In this work, we have developed a mild route to fabricate typically mesoporous Mo2C-C hybrid nanospheres based on a solvothermal synthesis and reduction-carbonization process. This work opens a low-temperature route to synthesize valuable carbides. The resultant Mo2C-C hybrid, for the first time, is used as an anode material in lithium ion batteries (LIBs). Compared with bulk Mo2C, the Mo2C-C hybrid exhibits much better electrochemical performance. Remarkably, the hybrid electrode can deliver a specific capacity of over 670 mA h g(-1) after 50 cycles at 100 mA g(-1), which is much higher than that of the bulk material (113 mA h g(-1)). Even cycled at a high current density of 1000 mA g(-1), high capacities of around 400-470 mA h g(-1) can still be retained for the Mo2C-C hybrid. It might benefit from the synergistic effect of the nanohybridization, effectively relieving the volume change during the repeated lithium insertion-extraction reactions and maintaining the integrity of the electrical connections. It is expected that the present synthesis strategy for the Mo2C-C hybrid can be extended to other nanostructured carbides with good energy storage performance.

Hierarchically nanostructured porous hollow microspheres of hydroxyapatite (HAP) are a promising biomaterial, owing to their excellent biocompatibility and porous hollow structure. Traditionally, synthetic hydroxyapatite is prepared by using an inorganic phosphorus source. Herein, we report a new strategy for the rapid, sustainable synthesis of HAP hierarchically nanostructured porous hollow microspheres by using creatine phosphate disodium salt as an organic phosphorus source in aqueous solution through a microwave-assisted hydrothermal method. The as-obtained products are characterized by powder X-ray diffraction (XRD), Fourier-transform IR (FTIR) spectroscopy, SEM, TEM, Brunauer-Emmett-Teller (BET) nitrogen sorptometry, dynamic light scattering (DLS), and thermogravimetric analysis (TGA). SEM and TEM micrographs show that HAP hierarchically nanostructured porous hollow microspheres consist of HAP nanosheets or nanorods as the building blocks and DLS measurements show that the diameters of HAP hollow microspheres are within the range 0.8-1.5 μm. The specific surface area and average pore size of the HAP porous hollow microspheres are 87.3 m(2) g(-1) and 20.6 nm, respectively. The important role of creatine phosphate disodium salt and the influence of the experimental conditions on the products were systematically investigated. This method is facile, rapid, surfactant-free and environmentally friendly. The as-prepared HAP porous hollow microspheres show a relatively high drug-loading capacity and protein-adsorption ability, as well as sustained drug and protein release, by using ibuprofen as a model drug and hemoglobin (Hb) as a model protein, respectively. These experiments indicate that the as-prepared HAP porous hollow microspheres are promising for applications in biomedical fields, such as drug delivery and protein adsorption.

Nowadays, oily wastewater and spilled oil have caused great threats on both ecosystem and human life. To address these severe problems, considerable efforts have been possessed on developing novel oil/water separation materials. The porous oil‐absorbent materials, especially the porous polydimethylsiloxane (PDMS) with excellent properties of easy fabrication and inherent hydrophobicity, have attracted tremendous attentions from worldwide. The conventional methods using salt or sugar as sacrificial template and water as solvent have been widely adopted to fabricate the porous PDMS sponge. Due to the inherent hydrophobicity of PDMS, the solvent of water hardly penetrates into the inside of PDMS, which results in the difficult and incomplete remove of the hard template. In this contribution, the 3D interconnected porous PDMS sponge is facilely prepared by utilizing a modified technique with the citric acid monohydrate as hard template and ethanol as solvent. The proposed approach is capable of removing the hard template efficiently and thoroughly, which demonstrates promising utilizations in practical applications.

In this paper, a facile and template-free one-step strategy has been developed to synthesize interconnected core-shell MoO 2 hierarchical microcapsules via a solvothermal route. The assynthesized MoO 2 microcapsules exhibit a core-shell hierarchical architecture, which integrates four beneficial features: carbon-free, hollow cavity, porous shell, and interconnected wall. Due to their unique nanostructure, when evaluated for lithium-storage properties, they exhibit a high specific capacity of 749.3 mA h g À1 in the first discharge at a rate of 1 C and high reversible capacity of 623.8 mA h g À1 after 50 cycles. Meanwhile, higher rate (2 C and 5 C) measurements show that the carbon-free, core-shell MoO 2 microcapsules exhibit much better rate capacity even compared to MoO 2 -C nanocomposites tested under the same conditions. This superior electrochemical performance of the assynthesized microcapsules could be ascribed to, on the one hand, their inherently metallic electrical resistivity, and on the other hand, their special structure, which not only provides short Li ion pathways and high electronic and ionic conductivity, and but also be able to accommodate large volume variation.