Diabatic transformation

In quantum chemistry, the solution of a set of coupled nuclear motion Schrödinger equations can be simplified by a diabatic transformation. Such a set of coupled equations, describing the (vibrational) motions of nuclei in a molecule, arises when the Born-Oppenheimer approximation breaks down. The term diabatic was coined in the early 1960s. Around that time shortcomings of the Born-Oppenheimer approximation (also known as the adiabatic approximation) became apparent and improvements of the adiabatic approximation were put forward under the name diabatic approximation. Linguistically the term is unfortunate because there is no connection whatsoever with the Greek word diabasis (going through).

Break-down of Born-Oppenheimer approximation

See the article Born-Oppenheimer approximation for more details.

The Born-Oppenheimer approximation, designed for the quantum mechanical computation of molecular properties, consists of two steps. In the first step the nuclei of a molecule are fixed in a certain constellation and the nuclear kinetic energies are dropped from the problem, i.e., the nuclei are assumed to be at rest. One or more electronic Schrödinger equations are solved yielding the corresponding (usually the lowest few) electronic energies. Changing sufficiently often the nuclear constellation of the molecule under study and solving the electronic Schrödinger equations over and over again, gives the electronic energies as functions of the nuclear coordinates. These functions are known as potential energy surfaces.

The second step of the original Born-Oppenheimer approximation consists of the solution of single (uncoupled) Schrödinger equations for the nuclei. In each of these equation the nuclear kinetic energy is reintroduced and one of the single potential energy surfaces (obtained from the first step) serves as potential. This simple approximation breaks down when the potential energy surfaces approach—or maybe even intersect—each other. In that case the nuclear motion equations, which are coupled by nuclear kinetic energy terms, may no longer be taken to be uncoupled, that is, the off-diagonal nuclear kinetic energy terms coupling the equations may no longer be neglected.

In short, when the Born-Oppenheimer approximation breaks down because of the presence of close lying potential energy surfaces, the solution of the nuclear motion problem requires the solution of a coupled set of Schrödinger equations. A diabatic transformation of this set of equations has the purpose of making them easier to solve. It is a linear (usually unitary) transformation applied to the coupled equations that minimizes the off-diagonal nuclear kinetic energy terms. However, at the same time the adiabatic potential energy surfaces that enter the equations (those that approach or intersect each other) are combined linearly to a new set of potentials, the diabatic potentials. In other words, a diabatic transformation is a unitary transformation from the adiabatic representation to the diabatic representation, in which the nuclear kinetic energy operator is a diagonal. In this representation, the coupling between the Schrödinger equations is now due to diabatic potential energy surfaces that are significantly easier to estimate numerically than the nuclear kinetic energy terms that appeared before transformation.

The diabatic potential energy surfaces are smooth, so that low order Taylor series expansions of the surfaces may be applied and capture much of the complexity of the original system. Unfortunately, in general a strictly diabatic transformation does not exist, it is not possible to transform the nuclear kinetic energy rigorously to zero. Hence, diabatic potentials generated from mixing linearly multiple electronic energy surfaces are generally not exact. These surfaces are sometimes called pseudo-diabatic potentials, but generally the term is not used unless it is necessary to highlight this subtlety. Hence, usually pseudo-diabatic potentials are synonymous with diabatic potentials.

Mathematical formulation

In order to introduce mathematically the diabatic transformation we assume now, for the sake of argument, that only two adiabatic potential energy surfaces (PES), E₁ and E₂, approach each other and that all other surfaces are well separated (do not come close to E₁ or E₂); the argument can be generalized to more surfaces.

Let the collection of electronic coordinates be indicated by r, while R indicates dependence on nuclear coordinates. Thus, we assume E₁(R) ≈ E₂(R) with corresponding orthonormal electronic eigenstates χ₁(r;R) and χ₂(r;R). In the absence of magnetic interactions these electronic states, which depend parametrically on the nuclear coordinates, may be taken to be real-valued functions.

