Temperature-Dependent Hydrogen Electrochemistry on Platinum Low-Index Single-Crystal Surfaces in Acid Solutions

TLDR

"At 274 K, exchange current densities increase in the order (111) ≪ (100) < (110), with (110) three times higher than (111); each face shows a distinct temperature‑dependent Tafel slope, and activation energies decrease in the same sequence, while the reaction follows a Tafel–Volmer mechanism on Pt(110) (Tafel step rate‑determining), a Heyrovsky–Volmer mechanism on Pt(100) (Heyrovsky step rate‑determining), and remains unresolved on Pt(111), where low activity and high activation energy are attributed to repulsive interactions between Had adatoms." Check sentence count: 3 sentences. Ensure each ends with period. No extra.

Abstract

The hydrogen evolution (HER) and the hydrogen oxidation reaction (HOR) were studied on platinum single crystals in a sulfuric acid solution over the temperature range 274−333 K. We found, for the first time, that at a fixed temperature (274 K) the exchange current densities (io) increase in the order (111) ≪ (100) < (110), with the io on the (110) surface being 3 times that on the (111) surface. We also found that each crystal face has an unique, temperature-dependent Tafel slope for the HOR, and that the activation energies for the HER and the HOR decrease in the sequence > > , the same sequence as the order of activity. These differences in activation energy with crystal face are attributed to structure-sensitive heats of adsorption of the active intermediate, Had, whose physical state is unclear. We analyzed the kinetic data with a model for the coupling of this unknown state, Had, with the well-known adsorbed state of hydrogen, Hupd, whose adsorption energy is strongly structure-sensitive. We concluded that on Pt(110), the reaction follows the Tafel−Volmer mechanism with the Tafel (recombination) step rate determining. On Pt(100), the reaction follows the Heyrovsky−Volmer sequence, with the Heyrovsky (ion−atom) reaction step being the rate-determining step. The reaction mechanism on Pt(111) could not, however, be resolved by analyzing the kinetic parameters. The relatively low activity and high activation energy for the (111) surface is attributed to strong repulsive interaction between Had adatoms on this surface.