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

Journal of Physics Conference Series

A typical oscillating perturbation on protonium

Herry Fridolin Lalus, Nila Prasetya Aryani

Published Jun 1, 2021• 2 citations
Publisher

Abstract

Abstract Protonium is a type of onium consisting of a proton (p) and an anti-proton ( <?CDATA $ \bar p $?> p ¯ ) which is called antiprotonic hydrogen. Since the proton and the anti-particle have the same mass, and each of them is a fermion, the Hamiltonian form of this system consists of the kinetic energy terms of each particle, the potential energy, and the spin interactions of both (hyperfine structure). To simplify the analysis, the Hamiltonian is then converted into a Hamiltonian which contains the relative motion terms of the two particles. This new Hamiltonian contains their reduced mass because the two particles orbit each other towards a certain center of mass. In the initial state, t < 0, the system is in the ground state and then at 0 < t < τ, the system is given a disturbance of the form <?CDATA $ V(t) = ({V_0} + {V_1}\,r\,\sin \theta \,{e^{i\phi }})\,\cos (\omega t)\,{\hat \sigma _p}.\hat x $?> V ( t ) = ( V 0 + V 1 r sin θ e i ϕ ) cos ( ω t ) σ ^ p . x ^ , where V 0 is a constant, V 1 is a constant and very small, <?CDATA $ {\hat \sigma _p} $?> σ ^ p is the Pauli matrix for proton, and <?CDATA $ \hat x $?> x ^ is the three-dimensional position operator in spherical coordinates. We analyze this system using a time-dependent perturbation theory that begins by defining the initial state, then calculating the transition amplitude for the new state when the perturbation is applied to the system. From the results of this calculation, we compute the system transition probability. We find that the transition probability of this system can only occur for the following quantum number terms, namely n even positive integer, l = 2,S = 1, and with the certain combinations of m and M.

