Formula that describes the transition rate from one energy eigenstate of a quantum system into other energy eigenstates
In quantum physics, Fermi's golden rule is a formula that describes the transition rate (the probability of a transition per unit time) from one energy eigenstate of a quantum system to a group of energy eigenstates in a continuum, as a result of a weak perturbation. This transition rate is effectively independent of time (so long as the strength of the perturbation is independent of time) and is proportional to the strength of the coupling between the initial and final states of the system (described by the square of the matrix element of the perturbation) as well as the density of states. It is also applicable when the final state is discrete, i.e. it is not part of a continuum, if there is some decoherence in the process, like relaxation or collision of the atoms, or like noise in the perturbation, in which case the density of states is replaced by the reciprocal of the decoherence bandwidth.
Although named after Enrico Fermi, most of the work leading to the "golden rule" is due to Paul Dirac, who formulated 20 years earlier a virtually identical equation, including the three components of a constant, the matrix element of the perturbation and an energy difference.[1][2] It was given this name because, on account of its importance, Fermi called it "golden rule No.2".[3]
Most uses of the term Fermi's golden rule are referring to "golden rule No.2", however, Fermi's "golden rule No.1" is of a similar form and considers the probability of indirect transitions per unit time.[4]
Fermi's golden rule describes a system that begins in an eigenstate | i {displaystyle |irangle } of an unperturbed Hamiltonian H0 and considers the effect of a perturbing Hamiltonian H' applied to the system. If H' is time-independent, the system goes only into those states in the continuum that have the same energy as the initial state. If H' is oscillating sinusoidally as a function of time (i.e. it is a harmonic perturbation) with an angular frequency , the transition is into states with energies that differ by from the energy of the initial state.
In both cases, the transition probability per unit of time from the initial state | i {displaystyle |irangle } to a set of final states | f {displaystyle |frangle } is essentially constant. It is given, to first-order approximation, by
where f | H | i {displaystyle langle f|H'|irangle } is the matrix element (in braket notation) of the perturbation H' between the final and initial states, and ( E f ) {displaystyle rho (E_{f})} is the density of states (number of continuum states divided by d E {displaystyle dE} in the infinitesimally small energy interval E {displaystyle E} to E + d E {displaystyle E+dE} ) at the energy E f {displaystyle E_{f}} of the final states. This transition probability is also called "decay probability" and is related to the inverse of the mean lifetime. Thus, the probability of finding the system in state | i {displaystyle |irangle } is proportional to e i f t {displaystyle e^{-Gamma _{ito f}t}} .
The standard way to derive the equation is to start with time-dependent perturbation theory and to take the limit for absorption under the assumption that the time of the measurement is much larger than the time needed for the transition.[5][6]
The golden rule is a straightforward consequence of the Schrdinger equation, solved to lowest order in the perturbation H' of the Hamiltonian. The total Hamiltonian is the sum of an original Hamiltonian H0 and a perturbation: H = H 0 + H ( t ) {displaystyle H=H_{0}+H'(t)} . In the interaction picture, we can expand an arbitrary quantum states time evolution in terms of energy eigenstates of the unperturbed system | n {displaystyle |nrangle } , with H 0 | n = E n | n {displaystyle H_{0}|nrangle =E_{n}|nrangle } .
We first consider the case where the final states are discrete. The expansion of a state in the perturbed system at a time t is | ( t ) = n a n ( t ) e i E n t / | n {displaystyle |psi (t)rangle =sum _{n}a_{n}(t)e^{-iE_{n}t/hbar }|nrangle } . The coefficients an(t) are yet unknown functions of time yielding the probability amplitudes in the Dirac picture. This state obeys the time-dependent Schrdinger equation:
Expanding the Hamiltonian and the state, we see that, to first order,
( H 0 + H i t ) n a n ( t ) | n e i t E n / = 0 , {displaystyle left(H_{0}+H'-mathrm {i} hbar {frac {partial }{partial t}}right)sum _{n}a_{n}(t)|nrangle e^{-mathrm {i} tE_{n}/hbar }=0,} where En and |n are the stationary eigenvalues and eigenfunctions of H0.
