Publications by authors named "Ji-Sen Jiang"

Radioactive cesium pollution have received considerable attention due to the increasing risks in development of the nuclear power plants in the world. Although various functional porous materials are utilized to adsorb Cs+ ions in water, Prussian blue analogues (PBAs) are an impressive class of candidates because of their super affinity of Cs+ ions. The adsorption ability of the PBAs strongly relate to the mesostructure and interstitial sites.

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Mesoporous magnetic Prussian Blue (PB) particles are good condidates for theragnostic nanomedicine. However, there are lack of efficient methods for fabrication of such materials. Here, we reported the synthesis of the mesoporous yolk-shell Fe3O4@PB particles by one-pot coordination replication and etching.

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While bulk-sized metal-organic frameworks (MOFs) face limits to their utilization in various research fields such as energy storage applications, nanoarchitectonics is believed to be a possible solution. It is highly challenging to realize MOF nanobubbles with monocrystalline frameworks. By a spatially controlled etching approach, here, we can achieve the synthesis of zeolitic imidazolate framework (ZIF-8) nanobubbles with a uniform size of less than 100 nm.

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Three-dimensional (3D) networks of graphitic carbon are promising materials for energy storage and conversion devices because of their high electrical conductivity, which is promoted by the good interconnection between the carbon particles. However, it is still difficult to directly synthesize such carbon networks. Herein, we report the novel synthesis of 3D graphitic carbon networks through the pyrolysis of nanosized ZIF-67 crystals.

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Despite a continuously growing interest in the integration of coordination polymer (CP) colloids toward functional materials, collective properties of the CP colloids have rarely been addressed mainly due to the difficulty in assembling pure CP colloids into superstructures with impressive mechanical strength. We demonstrated that CP nanoplates could stack together spontaneously upon drying the slurry of the nanoplates. The stacked CP nanoplates could work like polymeric adhesives.

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Metal cyanide coordination compounds are recognized as promising candidates for broad applications because of their tailorable and adjustable frameworks. Developing the nanostructure of a coordination compound may be an effective way to enhance the performance of that material in application-based roles. A controllable preferential etching method is described for synthesis of monocrystalline Prussian blue analogue (PBA) nanoframes, without the use of organic additives.

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Prussian blue (PB) mesocrystals with Na as the alkaline metal were synthesized and used as cathode materials in Na-ion batteries. The mesocrystalline structure endowed PB with very different phase change behavior and electrochemical performance in contrast to PB single-crystals in cyclic voltammograms and galvanostatic discharge/charge voltage profiles of PB/Na half-cells.

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Three-dimensional hierarchical Prussian blue composed of ultrathin nanosheets was successfully synthesized by employing a self-aggregation and oriented attachment strategy. The unique structure highly increases the exposure of micropores and metal sites of Prussian blue to guests, thus significantly enhancing its hetero-catalysis and adsorption properties compared to cubic and commercial counterparts.

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γ-Fe2O3/C nanocomposite was prepared through a convenient method by which one-pot synthesized Fe3O4/Starch was oxidized and carbonized by calcining at 250 °C. The γ-Fe2O3/C displayed strong magnetism and could adsorb organic molecules from aqueous solution effectively, thus it showed promising application in the dislodgement of organic pollutants in sewage. Adsorption isotherms and kinetics of methylene blue (MB) onto γ-Fe2O3/C were studied in a batch system.

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We have developed one versatile spatially confined self-assembly strategy to integrate cyanometallate-based coordination polymers with functional metal oxides into well-defined core@shell heterostructures. The structure, composition, size and morphology of the heterostructures could be facilely controlled. The obtained Fe3O4@Prussian blue heterostructure was evaluated as an appealing multifunctional thermal ablation agent exhibiting response to both magnetic field and light irradiation.

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Three-dimensional (3D) macroporous CuO structures composed of ultrathin nanosheets were successfully synthesized by employing a liquid-liquid interface as a two-dimensional (2D) nano-reactor. The macroporous structure helped CuO to retain the exposed surface during reactions, thus significantly enhancing the long term cycling performance both in photocatalysis and lithium ion batteries.

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An interface between toluene and water was utilized to synthesize ca. 10 nm thick of anatase TiO2 nanosheets (NSs) with 82% exposure of {001} facets. In this procedure, highly corrosive and toxic HF, which was generally used to prepare TiO2 NSs with largely exposed high energy facets, was avoided.

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Monocrystalline mesoporous BiFeO3 crystals were obtained via a multi-step single-crystal to single-crystal transformation of a coordination polymer, Bi[Fe(CN)6]·4H2O. This unique transformation process significantly decreased the crystallization temperature of perovskite oxide without losing high crystallinity.

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Core-shell structured FeO@C nanoparticles were fabricated by a facile one-pot hydrothermal route. The structure and component of the nanoparticles were fully characterized by transmission electron microscopy, X-ray diffraction, Mössbauer spectroscopy, Raman spectroscopy, thermogravimetric analysis, magnetometry and Brunauer-Emmett-Teller specific surface area measurements. The obtained FeO@C nanoparticles possessed favorable dispersibility, high saturation magnetization (61.

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We utilized a novel strategy, hierarchical structuring, to enhance the catalytic activity of coordination polymers. Hierarchical Prussian white crystals with hollow structures and kinked surfaces were synthesized by using a self-aggregation and etching strategy. The hierarchical structure significantly enhanced the catalytic activity of Prussian white in the degradation of methylene blue in comparison to the non-hierarchical Prussian white crystals.

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Homogeneous and stable magnetic nanofluids containing γ-Fe2O3 nanoparticles were prepared using a two-step method, and their thermal transport properties were investigated. Thermal conductivities of the nanofluids were measured to be higher than that of base fluid, and the enhanced values increase with the volume fraction of the nanoparticles. Viscosity measurements showed that the nanofluids demonstrated Newtonian behavior and the viscosity of the nanofluids depended strongly on the tested temperatures and the nanoparticles loadings.

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A new morphology of Prussian blue microcrystals has been prepared by selective etching. By thermal decomposition, PB has been transformed into mesoporous magnetic iron(III) oxide.

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Much interest has been attracted to the magnetic materials with porous structure because of their unique properties and potential applications. In this report, Fe3O4nanoporous particles assembled from small Fe3O4nanoparticles have been prepared by thermal decomposition of iron acetylacetonate in the presence of polyethylene glycol 4000. The size of the spherical nanoporous particles is 100-200 nm.

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By loading doxorubicin (DOX) on 5-carboxyl-fluorescein (FAM) labeled AGKGTPSLETTP peptide (A54) coupled starch-coated iron oxide nanoparticles (SIONs), we prepared a novel aqueous drug delivery system with both magnetic and biomolecular targeting, which was specific to human hepatocellular carcinoma cell line BEL-7402. The saturated extent of adsorption reached 2.0 mg DOX/mg A54-SIONs at 28 degrees C, which provided a rather high dose of DOX loading for application.

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As a homing peptide, A54 is the most effective peptide specific to the human hepatocellular carcinoma cell. Homing peptide labeled with green fluorescent protein (A54-GFP) was successfully immobilized on the surfaces of magnetic nanoparticles and characterized by Fourier transform infrared spectroscopy as well as fluorescence microscopy. The binding efficiency was analyzed by performing adsorption equilibrium and SDS-PAGE electrophoresis.

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