Publications by authors named "Junkuo Gao"

The development of materials with superior thermal insulation and flame retardancy is critical for industrial applications and daily life. Metal-organic framework (MOF)@poly(vinyl alcohol) (PVA) (MOF@PVA) aerogel composites have demonstrated remarkable thermal insulation and flame retardancy properties. In this work, MIL-53(Al) was directly mixed with PVA and formed by freeze-drying, and the influence of the pore structure on the thermal insulation and flame retardancy properties of the materials was investigated.

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The development of heterogeneous catalysts with abundant active sites is pivotal for enhancing the efficiency of photothermal CO conversion. Herein, we report the construction of CoN@ZIF-67 through the in situ pyrolysis of ZIF-67 under low-temperature pyrolysis conditions. During the pyrolysis process, the crystal structure of ZIF-67 is predominantly preserved concurrently with the formation of CoN nanoparticles (NPs) within the ZIF-67 pores.

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D-UiO-66-NIM with high proton conductivity has been synthesized through the dual strategy of defect engineering and ligand modification. Moreover, D-UiO-66-NIM exhibits good temperature cycling stability and durability in proton conductivity. This work has developed a new method to obtain efficient MOF-based proton conductors.

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Article Synopsis
  • The development of effective electrocatalysts for the oxygen evolution reaction (OER) is crucial for making hydrogen production via electrolysis cost-efficient, but existing catalysts struggle with performance and stability.
  • This study introduces a new method that uses a small amount of phosphorus to enhance the activity of NiFe nanochain arrays, enabling them to perform efficient water splitting even at high current densities for extended periods.
  • The modified electrodes achieve significantly low overpotentials, indicating they surpass existing benchmarks, marking a major step toward industrial applications of large-scale hydrogen production through electrolysis.
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Developing cost-efficient trifunctional catalysts capable of facilitating hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and oxygen reduction reaction (ORR) activity is essential for the progression of energy devices. Engineering these catalysts to optimize their active sites and integrate them into a cohesive system presents a significant challenge. This study introduces a nanoflower (NFs)-like carbon-encapsulated FeNiPt nanoalloy catalyst (FeNiPt@C NFs), synthesized by substituting Co ions with high-spin Fe ions in Hofmann-type metal-organic framework, followed by carbonization and pickling processes.

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A novel strategy was proposed to improve the performance of gas separation in nano-materials, by fabricating a core-shell structure out of the basic ionic liquid ([Emim][IDA]) and zeolitic imidazolate framework (ZIF-8). The [Emim][IDA]/ZIF-8 exhibits a remarkable CO adsorption capacity of 14 cm g at 298 K and 20 kPa, the ideal selectivity of CO/N is as high as 10 and CO/CH is 348 at 298 K and 100 kPa, which are much higher than the CO adsorption capacity (4.3 cm g) and the selectivity ( = 7.

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The processability and sustainability of proton conductors are two important indicators of their application. Here, MIL-91(Al) with an intrinsic proton conduction framework originating from protonated phosphonate groups was cross-linked with poly(vinyl alcohol) (PVA) to obtain MIL-91(Al) aerogel through freeze-drying. This simple and inexpensive strategy not only facilitated the processing of MIL-91(Al) powder but also resulted in a molded MIL-91(Al) aerogel having a high proton conductivity of 1.

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The development of high-efficiency heterojunction photocatalysts has been recognized as an effective approach to facilitate photocatalytic CO reduction. In this research, we successfully synthesized a novel multiflower-like ReS/NiAl-LDH heterojunction through a hydrothermal method. Remarkably, when exposed to visible-light irradiation, 2-ReS/NiAl-LDH demonstrated an exceptional CO production rate of 272.

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The global pursuit of sustainable energy is focused on producing hydrogen through electrocatalysis driven by renewable energy. Recently, High entropy alloys (HEAs) have taken the spotlight in electrolysis due to their intriguing cocktail effect, broad design space, customizable electronic structure, and entropy stabilization effect. The tunability and complexity of HEAs allow a diverse range of active sites, optimizing adsorption strength and activity for electrochemical water splitting.

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The cycloaddition of CO with epoxides driven by light irradiation is an intriguing approach to preparing cyclic carbonates. However, it remains a great challenge to achieve high photocatalytic efficiency in the absence of a cocatalyst. Herein, we explored a metal-organic-framework (MOF)-templated pyrolysis strategy to prepare uniform bromine ions/nitrogen-codoped carbon materials (Br-CN) as low-cost photocatalysts for CO cycloaddition.

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Rational design and fabrication of metal-organic framework-derived metal oxide (MO) materials featuring a hollow structure and active support can significantly enhance their catalytic activity for specific reactions. Herein, a series of CoO nanoparticles (NPs) immobilized in boron nitride (denoted as CoO@BN) with highly open and precisely controllable structures were constructed by an in situ self-assembly method combined with a controlled annealing process. The obtained CoO@BN not only possesses a hollow structure but also shows highly dispersed CoO NPs and high loadings of up to 34.

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The engineering of amorphous metal-organic frameworks (MOFs) offers potential opportunities for the construction of electrocatalysts for efficient oxygen evolution reaction (OER). Herein, highly efficient OER performance and durability in alkaline electrolyte are discovered for MOF-derived amorphous and porous electrocatalysts, which are synthesized in a brief procedure and can be facilely produced in scalable quantities. The structural inheritance of MOF amorphous catalysts is significant for the retention of catalytic sites and the diffusion of electrolytes, and the presence of Fe sites can change the electronic structure and effectively control the adsorption behavior of important intermediates, accelerating reaction kinetics.

