TY - JOUR
T1 - Highly Efficient Simultaneous Photocatalytic Reduction of CO2 and O2 from Air Using Conjugated Microporous Polymers with Ionic Imidazolium Sites
AU - Li, Waner
AU - Zhang, Tingting
AU - Feng, Chunyuan
AU - Chen, Mantao
AU - Sun, Zhaodi
AU - Handberg, Eric Storr Sage
AU - Wang, Bo
AU - Zhong, Lixiang
AU - Dai, Chunhui
N1 - Publisher Copyright:
© 2025 The Author(s). Energy & Environmental Materials published by John Wiley & Sons Australia, Ltd on behalf of Zhengzhou University.
PY - 2025
Y1 - 2025
N2 - Efficient photocatalytic reduction of CO2 is crucial to decrease the atmospheric concentration of CO2. Pairing this process with H2O2 production is of considerable importance for simultaneously producing value-added chemicals. However, the photocatalysts reported for such a process suffer from a high recombination rate of the surface/bulk charges, as well as inefficient enrichment and activation toward CO2 and O2, resulting in low conversion efficiency even in the presence of organic sacrificial agents and expensive metal co-catalysts. Herein, two 1,3,5-triphenylbenzene-based organic polymers with high ionic density and porosity are prepared through a facile Sonogashira polymerization. The ionic imidazolium sites embedded in the polymeric skeleton provide the two polymers (iCMP-1 and iCMP-2) with adsorptive selectivity for CO2/N2 up to 98–102 at 273 K, facilitating the enrichment of CO2 and O2 molecules around the catalytic centers, thus boosting their catalytic conversion directly from air under solar light (100 mW cm−2). Benefiting from the improved charge separation and broad light absorption, along with high CO2 and O2 uptake, iCMP-2 can deliver excellent CO and H2O2 yields (611.8 and 810.6 μmol h−1 g−1, respectively) under an atmosphere composed of water vapor and air without any co-catalysts.
AB - Efficient photocatalytic reduction of CO2 is crucial to decrease the atmospheric concentration of CO2. Pairing this process with H2O2 production is of considerable importance for simultaneously producing value-added chemicals. However, the photocatalysts reported for such a process suffer from a high recombination rate of the surface/bulk charges, as well as inefficient enrichment and activation toward CO2 and O2, resulting in low conversion efficiency even in the presence of organic sacrificial agents and expensive metal co-catalysts. Herein, two 1,3,5-triphenylbenzene-based organic polymers with high ionic density and porosity are prepared through a facile Sonogashira polymerization. The ionic imidazolium sites embedded in the polymeric skeleton provide the two polymers (iCMP-1 and iCMP-2) with adsorptive selectivity for CO2/N2 up to 98–102 at 273 K, facilitating the enrichment of CO2 and O2 molecules around the catalytic centers, thus boosting their catalytic conversion directly from air under solar light (100 mW cm−2). Benefiting from the improved charge separation and broad light absorption, along with high CO2 and O2 uptake, iCMP-2 can deliver excellent CO and H2O2 yields (611.8 and 810.6 μmol h−1 g−1, respectively) under an atmosphere composed of water vapor and air without any co-catalysts.
KW - air
KW - hydrogen peroxide generation
KW - imidazolium sites
KW - ionic-conjugated microporous polymers
KW - photocatalytic CO reduction
UR - http://www.scopus.com/pages/publications/105012019291
U2 - 10.1002/eem2.70114
DO - 10.1002/eem2.70114
M3 - Article
AN - SCOPUS:105012019291
SN - 2575-0348
JO - Energy and Environmental Materials
JF - Energy and Environmental Materials
ER -