Currently, however, there are relatively few such atomically layered solids. [ 2–5 ] Here, we report on 2D nanosheets, composed of a few Ti 3 C 2 layers and conical scrolls, produced by the room temperature exfoliation of Ti 3 AlC 2 in hydrofl uoric acid. The large elastic moduli predicted by ab initio simulation, and the possibility of varying their surface chemistries (herein they are terminated by hydroxyl and/or fl uorine groups) render these nanosheets attractive as polymer composite fi llers. Theory also predicts that their bandgap can be tuned by varying their surface terminations. The good conductivity and ductility of the treated powders suggest uses in Li-ion batteries, pseudocapacitors, and other electronic applications. Since Ti 3 AlC 2 is a member of a 60 + group of layered ternary carbides and nitrides known as the MAX phases, this discovery opens a door to the synthesis of a large number of other 2D crystals. Arguably the most studied freestanding 2D material is graphene, which was produced by mechanical exfoliation into single-layers in 2004. [ 1 ] Some other layered materials, such as hexagonal BN, [ 2 ] transition metal oxides, and hydroxides, [ 4 ] as well as clays, [ 3 ] have also been exfoliated into 2D sheets. Interestingly, exfoliated MoS 2 single layers were reported as early as in 1986. [ 5 ] Graphene is fi nding its way to applications ranging from supercapacitor electrodes [ 6 ] to reinforcement in composites. [ 7 ] Although graphene has attracted more attention than all other 2D materials combined, its simple chemistry and the weak van der Waals bonding between layers in multilayer structures limit its use. Complex, layered structures that contain more than one element may offer new properties because they

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Two‐Dimensional Nanocrystals Produced by Exfoliation of Ti 3 AlC 2

Electrocatalysis will play a key role in future energy conversion and storage technologies, such as water electrolysers, fuel cells and metal-air batteries. Molecular interactions between chemical reactants and the catalytic surface control the activity and efficiency, and hence need to be optimized; however, generalized experimental strategies to do so are scarce. Here we show how lattice strain can be used experimentally to tune the catalytic activity of dealloyed bimetallic nanoparticles for the oxygen-reduction reaction, a key barrier to the application of fuel cells and metal-air batteries. We demonstrate the core-shell structure of the catalyst and clarify the mechanistic origin of its activity. The platinum-rich shell exhibits compressive strain, which results in a shift of the electronic band structure of platinum and weakening chemisorption of oxygenated species. We combine synthesis, measurements and an understanding of strain from theory to generate a reactivity-strain relationship that provides guidelines for tuning electrocatalytic activity.

https://www.unicat.tu-berlin.de/fileadmin/user_upload/MAIN-bilder/UniCat/2_Research/24_Research_Highlights/NCHEM.623s.pdf

Lattice-strain control of the activity in dealloyed core–shell fuel cell catalysts

Acknowledgments Preface Introduction 1. Methods of investigation 2. Thermodynamic fundamentals 3. Mechanisms of oxidation 4. Oxidation of pure metals 5. Oxidation of alloys 6. Oxidation by oxidants other than oxygen 7. Reactions of metals in mixed environments 8. Hot corrosion 9. Erosion-corrosion of metals in oxidizing atmospheres 10. Protective coatings 11. Atmosphere control for the protection of metals during production processes Appendix A. Solution to Fick's second law for a semi-infinite solid Appendix B. Rigorous derivation of the kinetics of internal oxidation Appendix C. Effects of impurities on oxide defect structure Index.

Introduction to the high-temperature oxidation of metals

Materials whose dielectric constant varies spatially with submicrometer periodicity exhibit diffractive optical properties which are potentially valuable in a number of existing and emerging applications. Here, such systems are fabricated by exploiting the spontaneous crystallization of monodisperse silica spheres into close-packed arrays. By reliance on a vertical deposition technique to pack the spherical colloids into close-packed silica−air arrays, high quality samples can be prepared with thicknesses up to 50 μm. These samples are planar and thus suitable for optical characterization. Scanning electron microscopy (SEM) of these materials illustrates the close-packed ordering of the spherical colloids in planes parallel to the substrate; cross-sectional SEM micrographs of the arrays as well as optical methods are used to measure sample thickness and uniformity. Normal-incidence transmission spectra in the visible and near-infrared regions show distinct peaks due to diffraction from the colloidal layer...

Single-Crystal Colloidal Multilayers of Controlled Thickness

Paul Scherrer and Peter Debye developed powder X-ray diffraction together, but it was Scherrer who figured out how to determine the size of crystallites from the broadening of diffraction peaks.

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Bernard Dennis Cullity

Papers

Elements of X-ray diffraction