DOI
10.1088/1742-6596/1918/2/022023

Related papers

ATOMIC RADIATION

Mircea S. Rogalski, Stuart B. Palmer

During the presence of the radiation perturbation ( ),ˆ tV the Hamiltonian of the system becomes ( )tVHH ˆˆˆ 0 += (37.4) and, since the state of the system varies with time, we must adopt the time-dependent Schrödinger equation to be a basis for the perturbation theory, that is ( ) ( ) ( )0ˆ ˆti H V tt ∂Ψ ⎡ ⎤= + Ψ⎣ ⎦∂= t (37.5) We assume that Eq.(37.5) has normalized solutions which can be expanded in terms of the as 0kΨ t a t t a t e ε−Ψ = Ψ = Ψ∑ ∑ = (37.6) where the normalization condition on ( )tΨ gives a t =∑ (37.7) that is, ( ) 2ka t gives the probability that the system is in the state at time t. Substituting Eq.(37.6) into Eq.(37.5) yields da t ii a t e V t a t e dt ε εε ε− −⎡ ⎤ ⎡ ⎤− Ψ = +⎢ ⎥ ⎣ ⎦⎣ ⎦∑ ∑ = == = which reduces to da t i e V t a t e dt ε− k ε−Ψ = Ψ∑ ∑= == (37.8) In view of orthogonality of the stationary state eigenfunctions, multiplication by ( ) followed by integration over the configuration space gives da t i e a t e V t dt ε εδ− −= Ψ Ψ∑ ∑= == (37.9) Denoting the matrix elements of the perturbation operator between the stationary states n and k by ( ) ( )0 ˆnk n kV t V t 0= Ψ Ψ (37.10) we can rewrite Eq.(37.9) as da t i a t V t e dt ε ε−= ∑ == (37.11) which is a set of simultaneous differential equations of the first order for the coefficients ( ).na t If we assume that the system is in a definite stationary state at some 0iΨ particular time 0,t = and then it is allowed to interact with the radiation field, we obtain from Eq.(37.6) that ( ) ( )0 00 0i k k aΨ = Ψ = Ψk∑ Multiplying by and integrating gives ( )∗Ψ 0k ( )0ka kiδ= (37.12) that is, and for .( ) 10 =ia ( ) 00 =ka ik ≠ If we consider a time interval t sufficiently short for the coefficients in Eqs.(37.11) to be approximated by the form (37.12), which means that the term gives the greatest contribution to the sum and all other terms can be neglected, we have ( )tak ik = ( ) ( ) ( )0 0 /n ii tn nida ti V t edt ε ε−= == , ( ) ( ) ( )i i iida ti a t Vdt == t (37.13) and on integration we obtain ( ) ( ) ( ) (0 0 / 0 ia t V t e dt n iε ε ′− ′= − ≠∫ == ) , ( ) ( ) tdtVita iii ′′−= ∫ 0 1 = (37.14) The probability (29.29) that the system is in the state at time t, in other words, that coincides with is given by ( )tΨ ,0nΨ ( ) ( ) ( )2 20in n nP t t a t= Ψ Ψ = (37.15) and this is taken to be the probability of direct transition from state to state in a time t, induced by the presence of the radiation field. Assuming a transition where a photon is emitted, that is, we recall the Bohr condition (28.19), which reads ,00 ni εε > (37.16) inni ωεε ==− 00 so that Eqs.(37.14) can be rewritten as ( ) ( ) ( ) 0 n ni ia t V t e dt n iω ′−′ ′= − ≠∫= (37.17) ( ) ( ) 0 1 t i ii ia t V t dt′ ′= − ∫= As we can see from the above, the time-dependent perturbation theory is concerned with transitions that result from perturbation, between the unperturbed levels of the system, while time-independent perturbation theory calculates the stationary shifts in the energy levels. 37.2. FERMI'S GOLDEN RULE Consider the case of a constant perturbation, switched on at time The integrals (37.17) become straightforward, and we obtain .0=t ( ) ( ) ( )1ini tnin in Va t e n iωω −= − ≠= (37.18) ( ) tVita iii =−=1 Substituting Eqs.(37.18) into Eq.(37.6) gives, to a first approximation, the wave function of the atomic system as Vt e t e tωω − − ≠ Ψ = Ψ + − Ψ∑= = (37.19) The probability (37.15) of observing the system in the state at time t, for the coefficients given by Eq.(37.18), reduces to 0 nΨ( )tan ( ) ( 2/sin4 222 2 t V ni in ωω== ) (37.20) which means that transitions from state to states only take place if the matrix elements do not vanish. The plot of niV ( )tPin as a function of inω , given in Figure 37.1 for a perturbation which is on for a time t, suggests that the probability behaves like a Dirac δ -function as t approaches infinity. We may represent the δ -function as ( ) dxe t t 2 1lim 2/ 2/sin lim ωππω ω ( ) ( ininxi dxe in ωδωδπ ω 22/2 1 2/ === ∫ ∞ ∞− ) (37.21) where use was made of a property derived from the normalization condition, written as ( ) ( ) ( ) ( ) ( )u k kukudkuduu δδδδ 1or1 === ∫∫ ∞ P t( ) ω4π6π t2π in t-t-t 2π 4π t 6π t0 Figure 37.1. Dependence of the transition probability on frequency It follows from Figure 37.1 that, in the large-t limit, we have ,0≅inω and hence ( )2sin / 2 / 1.in int tω ω⎡ →⎣ ⎤⎦ Thus, one obtains ( ) ( ) ( ) ( ) (2 24sin / 2 sin / 2 sin / 2lim lim / 2 2/ 2 / 2in in in in int t in inin t t t tt ω ω ω )π πδ ω πδ ωω πωω→∞ →∞ ⎡ ⎤= =⎢ ⎥⎣ ⎦ = so that the transition probability becomes ( ) ( ) (2 2 0 022 2lim in ni in ni i nt t tP t V Vπ π )δ ω δ ε→∞ = = == ε− (37.23) It follows that the transitions take place between states of equal unperturbed energies The transition probability is proportional to the time interval t during which the perturbation is on, that is .00 in εε → ( )tPin approaches infinity as .∞→t Since no experiment lasts for an infinite time, it is the transition probability per unit time, called the transition rate , which is of particular interest. Normally, is part of a continuum, and hence, the transition might end in any state which belongs to a finite range of N final states, rather than in a particular state. We may then define the transition rate as ( )dNtP t P intni ∫∞→→ = 1lim (37.24) The integral over the final states is usually transformed into one over energy, if we define a density of states ( ) ,ρ ε representing the number of continuum states per energy interval, by taking ( )0ndN d 0nρ ε ε= (37.25) so that, substituting Eqs.(37.23) and (37.25), Eq.(37.24) gives ( ) ( ) ( ) ( )20 0 0 0 01 2limi n in n n ni n i ntP P t d Vt πρ ε ε ρ ε δ ε ε→ →∞= =∫ = − (37.26) This result is known as Fermi's golden rule, which states that transitions may occur only between states of equal energies for which the matrix elements of the perturbation operator do not vanish, and that the transition rate is proportional to both the square modulus of these matrix elements and the density of final states. 37.3. EMISSION AND ABSORPTION OF RADIATION Consider the transitions between stationary states which are induced by a harmonic perturbation of the form ( ) ( ) ( ) ( ) ( )( )titi eeArVtArVtV ωωωωω −+== GG ˆcosˆ2ˆ (37.27) It is assumed that the harmonic perturbation corresponds to the interaction of either the electric or magnetic field components of the incoming radiation with the electric or magnetic moment of the atom. Thus, the coupling between the system and the perturbing field can be taken in the form of a field amplitude ( )ωA times a displacement of the system ( ).ˆ rV G On substitution of Eq.(37.27) into Eq.(37.10) one obtains ( ) ( ) ( )( ) ( )( )titinititiinni eeAVeeArVtV ωωωω ωω −− +=+ΨΨ= 00 ˆ G (37.28) It follows from Eq.(37.17) that n ni ia t V A e e dtω ω ω ωω ′ ′− − − +⎡ ⎤ ′= − +⎣ ⎦∫= (37.29) inin eeAV 0 ⎥⎦ ⎤⎢⎣ ⎡ ++−= ωωωω ω ωωωω V A e eω ω ω ωω ω ω ω ω − − − +⎡ ⎤− −= +⎢ ⎥− +⎢ ⎥⎣ ⎦= If the atomic system is bathed into a radiation field of frequency ,inni ωωω −== which implies that according to the Bohr condition (37.16), the transition from state to state describes a process of induced absorption, where the energy of the system is increased by energy transfer from the radiation field to the atom. If 00 in εε > ,ni inω ω ω= = − the second term on the right-hand side of Eq.(37.29) grows without limit, so that the first term can be neglected.

