Ralph Kronig

Ralph Kronig (10 March 1904 – 16 November 1995) was a German physicist. He is noted for the discovery of particle spin and for his theory of X-ray absorption spectroscopy. His theories include the Kronig–Penney model, the Coster–Kronig transition and the Kramers–Kronig relations.

Ralph Kronig
Ralph de Laer Kronig (1904–1995)
Born10 March 1904 (1904-03-10)
Died16 November 1995 (1995-11-17) (aged 91)
NationalityGerman
CitizenshipUnited States
Germany
Alma materColumbia University
Known forDiscovery of particle spin
Kronig–Penney model
Coster–Kronig transition
Kramers–Kronig relations
AwardsMax Planck Medal (1962)
Scientific career
InstitutionsColumbia University
TU Delft
Doctoral advisorAlbert Potter Wills
Other academic advisorsWolfgang Pauli

Background

Ralph Kronig (later Ralph de Laer Kronig) was born on 10 March 1904 to German[1] parents (Harold Theodor Kronig, Augusta de Laer) in Dresden, Germany. He died in Zeist on 16 November 1995 at the age of 91. Kronig received his primary and high-school education in Dresden and went to New York City to study at Columbia University where he received his PhD in 1925 and subsequently became instructor (1925) and assistant professor (1927).

Early in Kronig's career he had encountered Paul Ehrenfest who, while visiting America in 1924, had advised the young physicist Ralph Kronig to revisit Europe. Kronig left for that continent later in 1924 and paid visits to the important centers for theoretical-physics research in Germany and Copenhagen. It was a time of great expansion in the development of quantum mechanics, and that development was taking place in Europe. Kronig was privileged to be a young, brilliant physicist in that glory-day of 20th century theoretical physics, which made it possible for him to live and work among the great physicists of that era (Bohr, Ehrenfest, Heisenberg, Pauli, Kramers).

In January 1925, when Kronig was a still a Columbia University PhD student, he first proposed electron spin after hearing Pauli in Tübingen. Werner Heisenberg and Wolfgang Pauli immediately hated the idea. They had just ruled out all imaginable actions from quantum mechanics. Now Kronig was proposing to set the electron rotating in space. Pauli especially ridiculed the idea of spin, saying that "it is indeed very clever but of course has nothing to do with reality". Faced with such criticism, Kronig decided not to publish his theory and the idea of electron spin had to wait for others to take the credit.[2] Ralph Kronig had come up with the idea of electron spin several months before Uhlenbeck and Goudsmit. Most textbooks credit these two Dutch physicists with the discovery. Ralph Kronig did not hold a grudge against Pauli for this turn of events. In fact, Kronig and Pauli remained friends for many years into the future. They exchanged many ideas in physics through letters. But it remains an historic fact that Kronig had told Pauli about electron spin before Pauli had published his paper showing that two electrons can inhabit the same orbital (W. Pauli, "On the Connexion between the Completion of Electron Groups in an Atom with the Complex Structure of Spectra", Z. Physik 31, 765ff, 1925). Months later when Uhlenbeck and Goudsmit came up with particle spin, it seemed to verify Pauli's paper. Together with Rabi, Kronig gave the first solution (1927) of the Schrödinger equation for the rigid symmetric top.

Werner Heisenberg in developing Quantum Mechanics involved Kronig in his seminal ideas of the theory. In the beginning of May 1925, Heisenberg wrote three times to Ralph Kronig, with whom he had cooperated a little earlier in Copenhagen on the spectral theory of multi-electron atoms. In the second letter, dated 5 May, Heisenberg wrote down in some detailed equations expressing the transition to his matrix mechanics.

In 1927, Kronig returned to Europe for good and worked in different prominent centres of research: Copenhagen, London, Zürich (where for a year he was Pauli's assistant). Around 1930 he settled in the Netherlands: first in Utrecht, then in Groningen, first as Dirk Coster's assistant, and from 1931 as an associate professor, and since 1939 as a full professor at the Delft University of Technology where he stayed until his retirement in 1969. Between 1959 and 1962 he was the rector of the university. He was recognized internationally by then as a renowned theorist who corresponded with the leading characters of that time and made interesting contributions to quantum mechanics and the application of it particularly on the physics of molecules and molecular spectra, an area on which he was the expert of those days. The Max Planck medal was awarded to Ralph Kronig in 1962.

Kronig was elected a member of the Royal Netherlands Academy of Arts and Sciences in 1946, in 1969 he became a foreign member.[3]

Among Ralph Kronig's substantial correspondence are many letters to and from the 20th century's greatest physicists that should be preserved for posterity and Kronig himself published many in books.

