Hollow microporous organic networks (H-MONs) were prepared by a template method using silica spheres. The shell thickness was delicately controlled by changing the synthetic conditions. The H-MONs were used as a template for the synthesis of nanoparticulate Co3O4 hollows which showed excellent catalytic performance in H2O2 oxidation.

The efficient electron injection by direct dye-to-TiO(2) charge transfer and strong adhesion of mussel-inspired synthetic polydopamine (PDA) dyes with TiO(2) electrode is demonstrated. Spontaneous self-polymerization of dopamine using dip-coating (DC) and cyclic voltammetry (CV) in basic buffer solution were applied to TiO(2) layers under a nitrogen atmosphere, which offers a facile and reliable synthetic pathway to make the PDA dyes, PDA-DC and PDA-CV, with conformal surface and perform an efficient dye-to-TiO(2) charge transfer. Both synthetic methods led to excellent photovoltaic results and the PDA-DC dye exhibited larger current density and efficiency values than those in the PDA-CV dye. Under simulated AM 1.5 G solar light (100 mW cm(-2)), a PDA-DC dye exhibited a short circuit current density of 5.50 mW cm(-2), corresponding to an overall power conversion efficiency of 1.2 %, which is almost 10 times that of the dopamine dye-sensitized solar cell. The PDA dyes showed strong adhesion with the nanocrystalline TiO(2) electrodes and the interface engineering of a dye-adsorbed TiO(2) surface through the control of the coating methods, reaction times and solution concentration maximized the overall conversion efficiency, resulting in a remarkably high efficiency.

Developing electrode materials with high-energy densities is important for the development of lithium-ion batteries. Here, we demonstrate a mesoporous molybdenum dioxide material with abnormal lithium-storage sites, which exhibits a discharge capacity of 1,814 mAh g−1 for the first cycle, more than twice its theoretical value, and maintains its initial capacity after 50 cycles. Contrary to previous reports, we find that a mechanism for the high and reversible lithium-storage capacity of the mesoporous molybdenum dioxide electrode is not based on a conversion reaction. Insight into the electrochemical results, obtained by in situ X-ray absorption, scanning transmission electron microscopy analysis combined with electron energy loss spectroscopy and computational modelling indicates that the nanoscale pore engineering of this transition metal oxide enables an unexpected electrochemical mass storage reaction mechanism, and may provide a strategy for the design of cation storage materials for battery systems.

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