Publications by authors named "Qingze Jiao"

Manganese-based oxides are be regarded as one of the most promising cathode materials for aqueous zinc ion batteries (AZIBs). A major restriction of manganese-based oxides in practical applications is their unsatisfied structural stability due to the irreversible manganese dissolution. Additionally, the poor electrical conductivity also limits the rate capability.

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The exploiting electrocatalysts for water/seawater electrolysis with remarkable activity and outstanding durability at industrial grade current density remains a huge challenge. Herein, CoMoN and Fe-doped CoMoN nanosheet arrays are in-situ grown on Ni foam, which possess plentiful holes, multilevel heterostructure, and lavish CoN/MoN@NF and Fe-CoN/MoN@NF interfaces. They require low overpotentials of 213 and 296 mV for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) under alkaline media to achieve current density of 800 mA cm, respectively, and both possess low Tafel slopes (51.

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The construction of yolk-shell composites with dielectric/magnetic multiple loss mechanisms has become a promising strategy to obtain high-efficiency microwave absorbing materials. An ideal microwave absorber should possess dielectric and magnetic loss abilities, thereby leading to the attenuation and absorption of incident electromagnetic radiation. Herein, the yolk-shell structured CoFeO@carbon (YS-CoFeO@C) and CoFe/FeO@carbon (YS-CoFe/FeO@C) composites were designed and synthesized through a series of processes, which include in-situ coating, heat-treating, etching and subsequent carbonization reduction reaction.

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As an efficient non-precious metal catalyst for the oxygen evolution reaction (OER), phosphides suffer from poor electrical conductivity, so it is still a challenge to reasonably design their structures to further improve their conductivity and OER performances. Here, we present a novel NiP/N-doped carbon@CoFeP/N-doped carbon composite (NiP/NC@CoFeP/NC) as electrocatalysts for OER. This elaborate structure consists of NiP/NC derived from Ni-MOF and CoFeP/NC derived from CoFe-Prussian blue analog MOF (Co-Fe PBA).

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It is highly challenging to design low-cost, efficient electrocatalysts for both oxygen evolution reaction (OER) and hydrogen evolution reaction (HER). Herein, a hierarchical heterostructure was constructed on three-dimensional (3D) Ni foam, which contains NiS nanorods decorated with both CoS and amorphous MoS nanosheets and NiS nanowires decorated with amorphous MoS nanosheets, namely, MoS@CoS@NiS/NF. The synergistic effects from the strong interactions of the heterointerface and unique hierarchical heterostructure endow the MoS@CoS@NiS/NF with abundant active sites and effective mass and electron transport pathways, resulting in excellent activity toward both HER and OER in 1 M KOH.

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Metal-organic-frameworks (MOFs) derived carbon or nitrogen-doped carbon (NC) materials are usually used as electromagnetic wave (EMW) absorbers. However, the effective control of the composition and structure of composites is still a major challenge for the development of high-performance EMW absorbing materials. In this work, core-shell structure and bimetallic composition Cu/nitrogen doped carbon @Co/ nitrogen doped carbon (Cu/NC@Co/NC) composites were designed and synthesized through the thermal decomposition of Cu-MOF@Co-MOF precursor.

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The growth of wafer-scale single-crystal two-dimensional transition metal dichalcogenides (TMDs) on insulating substrates is critically important for a variety of high-end applications. Although the epitaxial growth of wafer-scale graphene and hexagonal boron nitride on metal surfaces has been reported, these techniques are not applicable for growing TMDs on insulating substrates because of substantial differences in growth kinetics. Thus, despite great efforts, the direct growth of wafer-scale single-crystal TMDs on insulating substrates is yet to be realized.

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A novel pomegranate-like Ni-NSs@MSNSs nanocatalyst was successfully synthesized via a modified Stöber method, and its application in the hydrogenation of dicyclopentadiene (DCPD) was firstly reported. The Ni-NSs@MSNSs possessed a high specific area (658 m/g) and mesoporous structure (1.7-3.

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Fluorinated polyurethane (FPU) with a different fluorine content was prepared using perfluoropolyether glycols, poly(propylene glycol), and isophorone diisocyanate as starting materials, and 1,4-butanediol as a chain extender. The structure and molecular weight of FPU were characterized by Fourier transform infrared spectroscopy and gel permeation chromatography. A solution of FPU in xylene and cresol was then coated on copper wires using an enameled machine to prepare enameled wires.

