Abstract
The hydrogen evolution reaction (HER) is crucial for producing hydrogen gas via electrochemical water splitting. Among diverse strategies to activate the HER, single-atom catalysts (SACs) are efficient alternatives to conventional platinum catalysts, focusing on titanium carbide (TiC) as a support material with good redox and electronic stability. Using this, we conducted a comprehensive investigation of various SAC candidates, screening their thermodynamic stabilities and HER activities. These calculations revealed four possible transition metal (TM) (Pt, Pd, Au, and Ag)-embedded TiC candidates (TM@TiC) that are thermodynamically stable and further suggested that they exhibit an intriguing H*-passivated surface state, significantly improving HER activities. Notably, the Pt@TiC demonstrates superior activity, promoting H2 gas generation due to its unique H*-passivated surface, which enables a sustainable HER. Therefore, this work introduces a new SAC paradigm centered around the H*-passivated surface, expanding the conventional focus on a single TM site.
| Original language | English |
|---|---|
| Pages (from-to) | 2304-2310 |
| Number of pages | 7 |
| Journal | ACS Materials Letters |
| Volume | 6 |
| Issue number | 6 |
| DOIs | |
| State | Published - 3 Jun 2024 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
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