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February 14, 2026Exploration3 citationsOpen Access

Sunlight‐Driven Fixation of CO 2 to Cyclic Carbonates Using Carbon Dots as a Photothermal Catalyst

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RWRuijia WangHGHongda GuoTZTao Zhang

Key Points

  • To explore the use of carbon dots as a photothermal catalyst for CO2 fixation to cyclic carbonates utilizing natural sunlight.
  • Synthesis of carbon dots from gallic acid and polyethylenimine.
  • Catalytic cycloaddition of CO2 with epoxides.
  • Conducting reactions without solvents or additives under sunlight irradiation.
  • Assessment of catalytic stability and recyclability.
  • Scaling the reaction to 1000 mmol for evaluation.
  • Carbon dots effectively activated CO2 and epoxides under sunlight.
  • The process showed excellent stability and recyclability of the catalysts.
  • High conversion rates of CO2 to cyclic carbonates were achieved at mild temperatures.

Abstract

ABSTRACT 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.

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Cite This Study

Wang et al. (2026) studied this question.

synapsesocial.com/papers/699011172ccff479cfe57824https://doi.org/10.1002/exp.20250043
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