Analyzing the TiO2surface reactivity based on oxygen vacancies computed by DFT and DFTB methods.

Titanium dioxide is a key material in many fields, including technological, industrial and biomedical applications. Many of these applications are related to the surface reactivity of TiO2and involve its reducibility properties. Recently titania has been banned as a food additive due to its (nano)toxicity, and the release of reactive oxygen species plays a crucial role in many toxicological mechanisms. Determining chemical descriptors that account for the extension of reduction is necessary to understand such processes and necessary for predicting the reactivity of an unknown system. In the present work, we compute a set of chemical descriptors for selected surfaces of anatase and rutile TiO2. The aim is twofold: we want to provide chemically meaningful information on the surface reactivity, and benchmark the descriptors for twoab initioschemes. To do so, we compute the oxygen vacancy formation energy, and the corresponding electronic structure, in four slab models with two different computational schemes (DFT+Uand DFTB). In this way, we characterize the robustness of the dataset, with the purpose of scaling up to more realistic model systems such as nanoparticles or explicit solvent, which are too computationally demanding for state-of-the-art density functional theory approaches.

Complete Dynamic Reconstruction of C60, C70, and (C59N)2 Encapsulation into an Adaptable Supramolecular Nanocapsule.

The dynamic adaptability of tetragonal prismatic nanocapsule 18+ in the selective separation of fullerenes and endohedral metallofullerenes (EMFs) remains unexplored. Therefore, the essential molecular details of the fullerene recognition and binding process into the coordination capsule and the origins of fullerene selectivity remain elusive. In this work, the key steps of fullerene recognition and binding processes have been deciphered by designing a protocol which combines 1H-1H exchange spectroscopy (2D-EXSY) NMR experiments, long time-scale Molecular Dynamics (MD) and accelerated Molecular Dynamics (aMD) simulations, which are combined to completely reconstruct the spontaneous binding and unbinding pathways from nanosecond to second time-range. On one hand, binding (k'on) and unbinding (koff) rate constants were extracted from 1H-1H exchange spectroscopy (EXSY) NMR experiments for both C60 and C70. On the other hand, MD and aMD allowed monitoring the molecular basis of the encapsulation and guest competition processes at a very early stage under nonequilibrium conditions. The receptor capsule displays dynamical adaptability features similar to those observed in the process of biomolecular recognition in proteins. In addition, the encapsulation of bis-aza[60]fullerene (C59N)2 within a supramolecular coordination capsule has been studied for the first time, showcasing the pros and cons of the dumbbell-shaped guest in the dynamics of the encapsulation process and in the stability of the final bound adduct. The powerful combination of NMR, MD, and aMD methodologies allows to obtain a precise picture of the subtle events directing the encapsulation and is thus a predictive tool for understanding host-guest encapsulation and interactions in numerous supramolecular systems.