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Combined biomass valorization and hydrogen production in a photoelectrochemical cell

In a typical hydrogen-producing photoelectrochemical cell (PEC), water reduction at the cathode (producing hydrogen) is accompanied by water oxidation at the anode (producing oxygen). This anode reaction is, however, not kinetically favourable. Here we investigate the possibility of utilizing solar...

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Published in:Nature chemistry 2015-04, Vol.7 (4), p.328-333
Main Authors: Cha, Hyun Gil, Choi, Kyoung-Shin
Format: Article
Language:English
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Summary:In a typical hydrogen-producing photoelectrochemical cell (PEC), water reduction at the cathode (producing hydrogen) is accompanied by water oxidation at the anode (producing oxygen). This anode reaction is, however, not kinetically favourable. Here we investigate the possibility of utilizing solar energy for biomass conversion by performing the oxidation of 5-hydroxymethylfurfural (HMF) into 2,5-furandicarboxylic acid (FDCA) at the anode of a PEC. HMF is a key intermediate in biomass conversion, and FDCA is an important monomer for the production of numerous polymers. Using 2,2,6,6-tetramethylpiperidine-1-oxyl as a mediator, we obtained a near-quantitative yield and 100% Faradaic efficiency at ambient conditions without the use of precious-metal catalysts. This reaction is also thermodynamically and kinetically more favourable than water oxidation. Our results suggest that solar-driven biomass conversion can be a viable anode reaction that has the potential to increase both the efficiency and the utility of PECs constructed for solar-fuel production. Photoelectrochemical water-splitting produces hydrogen at the cathode and oxygen at the anode. The anode reaction is, however, kinetically unfavourable. Now, reduction of water at the cathode has been combined with oxidation of 5-hydroxymethylfurfural at the anode resulting in a photoelectrochemical cell that produces fuel and a useful platform chemical.
ISSN:1755-4330
1755-4349
DOI:10.1038/nchem.2194