11.2.1 Introduction

Ab initio quantum chemistry makes possible the study of gas-phase molecular properties from first principles. In liquid solution, however, these properties may change significantly, especially in polar solvents. Although it is possible to model solvation effects by including explicit solvent molecules in the quantum-chemical calculation (e.g. a super-molecular cluster calculation, averaged over different configurations of the molecules in the first solvation shell), such calculations are very computationally demanding. Furthermore, cluster calculations typically do not afford accurate solvation energies, owing to the importance of long-range electrostatic interactions. (Hybrid discrete/continuum models, which contain some explicit solvent, can be quite effective, however. ⁹⁶⁰ Pliego Jr. J. R., Riveros J. M.
Wiley Interdiscip. Rev.: Comput. Mol. Sci.
(2020), 10, pp. e1440. Link ^{, 911} Paul S. K., Herbert J. M.
J. Am. Chem. Soc.
(2021), 143, pp. 10189. Link ) Accurate prediction of solvation free energies is crucial for modeling of chemical reactions but also for relative conformational energies in solution.

Q-Chem contains several different implicit solvent models, which differ greatly in their level of sophistication. These are generally known as self-consistent reaction field (SCRF) models, because the continuum solvent establishes a “reaction field” (additional terms in the solute Hamiltonian) that depends upon the solute electron density, and must therefore be updated self-consistently during the iterative convergence of the wave function. The simplest and oldest of these models that is available in Q-Chem is the multipole expansion method, also known as a Kirkwood-Onsager model, ⁴⁹⁰ Herbert J. M.
Wiley Interdiscip. Rev.: Comput. Mol. Sci.
(2021), 11, pp. e1519. Link in which the solute molecule is placed inside of a spherical cavity and its electrostatic potential is represented in terms of a single-center multipole expansion. (This should not be confused with the Onsager model, in which a dipole approximation is used, and to avoid confusion the multipolar expansion method is better terminology.) More sophisticated models, which use a molecule-shaped cavity and the full molecular electrostatic potential, include the conductor-like PCM (C-PCM), ⁶⁷ Barone V., Cossi M.
J. Phys. Chem. A
(1998), 102, pp. 1995. Link ^{, 240} Cossi M. et al.
J. Comput. Chem.
(2003), 24, pp. 669. Link the conductor-like screening model (COSMO), the “surface and simulation of volume polarization for electrostatics” [SS(V)PE] model, ²¹¹ Chipman D. M.
J. Chem. Phys.
(2000), 112, pp. 5558. Link and the closely-related “integral equation formalism” (IEF-PCM). ¹⁶⁰ Cancès E., Mennucci B., Tomasi J.
J. Chem. Phys.
(1997), 107, pp. 3032. Link ^{, 161} Cancès E., Mennucci B.
J. Chem. Phys.
(2001), 114, pp. 4744. Link For an overview of all of these methods and their interconnections, see the review by Herbert. ⁴⁹⁰ Herbert J. M.
Wiley Interdiscip. Rev.: Comput. Mol. Sci.
(2021), 11, pp. e1519. Link

The C-PCM, IEF-PCM, and SS(V)PE are examples of what are called “apparent surface charge” SCRF models, and the term polarizable continuum models (PCMs), as popularized by Tomasi and coworkers, ¹¹⁹² Tomasi J., Mennucci B., Cammi R.
Chem. Rev.
(2005), 106, pp. 2999. Link is now used almost universally to refer to this class of solvation models. Q-Chem employs a Switching/Gaussian or “SwiG” implementation of these PCMs,^{661, 662, 664, 484, 659} which resolves a long-standing (though little-publicized) problem with standard PCMs, namely, that the boundary-element methods used to discretize the solute/continuum interface may lead to discontinuities in the potential energy surface for the solute molecule. These discontinuities inhibit convergence of geometry optimizations, introduce serious artifacts in vibrational frequency calculations, and make ab initio molecular dynamics calculations virtually impossible. ⁶⁶¹ Lange A. W., Herbert J. M.
J. Phys. Chem. Lett.
(2010), 1, pp. 556. Link ^{, 662} Lange A. W., Herbert J. M.
J. Chem. Phys.
(2010), 133, pp. 244111. Link In contrast, Q-Chem’s SwiG-PCMs afford potential energy surfaces that are rigorously continuous and smooth. Unlike earlier attempts to obtain smooth PCMs, the SwiG approach largely preserves the properties of the underlying integral-equation solvent models, so that solvation energies and molecular surface areas are hardly affected by the smoothing procedure.

