In situ X-ray diffraction monitoring of a mechanochemical reaction reveals a unique topology metal-organic framework.

Chemical and physical transformations by milling are attracting enormous interest for their ability to access new materials and clean reactivity, and are central to a number of core industries, from mineral processing to pharmaceutical manufacturing. While continuous mechanical stress during milling is thought to create an environment supporting nonconventional reactivity and exotic intermediates, such speculations have remained without proof. Here we use in situ, real-time powder X-ray diffraction monitoring to discover and capture a metastable, novel-topology intermediate of a mechanochemical transformation.

Design of multicomponent photocatalysts for hydrogen production under visible light using water-soluble titanate nanodisks.

We report the design of efficient multicomponent photocatalysts (MPs) for H2 production under visible light by using water-soluble ultrathin titanate nanodisks (TNDs) stabilized by tetraethylammonium cations (TEA(+)) as building blocks. The photocatalysts are designed in such a way to significantly enhance simultaneously the efficiency of the three main steps in the photocatalytic process i.e.

Visible light induced hydrogen generation using a hollow photocatalyst with two cocatalysts separated on two surface sides.

A hollow Fe2O3-TiO2-PtOx photocatalyst for visible light H2 generation was prepared from nanosized MIL-88B consisting of coordinatively unsaturated metal centers as a hard template. This photocatalyst is composed of hybrid metal oxide-TiO2 with controllable wall thickness and two different cocatalysts that are separately located on two surface sides.

Synthesis and engineering porosity of a mixed metal Fe2Ni MIL-88B metal-organic framework.

A new rational approach has been developed for the synthesis of a mixed metal MIL-88B metal-organic framework based on a neutral mixed metal cluster, such as Fe(2)Ni(μ(3)-O). Unlike the conventional negative charged single metal cluster, the use of the neutral mixed metal cluster as nodes in the framework avoids the need of a compensating anion inside the porous MIL-88B system; thus the mixed metal MIL-88B becomes porous. The flexibility of the mixed metal MIL-88B can be controlled by terminal ligands with different steric hindrance.

Novel route to size-controlled Fe-MIL-88B-NH2 metal-organic framework nanocrystals.

A new approach for the synthesis of uniform metal-organic framework (MOF) nanocrystals with controlled sizes and aspect ratios has been developed using simultaneously the non-ionic triblock co-polymer F127 and acetic acid as stabilizing and deprotonating agents, respectively. The alkylene oxide segments of the triblock co-polymer can coordinate with metal ions and stabilize MOF nuclei in the early stage of the formation of MOF nanocrystals. Acetic acid can control the deprotonation of carboxylic linkers during the synthesis and, thus, enables the control of the rate of nucleation, leading to the tailoring of the size and aspect ratio (length/width) of nanocrystals.