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CRC Press eBooks

Atomic Radiation

M.S. Rogalski, Stuart B. Palmer

Published Nov 5, 2020• 0 citations
Publisher

Abstract

The states of the atom, determined by the motion of electrons, are stationary in the presence of all internal atomic forces and of interactions with constant external fields. When electrons interact with the field associated with electromagnetic radiation, the atomic states are no longer stationary, and the time-dependent perturbation treatment has to be applied to calculate the effect produced by the radiation, which is a function of time. Consequently, as shown in Section 9.3 , the time evolution of the atom will be described in terms of transitions between the stationary states of the unperturbed atomic system.

DOI
10.1201/9781003078265-12

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

The interaction of atoms and radiation

D.G.C. Jones

The basic phenomena of interaction between atoms and e.m. fields can be discussed in some detail without the need of a detailed model of the atom. Absorption and stimulated emission of radiation can be explained satisfactorily by the theory, where a classical electromagnetic wave provides a time-dependent perturbation to the energy of the atomic electrons. Laser radiation appears to a very good approximation to be a classical travelling wave of well-defined amplitude and phase. The radiation produced by a continuous laser is a good approximation to a coherent state. For conventional sources of radiation, the interaction energy is small compared with the energy an electron possesses by virtue of the attraction to the atomic nucleus, so perturbation theory produces quite acceptable results. The quantum mechanical analogy to the distortion of the classical charge cloud is given by the writing down of a general state function for the system, Ψ.

Routledge eBooks•May 3, 2018•0 citations

Transitions

P. C. W. Davies, David S. Betts

In many practical cases a stationary system is perturbed in some way, inducing it to undergo transitions between the otherwise stationary states. Perhaps the best example concerns the radiative transitions of atomic electrons in which the disturbance of an external electromagnetic field causes the electrons to jump between energy levels, emitting or absorbing photons. Equation is a statement of the classical law of conservation of energy. The stimulated emission and absorption of radiation both have close classical analogues. If a simple harmonic oscillator is driven by a sinusoidal electromagnetic field it can gain or lose energy depending on phase angles. The existence of spontaneous emission implies that all excited states of electrical systems are unstable and will eventually decay to the ground state by photon emission. Quantum systems thus comply with the fundamental principle that physical systems tend to seek out their state of lowest energy and maximum entropy.

Routledge eBooks•Apr 27, 2018•0 citations

Radiative transition rates and selection rules

B. Henderson, G. F. Imbusch

Abstract Although the discussion in the preceding two chapters concentrated on the stationary states of an electronic system, the need to consider perturbations which mix stationary states and thereby excite transitions between these states was noted. In this chapter we apply time-dependent perturbation theory to estimate the rates of such transitions, first by developing a general formula for the transition probability between initial |i〉 and final |f〇 states; if the initial state |i〉 is lower in energy than |f〇 an absorption transition is involved, whereas if |f〇 is the lower state emission takes place. We then consider in some detail how such transitions are caused by interactions between the electronic system and the radiation field.

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The laser–atom interaction

Bruce W. Shore

As light passes an atom, it exerts forces on the charges, electrons, and nuclei that alter the atomic structure. These may be slight distortions (perturbations) of the electron cloud or they may be more severe, as described in subsequent sections of this monograph. We wish to determine those changes, given the radiation field, or to devise a radiation field that will produce specified changes. The changes to the atomic structure also affect the radiation that subsequently passes the atom. To describe those effects we must consider wave equations for radiation in the presence of altered atomic structure. More generally we must find self-consistent equations for the atoms and the field together, as discussed in Chaps. 21 and 22. Here we consider mathematical descriptions of the influence of coherent radiation on individual atoms, molecules, or other single quantum systems. Individual atoms Traditional sources of emission and absorption spectra, though revealing energy states of the constituent atoms and molecules, are macroscopic samples. One observes averaged characteristics of many individual particles, see Chap. 16. Quantum theory offers the basic formalism for dealing with individual atoms exposed to controlled radiation fields. Several experimental techniques provide acceptable approximations to this ideal. The following paragraphs note some of these examples. Vapors Neutral atoms or molecules in a vapor move freely along straight-line paths, interrupted by brief collisions that redirect the two collision partners. When the kinetic energies of the two partners are small, there can be no transfer of kinetic energy into internal energy of either particle – the collision is elastic .

Cambridge University Press eBooks•Sep 29, 2011•0 citations

The interaction of radiation and matter

P. M. Davidson

Abstract This paper is based on the idea that wave mechanics is primarily suitable for giving an indirect description of nature. The world to which the equations of the, theory here proposed are directly applicable is an unnatural one, containing sources and sinks of matter which give to its radiational laws a symmetry lacking in nature. The theory may be regarded as consisting of two postulates. The first (which may, if desired, be regarded as a definition) specifies the character and properties of an unnatural assembly of systems, each consisting of an electron in a static potential field U. It states that, of the energy radiated in an elementary solid angle of standard magnitude, the part which will pass through an analyzer which transmits the component of electric field in a given direction (perpendicular to the line of observation) is determined by applying the usual Schrödinger interpretations (of density, current and material energy) to a Schrödinger equation perturbed by a term which is a certain constant multiplied by the electric field, in that direction, acting on the electron, due to the potential field U. (For comparison with classical radiation theory, it will be noted that the perturbation term vanishes in any region in which, from the classical standpoint, the electron is not accelerated, in that direction, by the field U). In the process of specifying the radiation from the assembly, the Schrödinger interpretations will have specified also the nature and magnitude of the sources and sinks of electrons (each in a field U). Their presence is due, mathematically speaking, to the multiplying constant mentioned above being a complex quantity. From these results the properties of a natural assembly are specified by means of the second postulate, which states that when the sources and sinks are removed, any process which in their absence is meaningless or physically inconceivable will cease, and all other processes will remain unaffected. The calculation is readily extended to include the effect of an external field of radiation. The theory requires no representation of radiation other than the Maxwellian wave, and will be free from the difficulties encountered in other theories.

