4.8 Article

Challenges in Modeling Electrochemical Reaction Energetics with Polarizable Continuum Models

期刊

ACS CATALYSIS
卷 9, 期 2, 页码 920-931

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acscatal.8b02793

关键词

density functional theory; catalysis; electrocatalysis; electrochemistry; solvation

资金

  1. U.S. Department of Energy, Office of Basic Energy Science, Chemical Sciences, Geosciences, and Biosciences Division
  2. Joint Center for Artificial Photosynthesis, a DOE Energy Innovation Hub, through the Office of Science of the U.S. Department of Energy [DE-SC00004993]
  3. U.S. Department of Energy, Office of Science, Office of Advanced Scientific Computing Research, Scientific Discovery through Advanced Computing (SciDAC) program
  4. National Science Foundation Graduate Research Fellowship [DGE-114747]
  5. National Energy Research Scientific Computing Center (NERSC), a U.S. Department of Energy Office of Science User Facility [DE-AC02-05CH11231]

向作者/读者索取更多资源

A major challenge in the modeling of electrochemical phenomena is the accurate description of the interface between an electrolyte and a charged conductor. Polarizable continuum models (PCM) have been gaining popularity because they offer a computationally inexpensive method of modeling the electrolyte. In this Perspective, we discuss challenges from using one such model which treats the ions using a linearized Poisson-Boltzmann (LPB) distribution. From a physical perspective, this model places charge unphysically close to the surface and adsorbates, and it includes excessively steep ramping of the dielectric constant from the surface to the bulk solvent. Both of these issues can be somewhat mitigated by adjusting parameters built into the model, but in doing so, the resultant capacitance deviates from experimental values. Likewise, hybrid explicit-implicit approaches to the solvent may offer a more realistic description of hydrogen bonding and solvation to reaction intermediates, but the corresponding capacitances also deviate from experimental values. These deviations highlight the need for a careful adjustment of parameters in order to reproduce not only solvation energies but also other physical properties of solid-liquid interfaces. Continuum approaches alone also necessarily do not capture local variations in the electric field from cations at the interface, which can affect the energetics of intermediates with substantial dipoles or polarizability. Finally, since the double layer charge can be varied continuously, LPB/PCM models provide a way to determine electrochemical barriers at constant potential. However, double-layer charging and the atomic motion associated with reaction events occur on significantly different timescales. We suggest that more detailed approaches, such as the modified Poisson-Boltzmann model and/or the addition of a Stern layer, may be able to mitigate some but not all of the challenges discussed.

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