Schneider et al examine the mechanisms and materials of understanding titanium dioxide (TiO2) photocatalysis. They focus on topics such as time-resolved analysis of the photocatalytic process, the synthesis of TiO2 nanoparticles and nanoparticulate structures, and titanium-based single-site photocatalysts.
The halogen bond occurs when there is evidence of a net attractive interaction between an electrophilic region associated with a halogen atom in a molecular entity and a nucleophilic region in another, or the same, molecular entity. In this fairly extensive review, after a brief history of the interaction, we will provide the reader with a snapshot of where the research on the halogen bond is now, and, perhaps, where it is going. The specific advantages brought up by a design based on the use of the halogen bond will be demonstrated in quite different fields spanning from material sciences to biomolecular recognition and drug design.
The design, nanochemistry and ttheranostics applications of upconversion nanoparticles (UCNPs) were investigated and applied to health care technology. Among the topics addressed were DNA damage, photodynamic therapy for tumor destruction and photoluminescence spectroscopy.
The recent advances in electrocatalysis for oxygen reduction reaction (ORR) for proton exchange membrane fuel cells (PEMFCs) are thoroughly reviewed. This comprehensive Review focuses on the low- and non-platinum electrocatalysts including advanced platinum alloys, core shell structures, palladium-based catalysts, metal oxides and chalcogenides, carbon-based non-noble metal catalysts, and metal-free catalysts. The recent development of ORR electrocatalysts with novel structures and compositions is highlighted. The understandings of the correlation between the activity and the shape, size, composition, and synthesis method are summarized. For the carbon based materials, their performance and stability in fuel cells and comparisons with those of platinum are documented. The research directions as well as perspectives on the further development of more active and less expensive electrocatalysts are provided.
In recent decades, two new branches of coordination chemistry have emerged, metal-organic frameworks (MOF) and supramolecular coordination complexes (SCC). On the most basic level, both SCCs and MOFs share the design of metal nodes linked by organic ligands and such constructs can be broadly defined as metal-organic materials.