The nuclear kinetic energy is a sum over nuclei A with mass M_A,

$T_{\mathrm {n} }=\sum _{A}\sum _{\alpha =x,y,z}{\frac {P_{A\alpha }P_{A\alpha }}{2M_{A}}}\quad \mathrm {with} \quad P_{A\alpha }=-i\nabla _{A\alpha }=-i{\frac {\partial \quad }{\partial R_{A\alpha }}}.$

(Atomic units are used here and ∇_Aα is the a component of the gradient operator, short-hand for a differential.) By applying the Leibniz rule for differentiation, the matrix elements of T_n are (where coordinates are suppressed for clarity reasons):

$\mathrm {T_{n}} (\mathbf {R} )_{k'k}\equiv \langle \chi _{k'}|T_{n}|\chi _{k}\rangle _{(\mathbf {r} )}=\delta _{k'k}T_{\textrm {n}}+\sum _{A,\alpha }{\frac {1}{M_{A}}}\langle \chi _{k'}|{\big (}P_{A\alpha }\chi _{k}{\big )}\rangle _{(\mathbf {r} )}P_{A\alpha }+\langle \chi _{k'}|{\big (}T_{\mathrm {n} }\chi _{k}{\big )}\rangle _{(\mathbf {r} )}.$

The subscript r indicates that the integration inside the braket is over electronic coordinates only. The round brackets indicate the range of differentiation.

Assume that the off-diagonal matrix elements $\mathrm {T_{n}} (\mathbf {R} )_{12}=\mathrm {T_{n}} (\mathbf {R} )_{21}$ may not be neglected (in agreement with the assumption that only two surfaces approach each other, off-diagonal matrix elements with k, k′ > 2 are negligible, so that only a set of two coupled equations has to be considered). Upon making the expansion

$\Psi (\mathbf {r} ,\mathbf {R} )=\chi _{1}(\mathbf {r} ;\mathbf {R} )\Phi _{1}(\mathbf {R} )+\chi _{2}(\mathbf {r} ;\mathbf {R} )\Phi _{2}(\mathbf {R} ),$

the two coupled nuclear Schrödinger equations take the form (see the article Born-Oppenheimer approximation)

${\begin{pmatrix}E_{1}(\mathbf {R} )+\mathrm {T_{n}} (\mathbf {R} )_{11}&\mathrm {T_{n}} (\mathbf {R} )_{12}\\\mathrm {T_{n}} (\mathbf {R} )_{21}&E_{2}(\mathbf {R} )+\mathrm {T_{n}} (\mathbf {R} )_{22}\\\end{pmatrix}}{\boldsymbol {\Phi }}(\mathbf {R} )=E\,{\boldsymbol {\Phi }}(\mathbf {R} )\quad \mathrm {with} \quad {\boldsymbol {\Phi }}(\mathbf {R} )\equiv {\begin{pmatrix}\Phi _{1}(\mathbf {R} )\\\Phi _{2}(\mathbf {R} )\\\end{pmatrix}},\qquad \qquad (1)$

where E is the total (electronic plus nuclear motion) energy of the molecule.

In order to remove the problematic off-diagonal kinetic energy terms, two new orthonormal states are defined by a diabatic transformation of the adiabatic states χ₁(r;R) and χ₂(r;R)

${\begin{pmatrix}\varphi _{1}(\mathbf {r} ;\mathbf {R} )\\\varphi _{2}(\mathbf {r} ;\mathbf {R} )\\\end{pmatrix}}\equiv {\begin{pmatrix}\cos \gamma (\mathbf {R} )&\sin \gamma (\mathbf {R} )\\-\sin \gamma (\mathbf {R} )&\cos \gamma (\mathbf {R} )\\\end{pmatrix}}{\begin{pmatrix}\chi _{1}(\mathbf {r} ;\mathbf {R} )\\\chi _{2}(\mathbf {r} ;\mathbf {R} )\\\end{pmatrix}}$

where γ(R) is the diabatic angle. Transformation of the matrix of nuclear momentum $\langle \chi _{k'}|{\big (}P_{A\alpha }\chi _{k}{\big )}\rangle _{(\mathbf {r} )}$ for k′, k =1,2 gives for diagonal matrix elements:

$\langle {\varphi _{k}}|{\big (}P_{A\alpha }\varphi _{k}{\big )}\rangle _{(\mathbf {r} )}=0\quad {\textrm {for}}\quad k=1,\,2.$

These elements are zero because $\varphi _{k}$ is real and $P_{A\alpha }\,$ is Hermitian and pure-imaginary. The off-diagonal elements of the momentum operator satisfy,

$\langle {\varphi _{2}}|{\big (}P_{A\alpha }\varphi _{1}{\big )}\rangle _{(\mathbf {r} )}={\big (}P_{A\alpha }\gamma (\mathbf {R} ){\big )}+\langle \chi _{2}|{\big (}P_{A\alpha }\chi _{1}{\big )}\rangle _{(\mathbf {r} )}.$

Assume that a diabatic angle γ(R) exists, such that to a good approximation the right-hand side of the last equation vanishes,

${\big (}P_{A\alpha }\gamma (\mathbf {R} ){\big )}+\langle \chi _{2}|{\big (}P_{A\alpha }\chi _{1}{\big )}\rangle _{(\mathbf {r} )}=0$

i.e., $\varphi _{1}$ and $\varphi _{2}$ diagonalize the 2 x 2 matrix of the nuclear momentum. By the definition of Felix Smith $\varphi _{1}$ and $\varphi _{2}$ are diabatic states. (Smith was the first to define this concept; earlier the term diabatic was used somewhat loosely by Lichten.)

