Simon Cassidy

Abstract:

We use in situ synchrotron X-ray diffraction measurements to monitor the solvothermal crystallization mechanism of the aperiodic metal–organic framework TRUMOF-1. Following an initial incubation period, TRUMOF-1 forms as a metastable intermediate that subsequently transforms into an ordered product with triclinic crystal symmetry. We determine the structure of this ordered phase, which we call msw-TRUMOF-1, and show that it is related to TRUMOF-1 through topotactic reorganization of linker occupancies. Our results imply that the connectivity of TRUMOF-1 can be reorganized, as required for data storage and manipulation applications.

Abstract:

We report the magnetic behavior of the hybrid perovskites [Gua]Mn1–xFe2x/3□x/3(HCOO)3 (0 ≤ x ≤ 0.88), showing that vacancy ordering drives bulk ferrimagnetism for x > 0.6. The behavior is rationalized in terms of a simple microscopic model of percolation-induced ferrimagnetism. Monte Carlo simulations driven by this model reproduce the experimental dependence of magnetic susceptibility on x and show that, at intermediate compositions, domains of short-range vacancy order lead to the emergence of local magnetization. Our results open up a new avenue for the design of multiferroic hybrid perovskites.

Abstract:

We study the phenomenology of cooperative off-centering of K+ ions in potassiated Prussian blue analogues (PBAs). The principal distortion mechanism by which this off-centering occurs is termed a “K-ion slide”, and its origin is shown to lie in the interaction between local electrostatic dipoles that couple through a combination of electrostatics and elastic strain. Using synchrotron powder X-ray diffraction measurements, we determine the crystal structures of a range of low-vacancy K2M[Fe(CN)6] PBAs (M = Ni, Co, Fe, Mn, Cd) and establish an empirical link between composition, temperature, and slide-distortion magnitude. Our results reflect the common underlying physics responsible for K-ion slides and their evolution with temperature and composition. Monte Carlo simulations driven by a simple model of dipolar interactions and strain coupling reproduce the general features of the experimental phase behavior. We discuss the implications of our study for optimizing the performance of PBA K-ion battery cathode materials and also its relevance to distortions in other, conceptually related, hybrid perovskites.

Abstract:

We revisit the problem of polytypism in layered MX₂ materials, with a view to reinterpreting the phase space accessible to this family. Our starting point is to develop a simple, constructive, and compact label for the most commonly observed stacking arrangements, similar to the Glazer notation used to label tilt systems in perovskites. The key advantage of this label in the context of MX₂ systems is that it contains sufficient information to generate the corresponding stacking sequences uniquely. Using a related approach, we generate a Cartesian representation of the phase space containing all possible MX₂ polytypes, with the most common structures appearing as limiting cases. We argue that variation in, e.g., composition, temperature, or pressure may allow navigation of this phase space along continuous paths. This interpretation is shown to be consistent with the structural evolution of stacking-faulted MX₂ systems as a function in temperature and pressure. In this way, our study highlights the potential for controlling composition/structure/property relationships among layered MX₂ materials in ways that might not previously have been obvious.