This equation can be rewritten as a system of differential equations specifying the time evolution of the coefficients a n ( t ) {displaystyle a_{n}(t)} :
This equation is exact, but normally cannot be solved in practice.
For a weak constant perturbation H' that turns on at t = 0, we can use perturbation theory. Namely, if H = 0 {displaystyle H'=0} , it is evident that a n ( t ) = n , i {displaystyle a_{n}(t)=delta _{n,i}} , which simply says that the system stays in the initial state i {displaystyle i} .
For states k i {displaystyle kneq i} , a k ( t ) {displaystyle a_{k}(t)} becomes non-zero due to H 0 {displaystyle H'neq 0} , and these are assumed to be small due to the weak perturbation. The coefficient a i ( t ) {displaystyle a_{i}(t)} which is unity in the unperturbed state, will have a weak contribution from H {displaystyle H'} . Hence, one can plug in the zeroth-order form a n ( t ) = n , i {displaystyle a_{n}(t)=delta _{n,i}} into the above equation to get the first correction for the amplitudes a k ( t ) {displaystyle a_{k}(t)} :
whose integral can be expressed as
with k i ( E k E i ) / {displaystyle omega _{ki}equiv (E_{k}-E_{i})/hbar } , for a state with ai(0) = 1, ak(0) = 0, transitioning to a state with ak(t).
The probability of transition from the initial state (ith) to the final state (fth) is given by
It is important study a periodic perturbation with a given frequency {displaystyle omega } since arbitrary perturbations can be constructed from periodic perturbations of different frequencies. Since H ( t ) {displaystyle H'(t)} must be Hermitian, we must assume H ( t ) = F e i t + F e i t {displaystyle H'(t)=Fe^{-mathrm {i} omega t}+F^{dagger }e^{mathrm {i} omega t}} , where F {displaystyle F} is a time independent operator. The solution for this case is[7]
This expression is valid only when the denominators in the above expression is non-zero, i.e., for a given initial state with energy E i {displaystyle E_{i}} , the final state energy must be such that E f E i . {displaystyle E_{f}-E_{i}neq pm hbar omega .} Not only the denominators must be non-zero, but also must not be small since a f {displaystyle a_{f}} is supposed to be small.
Since the continuous spectrum lies above the discrete spectrum, E f E i > 0 {displaystyle E_{f}-E_{i}>0} and it is clear from the previous section, major role is played by the energies E f {displaystyle E_{f}} lying near the resonance energy E i + {displaystyle E_{i}+hbar omega } , i.e., when f i {displaystyle omega _{fi}approx omega } . In this case, it is sufficient to keep only the first term for a f ( t ) {displaystyle a_{f}(t)} . Assuming that perturbations are turned on from time t = 0 {displaystyle t=0} , we have then
The squared modulus of a f {displaystyle a_{f}} is
For large t {displaystyle t} , this will reduce to
a linear dependence on t {displaystyle t} .
The probability of transition from the ith state to final states lying in an interval d f {displaystyle dnu _{f}} (density of states in an infinitesimal element around E f {displaystyle E_{f}} ) is d w f i = | a f | 2 d f {displaystyle dw_{fi}=|a_{f}|^{2}dnu _{f}} . The transition probability per unit time is thus given by
The time dependence has vanished, and the constant decay rate of the golden rule follows.[8] As a constant, it underlies the exponential particle decay laws of radioactivity. (For excessively long times, however, the secular growth of the ak(t) terms invalidates lowest-order perturbation theory, which requires ak ai.)