CRC Press eBooks•Jan 8, 2014•0 citations

TIME-DEPENDENT PERTURBATION METHODS

Vishnu S. Mathur, Surendra Singh

We now consider systems for which the Hamiltonian contains time-dependent interaction terms. In such cases we cannot reduce the time-dependent Schro¨dinger equation to an eigenvalue equation. However, if the time-dependent terms can be regarded as small perturbations, we can develop a form of perturbation theory that can be used to calculate the effects of time-dependent terms. Consider a system for which the Hamiltonian may be written as the sum of a dominant unperturbed part Hˆ0 and a small perturbation Hˆ ′ as Hˆ = Hˆ0 + λHˆ ′(t) , (10.1.1) where the unperturbed Hamiltonian Hˆ0 is independent of time, whereas the perturbation Hˆ ′ may depend on time. The parameter 0 < λ < 1 has been introduced to keep track of various orders of approximations as in the case of time-independent perturbation theory discussed in Chapter 8. The basic idea is that a small perturbation to the Hamiltonian will produce a small change in the wave function. For a time-dependent perturbation, this change means that a system, initially in a particular eigenstate of Hˆ0, will find itself in a time-dependent admixture of the eigenstates. Thus the time-dependent perturbation causes the system to undergo transition to different eigenstates of Hˆ0. So for time-dependent perturbations our interest lies in calculating the probabilities for transition to different states.

Chapman & Hall/CRC eBooks•Dec 12, 2008•0 citations

Concerning the frequency shift associated with spin-exchange interaction in a quantum oscillator based on a beam of hydrogen atoms

A. V. Uspenskii

Radiophysics and Quantum Electronics•Sep 1, 1974•0 citations

A modified sinusoidal perturbation on a two distinguishable spin −12 particles system

