Reductive Hydrogenation of the Aqueous Rutile TiO2(110) Surface

Jun Cheng*, Xiandong Liu, Joost VandeVondele, Michiel Sprik

*Corresponding author for this work

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

At a semiconducting oxide water interface, two double layers (space charge layer and electric double layer) can develop near the interface. The double layer potentials can vary against the voltage and pH because they depend on the density of surface charges that have both electronic and protonic components. While the surface protonic charge density is determined by the acid-base equilibrium between the surface and the solution, electronic charges can also develop owing to the presence of electronic surface states that serve as traps for electrons and holes. A further complication is that the protonation and reduction (or deprotonation and oxidation) can couple at certain surface sites through proton coupled electron transfer (PCET) reactions. This is believed to be the cause of the observed (non-)Nernstian relation between the changes in electrode potentials and the pH, an approximately linear relationship with varying slopes depending on the nature of oxide surfaces. With the aim of addressing this issue, we present a first principles study for computation of the PCET energies of the reductive hydrogenation of the aqueous TiO2 surface. Our calculation shows that excess electrons and protons don't interact chemically at the interface, suggesting that the coupling between them is mainly electrostatic in nature. Our previous finding, on the other hand, showed that the electronic holes can chemically couple with protons through the terminal water. Combining these two results, we conclude that TiO2 may show different dependences of the electrode potentials on the pH at the cathodic and anodic voltage conditions.

Original languageEnglish
Pages (from-to)658-667
Number of pages10
JournalElectrochimica Acta
Volume179
Early online date2 Apr 2015
DOIs
Publication statusPublished - 10 Oct 2015

Fingerprint

Hydrogenation
Protons
Electrons
Oxides
Deprotonation
Electrodes
Water
Protonation
Surface states
Electric potential
Surface charge
Charge density
Electric space charge
Energy transfer
Electrostatics
titanium dioxide
Oxidation

Keywords

  • Density functional theory
  • Double layers
  • Interfaces
  • pKa
  • Redox potentials

ASJC Scopus subject areas

  • Electrochemistry
  • Chemical Engineering(all)

Cite this

Reductive Hydrogenation of the Aqueous Rutile TiO2(110) Surface. / Cheng, Jun; Liu, Xiandong; VandeVondele, Joost; Sprik, Michiel.

In: Electrochimica Acta, Vol. 179, 10.10.2015, p. 658-667.

Research output: Contribution to journalArticle

Cheng, Jun ; Liu, Xiandong ; VandeVondele, Joost ; Sprik, Michiel. / Reductive Hydrogenation of the Aqueous Rutile TiO2(110) Surface. In: Electrochimica Acta. 2015 ; Vol. 179. pp. 658-667.
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