Other solvent models available in Q-Chem include the “Langevin dipoles” model; ³³⁹ Florián J., Warshel A.
J. Phys. Chem. B
(1997), 101, pp. 5583. Link ^{, 340} Florián J., Warshel A.
J. Phys. Chem. B
(1999), 103, pp. 10282. Link as well as the SM8, ⁷⁹⁶ Marenich A. V. et al.
J. Chem. Theory Comput.
(2007), 3, pp. 2011. Link SM12, ⁷⁹⁴ Marenich A. V., Cramer C. J., Truhlar D. G.
J. Chem. Theory Comput.
(2013), 9, pp. 609. Link and SMD ⁷⁹³ Marenich A. V., Cramer C. J., Truhlar D. G.
J. Phys. Chem. B
(2009), 113, pp. 6378. Link models developed at the University of Minnesota. SM8 and SM12 are based upon the generalized Born method for electrostatics, augmented with atomic surface tensions intended to capture nonelectrostatic effects (cavitation, dispersion, exchange repulsion, and changes in solvent structure). These models have been carefully parameterized to reproduce experimental free energies of solvation. ²⁴² Cramer C. J., Truhlar D. G.
Acc. Chem. Res.
(2008), 41, pp. 760. Link The SMD model, in which the “D” is for “density”, combines IEF-PCM with similar nonelectrostatic corrections. Statistically speaking, SMD is not any more or less accurate than other SM$x$ models, ⁴⁹⁰ Herbert J. M.
Wiley Interdiscip. Rev.: Comput. Mol. Sci.
(2021), 11, pp. e1519. Link but has the advantage of being based on rigorous electrostatics derived from the solute’s exact SCF density. The SM12 and SMD models can each be used in arbitrary basis sets. The SM8 model uses generalized Born electrostatics based on “CM4” charges, ⁵⁹⁴ Kelly C. P., Cramer C. J., Truhlar D. G.
J. Chem. Theory Comput.
(2005), 1, pp. 1133. Link ^{, 888} Olson R. M. et al.
J. Chem. Theory Comput.
(2007), 3, pp. 2046–2054. Link which are themselves based on Löwdin atomic charges, and as such this model should only be used in the basis sets for which it was parameterized: 6-31G*, 6-31+G*, or 6-31+G**. (Other basis sets, if requested will use the 6-31G* parameters but this is not recommended.) The SM12 model also uses generalized Born electrostatics but substitutes CM4 charges for Hirshfeld charges; the latter are more stable with respect to changes in basis set and therefore SM12 is available in arbitrary basis sets. The trade-off is that an analytic gradient is available for SM8 but not SM12; see Table 11.2. An analytic gradient is available for SMD also.

Table 11.1 summarizes the implicit solvent models that are available in Q-Chem. Solvent models are invoked via the SOLVENT_METHOD keyword, as shown below. Additional details about each particular solvent model can be found in the sections that follow. In general, these methods are available for any SCF level of electronic structure theory, with the aforementioned caveat about basis sets for SM8. Post-Hartree–Fock calculations (such as MP2 or EOM-CC) can be performed by first running an SCF + PCM job, in which case the correlated wave function will employ MOs and Hartree-Fock energy levels that are polarized by the solvent. This represents a “zeroth-order” inclusion of the solvent effects at the correlated level of theory, but is perfectly adequate for many applications as higher-order corrections are usually small. ⁸¹⁷ Mewes J.-M., Herbert J. M., Dreuw A.
Phys. Chem. Chem. Phys.
(2017), 19, pp. 1644. Link ^{, 490} Herbert J. M.
Wiley Interdiscip. Rev.: Comput. Mol. Sci.
(2021), 11, pp. e1519. Link Table 11.2 also summarizes the availability of analytical energy gradients for implicit solvent models. (Finite-difference gradients and Hessians are requested automatically for calculations where the requisite analytic derivatives are not available.)

Note:  The format for specifying implicit solvent models changed significantly starting in Q-Chem version 4.2.1. This change was made in an attempt to simply and unify the input notation for a large number of different models.

Before going into detail about each of these models, a few potential points of confusion warrant mention, with regards to nomenclature. First, “PCM” refers to a family of models that includes C-PCM, COSMO, SS(V)PE, and IEF-PCM. The latter two models are formally equivalent at the level of integral equations, ¹⁶¹ Cancès E., Mennucci B.
J. Chem. Phys.
(2001), 114, pp. 4744. Link ^{, 490} Herbert J. M.
Wiley Interdiscip. Rev.: Comput. Mol. Sci.
(2021), 11, pp. e1519. Link but exhibit some some differences in their numerical implementation. ⁶⁶⁴ Lange A. W., Herbert J. M.
Chem. Phys. Lett.
(2011), 509, pp. 77. Link ^{, 1330} You Z.-Q. et al.
J. Chem. Phys.
(2015), 143, pp. 204104. Link ^{, 490} Herbert J. M.
Wiley Interdiscip. Rev.: Comput. Mol. Sci.
(2021), 11, pp. e1519. Link One or the other of these models can be selected by additional job control variables in a $pcm input section, as described in Section 11.2.3. COSMO is very similar to C-PCM but includes a correction for that part of the solute’s electron density that penetrates beyond the cavity (the so-called “outlying charge”), ⁶⁰⁷ Klamt A., Jonas V.
J. Chem. Phys.
(1996), 105, pp. 9972. Link although later work cast doubt on the theoretical justification for this and other ad hoc charge renormalization procedures. ²¹⁰ Chipman D. M.
J. Chem. Phys.
(1999), 110, pp. 8012. Link [The IEF-PCM and SS(V)PE methods already contain an implicit correction for outlying charge, as does the C-PCM method that is derived as an approximation to these models, ²¹⁰ Chipman D. M.
J. Chem. Phys.
(1999), 110, pp. 8012. Link ^{, 490} Herbert J. M.
Wiley Interdiscip. Rev.: Comput. Mol. Sci.
(2021), 11, pp. e1519. Link although this was not recognized at the time that COSMO was formulated. See Ref.  490 Herbert J. M.
Wiley Interdiscip. Rev.: Comput. Mol. Sci.
(2021), 11, pp. e1519. Link for a historical discussion of these developments.] In any case, COSMO is described in Section 11.2.8.

