Morse potential

The Morse potential, named after physicist Philip M. Morse, is a convenient interatomic interaction model for the potential energy of a diatomic molecule. It is a better approximation for the vibrational structure of the molecule than the quantum harmonic oscillator because it explicitly includes the effects of bond breaking, such as the existence of unbound states. It also accounts for the anharmonicity of real bonds and the non-zero transition probability for overtone and combination bands. The Morse potential can also be used to model other interactions such as the interaction between an atom and a surface. Due to its simplicity (only three fitting parameters), it is not used in modern spectroscopy. However, its mathematical form inspired the MLR (Morse/Long-range) potential, which is the most popular potential energy function used for fitting spectroscopic data.

Potential energy function

The Morse potential (blue) and harmonic oscillator potential (green). Unlike the energy levels of the harmonic oscillator potential, which are evenly spaced by ħω, the Morse potential level spacing decreases as the energy approaches the dissociation energy. The dissociation energy D_e is larger than the true energy required for dissociation D₀ due to the zero point energy of the lowest (v = 0) vibrational level.

The Morse potential energy function is of the form

${\displaystyle V'(r)=D_{e}(1-e^{-a(r-r_{e})})^{2}}$

Here ${\displaystyle r}$ is the distance between the atoms, ${\displaystyle r_{e}}$ is the equilibrium bond distance, ${\displaystyle D_{e}}$ is the well depth (defined relative to the dissociated atoms), and ${\displaystyle a}$ controls the 'width' of the potential (the smaller ${\displaystyle a}$ is, the larger the well). The dissociation energy of the bond can be calculated by subtracting the zero point energy ${\displaystyle E_{0}}$ from the depth of the well. The force constant (stiffness) of the bond can be found by Taylor expansion of ${\displaystyle V'(r)}$ around ${\displaystyle r=r_{e}}$ to the second derivative of the potential energy function, from which it can be shown that the parameter, ${\displaystyle a}$, is

${\displaystyle a={\sqrt {k_{e}/2D_{e}}},}$

where ${\displaystyle k_{e}}$ is the force constant at the minimum of the well.

Since the zero of potential energy is arbitrary, the equation for the Morse potential can be rewritten any number of ways by adding or subtracting a constant value. When it is used to model the atom-surface interaction, the energy zero can be redefined so that the Morse potential becomes

${\displaystyle V(r)=V'(r)-D_{e}=D_{e}(1-e^{-a(r-r_{e})})^{2}-D_{e}}$

which is usually written as

${\displaystyle V(r)=D_{e}(e^{-2a(r-r_{e})}-2e^{-a(r-r_{e})})}$

where ${\displaystyle r}$ is now the coordinate perpendicular to the surface. This form approaches zero at infinite ${\displaystyle r}$ and equals ${\displaystyle -D_{e}}$ at its minimum, i.e. ${\displaystyle r=r_{e}}$. It clearly shows that the Morse potential is the combination of a short-range repulsion term (the former) and a long-range attractive term (the latter), analogous to the Lennard-Jones potential.

Vibrational states and energies

Harmonic oscillator (grey) and Morse (black) potentials curves are shown along with their eigenfunctions (respectively green and blue for harmonic oscillator and morse) for the same vibrational levels for nitrogen.

Like the quantum harmonic oscillator, the energies and eigenstates of the Morse potential can be found using operator methods.[1] One approach involves applying the factorization method to the Hamiltonian.

To write the stationary states on the Morse potential, i.e. solutions ${\displaystyle \Psi _{n}(r)}$ and ${\displaystyle E_{n}}$ of the following Schrödinger equation:

${\displaystyle \left(-{\frac {\hbar ^{2}}{2m}}{\frac {\partial ^{2}}{\partial r^{2}}}+V(r)\right)\Psi _{n}(r)=E_{n}\Psi _{n}(r),}$

it is convenient to introduce the new variables:

${\displaystyle x=ar{\text{; }}x_{e}=ar_{e}{\text{; }}\lambda ={\frac {\sqrt {2mD_{e}}}{a\hbar }}{\text{; }}\varepsilon _{n}={\frac {2m}{a^{2}\hbar ^{2}}}E_{n}.}$

