TiO2-mediated visible-light-driven hydrogen evolution by ligand-capped Ru nanoparticles
Ru nanomaterials have recently emerged as potential substitutes for classical Pt-based cathodes for the hydrogen evolution reaction (HER). In this regard, nanoparticle surface-functionalization through the so-called organometallic approach is a promising strategy towards synthesizing tailored highly...
| Autores: | , , , , , , , , , |
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| Tipo de recurso: | artículo |
| Fecha de publicación: | 2020 |
| País: | España |
| Institución: | Universitat Autònoma de Barcelona |
| Repositorio: | Dipòsit Digital de Documents de la UAB |
| Idioma: | inglés |
| OAI Identifier: | oai:ddd.uab.cat:273904 |
| Acceso en línea: | https://ddd.uab.cat/record/273904 https://dx.doi.org/urn:doi:10.1039/d0se00446d |
| Access Level: | acceso abierto |
| Palabra clave: | SDG 7 - Affordable and Clean Energy |
| Sumario: | Ru nanomaterials have recently emerged as potential substitutes for classical Pt-based cathodes for the hydrogen evolution reaction (HER). In this regard, nanoparticle surface-functionalization through the so-called organometallic approach is a promising strategy towards synthesizing tailored highly active and durable HER (photo)electrocatalysts with limitless tunability. Herein, efficient (turnover numbers over 480 molH2 molRu-1 and a turnover frequency of 21.5 molH2 h-1 molRu-1; apparent quantum yield of 1.3%) and durable (. |
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