# Hydrogen adsorption at RuO2(110)

Source: [Hydrogen adsorption at RuO2(110)](<https://www.sota2.com/research/paper/68fa1e4e7a2b558e29321885>)

Collection index: [llms.txt](<https://www.sota2.com/research/llms.txt>)

Data updated: 2025-10-23T14:45:12.267Z

Authors: Qiang Sun, Karsten Reuter, Matthias Scheffler

Published: 2003-09-30T15:37:23.000Z

## Abstract

The structural, vibrational, energetic and electronic properties of hydrogen at the stoichiometric RuO2(110) termination are studied using density functional theory. The oxide surface is found to stabilize both molecular and dissociated H2. The most stable configuration in form of hydroxyl groups (monohydrides) at the undercoordinated O^br surface anions is at low temperatures accessed via a molecular state at the undercoordinated Ru^cus atoms (dihydrogen) and a second precursor in form of a water-like species (dihydride) at the O^br sites. This complex picture of the low-temperature dissociation kinetics of H2 at RuO2(110) is in agreement with existing data from high-resolution energy-loss spectroscopy and temperature programmed desorption. Hydrogen adsorption at O^br sites increases the reactivity of the neighboring Ru^cus sites, which are believed to be the active sites in catalytic oxidation reactions.

## Recorded benchmark results

A research result applies to its stated dataset, split, metric and evaluation configuration. Compare like-for-like settings, preserve the metric's unit and direction, and distinguish paper-reported results from independent reproduction. The best result recorded here is not a claim of exhaustive, current global coverage.

## Original sources and implementation

[Original paper](<https://arxiv.org/abs/cond-mat/0309714>)

[PDF](<https://arxiv.org/pdf/cond-mat/0309714.pdf>)