Emulsion polymerization derived organic photocatalysts for improved light-driven hydrogen evolution

• Published in: Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2019, Vol.7 (6), p.249-2496
• Main Authors: Aitchison, Catherine M, Sprick, Reiner Sebastian, Cooper, Andrew I
• Format: Article
• Language: English
• Subjects: Broadband; Catalysis; Catalytic activity; Electromagnetic absorption; Emulsion polymerization; Evolution; Hydrogen; Hydrogen evolution; Light scattering; Nanoparticles; Photocatalysis; Photocatalysts; Polymerization; Polymers
• ISSN: 2050-7488; 2050-7496; 2050-7496
• DOI: 10.1039/c8ta11383a

Here, we present the use of mini-emulsion polymerization to generate small particle analogues of three insoluble conjugated polymer photocatalysts. These materials show hydrogen evolution rates with a sacrificial donor under broadband illumination that are between two and three times higher than the corresponding bulk polymers. The most active emulsion particles displayed a hydrogen evolution rate of 60.6 mmol h −1 g −1 under visible light ( λ > 420 nm), which is the highest reported rate for an organic polymer. More importantly, the emulsion particles display far better catalytic lifetimes than previous polymer nanoparticles and they are also effective at high concentrations, allowing external quantum efficiencies as high as 20.4% at 420 nm. A limited degree of aggregation of the polymer particles maximizes the photocatalytic activity, possibly because of light scattering and enhanced light absorption. Here, we present the use of mini-emulsion polymerization to generate small particle analogues of three insoluble conjugated polymers for highly efficient photocatalytic hydrogen production.