Photomodulated Spatially Confined Chemical Reactivity in a Single Silver Nanoprism
Autor: | Vipul Bansal, Mandeep Singh, Rajesh Ramanathan, Murali Sastry, Sanje Mahasivam, Sushrut Bhanushali, Edwin L. H. Mayes, Billy J. Murdoch |
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Rok vydání: | 2020 |
Předmět: |
Materials science
Surface plasmon General Engineering General Physics and Astronomy Biasing 02 engineering and technology 010402 general chemistry 021001 nanoscience & nanotechnology 01 natural sciences Chemical reaction 0104 chemical sciences Ion Chemical physics Excited state Particle General Materials Science 0210 nano-technology Plasmon Excitation |
Zdroj: | ACS Nano. 14:11100-11109 |
ISSN: | 1936-086X 1936-0851 |
Popis: | Single-atom and single-particle catalysis is an area of considerable topical interest due to their potential in explaining important fundamental processes and applications across several areas. An interesting avenue in single-particle catalysis is spatial control of chemical reactivity within the particle by employing light as an external stimulus. To demonstrate this concept, we report galvanic replacement reactions (GRRs) as a spatial marker of subparticle chemical reactivity of a silver nanoprism with AuCl4- ions under optical excitation. The location of a GRR within a single Ag nanoprism can be spatially controlled depending on the plasmon mode excited. This leads to chemomorphological transformation of Ag nanoprisms into interesting Ag-Au structures. This spatial biasing effect is attributed to localized hot electron injection from the tips and edges of the silver nanoprisms to the adjacent reactants that correlate with excitation of different surface plasmon modes. The study also employs low-energy-loss EELS mapping to additionally probe the spatially confined redox reaction within a silver nanoprism. The findings presented here allow the visualization of a plasmon-driven subparticle chemical transformation with high resolution. The selective optical excitation of surface plasmon eigenmodes of anisotropic nanoparticles offers opportunities to spatially modulate chemical transformations mediated by hot electron transfer. |
Databáze: | OpenAIRE |
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