Herry Fridolin Lalus, Harti Umbu Mala, Antonius Suban Hali +1 more

Abstract We analyze a quantum system of two distinguishable spin − 1 2 particles subjected to modified sinusoidal perturbation of the form V ( t ) = ( V 0 + V 1 x + V 2 y + V 3 z ) e − γ t / τ cos ( ω t ) σ → 1 · x ^ ; 0 < t < τ ; where γ is a real positive number; V 0, V 1, V 2, V 3 are real constants and have very small values; x = r sin θ cos ϕ; y = r sin θ sin ϕ; = z = r cos θ; σ → 1 is the Pauli matrix for the first particle, and x ^ , is the three-dimensional position operator in spherical coordinates; V(t) is zero when t ≤ 0 and t ≥ τ. We use the time-dependent perturbation theory to solve this problem. Initially, we define the initial system state before being subjected to perturbation, namely | 000 ; 00 〉 , and the final state of the form | n l m ; S M 〉 ≡ | n l m 〉 | ⊗ S M 〉 . The total spin state | S M 〉 actually contains the linear combination of the states of each particle. Next, we calculate the expected value of 〈

Journal of Physics Conference Series•Sep 1, 2021•1 citation

Exact non-Born-Oppenheimer wave functions for three-particle Hookean systems with arbitrary masses

Xabier López, Jesús María Ugalde, Lorenzo Echevarría +1 more

A Hookean model of a three-body problem for particles with arbitrary masses and charges where two of them interact with each other through a Coulomb potential and with the third through a harmonic potential is presented. It is shown that a condition relating the masses to the harmonic coupling constants must be satisfied in order to render this problem separable. A general exact analytic solution written in terms of the relative interparticle coordinates is given as well as general expressions for the total and binding energies of this three-body system. We apply these results to examine electronic, muonic, antiprotonic, and pionic families of non-Born-Oppenheimer Hookean systems. The first contains the atoms or atomic ions: ${\mathrm{Ps}}^{\ensuremath{-}}({e}^{+}{e}^{\ensuremath{-}}{e}^{\ensuremath{-}})$, ${\mathrm{H}}^{\ensuremath{-}}({p}^{+}{e}^{\ensuremath{-}}{e}^{\ensuremath{-}})$, ${\mathrm{D}}^{\ensuremath{-}}({d}^{+}{e}^{\ensuremath{-}}{e}^{\ensuremath{-}})$, ${\mathrm{T}}^{\ensuremath{-}}({p}^{+}{e}^{\ensuremath{-}}{e}^{\ensuremath{-}})$, $^{4}\mathrm{He}(h{e}^{+2}{e}^{\ensuremath{-}}{e}^{\ensuremath{-}})$, and the following molecular ions: ${\mathrm{Ps}}_{2}^{+}({e}^{\ensuremath{-}}{e}^{+}{e}^{+})$, ${\mathrm{H}}_{2}^{+}({e}^{\ensuremath{-}}{p}^{+}{p}^{+})$, $\mathrm{H}{\mathrm{D}}^{+}({e}^{\ensuremath{-}}{d}^{+}{p}^{+})$, ${\mathrm{HT}}^{+}({e}^{\ensuremath{-}}{t}^{+}{p}^{+})$, ${\mathrm{DT}}^{+}({e}^{\ensuremath{-}}{d}^{+}{t}^{+})$, ${\mathrm{D}}_{2}^{+}({e}^{\ensuremath{-}}{d}^{+}{d}^{+})$, ${\mathrm{T}}_{2}^{+}({e}^{\ensuremath{-}}{t}^{+}{t}^{+})$. The muonic and antiprotonic families are similar to the electronic ones except that the species are formed replacing ${e}^{\ensuremath{-}}$ by ${\ensuremath{\mu}}^{\ensuremath{-}}$ or ${p}^{\ensuremath{-}}$. The pionic family comprises exotic atoms containing at least one pion. We also apply these results to two-electron three-dimensional spherical quantum dots and for these systems we examine the effect of electronic correlation, particularly on the singlet-triplet transitions and on the collective motion of the electrons and center of mass leading to ``floppy''dynamics.

