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Ruijia Wang
Ruijia Wang

Public Documents 2
Sunlight-driven Fixation of CO2 to Cyclic Carbonates Using Carbon Dots as a Photother...
Ruijia Wang
Hongda Guo

Ruijia Wang

and 12 more

February 23, 2025
Fixation of CO 2 through photocatalytic cycloaddition with epoxides to synthesize cyclic carbonates is an important but challenging process. In this work, carbon dots (CDs) synthesized from gallic acid and polyethylenimine are used for the efficient catalytic cycloaddition of CO 2 with epoxides in the absence of any solvent, additives, and halides, and importantly upon irradiation by natural sunlight. Specifically, carbon dots generated thermal energy and electrons upon solar irradiation, which together with their surface N-sites activated the inert CO 2. Meanwhile, epoxides were activated by the surface hydroxyl and carboxylic groups of the carbon dots, which reacted with activated CO 2 at solar thermal-induced high temperatures. The CDs shows excellent stability and recyclability during the catalysis. A 1000 mmol scale reaction for cyclic carbonate synthesis performed well upon irradiation with natural sunlight in the presence of CDs, showing great potential for the industrial application due to the simple, mild, and energy-saving process.
“All-in-one” carbon dots-based catalyst for converting CO2 to cyclic carbonates
Ruijia Wang
Jianyong Wan

Ruijia Wang

and 8 more

January 30, 2024
Converting CO2 with various epoxides to cyclic carbonates is extremely important. However, most of catalysts for such conversion either require complicated fabrication or are obtained from unsustainable sources. Motivated by this problem, we prepare biomass-based “all-in-one” carbon dots as nano-organocatalysts for firstly converting CO2 to cyclic carbonates. In this work, carbon dots (CD@KI) with high catalytic performance and good recyclability are prepared from sodium phytate (SP), polyethylenimine (PEI) and KI using one-pot hydrothermal treatment featuring cheap precursors and simple operation. Assisted by highly catalytic activity of CD@KI, up to 99.5% yield is achieved for converting CO2 and various epoxides to cyclic carbonates under mild conditions (solvent-free and 1 atm of CO2). Moreover, the conversion yield is maintained for reactions up to ten grams in scale. Significantly, by taking advantage of the inherent luminescence of CD@KI, the as-formed cyclic carbonates catalyzed by CD@KI can be directly converted to afterglow polymer composites.

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