Abstract
Fundamental understanding of the interaction between atoms and molecules with the surfaces
of oxides including semiconducting oxides is crucial for the development of several thermo-,
photo-, and electro-, catalytic reactions as well as any application where surfaces are exposed to
an environment beyond vacuum. While previous studies have postulated material features (descriptors)
that to some extent suggest the adsorption energy trends on semiconducting oxides,
a physics based model to describe the interaction of atoms and molecules with the surfaces of
these materials is still lacking. In this study, we perform a series of controlled in-silico experiments
involving doping of quintessential semiconducting oxides (SrTiO3, SrZrO3, and TiO2)
to identify the perturbation by the dopant to the electronic structure of the host oxide and its
resultant effect on the adsorption energies of simple atoms and molecules. We identify that a
combination of three surface features: unique surface resonance states of the host-metal and
lattice oxygen atoms of the terminating surface oxide layer as well as the gap states dominated
by the introduced dopants contribute to the adsorption energy in a concerted fashion.
We find that this intricate interplay between on the one hand host-metal and on the other
hand oxygen surface resonance states with the adsorbate, respectively, results in a deviation
from the well-established adsorbate scaling relations seen for NHx(x=0-2) and CHx(x=0-3) but
not OHx and SHx. Through this lens, we develop a physics based adsorption model hitherto
referred as the Generalized Concerted Coupling model (GCC-model). The introduced model
provides a physical understanding with an associated electronic structure descriptor rooted in
the unique surface resonances that accurately captures the adsorption energy trends on doped
semiconducting oxides. This paves the way for the atomistic design of doped semiconducting
oxides for different catalytic applications, including sustainable energy applications such as
electrochemical water-splitting.
Supplementary materials
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Supporting Information
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Supporting information to main text containing relevant Figures and Tables cross-referenced in main text.
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