Physical Review A•Oct 6, 2006•18 citations

Time-Dependent Perturbation Theory

Z. Ficek

Consider a two-level atom represented by the spin operators σ ^ ± , σ ^ Z , https://s3-euw1-ap-pe-df-pch-content-public-p.s3.eu-west-1.amazonaws.com/9780429092053/5e12ab0e-ba42-4caa-9bdf-6325e9117d3e/content/ineqn19_1.tif"/> interacting with a one-dimensional harmonic oscillator, represented by the creation and annihilation operators â † and â . The Hamiltonian of the system is given by ( 19.1 ) H ^ = 1 2 ℏ ω 0 σ ^ Z + ℏ w 0 ( a ^ † a ^ + 1 2 )− 1 2 i ℏ g + ( σ ^ + a ^ − σ ^ − a ^ † ) . https://s3-euw1-ap-pe-df-pch-content-public-p.s3.eu-west-1.amazonaws.com/9780429092053/5e12ab0e-ba42-4caa-9bdf-6325e9117d3e/content/eqn19_1.tif"/>

•Apr 27, 2016•0 citations
Abstract Protonium is a type of onium consisting of a proton (p) and an anti-proton ( <?CDATA $ \bar p $?> p ¯ ) which is called antiprotonic hydrogen. Since the proton and the anti-particle have the same mass, and each of them is a fermion, the Hamiltonian form of this system consists of the kinetic energy terms of each particle, the potential energy, and the spin interactions of both (hyperfine structure). To simplify the analysis, the Hamiltonian is then converted into a Hamiltonian which contains the relative motion terms of the two particles. This new Hamiltonian contains their reduced mass because the two particles orbit each other towards a certain center of mass. In the initial state, t < 0, the system is in the ground state and then at 0 < t < τ, the system is given a disturbance of the form <?CDATA $ V(t) = ({V_0} + {V_1}\,r\,\sin \theta \,{e^{i\phi }})\,\cos (\omega t)\,{\hat \sigma _p}.\hat x $?> V ( t ) = ( V 0 + V 1 r sin θ e i ϕ ) cos ( ω t ) σ ^ p . x ^ , where V 0 is a constant, V 1 is a constant and very small, <?CDATA $ {\hat \sigma _p} $?> σ ^ p is the Pauli matrix for proton, and <?CDATA $ \hat x $?> x ^ is the three-dimensional position operator in spherical coordinates. We analyze this system using a time-dependent perturbation theory that begins by defining the initial state, then calculating the transition amplitude for the new state when the perturbation is applied to the system. From the results of this calculation, we compute the system transition probability. We find that the transition probability of this system can only occur for the following quantum number terms, namely n even positive integer, l = 2,S = 1, and with the certain combinations of m and M.
During the presence of the radiation perturbation ( ),ˆ tV the Hamiltonian of the system becomes ( )tVHH ˆˆˆ 0 += (37.4) and, since the state of the system varies with time, we must adopt the time-dependent Schrödinger equation to be a basis for the perturbation theory, that is ( ) ( ) ( )0ˆ ˆti H V tt ∂Ψ ⎡ ⎤= + Ψ⎣ ⎦∂= t (37.5) We assume that Eq.(37.5) has normalized solutions which can be expanded in terms of the as 0kΨ t a t t a t e ε−Ψ = Ψ = Ψ∑ ∑ = (37.6) where the normalization condition on ( )tΨ gives a t =∑ (37.7) that is, ( ) 2ka t gives the probability that the system is in the state at time t. Substituting Eq.(37.6) into Eq.(37.5) yields da t ii a t e V t a t e dt ε εε ε− −⎡ ⎤ ⎡ ⎤− Ψ = +⎢ ⎥ ⎣ ⎦⎣ ⎦∑ ∑ = == = which reduces to da t i e V t a t e dt ε− k ε−Ψ = Ψ∑ ∑= == (37.8) In view of orthogonality of the stationary state eigenfunctions, multiplication by ( ) followed by integration over the configuration space gives da t i e a t e V t dt ε εδ− −= Ψ Ψ∑ ∑= == (37.9) Denoting the matrix elements of the perturbation operator between the stationary states n and k by ( ) ( )0 ˆnk n kV t V t 0= Ψ Ψ (37.10) we can rewrite Eq.