Mechanics can be founded on a principle relating the uncertainty delta-q in the trajectory of an observable particle to its motion relative to the observer. From this principle, p.delta-q=const., p being the q-conjugated momentum, mechanical laws are derived and the meaning of the Lagrangian and Hamiltonian functions are discussed. The connection between the presented principle and Hamilton's Least Action Principle is examined. Wave mechanics and Schrodinger equation appear without additional assumptions by choosing the representation for delta-q in the case the motion is not trajectory describable. The Cramer-Rao inequality serves that purpose. For a particle hidden from direct observation, the position uncertainty determined by the enclosing boundaries leads to thermodynamics in a straightforward extension of the presented formalism. The introduction of uncertainty in classical mechanics formulation enables the translation of mechanical laws into the wide ranging conceptual framework of information theory. The boundaries between classical mechanics, thermodynamics and quantum mechanics are defined in terms of informational changes associated with the system evolution. As a direct application of the proposed formulation upper bounds for the rate of information transfer are derived.
Mechanics can be founded on a principle relating the uncertainty delta-q in the trajectory of an observable particle to its motion relative to the observer. From this principle, p.delta-q=const., p being the q-conjugated momentum, mechanical laws are derived and the meaning of the Lagrangian and Hamiltonian functions are discussed. The connection between the presented principle and Hamilton's Least Action Principle is examined. Wave mechanics and Schrodinger equation appear without additional assumptions by choosing the representation for delta-q in the case the motion is not trajectory describable. The Cramer-Rao inequality serves that purpose. For a particle hidden from direct observation, the position uncertainty determined by the enclosing boundaries leads to thermodynamics in a straightforward extension of the presented formalism. The introduction of uncertainty in classical mechanics formulation enables the translation of mechanical laws into the wide ranging conceptual framework of information theory. The boundaries between classical mechanics, thermodynamics and quantum mechanics are defined in terms of informational changes associated with the system evolution. As a direct application of the proposed formulation upper bounds for the rate of information transfer are derived.
Mechanics can be founded in a principle stating the uncertainty in the position of an observable particle delta-q as a function of its motion relative to the observer, expressed in a trajectory representation . From this principle, p.delta-q=const., being p the q-conjugated momentum, mechanical laws are derived and the meaning of the Lagrangian and Hamiltonian functions are discussed. The connection between the presented principle and Hamilton's Least Action Principle is examined. For a particle hidden from direct observation, the position uncertainty is determined by the enclosing boundaries, and is, thus, disengaged from its momentum. Heat, as a non-mechanical magnitude, stem from this fact, and thermodynamical magnitudes have direct expression in the presented formalism. It is finally shown that in terms of Information Theory, mechanical laws have simple interpretation. Kinetic and potential energies are expressions of the information on momentum and position respectively, and the law of conservation of energy expresses the absence of information exchange in mechanical interactions.
Abstract We show that the formulations of non-relativistic quantum mechanics can be derived from an extended least action principle. The principle can be considered as an extension of the least action principle from classical mechanics by factoring in two assumptions. First, the Planck constant defines the minimal amount of action a physical system needs to exhibit during its dynamics in order to be observable. Second, there is constant vacuum fluctuation along a classical trajectory. A novel method is introduced to define the information metrics to measure additional observability due to vacuum fluctuations, which is then converted to an additional action through the first assumption. Applying the variational principle to minimize the total actions allows us to recover the basic quantum formulations including the uncertainty relation and the Schrödinger equation in the position representation. In the momentum representation, the same method can be applied to obtain the Schrödinger equation for a free particle while further investigation is still needed for a particle with an external potential. Furthermore, the principle brings in new results on two fronts. At the conceptual level, we find that the information metrics for vacuum fluctuations are responsible for the origin of the Bohm quantum potential. Even though the Bohm potential for a bipartite system is inseparable, the underlying vacuum fluctuations are local. Thus, inseparability of the Bohm potential does not justify a non-local causal relation between the two subsystems. At the mathematical level, quantifying the information metrics for vacuum fluctuations using more general definitions of relative entropy results in a generalized Schrödinger equation that depends on the order of relative entropy. The extended least action principle is a new mathematical tool. It can be applied to derive other quantum formalisms such as quantum scalar field theory.
