Abstract
Platinum-based catalysts have been considered the most effective electrocatalysts for the hydrogen evolution reaction in water splitting. However, platinum utilization in these electrocatalysts is extremely low, as the active sites are only located on the surface of the catalyst particles. Downsizing catalyst nanoparticles to single atoms is highly desirable to maximize their efficiency by utilizing nearly all platinum atoms. Here we report on a practical synthesis method to produce isolated single platinum atoms and clusters using the atomic layer deposition technique. The single platinum atom catalysts are investigated for the hydrogen evolution reaction, where they exhibit significantly enhanced catalytic activity (up to 37 times) and high stability in comparison with the state-of-the-art commercial platinum/carbon catalysts. The X-ray absorption fine structure and density functional theory analyses indicate that the partially unoccupied density of states of the platinum atoms' 5d orbitals on the nitrogen-doped graphene are responsible for the excellent performance.
Highlights
Platinum-based catalysts have been considered the most effective electrocatalysts for the hydrogen evolution reaction in water splitting
To further examine the effects of the N-dopants on the stability of the Pt atoms and clusters observed in Fig. 1 and to expand on the understanding of the N-dopant’s contribution to the hydrogen evolution reaction (HER), we have prepared atomic layer deposition (ALD)-deposited Pt on graphene nanosheets (GNs) for comparison
It can be suggested that the formation of larger particles on the GNs during the ALD procedure can be attributed to the weaker interaction between the Pt and the graphene support in contrast to the N-doped graphene support
Summary
Platinum-based catalysts have been considered the most effective electrocatalysts for the hydrogen evolution reaction in water splitting. The single platinum atom catalysts are investigated for the hydrogen evolution reaction, where they exhibit significantly enhanced catalytic activity (up to 37 times) and high stability in comparison with the state-of-the-art commercial platinum/carbon catalysts. Reducing the size of the Pt NPs to clusters or even single atoms could significantly decrease the noble metal usage and increase their catalytic activity, which is highly desirable to enhance the Pt utilization and decrease the cost of the electrocatalysts[17]. The single-atom catalysts exhibited a significantly improved catalytic activity towards methanol oxidation, up to 10 times greater than the state-of-the-art commercial carbon-supported Pt (Pt/C) catalysts[19]
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