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(June 30, 2021)

Double-hybrid density functional
theory
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J. Chem. Phys.

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pp. 034108.
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Phys. Chem. Chem. Phys.

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(DH-DFT) has demonstrated tremendous potential for approaching the chemical
accuracy with a computational cost comparable to the second-order
Møller-Plesset perturbation theory (MP2). In a DH-DFT, a Kohn-Sham (KS) DFT
calculation is performed first, followed by a treatment of non-local orbital
correlation energy at the level of second-order Møller-Plesset perturbation
theory (MP2).
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Phys. Rev.

(1934),
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pp. 618.
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This MP2 correlation correction includes a a
same-spin (ss) component, ${E}_{c}^{\mathrm{ss}}$, as well as an opposite-spin (os)
component, ${E}_{c}^{\mathrm{os}}$, which are added to the total energy obtained from
the KS-DFT calculation. Two scaling parameters, ${c}_{\mathrm{ss}}$ and ${c}_{\mathrm{os}}$, are
introduced in order to avoid double-counting correlation:

$${E}_{\text{DH-DFT}}={E}_{\text{KS-DFT}}+{c}_{\mathrm{ss}}{E}_{c}^{\mathrm{ss}}+{c}_{\mathrm{os}}{E}_{c}^{\mathrm{os}}$$ | (5.60) |

A starting point for understanding where a functional form like Eq. (5.60) might come from is the adiabatic connection formula that provides a rigorous way to define double-hybrid functionals. One considers an adiabatic path between the fictitious non-interacting KS reference system ($\lambda =0$) and the real physical system ($\lambda =1$), while holding the electron density fixed at its value for the real system, for all $\lambda $. Then

$${E}_{\mathrm{XC}}\left[\rho \right]={\int}_{0}^{1}{U}_{\mathrm{XC},\lambda}[\rho ]\mathit{d}\lambda ,$$ | (5.61) |

where ${U}_{\mathrm{XC},\lambda}$ is the exchange-correlation energy at a coupling strength $\lambda $, meaning that the exchange-correlation energy if the electron–electron terms in the Hamiltonian had the form $\lambda /{r}_{ij}$ rather than $1/{r}_{ij}$. Using a linear model of this quantity,

$${U}_{\mathrm{XC},\lambda}=a+b\lambda ,$$ | (5.62) |

one obtains the popular hybrid functional that includes the HF exchange (or
occupied orbitals) such as B3LYP.
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If one
further uses the Gorling-Levy’s perturbation theory (GL2) to define the initial
slope at $\lambda $= 0, one obtains the doubly hybrid functional form in
Eq. (5.60) that includes MP2 type perturbative terms (PT2) involving virtual orbitals:
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J. Chem. Theory Comput.

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$${U}_{\mathrm{XC},\lambda}={\frac{\partial {U}_{\mathrm{XC},\lambda}}{\lambda}|}_{\lambda =0}=2{E}_{\mathrm{C}}^{\mathrm{GL2}}.$$ | (5.63) |

The adiabatic connection formula has been used to develop double hybrid
functionals such as XYG3.
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Note that XYG3 as implemented in
Q-Chem uses B3LYP orbitals to generate the density and evaluate the PT2
terms. This is different from B2PLYP, an earlier doubly hybrid functional from
Grimme.
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J. Chem. Phys.

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The latter uses truncated KS orbitals while
XYG3 uses converged KS orbitals to evaluate the PT2 terms. The performance of
XYG3 is not only comparable to that of the G2 or G3 theory for thermochemistry,
but barrier heights and non-covalent interactions, including stacking
interactions, are also very well described by XYG3.
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Note: The recommended basis set for XYG3 is 6-311+G(3df,2p).

Due to the inclusion of PT2 terms, the cost of double-hybrid calculations is
formally $\mathcal{O}({N}^{5})$, as in conventional MP2, thereby not applicable to large
systems and partly losing DFT’s cost advantages. However, the highly successful
SOS-MP2 and local SOS-MP2 algorithms in Q-Chem can be leveraged to develop
double-hybrid functionals based on these $\mathcal{O}({N}^{4})$ methods. A version of
XYG3 that uses SOS-MP2 is the XYGJ-OS functional.
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Proc. Natl. Acad. Sci. USA

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This
functional has 4 parameters that are optimized using thermochemical data. It is
not only faster than XYG3, but comparable to XYG3 (or perhaps slightly better)
in accuracy. If the local SOS-MP2 algorithm is applied, the scaling of XYGJ-OS
is further reduced to $\mathcal{O}({N}^{3})$. Recently, XYGJ-OS became the first
double-hybrid functional whose analytic energy gradient has been derived and
implemented.
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J. Chem. Theory Comput.