Then, the Schrödinger equation takes the simple form:

${\displaystyle \left(-{\frac {\partial ^{2}}{\partial x^{2}}}+V(x)\right)\Psi _{n}(x)=\varepsilon _{n}\Psi _{n}(x),}$

${\displaystyle V(x)=\lambda ^{2}\left(e^{-2\left(x-x_{e}\right)}-2e^{-\left(x-x_{e}\right)}\right).}$

Its eigenvalues and eigenstates can be written as:[2]

${\displaystyle \varepsilon _{n}=-\left(\lambda -n-{\frac {1}{2}}\right)^{2},}$

where

${\displaystyle n=0,1,\ldots ,\left[\lambda -{\frac {1}{2}}\right],}$

with [x] denoting the largest integer smaller than x.

${\displaystyle \Psi _{n}(z)=N_{n}z^{\lambda -n-{\frac {1}{2}}}e^{-{\frac {1}{2}}z}L_{n}^{(2\lambda -2n-1)}(z),}$

where ${\displaystyle z=2\lambda e^{-\left(x-x_{e}\right)}{\text{; }}N_{n}=\left[{\frac {n!\left(2\lambda -2n-1\right)}{\Gamma (2\lambda -n)}}\right]^{\frac {1}{2}}}$ and ${\displaystyle L_{n}^{(\alpha )}(z)}$ is a generalized Laguerre polynomial:

${\displaystyle L_{n}^{(\alpha )}(z)={\frac {z^{-\alpha }e^{z}}{n!}}{\frac {d^{n}}{dz^{n}}}\left(z^{n+\alpha }e^{-z}\right)={\frac {\Gamma (\alpha +n+1)/\Gamma (\alpha +1)}{n!}}\,_{1}F_{1}(-n,\alpha +1,z),}$

There also exists the following important analytical expression for matrix elements of the coordinate operator (here it is assumed that ${\displaystyle m>n}$ and ${\displaystyle N=\lambda -{\frac {1}{2}}}$) [3]

${\displaystyle \left\langle \Psi _{m}|x|\Psi _{n}\right\rangle ={\frac {2(-1)^{m-n+1}}{(m-n)(2N-n-m)}}{\sqrt {\frac {(N-n)(N-m)\Gamma (2N-m+1)m!}{\Gamma (2N-n+1)n!}}}.}$

The eigenenergies in the initial variables have form:

${\displaystyle E_{n}=h\nu _{0}(n+1/2)-{\frac {\left[h\nu _{0}(n+1/2)\right]^{2}}{4D_{e}}}}$

where ${\displaystyle n}$ is the vibrational quantum number, and ${\displaystyle \nu _{0}}$ has units of frequency, and is mathematically related to the particle mass, ${\displaystyle m}$, and the Morse constants via

${\displaystyle \nu _{0}={\frac {a}{2\pi }}{\sqrt {2D_{e}/m}}.}$

Whereas the energy spacing between vibrational levels in the quantum harmonic oscillator is constant at ${\displaystyle h\nu _{0}}$, the energy between adjacent levels decreases with increasing ${\displaystyle v}$ in the Morse oscillator. Mathematically, the spacing of Morse levels is

${\displaystyle E_{n+1}-E_{n}=h\nu _{0}-(n+1)(h\nu _{0})^{2}/2D_{e}.\,}$

This trend matches the anharmonicity found in real molecules. However, this equation fails above some value of ${\displaystyle n_{m}}$ where ${\displaystyle E(n_{m}+1)-E(n_{m})}$ is calculated to be zero or negative. Specifically,

${\displaystyle n_{m}={\frac {2D_{e}-h\nu _{0}}{h\nu _{0}}}}$ integer part.

This failure is due to the finite number of bound levels in the Morse potential, and some maximum ${\displaystyle n_{m}}$ that remains bound. For energies above ${\displaystyle n_{m}}$, all the possible energy levels are allowed and the equation for ${\displaystyle E_{n}}$ is no longer valid.