Only the magnitude of the matrix element f | H | i {displaystyle langle f|H'|irangle } enters the Fermi's golden rule. The phase of this matrix element, however, contains separate information about the transition process.It appears in expressions that complement the golden rule in the semiclassical Boltzmann equation approach to electron transport.[9]
While the Golden rule is commonly stated and derived in the terms above, the final state (continuum) wave function is often rather vaguely described, and not normalized correctly (and the normalisation is used in the derivation). The problem is that in order to produce a continuum there can be no spatial confinement (which would necessarily discretise the spectrum), and therefore the continuum wave functions must have infinite extent, and in turn this means that the normalisation f | f = d 3 r | f ( r ) | 2 {displaystyle langle f|frangle =int d^{3}r|f(mathbf {r} )|^{2}} is infinite, not unity. If the interactions depend on the energy of the continuum state, but not any other quantum numbers, it is usual to normalise continuum wave-functions with energy {displaystyle epsilon } labelled | {displaystyle |epsilon rangle } , by writing | = ( ) {displaystyle langle epsilon |epsilon 'rangle =delta (epsilon -epsilon ')} where {displaystyle delta } is the Dirac delta function, and effectively a factor of the square-root of the density of states is included into | i {displaystyle |epsilon _{i}rangle } .[10] In this case, the continuum wave function has dimensions of 1 / {displaystyle 1/surd } [energy], and the Golden Rule is now
where i {displaystyle epsilon _{i}} refers to the continuum state with the same energy as the discrete state i {displaystyle i} . For example, correctly normalized continuum wave functions for the case of a free electron in the vicinity of a hydrogen atom are available in Bethe and Salpeter .[11]
The following paraphrases the treatment of Cohen-Tannoudji.[10] As before, the total Hamiltonian is the sum of an original Hamiltonian H0 and a perturbation: H = H 0 + H {displaystyle H=H_{0}+H'} . We can still expand an arbitrary quantum states time evolution in terms of energy eigenstates of the unperturbed system, but these now consist of discrete states and continuum states. We assume that the interactions depend on the energy of the continuum state, but not any other quantum numbers. The expansion in the relevant states in the Dirac picture is
where i = i / , = / {displaystyle omega _{i}=epsilon _{i}/hbar ,omega =epsilon /hbar } and i , {displaystyle epsilon _{i},epsilon } are the energies of states | i , | {displaystyle |irangle ,|epsilon rangle } . The integral is over the continuum C {displaystyle epsilon in C} , i.e. | {displaystyle |epsilon rangle } is in the continuum.
Substituting into the time-dependent Schrdinger equation
and premultiplying by i | {displaystyle langle i|} produces
where i = i | H | / {displaystyle Omega _{iepsilon }=langle i|H'|epsilon rangle /hbar } , and premultiplying by | {displaystyle langle epsilon '|} produces
We made use of the normalisation | = ( ) {displaystyle langle epsilon '|epsilon rangle =delta (epsilon '-epsilon )} .Integrating the latter and substituting into the former,
It can be seen here that d a i / d t {displaystyle da_{i}/dt} at time t {displaystyle t} depends on a i {displaystyle a_{i}} at all earlier times t {displaystyle t'} , i.e. it is non-Markovian. We make the Markov approximation, i.e. that it only depends on a i {displaystyle a_{i}} at time t {displaystyle t} (which is less restrictive than the approximation that a i {displaystyle a_{i}} 1 used above, and allows the perturbation to be strong)
where T = t t {displaystyle T=t-t'} and = i {displaystyle Delta =omega -omega _{i}} . Integrating over T {displaystyle T} ,
The fraction on the right is a nascent Dirac delta function, meaning it tends to ( i ) {displaystyle delta (epsilon -epsilon _{i})} as t {displaystyle tto infty } (ignoring its imaginary part which leads to an unimportant energy shift, while the real part produces decay [10]). Finally
which has solutions: a i ( t ) = exp ( i i t / 2 ) {displaystyle a_{i}(t)=exp(-Gamma _{ito epsilon _{i}}t/2)} , i.e., the decay of population in the initial discrete state is P i ( t ) = | a i ( t ) | 2 = exp ( i i t ) {displaystyle P_{i}(t)=|a_{i}(t)|^{2}=exp(-Gamma _{ito epsilon _{i}}t)} where
The Fermi golden rule can be used for calculating the transition probability rate for an electron that is excited by a photon from the valence band to the conduction band in a direct band-gap semiconductor, and also for when the electron recombines with the hole and emits a photon.[12] Consider a photon of frequency {displaystyle omega } and wavevector q {displaystyle {textbf {q}}} , where the light dispersion relation is = ( c / n ) | q | {displaystyle omega =(c/n)left|{textbf {q}}right|} and n {displaystyle n} is the index of refraction.
