4.8 Article

An Artificial Photosystem of Metal-Insulator-CTF Nanoarchitectures for Highly Efficient and Selective CO2 Conversion to CO

期刊

CHEMSUSCHEM
卷 15, 期 18, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cssc.202201107

关键词

CO2 conversion; CTAB; nanostructures; photocatalysis; self-assembly

资金

  1. National Natural Science Foundation of China [51672047, 21707173]
  2. Youth Talent Support Program of Fujian Province [00387077]
  3. National Natural Science Foundation of Fujian Province [2022J01110]

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In this study, an intelligent metal-insulator-semiconductor nano-architectural photosystem was constructed to efficiently convert CO2 into solar fuels under visible light. The system demonstrated a high CO evolution rate and selectivity, thanks to its larger surface area, improved visible-light response, and CO2 capture capacity.
It is of pivotal significance to explore robust photocatalysts to promote the photoreduction of CO2 into solar fuels. Herein, an intelligent metal-insulator-semiconductor (MIS) nano-architectural photosystem was constructed by electrostatic self-assembly between cetyltrimethylammonium bromide (CTAB) insulator-capped metal Ni nanoparticles (NPs) and covalent triazine-based frameworks (CTF-1). The metal-insulator-CTF composites unveiled a substantially higher CO evolution rate (1254.15 mu mol g(-1) h(-1)) compared with primitive CTF-1 (1.08 mu mol g(-1) h(-1)) and reached considerable selectivity (98.9 %) under visible-light irradiation. The superior photocatalytic CO2 conversion activity over Ni-CTAB-CTF nanoarchitecture could be attributed to the larger surface area, reinforced visible-light response, and CO2 capture capacity. More importantly, the Ni-CTAB-CTF nanoarchitecture endowed the photoexcited electrons on CTF-1 with the ability to tunnel across the thin CTAB insulating layer, directionally migrating to Ni NPs and thereby leading to the efficient separation of photogenerated electrons and holes in the photosystem. In addition, isotope-labeled ((CO2)-C-13) tracer results verified that the reduction products come from CO2 rather than the decomposition of the photocatalysts. This study opens a new avenue for establishing a highly efficient and selective artificial photosystem for CO2 conversion.

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