Below ${\displaystyle n_{m}}$, ${\displaystyle E_{n}}$ is a good approximation for the true vibrational structure in non-rotating diatomic molecules. In fact, the real molecular spectra are generally fit to the form¹

${\displaystyle E_{n}/hc=\omega _{e}(n+1/2)-\omega _{e}\chi _{e}(n+1/2)^{2}\,}$

in which the constants ${\displaystyle \omega _{e}}$ and ${\displaystyle \omega _{e}\chi _{e}}$ can be directly related to the parameters for the Morse potential.

As is clear from dimensional analysis, for historical reasons the last equation uses spectroscopic notation in which ${\displaystyle \omega _{e}}$ represents a wavenumber obeying ${\displaystyle E=hc\omega }$, and not an angular frequency given by ${\displaystyle E=\hbar \omega }$.

Morse/Long-range potential

An important extension of the Morse potential that made the Morse form very useful for modern spectroscopy is the MLR (Morse/Long-range) potential.[4] The MLR potential is used as a standard for representing spectroscopic and/or virial data of diatomic molecules by a potential energy curve. It has been used on N₂,[5] Ca₂,[6] KLi,[7] MgH,[8][9][10] several electronic states of Li₂,[4][11][12][13][9] Cs₂,[14][15] Sr₂,[16] ArXe,[9][17] LiCa,[18] LiNa,[19] Br₂,[20] Mg₂,[21] HF,[22][23] HCl,[22][23] HBr,[22][23] HI,[22][23] MgD,[8] Be₂,[24] BeH,[25] and NaH.[26] More sophisticated versions are used for polyatomic molecules.

See also

• Morse/Long-range potential
• Lennard-Jones potential
• Molecular mechanics

References

• ¹ CRC Handbook of chemistry and physics, Ed David R. Lide, 87th ed, Section 9, SPECTROSCOPIC CONSTANTS OF DIATOMIC MOLECULES pp. 9–82
• Morse, P. M. (1929). "Diatomic molecules according to the wave mechanics. II. Vibrational levels". Phys. Rev. 34. pp. 57–64. Bibcode:1929PhRv...34...57M. doi:10.1103/PhysRev.34.57.
• Girifalco, L. A.; Weizer, G. V. (1959). "Application of the Morse Potential Function to cubic metals". Phys. Rev. 114 (3). p. 687. Bibcode:1959PhRv..114..687G. doi:10.1103/PhysRev.114.687.
• Shore, Bruce W. (1973). "Comparison of matrix methods applied to the radial Schrödinger eigenvalue equation: The Morse potential". J. Chem. Phys. 59 (12). p. 6450. Bibcode:1973JChPh..59.6450S. doi:10.1063/1.1680025.
• Keyes, Robert W. (1975). "Bonding and antibonding potentials in group-IV semiconductors". Phys. Rev. Lett. 34 (21). pp. 1334–1337. Bibcode:1975PhRvL..34.1334K. doi:10.1103/PhysRevLett.34.1334.
• Lincoln, R. C.; Kilowad, K. M.; Ghate, P. B. (1967). "Morse-potential evaluation of second- and third-order elastic constants of some cubic metals". Phys. Rev. 157 (3). pp. 463–466. Bibcode:1967PhRv..157..463L. doi:10.1103/PhysRev.157.463.
• Dong, Shi-Hai; Lemus, R.; Frank, A. (2001). "Ladder operators for the Morse potential". Int. J. Quantum Chem. 86 (5). pp. 433–439. doi:10.1002/qua.10038.
• Zhou, Yaoqi; Karplus, Martin; Ball, Keith D.; Bery, R. Stephen (2002). "The distance fluctuation criterion for melting: Comparison of square-well and Morse Potential models for clusters and homopolymers". J. Chem. Phys. 116 (5). pp. 2323–2329. doi:10.1063/1.1426419.
• I.G. Kaplan, in Handbook of Molecular Physics and Quantum Chemistry, Wiley, 2003, p207.

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