English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Improving artificial photosynthesis in carbon nitride by gas-liquid-solid Interface management for full light-induced CO2 reduction to C1-C2 fuels and O2

MPS-Authors
/persons/resource/persons222674

Xiao,  Kai
Kolloidchemie, Max Planck Institute of Colloids and Interfaces, Max Planck Society;

/persons/resource/persons1057

Antonietti,  Markus
Markus Antonietti, Kolloidchemie, Max Planck Institute of Colloids and Interfaces, Max Planck Society;

/persons/resource/persons230732

Cao,  Shaowen
Markus Antonietti, Kolloidchemie, Max Planck Institute of Colloids and Interfaces, Max Planck Society;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)

Article.pdf
(Publisher version), 2MB

Supplementary Material (public)
There is no public supplementary material available
Citation

Xia, Y., Xiao, K., Cheng, B., Yu, J., Jiang, L., Antonietti, M., et al. (2020). Improving artificial photosynthesis in carbon nitride by gas-liquid-solid Interface management for full light-induced CO2 reduction to C1-C2 fuels and O2. ChemSusChem, 13(7), 1730-1734. doi:10.1002/cssc.201903515.


Cite as: https://hdl.handle.net/21.11116/0000-0005-9B97-2
Abstract
The activity and selectivity of simple photocatalysts for CO2 reduction were still limited by the insufficient photophysics of the catalysts, but also the low solubility and slow mass transport of gas molecules in/through aqueous solution. Herein, we present a way to overcome these limitation by constructing a triphase photocatalytic system, in which polymeric carbon nitride (CN) is immobilized onto a hydrophobic substrate, and the photocatalytic reduction reaction occurs at a gas-liquid-solid (CO2-water-catalyst) triple connection. It is found that the CN anchored onto the surface of a hydrophobic substrate exhibits an about 7.2-fold enhancement in the total CO2 conversion, with a rate of 415.50 ?mol m-2 h-1 under simulated solar light irradiation. This value corresponds to an overall photosynthetic efficiency for full water-CO2 conversion of 0.33%, i.e. very close to biological systems. Meanwhile, a remarkable enhancement of direct C2 hydrocarbon production, as well as a high CO2 conversion selectivity of 97.7% was observed. Going from water oxidation to phosphate oxidation, the quantum yield can be even increased to 1.28%.