Showing Kronig's great respect for Pauli, in one letter Ralph Kronig said regarding Pauli and the slim number of actual publications made by Pauli considering the extent of his work [translated from the German]:

"... his [Pauli's] publications contain however, which is understandable due to Pauli's unusually critical attitude, only a small part of the work really carried out by him. Pauli briefs in his papers on the finished results, but not on the long, often laborious way, which had led to them, and also not on incomplete attempts. A part of his work is only carried in a satisfying way in his extensive exchange of letters."

Stumm von Bordwehr (1989) gives a detailed description of the life and accomplishments of Kronig, even recounting how his name was changed to Ralph de Laer Kronig.

Scientific achievement

Ralph Kronig (1931, 1932), published the first theory of x-ray absorption fine structure, which contained some of the basic concepts of the modern interpretation. The Kronig-Penney Model (1931) is a one-dimensional model of a crystal that shows how the electrons in a crystal are dispersed into allowed and forbidden bands by scattering from the extended linear array of atoms. His first theory (1931) of EXAFS was the three-dimensional equivalent of this model. The theory showed that a photo electron traversing a crystal lattice would experience permitted and forbidden zones depending on its wavelength and, that even when the effect was averaged over all directions in the lattice, a residual structure should be observed. His theory was successful in predicting many generally observed features of the fine structure, including similar structure from similar lattices, inverse r2 dependence, correct r versus T dependence and increasing energy separation of the fine structure features with energy from the edge. The equation, which was re-derived in a more quantitative way in 1932 was simple to apply and interpret. Every experimenter found approximate agreement with the theory. There were always some absorption features close to that predicted by the possible lattice planes. However, the expected strong reflections (e. g. (100), (110), (111), etc. ) did not always correlate with the most intense absorption features as intuitively expected. Still, agreement was close enough to be tantalizing and everyone tested the agreement of their measured "Kronig structure" with the simple Kronig theory. In the Kronig equation, energy positions Wn correspond to the zone boundaries, i. e. not the absorption maxima or minima, but the first rise in each fine structure maximum. abg are the Miller indices, a is the lattice constant and q is the angle between the electron direction and the reciprocal lattice direction. When averaged over all directions with a non-polarized x-ray beam and a polycrystalline absorber, cos2q = 1. However, with a single crystal absorber and polarized x-rays the absorption features should be larger for specific crystal planes. This was another experimental variable that might verify the theory and many attempted to test it. Thus began the long record of publications in which Kronig structure was interpreted in terms of the simple Kronig theory. Until the 1970s fully 2% of the papers published in Phys. Rev. were devoted to x-ray absorption spectroscopy and most invoked Kronig's theory.

The short range order data of Hanawalt (1931b) stimulated Kronig (1932) to develop a theory for molecules. This model served as the starting point for all the subsequent short range order theories but few attempted to compare it to their data. Kronig's student, H. Petersen (1932, 1933) continued this work. Peterson's equation shows many of the features of the modern theory. This theory was applied to GeCl4 by Hartree, Kronig and Petersen (1934). A description of the Herculean efforts required to perform the calculations can be found in Stumm von Bordwehr (1989).

The Kramers–Kronig relation for dispersion was derived by Kronig (1926) independently of Kramers (1927).

Books published by Ralph Kronig

  • Correspondence with Niels Bohr, 1924–1953.
  • Textbook of physics. Under the editorship of R. Kronig in collaboration with J. De Boer [and others] With biographical notes and tables by J. Korringa.
  • The optical basis of the theory of valence / by R. de L. Kronig
  • Band spectra and molecular structure / by R. de L. Kronig
  • Oral history interview with Ralph de Laer Kronig, 1962 November 12

Notes

  1. H.B.G. Casimir (1996). "Ralph Kronig" (PDF). Huygens Institute, Royal Netherlands Academy of Arts and Sciences. pp. 55–60. Retrieved 5 February 2013.
  2. Bertolotti, Mario (2004). The History of the Laser. CRC Press. pp. 150–153. ISBN 9781420033403. Retrieved 22 March 2017.
  3. "R. Kronig (1904 - 1995)". Royal Netherlands Academy of Arts and Sciences. Retrieved 9 October 2016.

References

  • The Samuel A. Goudsmit Papers, 1921–1979 Box 59 Folder 48 Spin history correspondence: B. L. van der Waerden, Ralph Kronig, and George E. Uhlenbeck
  • A. Pais, in Physics Today (December 1989)
  • M. J. Klein, in Physics in the Making (North-Holland, Amsterdam, 1989)
  • Stumm von Bordwehr, R., Ann. Phys. Fr., 14 (1989), 377 – 466
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