Proceedings of the Royal Society of London A Mathematical and Physical Sciences•Dec 3, 1947•2 citations
The states of the atom, determined by the motion of electrons, are stationary in the presence of all internal atomic forces and of interactions with constant external fields. When electrons interact with the field associated with electromagnetic radiation, the atomic states are no longer stationary, and the time-dependent perturbation treatment has to be applied to calculate the effect produced by the radiation, which is a function of time. Consequently, as shown in Section 9.3 , the time evolution of the atom will be described in terms of transitions between the stationary states of the unperturbed atomic system.
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.
The basic phenomena of interaction between atoms and e.m. fields can be discussed in some detail without the need of a detailed model of the atom. Absorption and stimulated emission of radiation can be explained satisfactorily by the theory, where a classical electromagnetic wave provides a time-dependent perturbation to the energy of the atomic electrons. Laser radiation appears to a very good approximation to be a classical travelling wave of well-defined amplitude and phase. The radiation produced by a continuous laser is a good approximation to a coherent state. For conventional sources of radiation, the interaction energy is small compared with the energy an electron possesses by virtue of the attraction to the atomic nucleus, so perturbation theory produces quite acceptable results. The quantum mechanical analogy to the distortion of the classical charge cloud is given by the writing down of a general state function for the system, Ψ.
In many practical cases a stationary system is perturbed in some way, inducing it to undergo transitions between the otherwise stationary states. Perhaps the best example concerns the radiative transitions of atomic electrons in which the disturbance of an external electromagnetic field causes the electrons to jump between energy levels, emitting or absorbing photons. Equation is a statement of the classical law of conservation of energy. The stimulated emission and absorption of radiation both have close classical analogues. If a simple harmonic oscillator is driven by a sinusoidal electromagnetic field it can gain or lose energy depending on phase angles. The existence of spontaneous emission implies that all excited states of electrical systems are unstable and will eventually decay to the ground state by photon emission. Quantum systems thus comply with the fundamental principle that physical systems tend to seek out their state of lowest energy and maximum entropy.
Abstract Although the discussion in the preceding two chapters concentrated on the stationary states of an electronic system, the need to consider perturbations which mix stationary states and thereby excite transitions between these states was noted. In this chapter we apply time-dependent perturbation theory to estimate the rates of such transitions, first by developing a general formula for the transition probability between initial |i〉 and final |f〇 states; if the initial state |i〉 is lower in energy than |f〇 an absorption transition is involved, whereas if |f〇 is the lower state emission takes place. We then consider in some detail how such transitions are caused by interactions between the electronic system and the radiation field.
As light passes an atom, it exerts forces on the charges, electrons, and nuclei that alter the atomic structure. These may be slight distortions (perturbations) of the electron cloud or they may be more severe, as described in subsequent sections of this monograph. We wish to determine those changes, given the radiation field, or to devise a radiation field that will produce specified changes. The changes to the atomic structure also affect the radiation that subsequently passes the atom. To describe those effects we must consider wave equations for radiation in the presence of altered atomic structure. More generally we must find self-consistent equations for the atoms and the field together, as discussed in Chaps. 21 and 22. Here we consider mathematical descriptions of the influence of coherent radiation on individual atoms, molecules, or other single quantum systems. Individual atoms Traditional sources of emission and absorption spectra, though revealing energy states of the constituent atoms and molecules, are macroscopic samples. One observes averaged characteristics of many individual particles, see Chap. 16. Quantum theory offers the basic formalism for dealing with individual atoms exposed to controlled radiation fields. Several experimental techniques provide acceptable approximations to this ideal. The following paragraphs note some of these examples. Vapors Neutral atoms or molecules in a vapor move freely along straight-line paths, interrupted by brief collisions that redirect the two collision partners. When the kinetic energies of the two partners are small, there can be no transfer of kinetic energy into internal energy of either particle – the collision is elastic .
Abstract This paper is based on the idea that wave mechanics is primarily suitable for giving an indirect description of nature. The world to which the equations of the, theory here proposed are directly applicable is an unnatural one, containing sources and sinks of matter which give to its radiational laws a symmetry lacking in nature. The theory may be regarded as consisting of two postulates. The first (which may, if desired, be regarded as a definition) specifies the character and properties of an unnatural assembly of systems, each consisting of an electron in a static potential field U. It states that, of the energy radiated in an elementary solid angle of standard magnitude, the part which will pass through an analyzer which transmits the component of electric field in a given direction (perpendicular to the line of observation) is determined by applying the usual Schrödinger interpretations (of density, current and material energy) to a Schrödinger equation perturbed by a term which is a certain constant multiplied by the electric field, in that direction, acting on the electron, due to the potential field U. (For comparison with classical radiation theory, it will be noted that the perturbation term vanishes in any region in which, from the classical standpoint, the electron is not accelerated, in that direction, by the field U). In the process of specifying the radiation from the assembly, the Schrödinger interpretations will have specified also the nature and magnitude of the sources and sinks of electrons (each in a field U). Their presence is due, mathematically speaking, to the multiplying constant mentioned above being a complex quantity. From these results the properties of a natural assembly are specified by means of the second postulate, which states that when the sources and sinks are removed, any process which in their absence is meaningless or physically inconceivable will cease, and all other processes will remain unaffected. The calculation is readily extended to include the effect of an external field of radiation. The theory requires no representation of radiation other than the Maxwellian wave, and will be free from the difficulties encountered in other theories.