The old quantum theory is a collection of results from the years 1900–1925 which predate modern quantum mechanics. The theory was never complete or self-consistent, but was rather a set of heuristic corrections to classical mechanics. The theory is now understood as the semi-classical approximation to modern quantum mechanics. The main and final accomplishments of the old quantum theory were the determination of the modern form of the periodic table by Edmund Stoner and the Pauli Exclusion Principle which were both premised on the Arnold Sommerfeld enhancements to the Bohr model of the atom.
The main tool of the old quantum theory was the Bohr–Sommerfeld quantization condition, a procedure for selecting out certain states of a classical system as allowed states: the system can then only exist in one of the allowed states and not in any other state.
The old quantum theory was instigated by the 1900 work of Max Planck on the emission and absorption of light in a black body with his discovery of Planck’s law introducing his quantum of action, and began in earnest after the work of Albert Einstein on the specific heats of solids in 1907 brought him to the attention of Walther Nernst. Einstein, followed by Debye, applied quantum principles to the motion of atoms, explaining the specific heat anomaly.
In 1910, Arthur Erich Haas develops J. J. Thomson’s atomic model in his 1910 paper that outlined a treatment of the hydrogen atom involving quantization of electronic orbitals, thus anticipating the Bohr model (1913) by three years.
John William Nicholson is noted as the first to create an atomic model that quantized angular momentum as h/2π. Niels Bohr quoted him in his 1913 paper of the Bohr model of the atom.
In 1913, Niels Bohr displayed rudiments of the later defined correspondence principle and used it to formulate a model of the hydrogen atom which explained the line spectrum. In the next few years Arnold Sommerfeld extended the quantum rule to arbitrary integrable systems making use of the principle of adiabatic invariance of the quantum numbers introduced by Lorentz and Einstein.
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The course covers several exact, approximate, and numerical methods to solve the time-dependent molecular Schrödinger equation, and applications including calculations of molecular electronic spectra.
This course is an introduction to the non-perturbative bootstrap approach to Conformal Field Theory and to the Gauge/Gravity duality, emphasizing the fruitful interplay between these two ideas.
The Planck constant, or Planck's constant, is a fundamental physical constant of foundational importance in quantum mechanics. The constant gives the relationship between the energy of a photon and its frequency, and by the mass-energy equivalence, the relationship between mass and frequency. Specifically, a photon's energy is equal to its frequency multiplied by the Planck constant. The constant is generally denoted by . The reduced Planck constant, or Dirac constant, equal to divided by , is denoted by .
In chemistry and atomic physics, an electron shell may be thought of as an orbit that electrons follow around an atom's nucleus. The closest shell to the nucleus is called the "1 shell" (also called the "K shell"), followed by the "2 shell" (or "L shell"), then the "3 shell" (or "M shell"), and so on farther and farther from the nucleus. The shells correspond to the principal quantum numbers (n = 1, 2, 3, 4 ...) or are labeled alphabetically with the letters used in X-ray notation (K, L, M, ...).
The Stark effect is the shifting and splitting of spectral lines of atoms and molecules due to the presence of an external electric field. It is the electric-field analogue of the Zeeman effect, where a spectral line is split into several components due to the presence of the magnetic field. Although initially coined for the static case, it is also used in the wider context to describe the effect of time-dependent electric fields. In particular, the Stark effect is responsible for the pressure broadening (Stark broadening) of spectral lines by charged particles in plasmas.
Organic materials can tune the optical properties in layered (2D) hybrid perovskites, although their impact on photophysics is often overlooked. Here, we use transient absorption spectroscopy to probe the Dion−Jacobson (DJ) and Ruddlesden−Popper (RP) 2D pe ...
2023
This paper deals with the mathematical expressions called Sommerfeld integrals. Introduced by A. Sommerfeld in 1909, they are mathematically equivalent to inverse Hankel transforms. The original historical goal of these integrals was to provide an accurate ...
Piscataway2021
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The new trends for anomalous Nernst effect (ANE)-based thermoelectric devices require materials with large ANE values to realize the scalable generation of voltage. Recently, very large ANE values have been observed in single crystals of some novel magneti ...