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Properties of Transition Metals02:58

Properties of Transition Metals

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Transition metals are defined as those elements that have partially filled d orbitals. As shown in Figure 1, the d-block elements in groups 3–12 are transition elements. The f-block elements, also called inner transition metals (the lanthanides and actinides), also meet this criterion because the d orbital is partially occupied before the f orbitals.
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The periodic table arranges atoms based on increasing atomic number so that elements with the same chemical properties recur periodically. When their electron configurations are added to the table, a periodic recurrence of similar electron configurations in the outer shells of these elements is observed. Because they are in the outer shells of an atom, valence electrons play the most important role in chemical reactions. The outer electrons have the highest energy of the electrons in an atom...
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Coordination compounds and complexes exhibit different colors, geometries, and magnetic behavior, depending on the metal atom/ion and ligands from which they are composed. In an attempt to explain the bonding and structure of coordination complexes, Linus Pauling proposed the valence bond theory, or VBT, using the concepts of hybridization and the overlapping of the atomic orbitals. According to VBT, the central metal atom or ion (Lewis acid) hybridizes to provide empty orbitals of suitable...
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In Ultraviolet–Visible (UV–Vis) spectroscopy, the absorption of electromagnetic radiation is used to probe the electronic structure of molecules. This technique provides insights into molecular electronic transitions, particularly the movement of electrons between different molecular orbitals. Radiation is absorbed if the energy of the electromagnetic radiation passing through the molecule is precisely equal to the energy difference between the excited and ground states. During this...
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In Situ Transmission Electron Microscopy with Biasing and Fabrication of Asymmetric Crossbars Based on Mixed-Phased a-VOx
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Origin of Transitions Inversion in Rare-Earth Vanadates.

Xue-Jing Zhang1, Erik Koch2, Eva Pavarini1

  • 1Forschungszentrum Jülich, Peter Grünberg Institute, 52425 Jülich, Germany.

Physical Review Letters
|July 31, 2025
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Summary
This summary is machine-generated.

In rare earth vanadates (RVO3), lattice effects weaken, allowing spin interactions to dominate, causing magnetic ordering to precede orbital ordering (TN > TOO). This contrasts with most transition-metal oxides.

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Area of Science:

  • Condensed Matter Physics
  • Materials Science
  • Solid-State Chemistry

Background:

  • In most transition-metal oxides, orbital ordering (OO) typically precedes magnetic ordering (MO), with transition temperatures satisfying T_{N} < T_{OO}.
  • The rare earth vanadate (RVO3) series presents an anomaly, exhibiting an inversion where magnetic ordering precedes orbital ordering (T_{N} > T_{OO}) as the rare earth ionic radius (R_{I}) increases.
  • The underlying physical mechanism driving this inversion in vanadates has remained unexplained.

Purpose of the Study:

  • To elucidate the fundamental reason behind the inverted ordering temperatures (T_{N} > T_{OO}) observed in the RVO3 series.
  • To identify the specific interplay of interactions that leads to this rare phenomenon.
  • To establish criteria for discovering similar inverted ordering phenomena in other material systems.

Main Methods:

  • Analysis based on the decomposition of the order parameter into irreducible tensors.
  • Investigating the competition between lattice effects and spin-spin interactions.
  • Examining the influence of rare earth ionic radius (R_{I}) on the relative strengths of these interactions.

Main Results:

  • In RVO3, increasing R_{I} weakens lattice effects, diminishing their influence on orbital physics.
  • Concurrently, orbital-independent dipolar spin-spin interactions become dominant for antiferromagnetic spin order.
  • This balance leads to the observed inversion, where magnetic ordering precedes orbital ordering (T_{N} > T_{OO}).

Conclusions:

  • The T_{N} > T_{OO} inversion in RVO3 is driven by the ineffectiveness of lattice effects and the dominance of spin-spin interactions as R_{I} increases.
  • This mechanism explains the rarity of this phenomenon and provides guidelines for identifying it in other materials.
  • These vanadate systems serve as ideal platforms for studying unconventional orbital phases due to the unique balance of interactions.