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Surface-active heteropolyacid-based ionic liquids with varying alkyl carbon chains were synthesized, which were subsequently analyzed. The desulfurization of fuels was investigated utilizing various surface-active heteropolyacid-based ionic liquids, and acetonitrile was used as the extractant for the coupling of ODS and EDS. The influences of the alkyl group, surface activity, and hydrophobicity of ionic liquids on sulfur removal were studied.

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Transition-metal compounds/carbon hybrids with high electrocatalytic capability possess attractive potential as a counter electrode (CE) for dye-sensitized solar cells (DSSCs). However, the simple structure and agglomeration always result in poor performance. Herein, cobalt selenides confined in hollow N-doped porous carbon interconnected by carbon nanotubes (CNTs) with cobalt selenides encapsulated inside (denoted as CoSe@NPC/CoSe@CNTs) are formed through pyrolysis and selenization process.

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A novel ionic liquid immobilized on a magnetic polymer microsphere catalyst is reported in this paper. The obtained core-shell-shell catalyst consisted of magnetic nanoparticles (MNPs) as the core, catalytic inert St-co-DVB as the intermediate protective layer, and cross-linked polyaryl imidazole ionic liquids as the active catalytic layer located at the outermost [Im[OH]/MNPs@P(St-DVB)@P(VBC-DVB)]. This catalyst exhibited a high ion-exchange rate (64.

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Developing lightweight and broadband microwave absorbers for dealing with serious electromagnetic radiation pollution is a great challenge. Here, a novel Fe-Co/N-doped carbon/reduced graphene oxide (Fe-Co/NC/rGO) composite with hierarchically porous structure was designed and synthetized by in situ growth of Fe-doped Co-based metal organic frameworks (Co-MOF) on the sheets of porous cocoon-like rGO followed by calcination. The Fe-Co/NC composites are homogeneously distributed on the sheets of porous rGO.

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The design and development of low-cost, highly efficient, and stable electrocatalysts to take the place of noble-metal catalysts for the oxygen evolution reaction (OER) remain a significant challenge. Herein, the synthesis of yolk-shell-structured binary transition metal phosphide Co Fe P with different Co/Fe ratios by phosphidation of a cobalt ferrite precursor is reported. The as-synthesized Co Fe P catalysts were used for the OER.

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Quantitatively mapping and monitoring the strain distribution in 2D materials is essential for their physical understanding and function engineering. Optical characterization methods are always appealing due to unique noninvasion and high-throughput advantages. However, all currently available optical spectroscopic techniques have application limitation, e.

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A novel porous cocoon-like reduced graphene oxide (rGO) with high porosity and low density was fabricated by a simple and green reduction reaction using ascorbic acid as the reductant in combination with a freeze-drying process without annealing. The bulk density of porous cocoon-like rGO is only 28.49 mg/cm, and the porosity reaches 94.

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The oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) are considered to be cornerstones of many energy conversion and storage technologies. It is difficult studying high-performance nonprecious materials as cost-effective bifunctional electrocatalysts for both the OER and ORR in future practical applications. In this study, NiCoS hollow spheres (NiCoS HSs) were fabricated via an effective and facile one-pot "green" approach in an N, N-dimethylformamide-ethylene glycol binary solution.

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In the present work, a cell environment which mimicked the real body environment according to the concentration radio between serum albumin and hemoglobin was built, and the cell morphology, the membrane deformation capacity, and the structure of intracellular hemoglobin of single human living erythrocyte under the effect of pH and serum albumin were studied. It was found that at different suspension pH, the magnitude of variations in cell shape and membrane deformation capacity changes with the structural changes of the intracellular hemoglobin. At pH 4.

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The hollow Co(3)O(4) microspheres were prepared by a gas-liquid diffusion reaction in the presence of ionic liquid [Bmim][BF(4)] in combination with calcination at 300 °C. Their structures and morphologies were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, Raman spectrometry, and X-ray photoelectron spectroscopy. The growth mechanism of hollow Co(3)O(4) microspheres was proposed.

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Pentanitromonoformylhexaazaisowurtzitane (PNMFIW) was synthesized by the nitrolysis of tetraacetyldiformylhexaazaisowurtzitane (TADFIW) in mixed nitric and sulfuric acids and structurally characterized by element analysis, FT-IR, MS and (1)H NMR. Single crystals of PNMFIW were grown from aqueous solution employing the technique of controlled evaporation. PNMFIW belongs to the orthorhombic system having four molecules in the unit cell, with space group P2(1)2(1)2(1) and the lattice parameters a=8.

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