Two implementations of the SS(V)PE model are also available. The PCM implementation (which is requested by setting SOLVENT_METHOD = PCM in conjunction with appropriate job-control variables in the $pcm input section) uses a solute cavity constructed from atom-centered spheres, in keeping with other PCMs. On the other hand, setting SOLVENT_METHOD = ISOSVP requests an SS(V)PE calculation in which the solute cavity is defined by an isocontour of the solute’s own electron density. ²⁰⁸ Chipman D. M., Dupuis M.
Theor. Chem. Acc.
(2002), 107, pp. 90. Link ^{, 204} Chen F., Chipman D. M.
J. Chem. Phys.
(2003), 119, pp. 10289. Link ^{, 213} Chipman D. M.
J. Chem. Phys.
(2006), 124, pp. 224111. Link This is an appealing, one-parameter cavity construction that avoid many of the problems with cusps in “van der Waals” cavity surfaces that are constructed from atom-centered spheres, and the isodensity implementation of SS(V)PE forms the basis of a physics-based continuum solvation model called CMIRS that is described in Section 11.2.7. ⁹⁶⁷ Pomogaeva A., Chipman D. M.
J. Chem. Theory Comput.
(2011), 7, pp. 3952. Link ^{, 968} Pomogaeva A., Chipman D. M.
J. Phys. Chem. A
(2013), 117, pp. 5812. Link ^{, 969} Pomogaeva A., Chipman D. M.
J. Chem. Theory Comput.
(2014), 10, pp. 211. Link ^{, 970} Pomogaeva A., Chipman D. M.
J. Phys. Chem. A
(2015), 119, pp. 5173. Link ^{, 1327} You Z.-Q., Herbert J. M.
J. Chem. Theory Comput.
(2016), 12, pp. 4338. Link CMIRS is competitive in accuracy (for solvation free energies) with the best-available SM$x$ solvation models, ⁴⁹⁰ Herbert J. M.
Wiley Interdiscip. Rev.: Comput. Mol. Sci.
(2021), 11, pp. e1519. Link despite using far fewer fitting parameters. However, analytic energy gradients are not available for the isodensity cavity construction and therefore not available for CMIRS, whereas these gradients are available when the cavity surface is constructed from atom-centered spheres.

Regarding the accuracy of these models for solvation free energies ($\mathrm{\Delta }{G}_{298}$), the SM$x$ models generally achieve sub-kcal/mol accuracy for neutral molecules, based on comparison to a large database of experimental values, although average errors for ions are more like 4 kcal/mol. ²⁴² Cramer C. J., Truhlar D. G.
Acc. Chem. Res.
(2008), 41, pp. 760. Link ^{, 490} Herbert J. M.
Wiley Interdiscip. Rev.: Comput. Mol. Sci.
(2021), 11, pp. e1519. Link (Note that the SM12 and SMD models generally do not improve too much upon SM8 in any statistical sense, ⁷⁹³ Marenich A. V., Cramer C. J., Truhlar D. G.
J. Phys. Chem. B
(2009), 113, pp. 6378. Link ^{, 794} Marenich A. V., Cramer C. J., Truhlar D. G.
J. Chem. Theory Comput.
(2013), 9, pp. 609. Link but do extend these models to arbitrary basis sets whereas SM8 is limited to a few small basis sets.) To achieve accuracy comparable to the SM$x$ models within the PCM class of solvent models, nonelectrostatic terms must be added. ⁴⁹⁰ Herbert J. M.
Wiley Interdiscip. Rev.: Comput. Mol. Sci.
(2021), 11, pp. e1519. Link Among the various PCMs described above, the only one that constitutes a “black box” model for solvation energies is CMIRS, which slightly outperforms the SM$x$ models in a statistical sense, ¹³²⁷ You Z.-Q., Herbert J. M.
J. Chem. Theory Comput.
(2016), 12, pp. 4338. Link ^{, 490} Herbert J. M.
Wiley Interdiscip. Rev.: Comput. Mol. Sci.
(2021), 11, pp. e1519. Link although it is only available for a few solvents.

The following sections provide more details regarding theory and job control for the various implicit solvent models that are available in Q-Chem. Ref.  490 Herbert J. M.
Wiley Interdiscip. Rev.: Comput. Mol. Sci.
(2021), 11, pp. e1519. Link contains both formal comparisons amongst these models as well as a side-by-side comparison of the accuracy of solvation free energies.