(37.9) as da t i a t V t e dt ε ε−= ∑ == (37.11) which is a set of simultaneous differential equations of the first order for the coefficients ( ).na t If we assume that the system is in a definite stationary state at some 0iΨ particular time 0,t = and then it is allowed to interact with the radiation field, we obtain from Eq.(37.6) that ( ) ( )0 00 0i k k aΨ = Ψ = Ψk∑ Multiplying by and integrating gives ( )∗Ψ 0k ( )0ka kiδ= (37.12) that is, and for .( ) 10 =ia ( ) 00 =ka ik ≠ If we consider a time interval t sufficiently short for the coefficients in Eqs.(37.11) to be approximated by the form (37.12), which means that the term gives the greatest contribution to the sum and all other terms can be neglected, we have ( )tak ik = ( ) ( ) ( )0 0 /n ii tn nida ti V t edt ε ε−= == , ( ) ( ) ( )i i iida ti a t Vdt == t (37.13) and on integration we obtain ( ) ( ) ( ) (0 0 / 0 ia t V t e dt n iε ε ′− ′= − ≠∫ == ) , ( ) ( ) tdtVita iii ′′−= ∫ 0 1 = (37.14) The probability (29.29) that the system is in the state at time t, in other words, that coincides with is given by ( )tΨ ,0nΨ ( ) ( ) ( )2 20in n nP t t a t= Ψ Ψ = (37.15) and this is taken to be the probability of direct transition from state to state in a time t, induced by the presence of the radiation field. Assuming a transition where a photon is emitted, that is, we recall the Bohr condition (28.19), which reads ,00 ni εε > (37.16) inni ωεε ==− 00 so that Eqs.(37.14) can be rewritten as ( ) ( ) ( ) 0 n ni ia t V t e dt n iω ′−′ ′= − ≠∫= (37.17) ( ) ( ) 0 1 t i ii ia t V t dt′ ′= − ∫= As we can see from the above, the time-dependent perturbation theory is concerned with transitions that result from perturbation, between the unperturbed levels of the system, while time-independent perturbation theory calculates the stationary shifts in the energy levels. 37.2. FERMI'S GOLDEN RULE Consider the case of a constant perturbation, switched on at time The integrals (37.17) become straightforward, and we obtain .0=t ( ) ( ) ( )1ini tnin in Va t e n iωω −= − ≠= (37.18) ( ) tVita iii =−=1 Substituting Eqs.(37.18) into Eq.(37.6) gives, to a first approximation, the wave function of the atomic system as Vt e t e tωω − − ≠ Ψ = Ψ + − Ψ∑= = (37.19) The probability (37.15) of observing the system in the state at time t, for the coefficients given by Eq.(37.18), reduces to 0 nΨ( )tan ( ) ( 2/sin4 222 2 t V ni in ωω== ) (37.20) which means that transitions from state to states only take place if the matrix elements do not vanish. The plot of niV ( )tPin as a function of inω , given in Figure 37.1 for a perturbation which is on for a time t, suggests that the probability behaves like a Dirac δ -function as t approaches infinity. We may represent the δ -function as ( ) dxe t t 2 1lim 2/ 2/sin lim ωππω ω ( ) ( ininxi dxe in ωδωδπ ω 22/2 1 2/ === ∫ ∞ ∞− ) (37.21) where use was made of a property derived from the normalization condition, written as ( ) ( ) ( ) ( ) ( )u k kukudkuduu δδδδ 1or1 === ∫∫ ∞ P t( ) ω4π6π t2π in t-t-t 2π 4π t 6π t0 Figure 37.1. Dependence of the transition probability on frequency It follows from Figure 37.1 that, in the large-t limit, we have ,0≅inω and hence ( )2sin / 2 / 1.in int tω ω⎡ →⎣ ⎤⎦ Thus, one obtains ( ) ( ) ( ) ( ) (2 24sin / 2 sin / 2 sin / 2lim lim / 2 2/ 2 / 2in in in in int t in inin t t t tt ω ω ω )π πδ ω πδ ωω πωω→∞ →∞ ⎡ ⎤= =⎢ ⎥⎣ ⎦ = so that the transition probability becomes ( ) ( ) (2 2 0 022 2lim in ni in ni i nt t tP t V Vπ π )δ ω δ ε→∞ = = == ε− (37.23) It follows that the transitions take place between states of equal unperturbed energies The transition probability is proportional to the time interval t during which the perturbation is on, that is .00 in εε → ( )tPin approaches infinity as .