![]() ![]() in International Tables for Crystallography Volume H: Powder Diffraction Ch. Crystallography Open Database - an open-access collection of crystal structures. This work is the primary reference to the contents and structure of the Powder Diffraction File database, which should be used to cite the database. The Powder Diffraction File: a quality materials characterization database. Structure determination of disordered materials from diffraction data. Ab initio determination of solid-state nanostructure. Structure determination from powder diffraction data. DEBUSSY: a Debye user system for nanocrystalline materials. The crystallography of correlated disorder. Evaluation of the Detectability and Quantification of Respirable Crystalline Silica by X-ray Powder Diffraction Methods (Cambridge Univ. GSAS II: the genesis of a modern open source all purpose crystallography software package. Principles and Applications of Powder Diffraction (Wiley, 2008). This work is an excellent introduction to powder diffraction for the beginner.Ĭlearfield, A., Reibenspies, J. Fundamentals of Powder Diffraction and Structural Characterization of Materials 2nd edn (Springer, 2009). Modern Diffraction Methods (Wiley-VCH, 2013). Introduction to X-Ray Powder Diffractometry (Wiley-Interscience, 1996). X-ray Diffraction by Polycrystalline Materials (ISTE, 2006). Elements of X-ray Diffraction 3rd edn (Prentice Hall, 2001). This work is the classic reference textbook on powder diffraction.Ĭullity, B. X -Ray Diffraction Procedures for Polycrystalline and Amorphous Materials (Wiley-Interscience, 1974). Clays in the Critical Zone (Cambridge Univ. This work is the initial description of what is now known as the Rietveld method.Ĭline, J. Line profiles of neutron powder-diffraction peaks for structure refinement. A photoinduced metal-like phase of monoclinic VO 2 revealed by ultrafast electron diffraction. Origin of additional capacities in metal oxide lithium-ion battery electrodes. Pair distribution function computed tomography. Dynamic X-ay diffraction computed tomography reveals real-time insight into catalyst active phase evolution. Radial distribution function imaging by STEM diffraction: phase mapping and analysis of heterogeneous nanostructured glasses. Four-dimensional scanning transmission electron microscopy (4D-STEM): From scanning nanodiffraction to ptychography and beyond. This work is a guide for beginners in the pair distribution function analysis of imperfect crystals, but also useful for more advanced users and those who apply Powder Diffraction File analysis to liquids and glasses.īragg, W. Underneath the Bragg Peaks: Structural Analysis of Complex Materials 2nd edn (Elsevier, 2012). Diffraction Analysis of the Microstructure of Materials (Springer, 2004).Įgami, T. This recent comprehensive review of powder diffraction theory, practice and applications is the primary reference for both beginners and advanced users. International Tables for Crystallography Volume H: Powder Diffraction (International Union of Crystallography, 2019). Powder Diffraction: Theory and Practice (eds Dinnebier, R. A century of powder diffraction: a brief history. Major applications of qualitative and quantitative phase analysis, structure solution, size/strain/nanostructure analysis using peak profiles, texture analysis and pair distribution function analysis are introduced.Įtter, M. Methods for obtaining suitable powder specimens are summarized. ![]() The major features of contemporary laboratory powder diffractometers are described. For powder diffraction, everything is a sample the technique is commonly applied to characterize minerals, ceramics, metals and alloys, catalysts, polymers, pharmaceuticals, organic compounds, environmental and forensic samples, among others. Abandoning the crystallographic model provides information about local structure, by pair distribution function analysis. ![]() Non-idealities in the intensities give information on texture. The peak profiles contain information about crystallite size, strain and nanostructure. Crystal structures can be solved using powder diffraction data and refined by the Rietveld method. Unit cells can be derived from the peak positions. Quantitative phase analysis can be obtained by detailed analysis of the intensities. The positions and relative intensities of the peaks yield a fingerprint that can be used for qualitative phase analysis. Because the physics behind diffraction is well understood, an exceptionally large amount of information can be obtained from a single measurement. Powder diffraction is a non-destructive technique, which is experimentally simple in principle. ![]()
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