Pd-Ru pair on Pt surface for promoting hydrogen oxidation and evolution in alkaline media.
Longsheng CaoFernando A SotoDan LiTao DengEnyuan HuXiner LuDavid A CullenNico EidsonXiao-Qing YangKai HePerla B BalbuenaChunsheng WangPublished in: Nature communications (2024)
Hydrogen oxidation reaction in alkaline media is critical for alkaline fuel cells and electrochemical ammonia compressors. The slow hydrogen oxidation reaction in alkaline electrolytes requires large amounts of scarce and expensive platinum catalysts. While transition metal decoration can enhance Pt catalysts' activity, it often reduces the electrochemical active surface area, limiting the improvement in Pt mass activity. Here, we enhance Pt catalysts' activity without losing surface-active sites by using a Pd-Ru pair. Utilizing a mildly catalytic thermal pyrolysis approach, Pd-Ru pairs are decorated on Pt, confirmed by extended X-ray absorption fine structure and high-angle annular dark-field scanning transmission electron microscopy. Density functional theory and ab-initio molecular dynamics simulations indicate preferred Pd and Ru dopant adsorption. The Pd-Ru decorated Pt catalyst exhibits a mass-based exchange current density of 1557 ± 85 A g -1 metal for hydrogen oxidation reaction, demonstrating superior performance in an ammonia compressor.
Keyphrases
- visible light
- transition metal
- highly efficient
- electron microscopy
- electron transfer
- anaerobic digestion
- molecular dynamics simulations
- ionic liquid
- density functional theory
- energy transfer
- hydrogen peroxide
- gold nanoparticles
- high resolution
- room temperature
- reduced graphene oxide
- quantum dots
- induced apoptosis
- molecular dynamics
- air pollution
- oxidative stress
- nitric oxide
- heavy metals
- cell death
- risk assessment
- cell cycle arrest
- magnetic resonance
- municipal solid waste
- carbon dioxide
- crystal structure
- contrast enhanced
- liquid chromatography
- solid state