∞→t Since no experiment lasts for an infinite time, it is the transition probability per unit time, called the transition rate , which is of particular interest. Normally, is part of a continuum, and hence, the transition might end in any state which belongs to a finite range of N final states, rather than in a particular state. We may then define the transition rate as ( )dNtP t P intni ∫∞→→ = 1lim (37.24) The integral over the final states is usually transformed into one over energy, if we define a density of states ( ) ,ρ ε representing the number of continuum states per energy interval, by taking ( )0ndN d 0nρ ε ε= (37.25) so that, substituting Eqs.(37.23) and (37.25), Eq.(37.24) gives ( ) ( ) ( ) ( )20 0 0 0 01 2limi n in n n ni n i ntP P t d Vt πρ ε ε ρ ε δ ε ε→ →∞= =∫ = − (37.26) This result is known as Fermi's golden rule, which states that transitions may occur only between states of equal energies for which the matrix elements of the perturbation operator do not vanish, and that the transition rate is proportional to both the square modulus of these matrix elements and the density of final states. 37.3. EMISSION AND ABSORPTION OF RADIATION Consider the transitions between stationary states which are induced by a harmonic perturbation of the form ( ) ( ) ( ) ( ) ( )( )titi eeArVtArVtV ωωωωω −+== GG ˆcosˆ2ˆ (37.27) It is assumed that the harmonic perturbation corresponds to the interaction of either the electric or magnetic field components of the incoming radiation with the electric or magnetic moment of the atom. Thus, the coupling between the system and the perturbing field can be taken in the form of a field amplitude ( )ωA times a displacement of the system ( ).ˆ rV G On substitution of Eq.(37.27) into Eq.(37.10) one obtains ( ) ( ) ( )( ) ( )( )titinititiinni eeAVeeArVtV ωωωω ωω −− +=+ΨΨ= 00 ˆ G (37.28) It follows from Eq.(37.17) that n ni ia t V A e e dtω ω ω ωω ′ ′− − − +⎡ ⎤ ′= − +⎣ ⎦∫= (37.29) inin eeAV 0 ⎥⎦ ⎤⎢⎣ ⎡ ++−= ωωωω ω ωωωω V A e eω ω ω ωω ω ω ω ω − − − +⎡ ⎤− −= +⎢ ⎥− +⎢ ⎥⎣ ⎦= If the atomic system is bathed into a radiation field of frequency ,inni ωωω −== which implies that according to the Bohr condition (37.16), the transition from state to state describes a process of induced absorption, where the energy of the system is increased by energy transfer from the radiation field to the atom. If 00 in εε > ,ni inω ω ω= = − the second term on the right-hand side of Eq.(37.29) grows without limit, so that the first term can be neglected.
We now consider systems for which the Hamiltonian contains time-dependent interaction terms. In such cases we cannot reduce the time-dependent Schro¨dinger equation to an eigenvalue equation. However, if the time-dependent terms can be regarded as small perturbations, we can develop a form of perturbation theory that can be used to calculate the effects of time-dependent terms. Consider a system for which the Hamiltonian may be written as the sum of a dominant unperturbed part Hˆ0 and a small perturbation Hˆ ′ as Hˆ = Hˆ0 + λHˆ ′(t) , (10.1.1) where the unperturbed Hamiltonian Hˆ0 is independent of time, whereas the perturbation Hˆ ′ may depend on time. The parameter 0 < λ < 1 has been introduced to keep track of various orders of approximations as in the case of time-independent perturbation theory discussed in Chapter 8. The basic idea is that a small perturbation to the Hamiltonian will produce a small change in the wave function. For a time-dependent perturbation, this change means that a system, initially in a particular eigenstate of Hˆ0, will find itself in a time-dependent admixture of the eigenstates. Thus the time-dependent perturbation causes the system to undergo transition to different eigenstates of Hˆ0. So for time-dependent perturbations our interest lies in calculating the probabilities for transition to different states.
