Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

PrPh

Phenomenological Derivation of the Schr¨ odinger Equation

Fernando Ogiba

Published Oct 1, 2011• 4 citations
OpenAlex

Abstract

The Schrödinger equation is derived classically assuming that particles present local \nrandom spatial fluctuations compatible with the presence of the zero-point field. With- \nout specifying the forces arising from this permanent matter-field interaction but ex- \nploring its fundamental properties (homogeneity, isotropy and random aspect) to justify \nthe emergence of the continuity equation in one-particle context, these fluctuations are \ndescribed in terms of the probability density. Specifically, the starting point is the as- \nsumption that the local activities, which turn the path followed by the particle totally \nunpredictable, must be associated with an energy proportional to \n@ \nP \n=@ \nt \n. The polar form \nof the wave function, which connects the obtained classical equations with the corre- \nsponding quantum equation, emerges as a by-product of the approach.

Related papers

Perceptions of the Schrodinger Equation

Spyros Efthimiades

The Schrodinger equation has been considered to be a postulate of quantum physics, but it is also perceived and derived heuristically as the quantum equivalent of the classical energy relation. We indicate that the Schrodinger equation cannot be a physical postulate, and we show that the heuristic derivations wrongly consider that the particle kinetic energy is proportional to the square of the momentum operator acting on the wavefunction. The correct term is proportional to the square of the momentum. Analyzing particle interactions, we realize that particles have multiple virtual motions and that each motion is accompanied by a wave that has constant amplitude. Accordingly, we define the wavefunction as the superposition of the virtual waves of the particle. As a result, quantum mechanics becomes a local and global theory, while in the traditional formulation it is a local theory. In several interaction settings we can tell what particle motions arise and explain the outcomes in simple and tangible terms. Most importantly, the mathematical foundation of quantum mechanics becomes clear and justified, and we derive the Schrodinger, Dirac, etc. equations as the conditions the wavefunction must satisfy at each space-time point in order to fulfill the respective total energy equation.

arXiv:1307.6108•Bulletin of the American Physical Society•Jul 23, 2013•0 citations

Derivation of the Schrodinger equation from fundamental principles

Wenzhuo Zhang, Anatoly Svidzinsky

Schrodinger path to the quantum mechanical wave equation was heuristic and guided more by physical intuition than formal deduction. Here we derive the Schrodinger equation for the particle wave function, assuming that it has a meaning of the probability amplitude to find the particle at time t at point r and the relations E=hw, p=hk expressing particle energy and momentum in terms of the frequency and wave vector of the associated probability wave.

quant-pharXiv:2603.27041•Mar 31, 2026

The Logical Origin of the Schrödinger Equation

H.-K. Chan

This paper derives the non-relativistic time-dependent Schrödinger equation as the logically unavoidable dynamical law for de Broglie matter waves, extending the reconstruction begun in the companion work “The Logical Origin of the de Broglie Matter Wave and its Physical Meaning (the Born Rule)” (Chan, 2026). Starting from the same minimal premises—continuous position in real space, Fourier conjugacy (and the logical uncertainty principle), translation invariance via Noether’s theorem, and probability conservation via statistical energy flux—the Schrödinger equation follows deductively once norm preservation and classical non-relativistic correspondence are enforced. The derivation proceeds in clear stages: Plane-wave solutions for free particles and constant potentials, Quadratic dispersion relation from classical kinematics, Exact local plane-wave structure (defined via phase gradients) that must hold at every point for any smooth wave function, The unique linear differential operator of order ≤ 2 that consistently “glues” these local structures across smooth external potentials V(x,t) while preserving the L²-norm (unitarity). No canonical quantization, operator promotion, commutation relations, or postulated wave equations are used. The Born rule is taken as already established from the prior paper and serves only to constrain unitary evolution. The Schrödinger equation thus emerges not as an empirical postulate or convenient ansatz, but as the mathematically and symmetrically forced description of indivisible particles propagating in continuous, translationally invariant (or smoothly perturbed) space. Domain of validity and natural limitations (non-relativistic kinematics, smooth potentials, single-particle/mean-field regime, closed-system unitarity) are explicitly delineated.

•Mar 24, 2026•0 citations

Quantum mechanical motion of classical particles

V. D. Rusov, Konstantin Alexandrovich Lukin

The Schrödinger equation for the particle wave function introduced via its action was derived from Newton equation for a point-like particle moving under effect of both potential force and fluctuation-dissipative environment, provided considering only stable motion of the particle. The model considered assumes existence of wave function as a physical field rather than just a mathematical abstraction.

Journal of Physics Conference Series•May 10, 2012•0 citations

Classical Mechanics Theory and Schrödinger's Equation: A Derivation of Relations

J. Q. Li, Yanchun Yu

This study examines integrating the Schrödinger equation with classical mechanics using a virtual axis-to-dimensional expansion. One-dimensional material fluctuations are viewed in a two-dimensional plane, explaining the random nature of these fluctuations and their spatial and temporal trajectories. A quantum-consistent force field is proposed, with its strength determined by the Planck constant and inversely proportional to the distance from the stationary point. Newton's second law is applied to establish a second-order linear differential equation for material fluctuations, from which the standard one-dimensional Schrödinger equation is derived, showing their equivalence. The study extends the three-dimensional Schrödinger equation to include external forces and explains quantum phenomena like energy levels and transitions through particle trajectory changes. This approach connects classical mechanics and quantum mechanics, offering a concise and intuitive formulation with clear physical significance.

