Powder samples of Ag3LiIr2O6 and Ag3LiRu2O6 were synthesized from α-Li2IrO3 and Li2RuO3 respectively by ion exchange in an AgNO3 melt. The crystal structures of the title compounds were solved from high resolution laboratory X-ray powder diffraction (XRPD) patterns and from pair distribution function (PDF) analysis using synchrotron X-ray powder diffraction data. In both crystal structures edge sharing LiO6/3- and (Ir/Ru)O6/3-octahedra form honeycomb like layers that are stacked in a staggered fashion. Silver cations, situated in-between the layers mediate the interlayer interactions by linear O-Ag-O bonds. Anisotropic peak broadening in the XRPD patterns and diffuse scattering occurring as streaks in the precession electron diffraction (PED) patterns indicate the presence of stacking faults, which could be also visualized by high resolution transmission electron microscopy (HRTEM). Possible alternative stacking sequences were derived from the ideal crystal and incorporated into a microstructure model. By applying a supercell approach that randomly generates and averages stacking sequences based on transition probabilities and combining it with a grid search algorithm, the microstructures, i.e. the degrees of faulting in the structures of the title compounds were refined to the measured XRPD data. In result the crystal structures of Ag3LiIr2O6 and Ag3LiRu2O6 were found to be vastly faulted with almost no coherence of the stacked layers.

Download full-text PDF

Source
http://dx.doi.org/10.1039/c9dt01789eDOI Listing

Publication Analysis

Top Keywords

crystal structures
12
stacking faults
8
ag3liir2o6 ag3liru2o6
8
structures title
8
title compounds
8
high resolution
8
x-ray powder
8
powder diffraction
8
xrpd patterns
8
stacking sequences
8

Similar Publications

A new Donor-Acceptor type pyrazinacene derivative (1) featuring strong ICT was synthesized by linking electron-donating triphenylamine (TPA) and electron-accepting CN groups via a pyrazinacene core. The compound exhibits a dramatic color change from greenish blue to red-violet upon selective recognition of naphthalene (3) to form a 1:1 co-crystal (1•3). This color change is induced by intermolecular CT between pyrazinacene and naphthalene's aromatic moieties, driven by π-hole···π interactions.

View Article and Find Full Text PDF

Enterovirus-D68 (EV68) continues to present as a global health issue causing respiratory illness and outbreaks associated with long-lasting neurological disease, with no antivirals or specific treatment options. The development of antiviral therapeutics, such as small-molecule inhibitors that target conserved proteins like the enteroviral 3C protease, remains to be achieved. While various 3C inhibitors have been investigated, their design does not consider the potential emergence of drug resistance mutations.

View Article and Find Full Text PDF

: The co-formulation of active pharmaceutical ingredients (APIs) is a growing strategy in biopharmaceutical development, particularly when it comes to improving solubility and bioavailability. This study explores a co-precipitation method to prepare co-formulated crystals of griseofulvin (GF) and dexamethasone (DXM), utilizing nanostructured, functionalized polylactic glycolic acid (PLGA) as a solubility enhancer. : An antisolvent precipitation technique was employed to incorporate PLGA at a 3% concentration into the co-formulated GF and DXM, referred to as DXM-GF-PLGA.

View Article and Find Full Text PDF

In organic solar cells, the aggregation and crystallization of polymers are significant for bulk heterojunction. Blending with acceptor materials, polymer donor materials can adjust their aggregation by the movement of the chain segments. In this paper, the unfused structures based on thiophene and carbazole are respectively designed and introduced into the donor-acceptor copolymer donor materials to investigate the influence of flexible and rigid structures on polymer-aggregation leading photoelectric performance.

View Article and Find Full Text PDF

Adsorption and Bulk Assembly of Quaternized Hydroxyethylcellulose-Anionic Surfactant Complexes on Negatively Charged Substrates.

Polymers (Basel)

January 2025

Departamento de Química Física, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Ciudad Universitaria, Plaza de la Ciencias s/n, 28040 Madrid, Spain.

This study examines the adsorption and bulk assembly behaviour of quaternized hydroxyethylcellulose ethoxylate (QHECE)-sodium dodecyl sulphate (SDS) complexes on negatively charged substrates. Due to its quaternized structure, QHECE, which is used in several industries, including cosmetics, exhibits enhanced electrostatic interactions. The phase behaviour and adsorption mechanisms of QHECE-SDS complexes are investigated using model substrates that mimic the wettability and surface charge of damaged hair fibres.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!