Using the Coulomb gauge where A = 0 {displaystyle nabla cdot {textbf {A}}=0} and V = 0 {displaystyle V=0} , the vector potential of the EM wave is given by A = A 0 e i ( q r t ) + C {displaystyle {textbf {A}}=A_{0}{vec {epsilon }}e^{i({textbf {q}}cdot {textbf {r}}-omega t)}+C} where the resulting electric field is
For a charged particle in the valence band, the Hamiltonian is
where V ( r ) {displaystyle V({textbf {r}})} is the potential of the crystal. If our particle is an electron ( Q = e {displaystyle Q=-e} ) and we consider process involving one photon and first order in A {displaystyle {textbf {A}}} . The resulting Hamiltonian is
where H {displaystyle H'} is the perturbation of the EM wave.
From here on we have transition probability based on time-dependent perturbation theory that
where {displaystyle {vec {epsilon }}} is the light polarization vector. From perturbation it is evident that the heart of the calculation lies in the matrix elements shown in the braket.
For the initial and final states in valence and conduction bands respectively, we have | i = v , k i , s i ( r ) {displaystyle |irangle =Psi _{v,{textbf {k}}_{i},s_{i}}({textbf {r}})} and | f = c , k f , s f ( r ) {displaystyle |frangle =Psi _{c,{textbf {k}}_{f},s_{f}}({textbf {r}})} , and if the H {displaystyle H'} operator does not act on the spin, the electron stays in the same spin state and hence we can write the wavefunctions as Bloch waves so
where N {displaystyle N} is the number of unit cells with volume 0 {displaystyle Omega _{0}} . Using these wavefunctions and with some more mathematics, and focusing on emission (photoluminescence) rather than absorption, we are led to the transition rate
where c v {displaystyle {boldsymbol {mu }}_{cv}} is the transition dipole moment matrix element is qualitatively the expectation value c | ( charge ) ( distance ) | v {displaystyle langle c|({text{charge}})times ({text{distance}})|vrangle } and in this situation takes the form
Finally, we want to know the total transition rate ( ) {displaystyle Gamma (omega )} . Hence we need to sum over all initial and final states (i.e. an integral of the Brillouin zone in the k-space), and take into account spin degeneracy, which through some mathematics results in
( ) = 4 ( e A 0 m 0 ) 2 | c v | 2 c v ( ) {displaystyle Gamma (omega )={frac {4pi }{hbar }}left({frac {eA_{0}}{m_{0}}}right)^{2}|{vec {epsilon }}cdot {boldsymbol {mu }}_{cv}|^{2}rho _{cv}(omega )}
where c v ( ) {displaystyle rho _{cv}(omega )} is the joint valence-conduction density of states (i.e. the density of pair of states; one occupied valence state, one empty conduction state). In 3D, this is
but the joint DOS is different for 2D, 1D, and 0D.
Finally we note that in a general way we can express the Fermi golden rule for semiconductors as[13]
In a scanning tunneling microscope, the Fermi golden rule is used in deriving the tunneling current. It takes the form
where M {displaystyle M} is the tunneling matrix element.
When considering energy level transitions between two discrete states, Fermi's golden rule is written as
where g ( ) {displaystyle g(hbar omega )} is the density of photon states at a given energy, {displaystyle hbar omega } is the photon energy, and {displaystyle omega } is the angular frequency. This alternative expression relies on the fact that there is a continuum of final (photon) states, i.e. the range of allowed photon energies is continuous.[14]
Fermi's golden rule predicts that the probability that an excited state will decay depends on the density of states. This can be seen experimentally by measuring the decay rate of a dipole near a mirror: as the presence of the mirror creates regions of higher and lower density of states, the measured decay rate depends on the distance between the mirror and the dipole.[15][16]
See more here:
Fermi's golden rule - Wikipedia
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