Toward Chemical Accuracy for Chemi- and Physisorption with an Efficient Density Functional

Understanding molecular adsorption on surfaces underpins many problems in chemistry and materials science. Accurately and efficiently describing the adsorption has been a challenging task for first-principles methods as the process can involve both short-range chemical bond formations and long-range physical interactions, e.g., van der Waals (vdW) interaction. Density functional theory presents an appealing choice for modeling adsorption reactions, although calculations with many exchange-correlation density functional approximations struggle to accurately describe both chemical and physical molecular adsorptions. Here, we propose an efficient density functional approximation that is accurate for both chemical and physical adsorption by concurrently optimizing its semilocal component and the long-range vdW correction against the prototypical adsorption CO/Pt(111) and Ar<sub>2</sub> binding energy curve. The resulting function opens the door to accurate and efficient modeling of general molecular adsorption.

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Publication Details

Journal
The Journal of Physical Chemistry C
Published
2026-02-17
DOI
https://doi.org/10.1021/acs.jpcc.5c08744
Primary Topic
Surface Chemistry and Catalysis
Type
article
Field-Weighted Citation Impact
0.00

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article

Toward Chemical Accuracy for Chemi- and Physisorption with an Efficient Density Functional

A. K. Patra, James W. Furness, Ruiqi Zhang, Jianwei Sun et al.
The Journal of Physical Chemistry C
Surface Chemistry and Catalysis
article

Toward Chemical Accuracy for Chemi- and Physisorption with an Efficient Density Functional

A. K. Patra, James W. Furness, Ruiqi Zhang, Jianwei Sun, Manish Kothakonda, Qing Zhao, Jinliang Ning
article en

Abstract

Understanding molecular adsorption on surfaces underpins many problems in chemistry and materials science. Accurately and efficiently describing the adsorption has been a challenging task for first-principles methods as the process can involve both short-range chemical bond formations and long-range physical interactions, e.g., van der Waals (vdW) interaction. Density functional theory presents an appealing choice for modeling adsorption reactions, although calculations with many exchange-correlation density functional approximations struggle to accurately describe both chemical and physical molecular adsorptions. Here, we propose an efficient density functional approximation that is accurate for both chemical and physical adsorption by concurrently optimizing its semilocal component and the long-range vdW correction against the prototypical adsorption CO/Pt(111) and Ar<sub>2</sub> binding energy curve. The resulting function opens the door to accurate and efficient modeling of general molecular adsorption.

The Journal of Physical Chemistry CVol. 130(8)
Tulane University (US), University of Delaware (US), Universidad del Noreste (MX)
U.S. Department of Energy, National Energy Research Scientific Computing Center, Office of Science, American Chemical Society Petroleum Research Fund, Basic Energy Sciences
Openalex Percentile: Top 53%
Surface Chemistry and Catalysis
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