Abstract We analyze a quantum system of two distinguishable spin − 1 2 particles subjected to modified sinusoidal perturbation of the form V ( t ) = ( V 0 + V 1 x + V 2 y + V 3 z ) e − γ t / τ cos ( ω t ) σ → 1 · x ^ ; 0 < t < τ ; where γ is a real positive number; V 0, V 1, V 2, V 3 are real constants and have very small values; x = r sin θ cos ϕ; y = r sin θ sin ϕ; = z = r cos θ; σ → 1 is the Pauli matrix for the first particle, and x ^ , is the three-dimensional position operator in spherical coordinates; V(t) is zero when t ≤ 0 and t ≥ τ. We use the time-dependent perturbation theory to solve this problem. Initially, we define the initial system state before being subjected to perturbation, namely | 000 ; 00 〉 , and the final state of the form | n l m ; S M 〉 ≡ | n l m 〉 | ⊗ S M 〉 . The total spin state | S M 〉 actually contains the linear combination of the states of each particle. Next, we calculate the expected value of 〈
A Hookean model of a three-body problem for particles with arbitrary masses and charges where two of them interact with each other through a Coulomb potential and with the third through a harmonic potential is presented. It is shown that a condition relating the masses to the harmonic coupling constants must be satisfied in order to render this problem separable. A general exact analytic solution written in terms of the relative interparticle coordinates is given as well as general expressions for the total and binding energies of this three-body system. We apply these results to examine electronic, muonic, antiprotonic, and pionic families of non-Born-Oppenheimer Hookean systems. The first contains the atoms or atomic ions: ${\mathrm{Ps}}^{\ensuremath{-}}({e}^{+}{e}^{\ensuremath{-}}{e}^{\ensuremath{-}})$, ${\mathrm{H}}^{\ensuremath{-}}({p}^{+}{e}^{\ensuremath{-}}{e}^{\ensuremath{-}})$, ${\mathrm{D}}^{\ensuremath{-}}({d}^{+}{e}^{\ensuremath{-}}{e}^{\ensuremath{-}})$, ${\mathrm{T}}^{\ensuremath{-}}({p}^{+}{e}^{\ensuremath{-}}{e}^{\ensuremath{-}})$, $^{4}\mathrm{He}(h{e}^{+2}{e}^{\ensuremath{-}}{e}^{\ensuremath{-}})$, and the following molecular ions: ${\mathrm{Ps}}_{2}^{+}({e}^{\ensuremath{-}}{e}^{+}{e}^{+})$, ${\mathrm{H}}_{2}^{+}({e}^{\ensuremath{-}}{p}^{+}{p}^{+})$, $\mathrm{H}{\mathrm{D}}^{+}({e}^{\ensuremath{-}}{d}^{+}{p}^{+})$, ${\mathrm{HT}}^{+}({e}^{\ensuremath{-}}{t}^{+}{p}^{+})$, ${\mathrm{DT}}^{+}({e}^{\ensuremath{-}}{d}^{+}{t}^{+})$, ${\mathrm{D}}_{2}^{+}({e}^{\ensuremath{-}}{d}^{+}{d}^{+})$, ${\mathrm{T}}_{2}^{+}({e}^{\ensuremath{-}}{t}^{+}{t}^{+})$. The muonic and antiprotonic families are similar to the electronic ones except that the species are formed replacing ${e}^{\ensuremath{-}}$ by ${\ensuremath{\mu}}^{\ensuremath{-}}$ or ${p}^{\ensuremath{-}}$. The pionic family comprises exotic atoms containing at least one pion. We also apply these results to two-electron three-dimensional spherical quantum dots and for these systems we examine the effect of electronic correlation, particularly on the singlet-triplet transitions and on the collective motion of the electrons and center of mass leading to ``floppy''dynamics.
Consider a two-level atom represented by the spin operators σ ^ ± , σ ^ Z , https://s3-euw1-ap-pe-df-pch-content-public-p.s3.eu-west-1.amazonaws.com/9780429092053/5e12ab0e-ba42-4caa-9bdf-6325e9117d3e/content/ineqn19_1.tif"/> interacting with a one-dimensional harmonic oscillator, represented by the creation and annihilation operators â † and â . The Hamiltonian of the system is given by ( 19.1 ) H ^ = 1 2 ℏ ω 0 σ ^ Z + ℏ w 0 ( a ^ † a ^ + 1 2 )− 1 2 i ℏ g + ( σ ^ + a ^ − σ ^ − a ^ † ) . https://s3-euw1-ap-pe-df-pch-content-public-p.s3.eu-west-1.amazonaws.com/9780429092053/5e12ab0e-ba42-4caa-9bdf-6325e9117d3e/content/eqn19_1.tif"/>