The usual Heisenberg uncertainty relation, ΔX ΔP ≥ ℏ/2, may be replaced by an exact equality for suitably chosen measures of position and momentum uncertainty, which is valid for all wavefunctions. This exactuncertainty relation, δX ΔPnc ≡ ℏ/2, can be generalised to other pairs of conjugate observables such as photon number and phase, and is sufficiently strong to provide the basis for moving from classical mechanics to quantum mechanics. In particular, the assumption of a nonclassical momentum fluctuation, having a strength which scales inversely with uncertainty in position, leads from the classical equations of motion to the Schrödinger equation.
Abstract Quantum thermodynamics describes dynamic processes by means of the operators of entropy production P and time t . P and t do not commute. It exists the non-vanishing t–P commutator [ t , P ]=ik. Here the Boltzmann constant k has the physical meaning of a quantum of entropy. The t–P commutator immediately leads us to the t–P uncertainty relation ΔtΔP≥k/2. Hence the observables t and P are not sharply defined simultaneously. Similar uncertainty relations can also be expected for other pairs of conjugate variables with products of the physical meaning of an entropy. The free energy F and the reciprocal temperature (1/T) are the respective conjugate variables of an isolated system of many particles, which leads us to the F–(1/T) uncertainty relation ǀΔFǁΔ(1/T)ǀ≥k/2. It can be traced back to the t–P uncertainty relation mentioned above. In this way the Helmholtz free energy F and the temperatur T are introduced into quantum thermodynamics. The uncertainties ǀΔFǀ→0 and ǀΔTǀ→0 are negligible at low temperatures T→0, and quantum thermodynamics turns into the time-independent classical thermodynamics. Against this the uncertainties ǀΔFǀ→∞ and ǀΔTǀ→∞ grow unlimited at high temperatures T→∞, and classical thermodynamics loses its sense. In the limit of one particle the uncertainties cannot be neglected even at low temperatures. However a detailed discussion shows that the free energy f of a single particle vanishes within the whole range of temperatures T. This defines the particle entropy σ=ε/T=ak. The dimensionless entropy number a connects the particle energy ε=akT with the temperature T. The entropy number a of a single (s) independent particle can be calculated with the extended, temperature-dependent Schrödinger equation A s φ=aφ. Here A s=−(Λ 2/4π)∇2 means the dimensionless entropy operator describing the entropy number a and thus the particle entropy σ=ak. Λ is the thermal de Broglie wave length. Finally we calculate by means of quantized particle entropies σ the internal energy E, the Helmholtz free energy F, the entropy S, the chemical potential μ, and the equation of state of an ideal gas of N monatomic free particles in full agreement with classical thermodynamics. We also calculate the partition function q=V/Λ 3 of a single free particle within the volume V. Here Λ 3 is a small volume element taking into account the wave–particle dualism of a single free particle of mass m at temperature T. Extension to a system of N free particles leads us to a simple geometrical model and to the conclusion that an ideal gas of independent particles becomes instable below a critical temperature T C. T C corresponds to the critical temperature T BE of Bose–Einstein condensation.
We demonstrate two points: 1) the formalism of quantum mechanics can be understood simply as a structure for the expression of the physical notion that not all observables can have values simultaneously; 2) the specific uncertainty relations can be derived (rigorously) by combination of the invariance principle with a general uncertainty relation based only on the existence of unspecified pairs of conjugate observables. For this purpose, we present a formulation of quantum mechanics based strictly on the invariance principle and a “weak” statement of the uncertainty principle that asserts only the existence of incompatible (conjugate) observables without specifying which observables are incompatible. We go on to show that the invariance principle can be used to develop the equations of motion of the theory, including the Klein-Gordon and Schrodinger equations.
Uncertainty relations represent a foundational principle in quantum mechanics, imposing inherent limits on the precision with which \textit{mechanically} conjugate variables such as position and momentum can be simultaneously determined. This work establishes analogous relations for \textit{thermodynamically} conjugate variables -- specifically, a classical intensive parameter θ and its corresponding extensive quantum operator O^ -- in equilibrium states. We develop a framework to derive a rigorous thermodynamic uncertainty relation for such pairs, where the uncertainty of the classical parameter θ is quantified by its quantum Fisher information Fθ. The framework is based on an exact integral representation that relates Fθ to the autocorrelation function of operator O^. From this representation, we derive a tight upper bound for the quantum Fisher information, which yields a thermodynamic uncertainty relation: ΔθΔO≥kBT with ΔO≡∂θ⟨O^⟩Δθ and T is the system temperature. The result establishes a fundamental precision limit for quantum sensing and metrology in thermal systems, directly connecting it to the thermodynamic properties of linear response and fluctuations.