Journal of Engineering and Technological Sciences•Sep 23, 2025•1 citation

Deriving the Schrödinger Equation

Steven M. Pascal

The Schrödinger equation was really postulated rather than derived. But we can see why it was postulated. It has been proven to be valid, in that it provides information about small, slow moving particles subject to a wide variety of potentials. The derivation of the time-dependent Schrödinger equation (TDSE) follows rather directly from assuming a free particle wave: Ψ = e i(kx-ωt) . If this wave function is plugged into the classical wave equation, and quantum principles are used, the two sides of the equation are not equal (this means this function does not "solve" the equation). The quantum principles required are an understanding of the photoelectric effect (by which E = ħω) and the de Broglie hypothesis (λ = h/p). Using these relationships, we show that one derivative of time is equal to a double derivative with respect to position, with a few proportionality factors mixed in. Thus, the TDSE for a free particle is just a statement that kinetic energy equals total energy . For a non-free particle (subject to a potential), potential must merely be added to the left-hand side of the equation, to yield kinetic energy plus potential energy equals total energy .

CRC Press eBooks•Jul 12, 2023•0 citations
The Schrödinger equation is derived classically assuming that particles present local \nrandom spatial fluctuations compatible with the presence of the zero-point field. With- \nout specifying the forces arising from this permanent matter-field interaction but ex- \nploring its fundamental properties (homogeneity, isotropy and random aspect) to justify \nthe emergence of the continuity equation in one-particle context, these fluctuations are \ndescribed in terms of the probability density. Specifically, the starting point is the as- \nsumption that the local activities, which turn the path followed by the particle totally \nunpredictable, must be associated with an energy proportional to \n@ \nP \n=@ \nt \n. The polar form \nof the wave function, which connects the obtained classical equations with the corre- \nsponding quantum equation, emerges as a by-product of the approach.
The Schrodinger equation has been considered to be a postulate of quantum physics, but it is also perceived and derived heuristically as the quantum equivalent of the classical energy relation. We indicate that the Schrodinger equation cannot be a physical postulate, and we show that the heuristic derivations wrongly consider that the particle kinetic energy is proportional to the square of the momentum operator acting on the wavefunction. The correct term is proportional to the square of the momentum. Analyzing particle interactions, we realize that particles have multiple virtual motions and that each motion is accompanied by a wave that has constant amplitude. Accordingly, we define the wavefunction as the superposition of the virtual waves of the particle. As a result, quantum mechanics becomes a local and global theory, while in the traditional formulation it is a local theory. In several interaction settings we can tell what particle motions arise and explain the outcomes in simple and tangible terms. Most importantly, the mathematical foundation of quantum mechanics becomes clear and justified, and we derive the Schrodinger, Dirac, etc. equations as the conditions the wavefunction must satisfy at each space-time point in order to fulfill the respective total energy equation.
This paper derives the non-relativistic time-dependent Schrödinger equation as the logically unavoidable dynamical law for de Broglie matter waves, extending the reconstruction begun in the companion work “The Logical Origin of the de Broglie Matter Wave and its Physical Meaning (the Born Rule)” (Chan, 2026). Starting from the same minimal premises—continuous position in real space, Fourier conjugacy (and the logical uncertainty principle), translation invariance via Noether’s theorem, and probability conservation via statistical energy flux—the Schrödinger equation follows deductively once norm preservation and classical non-relativistic correspondence are enforced. The derivation proceeds in clear stages: Plane-wave solutions for free particles and constant potentials, Quadratic dispersion relation from classical kinematics, Exact local plane-wave structure (defined via phase gradients) that must hold at every point for any smooth wave function, The unique linear differential operator of order ≤ 2 that consistently “glues” these local structures across smooth external potentials V(x,t) while preserving the L²-norm (unitarity). No canonical quantization, operator promotion, commutation relations, or postulated wave equations are used. The Born rule is taken as already established from the prior paper and serves only to constrain unitary evolution. The Schrödinger equation thus emerges not as an empirical postulate or convenient ansatz, but as the mathematically and symmetrically forced description of indivisible particles propagating in continuous, translationally invariant (or smoothly perturbed) space. Domain of validity and natural limitations (non-relativistic kinematics, smooth potentials, single-particle/mean-field regime, closed-system unitarity) are explicitly delineated.
This study examines integrating the Schrödinger equation with classical mechanics using a virtual axis-to-dimensional expansion. One-dimensional material fluctuations are viewed in a two-dimensional plane, explaining the random nature of these fluctuations and their spatial and temporal trajectories. A quantum-consistent force field is proposed, with its strength determined by the Planck constant and inversely proportional to the distance from the stationary point. Newton's second law is applied to establish a second-order linear differential equation for material fluctuations, from which the standard one-dimensional Schrödinger equation is derived, showing their equivalence. The study extends the three-dimensional Schrödinger equation to include external forces and explains quantum phenomena like energy levels and transitions through particle trajectory changes. This approach connects classical mechanics and quantum mechanics, offering a concise and intuitive formulation with clear physical significance.
The Schrödinger equation was really postulated rather than derived. But we can see why it was postulated. It has been proven to be valid, in that it provides information about small, slow moving particles subject to a wide variety of potentials. The derivation of the time-dependent Schrödinger equation (TDSE) follows rather directly from assuming a free particle wave: Ψ = e i(kx-ωt) . If this wave function is plugged into the classical wave equation, and quantum principles are used, the two sides of the equation are not equal (this means this function does not "solve" the equation). The quantum principles required are an understanding of the photoelectric effect (by which E = ħω) and the de Broglie hypothesis (λ = h/p). Using these relationships, we show that one derivative of time is equal to a double derivative with respect to position, with a few proportionality factors mixed in. Thus, the TDSE for a free particle is just a statement that kinetic energy equals total energy . For a non-free particle (subject to a potential), potential must merely be added to the left-hand side of the equation, to yield kinetic energy plus potential energy equals total energy .