Photoredox Cascade Catalyst for Efficient Hydrogen Production with Biomass Photoreforming

Author:

Kobayashi Atsushi1ORCID

Affiliation:

1. Department of Chemistry Faculty of Science Hokkaido University North-10 West-8, Kita-ku 060-0810 Sapporo Japan

Abstract

AbstractBiomass photoreforming is a promising method to provide both a clean energy resource in the form of hydrogen (H2) and valuable chemicals as the results of water reduction and biomass oxidation. To overcome the poor contact between heterogeneous photocatalysts and biomass substrates, we fabricated a new photoredox cascade catalyst by combining a homogeneous catalyst, 2,2,6,6‐tetramethylpiperidine 1‐oxyl (TEMPO), and a heterogeneous dual‐dye sensitized photocatalyst (DDSP) composed of two Ru(II)‐polypyridine photosensitizers (RuP6 and RuCP6) and Pt‐loaded TiO2 nanoparticles. During blue‐light irradiation (λ=460±15 nm; 80 mW), the DDSP photocatalytically reduced aqueous protons to form H2 and simultaneously oxidized TEMPO radicals to generate catalytically active TEMPO+. It oxidized biomass substrates (water‐soluble glycerol and insoluble cellulose) to regenerate TEMPO. In the presence of N‐methyl imidazole as a proton transfer mediator, the photocatalytic H2 production activities for glycerol and cellulose reforming reached 2670 and 1590 μmol H2 (gTiO2)−1 h−1, respectively, which were comparable to those of state‐of‐the‐art heterogeneous photocatalysts.

Funder

ENEOS Hydrogen Trust Fund

Casio Science Promotion Foundation

Iwatani Naoji Foundation

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

General Chemistry,Catalysis

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