The internal disorder of a D-dimensional hydrogenic system, which is strongly associated to the non-uniformity of the quantum-mechanical density of its physical states, is investigated by means of the shape complexity in the two reciprocal spaces. This quantity, which is the product of the disequilibrium and the Shannon entropic power, is mathematically expressed for both ground and excited stationary states in terms of certain entropic functionals of Laguerre and Gegenbauer (or ultraspherical) polynomials. Emphasis is made in the ground and circular states.
The internal disorder of a D-dimensional hydrogenic system, which is strongly associated to the non-uniformity of the quantum-mechanical density of its physical states, is investigated by means of the shape complexity in the two reciprocal spaces. This quantity, which is the product of the disequilibrium and the Shannon entropic power, is mathematically expressed for both ground and excited stationary states in terms of certain entropic functionals of Laguerre and Gegenbauer (or ultraspherical) polynomials. Emphasis is made in the ground and circular states.
The internal disorder of hydrogenic Rydberg atoms as contained in their position and momentum probability densities is examined by means of the following information-theoretic spreading quantities: the radial and logarithmic expectation values, the Shannon entropy, and the Fisher information. As well, the complexity measures of Crámer-Rao, Fisher-Shannon, and López Ruiz-Mancini-Calvet types are investigated in both reciprocal spaces. The leading term of these quantities is rigorously calculated by use of the asymptotic properties of the concomitant entropic functionals of the Laguerre and Gegenbauer orthogonal polynomials which control the wavefunctions of the Rydberg states in both position and momentum spaces. The associated generalized Heisenberg-like, logarithmic and entropic uncertainty relations are also given. Finally, application to linear (l = 0), circular (l = n − 1), and quasicircular (l = n − 2) states is explicitly done.
Abstract Rydberg atoms and excitons are composed so that they have a hydrogenic energy level structure governed by the Rydberg formula. They are relevant per se and for their numerous applications, e.g. facilitating the creation of novel quantum devices in quantum technologies which are inherently robust, miniature, and scalable (basically because they exist in solid-state platforms) and the realization of synthetic dimensions in numerous quantum-mechanical systems, giving rise to quantum matter which can behave as if it were in dimensions other than three. However the quantification of their internal disorder is scarcely known. Here we show and review the knowledge of dispersion, entanglement, physical entropies (Rényi, Shannon) and complexity-like measures of D-dimensional Rydberg systems with D ⩾ 2 in both position and momentum spaces. These uncertainty quantifiers are expressed in terms of D, the potential strength and the hyperquantum numbers of the Rydberg states. This has been possible because of the fine asymptotics of algebraic functionals the Laguerre and Gegenbauer polynomials which, together with the hyperspherical harmonics, control the Rydberg wavefunctions.
The Cramér-Rao, Fisher-Shannon and LMC shape complexity measures have been recently shown to play a relevant role to study the internal disorder of finite many-body systems (e.g., atoms, molecules, nuclei). They highlight amongst the bunch of complexities appeared in the literature by their mathematical simplicity and transparent physical interpretation. They are composed by two spreading measures (variance, Fisher information and Shannon entropies) of the single-particle probability density of the systems. Here we discuss the physico-mathematical knowledge of these two-component complexities for hydrogenic systems with standard (D=3) and non-standard dimensionalities. These systems include not only the hydrogen atom and its isoelectronic series but also a large diversity of quantum systems such as, e.g. exotic atoms, antimatter atoms, some qubits systems and Rydberg atoms, ions and molecules.
The various facets of the internal disorder of quantum systems can be described by means of the Rényi entropies of their single-particle probability density according to modern density functional theory and quantum information techniques. In this work, we first show the lower and upper bounds for the Rényi entropies of general and central-potential quantum systems, as well as the associated entropic uncertainty relations. Then, the Rényi entropies of multidimensional oscillator and hydrogenic-like systems are reviewed and explicitly determined for all bound stationary position and momentum states from first principles (i.e., in terms of the potential strength, the space dimensionality and the states's hyperquantum numbers). This is possible because the associated wavefunctions can be expressed by means of hypergeometric orthogonal polynomials. Emphasis is placed on the most extreme, non-trivial cases corresponding to the highly excited Rydberg states, where the Rényi entropies can be amazingly obtained in a simple, compact, and transparent form. Powerful asymptotic approaches of approximation theory have been used when the polynomial's degree or the weight-function parameter(s) of the Hermite, Laguerre, and Gegenbauer polynomials have large values. At present, these special states are being shown of increasing potential interest in quantum information and the associated quantum technologies, such as e.g., quantum key distribution, quantum computation, and quantum metrology.
Abstract The entropic uncertainty measures of the multidimensional hydrogenic states quantify the multiple facets of the spatial delocalization of the electronic probability density of the system. The Shannon entropy is the most adequate uncertainty measure to quantify the electronic spreading and to mathematically formalize the Heisenberg uncertainty principle, partially because it does not depend on any specific point of their multidimensional domain of definition. In this work, the radial and angular parts of the Shannon entropies for all the discrete stationary states of the multidimensional hydrogenic systems are obtained from first principles; that is, they are given in terms of the states' principal and magnetic hyperquantum numbers ( n , μ 1 , μ 2 , …, μ D− 1 ), the system's dimensionality D and the nuclear charge Z in an analytical, compact form. Explicit expressions for the total Shannon entropies are given for the quasi‐spherical states, which conform to a relevant class of specific states of the D ‐dimensional hydrogenic system characterized by the hyperquantum numbers μ 1 = μ 2 … = μ D− 1 = n − 1, including the ground state.
Abstract There exists an increasing interest on the dimensionality dependence of the entropic properties for the stationary states of the multidimensional quantum systems in order to contribute to its emergent informational representation, which extends and complements the standard energetic representation. Nowadays, this is specially so for high‐dimensional systems as they have been recently shown to be very useful in both scientific and technological fields. In this work, the Shannon entropy of the discrete stationary states of the high‐dimensional harmonic (ie, oscillator‐like) and hydrogenic systems is analytically determined in terms of the dimensionality, the potential strength, and the state's hyperquantum numbers. We have used an information‐theoretic methodology based on the asymptotics of some entropy‐like integral functionals of the orthogonal polynomials and hyperspherical harmonics which control the wave functions of the quantum states, when the polynomial parameter is very large; this is basically because such a parameter is a linear function of the system's dimensionality. Finally, it is shown that the Shannon entropy of the D‐dimensional harmonic and hydrogenic systems has a logarithmic growth rate of the type D log D when D → ∞.