TY - JOUR
T1 - Solution-processable polymers of intrinsic microporosity for gas-phase carbon dioxide photoreduction
AU - Moruzzi, Floriana
AU - Zhang, Weimin
AU - Purushothaman, Balaji
AU - Gonzalez-Carrero, Soranyel
AU - Aitchison, Catherine M.
AU - Willner, Benjamin
AU - Ceugniet, Fabien
AU - Lin, Yuanbao
AU - Kosco, Jan
AU - Chen, Hu
AU - Tian, Junfu
AU - Alsufyani, Maryam
AU - Gibson, Joshua S.
AU - Rattner, Ed
AU - Baghdadi, Yasmine
AU - Eslava, Salvador
AU - Neophytou, Marios
AU - Durrant, James R.
AU - Steier, Ludmilla
AU - McCulloch, Iain
N1 - Publisher Copyright:
© 2023, The Author(s).
PY - 2023/12
Y1 - 2023/12
N2 - Four solution-processable, linear conjugated polymers of intrinsic porosity are synthesised and tested for gas phase carbon dioxide photoreduction. The polymers’ photoreduction efficiency is investigated as a function of their porosity, optical properties, energy levels and photoluminescence. All polymers successfully form carbon monoxide as the main product, without the addition of metal co-catalysts. The best performing single component polymer yields a rate of 66 μmol h−1 m−2, which we attribute to the polymer exhibiting macroporosity and the longest exciton lifetimes. The addition of copper iodide, as a source of a copper co-catalyst in the polymers shows an increase in rate, with the best performing polymer achieving a rate of 175 μmol h−1 m−2. The polymers are active for over 100 h under operating conditions. This work shows the potential of processable polymers of intrinsic porosity for use in the gas phase photoreduction of carbon dioxide towards solar fuels.
AB - Four solution-processable, linear conjugated polymers of intrinsic porosity are synthesised and tested for gas phase carbon dioxide photoreduction. The polymers’ photoreduction efficiency is investigated as a function of their porosity, optical properties, energy levels and photoluminescence. All polymers successfully form carbon monoxide as the main product, without the addition of metal co-catalysts. The best performing single component polymer yields a rate of 66 μmol h−1 m−2, which we attribute to the polymer exhibiting macroporosity and the longest exciton lifetimes. The addition of copper iodide, as a source of a copper co-catalyst in the polymers shows an increase in rate, with the best performing polymer achieving a rate of 175 μmol h−1 m−2. The polymers are active for over 100 h under operating conditions. This work shows the potential of processable polymers of intrinsic porosity for use in the gas phase photoreduction of carbon dioxide towards solar fuels.
UR - http://www.scopus.com/inward/record.url?scp=85161677355&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85161677355&partnerID=8YFLogxK
U2 - 10.1038/s41467-023-39161-6
DO - 10.1038/s41467-023-39161-6
M3 - Article
C2 - 37301872
AN - SCOPUS:85161677355
SN - 2041-1723
VL - 14
JO - Nature communications
JF - Nature communications
IS - 1
M1 - 3443
ER -