Journal
CHEMICAL COMMUNICATIONS
Volume 57, Issue 51, Pages 6233-6236Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1cc02491d
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Funding
- European Research Council [802769]
- Israeli Ministry of Energy
- Azrieli Foundation
- Hebrew University Center for Nanoscience and Nanotechnology PhD Scholarship
- European Research Council (ERC) [802769] Funding Source: European Research Council (ERC)
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The study investigated the impact of surface-adsorbate interactions on the adsorption geometry of stilbene-NHCs monolayers and its influence on surface potential. It was found that stilbene-NHCs on Au film accumulated in a vertical orientation for high photoisomerization efficiency, while strong metal-adsorbate interactions on Pt film led to a flat-lying adsorption geometry that quenched the photo-induced response.
Self-assembly of photo-responsive molecules is a robust technology for reversibly tuning the properties of functional materials. Herein, we probed the crucial role of surface-adsorbate interactions on the adsorption geometry of stilbene-functionalized N-heterocyclic carbenes (stilbene-NHCs) monolayers and its impact on surface potential. Stilbene-NHCs on Au film accumulated in a vertical orientation that enabled high photoisomerization efficiency and reversible changes in surface potential. Strong metal-adsorbate interactions led to flat-lying adsorption geometry of stilbene-NHCs on Pt film, which quenched the photo-isomerization influence on surface potential. It is identified that photo-induced response can be optimized by positioning the photo-active group in proximity to weakly-interacting surfaces.
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