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...

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Bibliographic Details
Authors: Romero Fernández, Nuria|||0000-0002-2704-7779; Barrach Guerra, Renan|||0000-0002-2034-4201; Gil Jiménez, Laia|||0000-0003-0870-4064; Drouet, Samuel|||0000-0003-1814-7556; Salmeron-Sànchez, Ivan; Illa, Ona|||0000-0001-7390-4893; Philippot, Karine|||0000-0002-8965-825X; Natali, Mirco|||0000-0002-6638-978X; García-Antón, Jordi|||0000-0002-2401-0401; Sala, Xavier|||0000-0002-7779-6313
Format: Article
Publication date:2020
Country:España
Institution:Universitat Autònoma de Barcelona
Repository:Dipòsit Digital de Documents de la UAB
Language:English
OAI Identifier:oai:ddd.uab.cat:273904
Online Access:https://ddd.uab.cat/record/273904
https://dx.doi.org/urn:doi:10.1039/d0se00446d
Access Level:Open access
Keyword:SDG 7 - Affordable and Clean Energy
Description
Summary: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 (.