Synthesis of boron-doped porous carbons improves CO2 capture, indicating environmental benefits.
Porous carbons have garnered significant attention for their excellent performance in carbon capture applications, which is attributed to their distinctive textural and physicochemical characteristics. The design of heteroatom-doped porous carbons derived from renewable biomass precursors represents a promising direction for sustainable materials development. By integrating eco-friendly synthesis strategies with cost-effective processing routes, such materials can be tailored to exhibit enhanced porosity, surface chemistry, and adsorption capacity. In this context, the current study presents the synthesis of boron-doped porous carbons via a KOH activation process, utilizing water chestnut shells as the carbon precursor and boric acid as the boron source. The synthesized porous carbons exhibit a well-developed porous structure and rich boron functionalities. Their performance was systematically evaluated for CO₂ adsorption. Notably, the maximum CO₂ adsorption capacities reached 4.82 mmol g⁻¹ and 7.01 mmol g⁻¹ at 25 °C and 0 °C under 1 bar pressure, respectively, which is primarily attributed to the well-developed narrow microporosity, with boric acid playing an indirect role in regulating pore formation during the activation. Finally, the underlying mechanisms contributing to the superior CO₂ adsorption performance are comprehensively discussed. In this study, boron-doped porous carbons derived from water chestnut shells exhibit a strong potential as sustainable and efficient sorbents for carbon capture.
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Wang et al. (2026) studied this question.
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