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Wyświetlanie 1-2 z 2
Tytuł:
Disentangling chemical pressure and superexchange effects in lanthanide–organic valence tautomerism
Autorzy:
Viborg, Anton
Pryds, Nini
Pedersen, Kasper S.
Wilhelm, Fabrice
Chanda, Amit
Pinkowicz, Dawid
Dunstan, Maja A.
Yutronkie, Nathan J.
Rogalev, Andrei
Trier, Felix
Opis:
Valence tautomerism in molecule-based f-block materials remains virtually elusive. As a result, the effects driving and controlling the valence conversion phenomenon are poorly understood. Herein, we unravel these fundamental factors by systematic chemical modification of a bona fide lanthanide coordination solid, SmI2(pyrazine)2(tetrahydrofuran), in which a complete, temperature-driven conversion between Sm(II) and Sm(III) occurs abruptly around 200 K. Solid solutions incorporating either divalent, diamagnetic metal ions or Sm(III) ions feature disparate behavior. Substitution with redox-inactive, divalent metal ions invariably leads to lower conversion temperatures and reduced cooperativity. In contrast, incorporation of redox-inactive Sm(III) ions leads to trapped pyrazine anion radicals in the ligand scaffold, shifting the valence tautomeric conversion phenomenon towards higher temperature with virtually no loss of cooperativity. These materials are rare examples of lanthanide–organic materials hosting mixed valency in both the lanthanide and organic scaffold, affording switchable conductivity associated with the valence tautomeric conversion.
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł
Tytuł:
Molecular alloying drives valence change in a van der Waals antiferromagnet
Autorzy:
Perlepe, Panagiota
Viborg, Anton
Christensen, Niels B.
Brechin, Euan K.
Pryds, Nini
Wong, Siena
Clérac, Rodolphe
Trier, Felix
Jinschek, Joerg R.
Rogalev, Andrei
Stampe, Kirstine A.
Manvell, Anna S.
Kubus, Mariusz
Pedersen, Kasper S.
Aribot, Frédéric
McPherson, James N.
Baran, Volodymyr
Le, Manh Duc
Chanda, Amit
Deylamani, Sara Talebi
Wan, Wenjie
Voigt, Laura
Coletta, Marco
Walker, Helen C.
Wilhelm, Fabrice
McMonagle, Charles J.
Pinkowicz, Dawid
Probert, Michael R.
Dunstan, Maja A.
Yutronkie, Nathan J.
Senyshyn, Anatoliy
Opis:
Bespoke van der Waals (vdW) crystals provide command over the confinement and transport of charge, spin, and heat within and between two-dimensional (2D) layers. We report a novel functionality in vdW crystals by actuating valence changes through molecular alloying. The net materials $Cr(pyrazine)_{2} Br_{2}$ and $Cr(pyrazine)_{2}I_{2}$ are aliovalent, hosting Cr(III) and Cr(II), respectively, due to disparate crystal field potentials. Pressurizing and thereby strengthening of the crystal field compresses the $Cr(pyrazine)_{2}I_{2}$ layers significantly, but no Cr valence change is induced. However, alloyed $Cr(pyrazine)_{2}I_{2−x}Br_{x}$ phases exhibit hysteretic and tunable Cr(II) ⇄ Cr(III) interconversions with concomitant charge injection into the net. The valence switch manifests drastic changes to the magnetization and the electrical conductivity, which varies by up to five orders of magnitude during the valence conversion. This use of coordination chemistry addresses a gap in vdW and 2D materials science, where electronic structure engineering via valence change events has remained elusive.
Dostawca treści:
Repozytorium Uniwersytetu Jagiellońskiego
Artykuł
    Wyświetlanie 1-2 z 2

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