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Microflora within cancer cells plays a pivotal role in promoting metastasis of cancer. However, contemporary anticancer research often overlooks the potential benefits of combining anticancer and antibacterial agents. Consequently, a metal-organic framework Cu-Cip with cuproptosis and antibacterial properties was synthesized for cancer therapy.

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Materials with enzyme-like activity have received a lot of attention in the field of tumor catalytic therapy. Here, biocompatible core-shell MOF CSMnP with two valence states of Mn ion, which could process chemodynamic therapy (CDT), was designed and synthesized. Besides, it could also promote a series of catalytic processes in the tumor microenvironment (TME).

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A novel metal-organic framework (MOF) Zn-PBC (HPBC = pyridine-3,5-bis(phenyl-4-carboxylic acid)) was designed and synthesized a solvothermal reaction with the HPBC ligand, and produced a strong fluorescence. The material exhibited good stability and an ideal luminescent property in water. In addition, it was found that Zn-PBC displayed a different fluorescent response to different types of amino acids, and the mechanism was investigated.

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The development of efficient and low-cost catalysts for cathodic oxygen reduction reaction (ORR) in Zn-air battery (ZAB) is a key factor in reducing costs and achieving industrialization. Here, a novel segregated CoNiPt alloy embedded in N-doped porous carbon with a nanoflowers (NFs)-like hierarchy structure is synthesized through pyrolyzing Hofmann-type metal-organic frameworks (MOFs). The unique hierarchical NFs structure exposes more active sites and facilitates the transportation of reaction intermediates, thus accelerating the reaction kinetics.

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Developing hydrogen-bonded organic frameworks (HOFs) that combine functional sites, size control, and storage capability for targeting gas molecule capture is a novel and challenging venture. However, there is a lack of effective strategies to tune the hydrogen-bonded network to achieve high-performance HOFs. Here, a series of HOFs termed as HOF-ZSTU-M (M=1, 2, and 3) with different pore structures are obtained by introducing structure-directing agents (SDAs) into the hydrogen-bonding network of tetrakis (4-carboxyphenyl) porphyrin (TCPP).

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As a rich green energy source, natural gas is widely used in many fields such as the chemical industry, automobile energy, and daily life. However, it is very challenging to separate and recover CH and CH from natural gas. Metal-organic frameworks (MOFs) as an emerging type of multi-pore porous materials show huge potential in gas adsorption separation.

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Hydrogen-bonded organic frameworks (HOFs), as an emerging porous material, have attracted increasing research interest in fluorescence sensing due to their inherent fluorescence emission units with unique physicochemical properties. Herein, based on the organic building block 3,3',5,5'-tetrakis-(4-carboxyphenyl)-1,1'-biphenyl (HTCBP), the porous material HOF-TCBP was successfully synthesized using hydrogen bond self-assembly in a DMF solution. The fluorescence properties of the HOF-TCBP solution showed that when the concentration was high, excimers were easily formed, the PL emission was red-shifted, and the fluorescence intensity became weaker.

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Bi O Se is the most promising 2D material due to its semiconducting feature and high mobility, making it propitious channel material for high-performance electronics that demands highly crystalline Bi O Se at low-growth temperature. Here, a low-temperature salt-assisted chemical vapor deposition approach for growing single-domain Bi O Se on a millimeter scale with thicknesses of multilayer to monolayer is presented. Because of the advantage of thickness-dependent growth, systematical scrutiny of layer-dependent Raman spectroscopy of Bi O Se from monolayer to bulk is investigated, revealing a redshift of the A mode at 162.

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Oxygen evolution reaction (OER) represents a highly important electrochemical transformation in energy storage and conversion technologies. Considering the low rate of this four-electron half-reaction, there is a demand for efficient, stable, and noble-metal-free electrocatalysts to improve the kinetic and economical parameters. In this work, a new pillared-MOF@NiV-LDH nanocomposite based on a Co metal-organic framework (pillared-MOF) and heterometallic Ni/V-layered double hydroxide (NiV-LDH) was assembled via a simple protocol, characterized, and explored as an electrocatalyst in OER.

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For the advancement of laser technologies and optical engineering, various types of new inorganic and organic materials are emerging. Metal-organic frameworks (MOFs) reveal a promising use in nonlinear optics, given the presence of organic linkers, metal cluster nodes, and possible delocalization of π-electron systems. These properties can be further enhanced by the inclusion of solely inorganic materials such as polyoxometalates as prospective low-cost electron-acceptor species.

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The removal of impurity gases (N , CO ) in natural gas is critical to the efficient use of natural gas. In this work, the selective adsorption for N and CO over CH on MIL-100 (M) (M= Cr, Cr, Fe, In, Sc, V) is studied by density functional theory (DFT) calculations. The calculated adsorption energy of the large-size cluster model (LC) of MIL-100 (M) shows that the MIL-100 ( Cr) is the best at the refinement of natural gas due to the lower adsorption energy of CH (-2.

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Metal-organic frameworks (MOFs) and their derived powder catalysts are prone to agglomerate and difficult to recycle in water, thus resulting in their low utilization and secondary pollution in water treatment. Herein, a composite aerogel (CoFe0.8@NCNT@CA) loaded with bimetallic MOF-derived carbon nanotubes on cellulose aerogel was developed for activating peroxymonosulfate (PMS) to degrade tetracycline (TC).

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Photocatalytic hydrogen production using stable metal-organic frameworks (MOFs), especially the titanium-based MOFs (Ti-MOFs) as photocatalysts is one of the most promising solutions to solve the energy crisis. However, due to the high reactivity and harsh synthetic conditions, only a limited number of Ti-MOFs have been reported so far. Herein, we synthesized a new amino-functionalized Ti-MOFs, named NH-ZSTU-2 (ZSTU stands for Zhejiang Sci-Tech University), for photocatalytic hydrogen production under visible light irradiation.

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