TY - JOUR
T1 - Polythiacalixarene-Embedded Gold Nanoparticles for Visible-Light-Driven Photocatalytic CO2Reduction
AU - Skorjanc, Tina
AU - Kamal, Khaja Mohaideen
AU - Alkhoori, Ayesha
AU - Mali, Gregor
AU - Mohammed, Abdul Khayum
AU - Asfari, Zouhair
AU - Polychronopoulou, Kyriaki
AU - Likozar, Blaž
AU - Trabolsi, Ali
AU - Shetty, Dinesh
N1 - Publisher Copyright:
© 2022 American Chemical Society.
PY - 2022/7/13
Y1 - 2022/7/13
N2 - Metal nanoparticles are potent reaction catalysts, but they tend to aggregate, thereby limiting their catalytic efficiency. Their coordination with specific functional groups within a porous structure prevents their aggregation and facilitates the mass flow of catalytic starting materials and products. Herein, we use a thiacalix[4]arene-based polymer as a porous support with abundant docking sites for Au nanoparticles. The sulfur atoms bridging the phenolic subunits of thiacalix[4]arene serve as Lewis basic sites that coordinate Au atoms. Therefore, this approach takes advantage of the functional groups inherent in the monomer and avoids laborious postsynthetic modifications of the polymer. The presented system was tested for visible-light-driven photocatalytic CO2 reduction, where it showed adequate ability to generate 6.74 μmol g-1 CO over the course of 4 h, while producing small amounts of the CH4 product. This study aims to stimulate interest in the design and development of synthetically simpler porous polymer supports for various metal nanoparticles in catalytic and other applications.
AB - Metal nanoparticles are potent reaction catalysts, but they tend to aggregate, thereby limiting their catalytic efficiency. Their coordination with specific functional groups within a porous structure prevents their aggregation and facilitates the mass flow of catalytic starting materials and products. Herein, we use a thiacalix[4]arene-based polymer as a porous support with abundant docking sites for Au nanoparticles. The sulfur atoms bridging the phenolic subunits of thiacalix[4]arene serve as Lewis basic sites that coordinate Au atoms. Therefore, this approach takes advantage of the functional groups inherent in the monomer and avoids laborious postsynthetic modifications of the polymer. The presented system was tested for visible-light-driven photocatalytic CO2 reduction, where it showed adequate ability to generate 6.74 μmol g-1 CO over the course of 4 h, while producing small amounts of the CH4 product. This study aims to stimulate interest in the design and development of synthetically simpler porous polymer supports for various metal nanoparticles in catalytic and other applications.
KW - COreduction
KW - nanoparticles
KW - photocatalysis
KW - porous polymers
KW - thiacalixarene
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U2 - 10.1021/acsami.2c05606
DO - 10.1021/acsami.2c05606
M3 - Article
C2 - 35713305
AN - SCOPUS:85133977673
SN - 1944-8244
VL - 14
SP - 30796
EP - 30801
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 27
ER -