By a small change of notation these differential equations for γ(R) can be rewritten in the following more familiar form reminiscent of Newton's equations,

$\nabla _{A\alpha }V(\mathbf {R} )+F_{A\alpha }(\mathbf {R} )=0\quad \mathrm {with} \;\;V(\mathbf {R} )\equiv \gamma (\mathbf {R} )\;\;\mathrm {and} \;\;F_{A\alpha }(\mathbf {R} )\equiv \langle \chi _{2}|{\big (}iP_{A\alpha }\chi _{1}{\big )}\rangle _{(\mathbf {r} )}.$

It is well-known that the differential equations have a solution (i.e., the "potential"   V exists) if and only if the vector field ("force")   F_Aα(R) is irrotational,

$\nabla _{A\alpha }F_{B\beta }(\mathbf {R} )-\nabla _{B\beta }F_{A\alpha }(\mathbf {R} )=0.$

It can be shown that these conditions are rarely ever satisfied, so that a strictly diabatic transformation rarely ever exists. It is common to use approximate functions $\gamma (\mathbf {R} )$ leading to pseudo diabatic states.

Under the assumption that the momentum operators are represented exactly by 2 x 2 matrices, which is consistent with neglect of off-diagonal elements other than the (1,2) element, and the assumption of "strict" (not pseudo) diabaticity, it can be shown that

Failed to parse (SVG (MathML can be enabled via browser plugin): Invalid response ("Math extension cannot connect to Restbase.") from server "https://wikimedia.org/api/rest_v1/":): {\displaystyle \langle \varphi_{k'} | T_n | \varphi_k \rangle_{(\mathbf{r})} = \delta_{k'k} T_n. }

On the basis of the diabatic states the nuclear motion problem [Eq. (1)]   takes the following form

Failed to parse (SVG (MathML can be enabled via browser plugin): Invalid response ("Math extension cannot connect to Restbase.") from server "https://wikimedia.org/api/rest_v1/":): {\displaystyle \left[ \begin{pmatrix} T_\mathrm{n}+ \frac{E_{1}(\mathbf{R})+E_{2}(\mathbf{R})}{2} & 0 \\ 0 & T_\mathrm{n} + \frac{E_{1}(\mathbf{R})+E_{2}(\mathbf{R})}{2} \end{pmatrix} + \frac{E_{2}(\mathbf{R})-E_{1}(\mathbf{R})}{2} \begin{pmatrix} \cos2\gamma(\mathbf{R}) & \sin2\gamma(\mathbf{R}) \\ \sin2\gamma(\mathbf{R}) & -\cos2\gamma(\mathbf{R}) \end{pmatrix} \right] \tilde{\boldsymbol{\Phi}}(\mathbf{R}) = E \tilde{\boldsymbol{\Phi}}(\mathbf{R}). }

It is important to note that the off-diagonal elements (that appear only in the second term on the left-hand side) depend on the diabatic angle and adiabatic electronic energies only. The adiabatic surfaces E₁(R) and E₂(R) are PESs obtained from clamped nuclei electronic structure calculations and T_n is the usual nuclear kinetic energy operator defined above.

Finding approximations for γ(R) is the remaining problem before a solution of the coupled nuclear Schrödinger equations can be attempted. Much of the current research in quantum chemistry is devoted to this determination. Once γ(R) has been found and the coupled equations have been solved, the final vibronic (vibration—i.e., nuclear motion—plus electronic) wave function in the diabatic approximation is

Failed to parse (SVG (MathML can be enabled via browser plugin): Invalid response ("Math extension cannot connect to Restbase.") from server "https://wikimedia.org/api/rest_v1/":): {\displaystyle \Psi(\mathbf{r},\mathbf{R}) = \varphi_1(\mathbf{r};\mathbf{R})\tilde\Phi_1(\mathbf{R})+ \varphi_2(\mathbf{r};\mathbf{R})\tilde\Phi_2(\mathbf{R}). }