Carbon Nanotube-Graphitic Carbon Nitride Hybrid Films for Flavoenzyme-Catalyzed Photoelectrochemical Cells

Journal Article (2017)
Author(s)

Eun Jin Son (Korea Advanced Institute of Science and Technology)

Sahng Ha Lee (Korea Advanced Institute of Science and Technology)

Su Keun Kuk (Korea Advanced Institute of Science and Technology)

M. Pesic (TU Delft - BT/Biocatalysis)

Da Som Choi (Korea Advanced Institute of Science and Technology)

Jong Wan Ko (Korea Advanced Institute of Science and Technology)

Kayoung Kim (Korea Advanced Institute of Science and Technology)

F. Hollmann (TU Delft - BT/Biocatalysis)

Chan Park (Korea Advanced Institute of Science and Technology)

Research Group
BT/Biocatalysis
Copyright
© 2017 Eun Jin Son, Sahng Ha Lee, Su Keun Kuk, M. Pesic, Da Som Choi, Jong Wan Ko, Kayoung Kim, F. Hollmann, Chan Beum Park
DOI related publication
https://doi.org/10.1002/adfm.201705232
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Publication Year
2017
Language
English
Copyright
© 2017 Eun Jin Son, Sahng Ha Lee, Su Keun Kuk, M. Pesic, Da Som Choi, Jong Wan Ko, Kayoung Kim, F. Hollmann, Chan Beum Park
Research Group
BT/Biocatalysis
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Abstract

In green plants, solar-powered electrons are transferred through sophistically arranged photosystems and are subsequently channelled into the Calvin cycle to generate chemical energy. Inspired by the natural photosynthetic scheme, a photoelectrochemical cell (PEC) is constructed configured with protonated graphitic carbon nitride (p-g-C3N4) and carbon nanotube hybrid (CNT/p-g-C3N4) film cathode, and FeOOH-deposited bismuth vanadate (FeOOH/BiVO4) photoanode for the production of industrially useful chiral alkanes using an old yellow enzyme homologue from Thermus scotoductus (TsOYE). In the biocatalytic PEC platform, photoexcited electrons provided by the FeOOH/BiVO4 photoanode are transferred to the robust and self-standing CNT/p-g-C3N4 hybrid film that electrocatalytically reduces flavin mononucleotide (FMN) mediator. The p-g-C3N4 promotes a two-electron reduction of FMN coupled with an accelerated electron transfer by the conductive CNT network. The reduced FMN subsequently delivers the electrons to TsOYE for the highly enantioselective conversion of ketoisophorone to (R)-levodione. Under light illumination (>420 nm) and external bias, (R)-levodione is synthesized with the enantiomeric excess value of above 83%, not influenced by the scale of applied bias, simultaneously exhibiting stable and high current efficiency. The results suggest that the biocatalytic PEC made up of economical materials can selectively synthesize high-value organic chemicals using water as an electron donor.

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