Nanocomposite tectons as unifying systems for nanoparticle assembly.

Nanocomposite tectons (NCTs) are nanocomposite building blocks consisting of nanoparticle cores functionalized with a polymer brush, where each polymer chain terminates in a supramolecular recognition group capable of driving particle assembly. Like other ligand-driven nanoparticle assembly schemes (for example those using DNA-hybridization or solvent evaporation), NCTs are able to make colloidal crystal structures with precise particle organization in three dimensions. However, despite the similarity of NCT assembly to other methods of engineering ordered particle arrays, the crystallographic symmetries of assembled NCTs are significantly different.

Construction of a quantitative relation between structural relaxation and dynamic heterogeneity by vibrational dynamics in glass-forming liquids and polymers.

The structural relaxation slows down drastically upon approaching the glass transition, accompanied by the significant growth of dynamic heterogeneity. The fundamental question of elusiveness and interest is whether there exists an underlying quantitative relationship between structural relaxation and dynamic heterogeneity. Here, we reveal that which is related to the reduced mean square displacements to overcome the energy barriers of activated jumps, instead of the kinetic fragility , is the genuine key parameter connecting dynamic heterogeneity with structural relaxation for varying types of glass formers.