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Other more empirical double-hybrid functionals have been implemented in
Q-Chem. Among the $\omega $B97 series of functionals,
$\omega $B97X-2
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J. Chem. Phys.

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is a long-range corrected double
hybrid that can greatly reduce the self-interaction errors (due to its high
fraction of HF exchange), and has been shown significantly superior to other
functionals for systems with both bonded and non-bonded interactions. Due to
the sensitivity of PT2 correlation energy with respect to the choices of basis
sets, $\omega $B97X-2 was parameterized with two different basis
sets: the $\omega $B97X-2(LP) was parameterized for use with
6-311++G(3df,3pd), while $\omega $B97X-2(TQZ) was parameterized with
the T/Q (triple-$\zeta $/quadruple-$\zeta $) extrapolation to the basis set
limit. A careful reading of Ref. 181 is highly advised
before using either of these two functionals.

Job control variables for double-hybrid DFT are described below. Note that the PT2 correlation energy can also be computed with the efficient resolution-of-identity (RI) methods. Since Q-Chem 5.2, RIMP2 can be invoked simply by specifying auxiliary basis set using AUX_BASIS_CORR. See Section 6.6.

DH

Controls the application of DH-DFT scheme.

TYPE:

LOGICAL

DEFAULT:

FALSE

OPTIONS:

FALSE (or 0)
Do not apply the DH-DFT scheme
TRUE (or 1)
Apply DH-DFT scheme

RECOMMENDATION:

NONE

The following to *$rem* variables pertain to the
$\omega $B97X-2(LP) and $\omega $B97X-2(TQZ) functionals.

SSS_FACTOR

Controls the strength of the same-spin component of PT2 correlation energy.

TYPE:

INTEGER

DEFAULT:

0

OPTIONS:

$n$
Corresponding to ${c}_{\mathrm{ss}}=n/{10}^{6}$ in Eq. (5.60).

RECOMMENDATION:

NONE

SOS_FACTOR

Controls the strength of the opposite-spin component of PT2 correlation energy.

TYPE:

INTEGER

DEFAULT:

0

OPTIONS:

$n$
Corresponding to ${c}_{\mathrm{os}}=n/{10}^{6}$ in Eq. (5.60).

RECOMMENDATION:

NONE

$molecule 0 1 H Li H 1.6 $end $rem EXCHANGE B2PLYP BASIS cc-pvtz AUX_BASIS rimp2-cc-pvtz $end @@@ $molecule read $end $rem EXCHANGE B2PLYP BASIS cc-pvtz $end

$molecule 0 1 H Li H 1.6 $end $rem EXCHANGE omegaB97X-2(TQZ) BASIS cc-pvqz AUX_BASIS rimp2-cc-pvqz $end @@@ $molecule read $end $rem EXCHANGE omegaB97X-2(TQZ) BASIS cc-pvqz $end

In the following example of XYG3, Q-Chem automatically performs a B3LYP calculation first, then uses the resulting orbitals to evaluate the PT2 correlation terms. Once can also use XYG3 combined with the RI approximation; use EXCHANGE = XYG3RI to do so, along with an appropriate choice of auxiliary basis set.

$molecule 0 1 N 0.000000 0.000000 0.547775 N 0.000000 0.000000 -0.547775 $end $rem EXCHANGE xyg3 BASIS 6-311+G(3df,2p) $end

The next example illustrates XYGJ-OS. This functional uses the RI approximation by default, so it is necessary to specify an auxiliary basis set.

$molecule 0 1 N 0.000000 0.000000 0.547775 N 0.000000 0.000000 -0.547775 $end $rem EXCHANGE xygjos BASIS 6-311+G(3df,2p) AUX_BASIS rimp2-cc-pVTZ PURECART 1111 TIME_MP2 true $end

The final example uses the local version of XYGJ-OS, which is the same as the original XYGJ-OS but with the use of the attenuated Coulomb metric to solve the RI coefficients. Here, the keyword omega determines the locality of the metric.

$molecule 0 1 N 0.000 0.000 0.54777500 N 0.000 0.000 -0.54777500 $end $rem EXCHANGE lxygjos BASIS 6-311+G(3df,2p) AUX_BASIS rimp2-cc-pVTZ OMEGA 200 PURECART 1111 $end