| Literature DB >> 30018065 |
Hua He1, Chuck-Hou Yee2, Daniel E McNally3, Jack W Simonson4, Shelby Zellman1, Mason Klemm1, Plamen Kamenov3, Gayle Geschwind3, Ashley Zebro3, Sanjit Ghose5, Jianming Bai5, Eric Dooryhee5, Gabriel Kotliar2, Meigan C Aronson6.
Abstract
The lack of a mechanistic framework for chemical reactions forming inorganic extended solids presents a challenge to accelerated materials discovery. We demonstrate here a combined computational and experimental methodology to tackle this problem, in which in situ X-ray diffraction measurements monitor solid-state reactions and deduce reaction pathways, while theoretical computations rationalize reaction energetics. The method has been applied to the La2CuO4-x S x (0 ≤ x ≤ 4) quaternary system, following an earlier prediction that enhanced superconductivity could be found in these new lanthanum copper(II) oxysulfide compounds. In situ diffraction measurements show that reactants containing Cu(II) and S(2-) ions undergo redox reactions, leaving their ions in oxidation states that are incompatible with forming the desired new compounds. Computations of the reaction energies confirm that the observed synthetic pathways are indeed favored over those that would hypothetically form the suggested compounds. The consistency between computation and experiment in the La2CuO4-x S x system suggests a role for predictive theory: to identify and to explicate new synthetic routes for forming predicted compounds.Entities:
Keywords: Materials by Design; electronic structure calculations; in situ X-ray studies
Year: 2018 PMID: 30018065 PMCID: PMC6077747 DOI: 10.1073/pnas.1800284115
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205