utilized a simple hydrothermal method to synthesize 3D NiCo-LDH nanosheets on nickel foam and subsequently converted them into the PBA@NiCo-LDH/NF nanocomposite through a thermal ion-exchange process.
  • The resulting electrode showed outstanding electrochemical performance, boasting an area specific capacitance of 2004.26 mF cm at 1 mA cm, significantly surpassing the individual components' performance, highlighting the effectiveness and importance of composite electrode development.
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While many metal oxalate salts are known, few are known to form zeolite-type topologies. The construction of zeolite types, especially those with low framework density such as RHO, from linear ligands is generally perceived as less likely, because the 180° metal-ligand-metal geometry deviates too much from the established strategy of using ligands with bent coordination geometry (centered around 145°) to mimic the geometry in natural zeolites. We show the general feasibility of using linear ligands for the synthesis of zeolite types by reporting a family of indium oxalate salts with multiple zeolite topologies, including RHO, GIS, and ABW.

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High-quality graphene@prussian blue (G@PB) nanocomposite sheets have been successfully fabricated via a one-step in situ hydrothermal method, in which uniform PB nanoparticles completely covered both sides of graphene sheets through control of the etching of the raw material and growth of the target products. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM) and thermogravimetric analysis (TGA) demonstrated effective combination. A series of G@PB nanocomposite sheets with different graphene contents as well as other PB/carbonaceous composites and mixed G@PB materials provided adequate proof for the synergetic effect of graphene and Prussian blue in G@PB nanocomposite sheets as well as the important effect of each composite on the electrochemical performance; graphene not only prevented the agglomeration of PB nanoparticles but also provided conductive network for fast electron transport, which was verified by the IR voltage drop and EIS test.

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A non-luminescent 3d-4f heterobimetallic CuEu organic framework (NBU-8) was designedly synthesized with Cu2+ ions as a fluorescence quencher. NBU-8 as a sensor realized selective light recovery with a "turn-on" luminescence response toward N,N'-dimethylformamide (DMF) even in the presence of other amide molecules.

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A novel hierarchical nanoarray material based on a two-dimensional metal-organic framework (Ni-CAT) and a layered double hydroxide (NiCo-LDH) was fabricated on a nickel foam substrate. By taking advantage of the regular nanostructure and making full use of the high porosity and excellent conductivity, the hybrid material exhibits a high areal capacitance for a supercapacitor (3200 mF cm at 1 mA cm).

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KCe[FeII(CN)6]·4H2O (CePBA), a Prussian blue analogue, was successfully synthesized with various morphologies and different sizes. CePBA, when used as a heterogeneous catalyst, can rapidly and completely degrade a large number of methylene blue molecules in 30 seconds: 14.5 mg of MB (for each 5 mg of catalyst).

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A highly luminescent porous metal-organic framework Cd(L)(4-PTZ)(DMF), labeled as NBU-9, has been designedly synthesized based on Cd(NO)·4HO and mixed ligands of 4-(1 H-tetrazol-5-yl)pyridine (4-HPTZ) with N-coordinated sites and thiophene-2,5-dicarboxylic acid (HL) with heteroatomic (S) ring and carboxylate groups in N, N-dimethylformamide (DMF) at 100 °C for 3 days. The interesting result is that this compound NBU-9 can be also obtained via the mixed raw materials of Cd(NO)·4HO, 4-cyanopyridine, NaN, and HL under solvothermal condition at a higher temperature of 140 °C for 3 days, involving in situ ligand synthesis of 4-HPTZ. Its structure was indentified by single-crystal X-ray study, powder X-ray diffraction, element analysis, and TGA results.

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Electrode materials for supercapacitors with one-dimensional porous nanostructures, such as nanowires and nanotubes, are very attractive for high-efficiency storage of electrochemical energy. Herein, ultralong Cu-based porous coordination polymer nanowires (copper-l-aspartic acid) were used as the electrode material for supercapacitors, for the first time. The as-prepared material exhibits a high specific capacitance of 367 F g at 0.

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To explore catalysts combining highly accessible specific surface areas with low recombination of the photo-induced electron-hole pairs, a novel SiO@PDA@BiOBr composite photocatalyst with a hierarchical core-shell structure was prepared by a facile solvothermal method. The catalyst shows a superior performance on photodegradation of Rhodamine B under visible light irradiation, especially for SiO@PDA-2@BiOBr with the reactant kinetics constant (k = 0.0487 min).

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A hierarchical NiO/NiMn-LDH nanosheet array on Ni foam was prepared via a facile two-step approach and exhibited a high specific capacitance (937 F g at 0.5 A g) and good cycling stability (91% retention after 1000 cycles at 5 A g). The improved electrochemical performance is benefited from the synergistic properties of hierarchical NiO/LDH nanosheet composites on a conductive substrate.

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Metal-organic frameworks (MOFs) are considered as suitable materials for various applications in the area of photocatalysis. On the other hand, 2D BiOBr materials are efficient for the photodegradation of organic dyes under visible light illumination. In this work, BiOBr/NH-MIL-125(Ti) composite photocatalysts with different NH-MIL-125(Ti) content were prepared by incorporating NH-MIL-125(Ti) with BiOBr using a co-precipitation method.

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Metal-organic frameworks (MOFs) as chemical sensors have developed rapidly in recent years. There have been many papers concerning this field and interest is still growing. The reason is that the specific merits of MOFs can be utilized to enhance sensitivity and selectivity by various energy/charge transfers occurring among different ligands, ligand, and metal centers, such as from ligands to metal centers or metal centers to ligands, as well as from MOF skeletons to guest species.

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A hexagonal nanosheet LDH@ZIF-8 composite was fabricated by in situ growth of ZIF-8 on Zn-Al LDH without adding any zinc precursor, and exhibited a CO2 adsorption capacity of 1.0 mmol g(-1) at room temperature and 1 bar, which was significantly higher than that of pure Zn-Al LDH or ZIF-8, indicating a synergy between ZIF-8 and Zn-Al LDH.

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