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Visible‐Light‐Driven Hydrogen Evolution Using Planarized Conjugated Polymer Photocatalysts
Authors:Dr Reiner Sebastian Sprick  Dr Baltasar Bonillo  Rob Clowes  Pierre Guiglion  Nick J Brownbill  Dr Benjamin J Slater  Dr Frédéric Blanc  Dr Martijn A Zwijnenburg  Prof Dave J Adams  Prof Andrew I Cooper
Institution:1. Department of Chemistry and Centre for Materials Discovery, University of Liverpool, Liverpool, UK;2. Department of Chemistry, University College London, London, UK;3. Stephenson Institute for Renewable Energy, University of Liverpool, Liverpool, UK
Abstract:Linear poly(p‐phenylene)s are modestly active UV photocatalysts for hydrogen production in the presence of a sacrificial electron donor. Introduction of planarized fluorene, carbazole, dibenzob,d]thiophene or dibenzob,d]thiophene sulfone units greatly enhances the H2 evolution rate. The most active dibenzob,d]thiophene sulfone co‐polymer has a UV photocatalytic activity that rivals TiO2, but is much more active under visible light. The dibenzob,d]thiophene sulfone co‐polymer has an apparent quantum yield of 2.3 % at 420 nm, as compared to 0.1 % for platinized commercial pristine carbon nitride.
Keywords:conjugated polymer  extended conjugation  photocatalysis  planarization  water splitting
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