Abstract
The generation of chemical species from gases, noble metals and light interacting with localized surface plasmons represents a new paradigm for achieving low energy sustainable reaction pathways. Here, we demonstrate that the dissociation reaction of H 2 meditated by the decay of localized surface plasmons of gold nanoparticles leads to the generation of a new material as detected by a change in the optical properties of the gold nanostructures. The effective permittivity measured by in situ spectroscopic ellipsometry shows a blue-shift of 0.02 eV in the surface plasmon resonance, demonstrating the plausible formation of a metastable gold hydride layer on the surface of nanoparticles following the dissociation of H 2 . The formation of this gold hydride through the interaction of gold with atomic H is supported by first-principles simulations. These calculations do not indicate a significant charge transfer upon hydrogenation of the (111) surface but rather large Friedel charge oscillations within the gold layer. Moreover, our blue-shift is produced by the formation of a hydride leading to changes in critical band gaps in the electronic structure. For a coverage of 11%, the calculated peak of the imaginary part of the ZZ-component of the dielectric tensor undergoes a blue shift of 28 nm from a hydrogen free peak at 574 nm.
Original language | English (US) |
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Pages (from-to) | 4287-4292 |
Number of pages | 6 |
Journal | ChemistrySelect |
Volume | 4 |
Issue number | 14 |
DOIs | |
State | Published - Apr 16 2019 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- General Chemistry
Keywords
- Ab initio calculations
- Ellipsometry
- Gold
- Hydride