A thiophene-modified doubleshell hollow g-CN nanosphere boosts NADH regeneration synergistic enhancement of charge excitation and separation
Low efficiency in photo-regeneration of redox-active cofactors is a crucial bottleneck in restricting artificial bio-photosynthesis of fuel systems from practical applications. We herein developed novel thiophene-modified doubleshell hollow g-C 3 N 4 nanospheres (ATCN-DSCN) via synergistically enhan...
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Veröffentlicht in: | Catalysis science & technology 2019-04, Vol.9 (8), p.1911-1921 |
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Zusammenfassung: | Low efficiency in photo-regeneration of redox-active cofactors is a crucial bottleneck in restricting artificial bio-photosynthesis of fuel systems from practical applications. We herein developed novel thiophene-modified doubleshell hollow g-C
3
N
4
nanospheres (ATCN-DSCN)
via
synergistically enhancing both the charge excitation and separation processes to efficiently photo-regenerate nicotinamide adenine dinucleotide (NADH), which was then utilized as the cofactor by formate dehydrogenase (FDH) to reduce CO
2
to form formic acid. The ATCN-DSCN material exhibited outstanding optical and photoelectrical properties, enabling a NADH yield of ∼74%, which was ∼40 times higher than that of the bulk C
3
N
4
(∼1.76%). ATCN-DSCN enabled a turnover frequency (TOF) of 2.950 h
−1
, which, to the best of our knowledge, is the highest record of TOF for the photo-regeneration of NADH. For the artificial bio-photoreduction of CO
2
, sustainable conversion of CO
2
to formic acid was achieved with a final formic acid concentration of 290.0 μM after 9 hours of light illumination. The excellent optical and photoelectrical properties of the ATCN-DSCN were enabled by the synergistic effect between the specific porous multishell hollow structure and thiophene ring incorporation, which endowed ATCN-DSCN enhanced light absorption and improved charge separation with boosted photocatalytic regeneration of NADH.
ATCN-DSCN enabled boosted NADH photo-regeneration and FDH-assisted CO
2
reduction. |
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ISSN: | 2044-4753 2044-4761 |
DOI: | 10.1039/c9cy00180h |