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Dive into the research topics where J. H. van Santen is active.

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Featured researches published by J. H. van Santen.


Physica D: Nonlinear Phenomena | 1950

Ferromagnetic compounds of manganese with perovskite structure

G.H. Jonker; J. H. van Santen

Abstract Various manganites of the general formula La 3+ Mn 3+ O 3 2− -Me 2+ Mn 4+ O 3 2− have been prepared in the form of polycrystalline products. Perovskite structures were found, i.a. for all mixed crystals LaMnO 3 CaMnO 3 , for LaMnO 3 SrMnO 3 containing up to 70% SrMnO 3 , and for LaMnO 3 BaMnO 3 containing less than 50% BaMnO 3 . The mixed crystals with perovskite structure are ferromagnetic. Curves for the Curie temperature versus composition and saturation versus composition are given for LaMnO 3 CaMnO 3 , LaMnO 3 SrMnO 3 , and LaMnO 3 BaMnO 3 . Both types of curves show maxima between 25 and 40% Me 2+ Mn 4+ O 3 2− ; here all 3 d electrons available contribute with their spins to the saturation magnetization. The ferromagnetic properties can be understood as the result of a strong positive Mn 3+ Mn 4+ exchange interaction combined with a weak Mn 3+ Mn 3+ interaction and a negative Mn 4+ Mn 4+ interaction. The Mn 3+ Mn 4+ interaction, presumably of the indirect exchange type, is thought to be the first clear example of positive exchange interaction in oxidic substances.


Physica D: Nonlinear Phenomena | 1953

Magnetic compounds wtth perovskite structure III. ferromagnetic compounds of cobalt

G.H. Jonker; J. H. van Santen

Synopsis Polycrystalline mixed crystals (La, Sr) CoO 3 have been prepared. Perovskite structure is found for all compositions. Ferromagnetism is observed for intermediate Sr concentrations. Curves are given for the saturation magnetizations, the paramagnetic Curie temperatures, and the effective paramagnetic moments as a function of composition. It is suggested that the ferromagnetism observed is caused essentially by a positive Co 3+ — Co 4+ interaction. The sign of the exchange interaction is discussed in connection with the theories of Anderson and Polder, and of Zener.


Physica D: Nonlinear Phenomena | 1948

On a generalization of the Lorentz-Lorenz formula

J. H. van Santen; W Opechowski

Abstract The well-known Lorentz-Lorenz formula holds only for a crystal in which all atoms have environments with cubic symmetry. In this paper a derivation is given of an analogous formula, valid for the more general case that the environments of atoms are not necessarily cubic, the macroscopic symmetry of the crystal being still cubic. The formula is applied to the perovskite lattice.


Physica D: Nonlinear Phenomena | 1950

Electrical conductivity of ferromagnetic compounds of manganese with perovskite structure

J. H. van Santen; G.H. Jonker


Journal of Chemical Physics | 1948

Cation Arrangement in Spinels

E. J. W. Verwey; F.R. de Boer; J. H. van Santen


Journal of Chemical Physics | 1950

The Electrostatic Contribution to the Lattice Energy of Some Ordered Spinels

F.R. de Boer; J. H. van Santen; E. J. W. Verwey


Recueil des Travaux Chimiques des Pays-Bas | 2010

The entropy of liquid mixtures: I. The theory of Raoult's Law

A. J. Staverman; J. H. van Santen


Recueil des Travaux Chimiques des Pays-Bas | 2010

Some remarks on the ionic radii of iron-group elements. The influence of crystalline field

J. H. van Santen; J. S. van Wieringen


Physica D: Nonlinear Phenomena | 1963

Note on the Koch and Wagner effect in lead chloride single crystals

K.J. de Vries; J. H. van Santen


Il Nuovo Cimento | 1958

Dielectric relaxation of lattice defects in crystals

Y. Haven; J. H. van Santen

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F.R. de Boer

University of Amsterdam

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