Magnetic pair distribution function analysis: introduction and applications

2014 ◽  
Vol 70 (a1) ◽  
pp. C1459-C1459
Author(s):  
Benjamin Frandsen ◽  
Xiaohao Yang ◽  
Simon Billinge

Short-range magnetic correlations play a crucial role in a variety of condensed matter phenomena, yet they remain notoriously difficult to investigate experimentally. Quantitative analysis of the diffuse scattering of neutrons from local magnetic correlations represents a viable but challenging route toward revealing short-range magnetic order in complex materials. Reverse Monte Carlo techniques that iteratively fit randomly generated structural models in momentum space have been used successfully [1], demonstrating that diffuse magnetic scattering can be rich in information. Recently [2], we developed a real-space approach to investigating local magnetic correlations, which we call magnetic pair distribution function (mPDF) analysis in analogy to the more familiar atomic pair distribution function. This experimentally accessible quantity reveals magnetic correlations directly in real space and places diffuse and Bragg scattering on equal footing, thereby gaining sensitivity to both short- and long-range magnetic order. Here we present the basic theory behind mPDF analysis and provide several examples of its utility using both simulated and experimentally measured data on several interesting magnetic systems, including a canonical antiferromagnetic, a spin glass, and a spin ice. We discuss the potential impact that mPDF methods may have on current and future research interests in magnetism.

2020 ◽  
Author(s):  
Anuradha Pallipurath ◽  
Francesco Civati ◽  
Jonathan Skelton ◽  
Dean Keeble ◽  
Clare Crowley ◽  
...  

X-ray pair distribution function analysis is used with first-principles molecular dynamics simulations to study the co-operative H<sub>2</sub>O binding, structural dynamics and host-guest interactions in the channel hydrate of diflunisal.


2020 ◽  
Vol 2 (6) ◽  
pp. 2234-2254 ◽  
Author(s):  
Troels Lindahl Christiansen ◽  
Susan R. Cooper ◽  
Kirsten M. Ø. Jensen

We review the use of pair distribution function analysis for characterization of atomic structure in nanomaterials.


2016 ◽  
Vol 116 (19) ◽  
Author(s):  
Benjamin A. Frandsen ◽  
Michela Brunelli ◽  
Katharine Page ◽  
Yasutomo J. Uemura ◽  
Julie B. Staunton ◽  
...  

2021 ◽  
Author(s):  
Theodosios Famprikis ◽  
Houssny Bouyanfif ◽  
Pieremanuele Canepa ◽  
James Dawson ◽  
Mohamed Zbiri ◽  
...  

Solid electrolytes are crucial for next generation solid state batteries and Na<sub>3</sub>PS<sub>4</sub> is one of the most promising Na<sup>+</sup> conductors for such applications. In this contribution, we present a detailed investigation of the evolution in structure and dynamics of Na<sub>3</sub>PS<sub>4</sub> under the effect of temperature in the range 30 < T < 600 °C through combined experimental-computational analysis. Although x ray Bragg diffraction experiments indicate a second order phase transition from the tetragonal ground state (α, P-42<sub>1</sub>c) to the cubic polymorph (β, I-43m), pair distribution function analysis in real space and Raman spectroscopy indicate remnants of tetragonal character in the range 250 < T < 500 °C which we attribute to dynamic local tetragonal distortions. The first order phase transition to the mesophasic high temperature polymorph (γ, Fddd) is associated with a sharp volume increase and the onset of liquid like diffusive dynamics for sodium-cations (translative) and thiophosphate-polyanions (rotational) evident by inelastic neutron- and Raman- spectroscopies, as well as pair-distribution function and molecular dynamics. These results shed light on the rich polymorphism in Na<sub>3</sub>PS<sub>4</sub> and are relevant for a host of high performance materials deriving from the Na<sub>3</sub>PS<sub>4</sub> structural archetype.<br>


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