Proton Acidity and Proton Mobility in ECR-40, a Silicoaluminophosphate that Violates Löwenstein's Rule

Abstract

The silicoaluminophosphate zeotype ECR-40 contains linkages of AlO4 tetrahedra via a common oxygen atom, thereby violating the famous “Löwenstein's rule”. In this work, a combination of static density functional theory (DFT) calculations and DFT-based ab-initio molecular dynamics (AIMD) simulations were employed to study the acidity and mobility of protons associated with such unusual linkages. It was found that the Al-O-Al linkages are preferentially protonated, as deprotonation causes a local accumulation of negative charge. The protons at these linkages possess a somewhat lower Brønsted acidity than those at Si-O-Al links. AIMD simulations for fully hydrated ECR-40 predicted a partial deprotonation of the Al-O-Al linkages, whereas Si-O-Al linkages were fully deprotonated. Frequently, a coordination of water molecules to framework Al atoms was observed in the vicinity of the Al-O-Al links. Hence, these linkages appear prone to break upon dehydration, potentially explaining why Löwenstein's rule is mostly obeyed in materials formed in aqueous media.