Applying Mechanochemistry for Bottom‐Up Synthesis and Host–Guest Surface Modification of Semiconducting Nanocrystals: A Case of Water‐Soluble β‐Cyclodextrin‐Coated Zinc Oxide

Mechanochemistry has recently emerged as an environmentally friendly solventless synthesis method enabling a variety of transformations including those impracticable in solution. However, its application in the synthesis of well‐defined nanomaterials remains very limited. Here, we report a new bottom‐up mechanochemical strategy to rapid mild‐conditions synthesis of organic ligand‐coated ZnO nanocrystals (NCs) and their further host–guest modification with β‐cyclodextrin (β‐CD) leading to water‐soluble amide‐β‐CD‐coated ZnO NCs. The transformations can be achieved by either one‐pot sequential or one‐step three‐component process. The developed bottom‐up methodology is based on employing oxo‐zinc benzamidate, [Zn₄(μ₄‐O)(NHOCPh)₆], as a predesigned molecular precursor undergoing mild solid‐state transformation to ZnO NCs in the presence of water in a rapid, clean and sustainable process.     

A Surfactants Walk to Work: Modes of Action of Citrate Controlling (10–10) and (000–1) Zinc Oxide Surface Growth from Solution

Molecular dynamics simulations unravel the association of citrate to (10–10) and (000–1) growth fronts of zinc oxide and demonstrate an unexpected mobility of the surfactant. Citrate association to perfectly planar (10–10) and (000–1) ZnO‐ethanol interfaces was found to be favored over dissociation by 1.5–2 eV hence suggesting strongly bound, immobilized surfactants. However, intramolecular stress prevents binding of all three carboxyl groups to planar surfaces and the typical arrangement is that of two carboxyl‐Zn contacts (including two salt bridges each) whilst the remaining carboxyl group is dangling into the solvent. As a consequence, the surfactant exhibits a “walking” mechanism to move along the surface by exchanging the role of its carboxyl groups. This finding has strong implications for the role of citrate during crystal growth as illustrated by a recently developed simulation scheme based on hundreds of individual Zn²⁺ and OH^– ion association steps. In particular, for the (10–10) surface – which grows via formation of ridges embedded by {10–10} faces – these simulations show how citrate ions move towards steps and bind to the growth front by additional 4 eV per surfactant molecule.