4.7 Article

Gradient synthesis of carbon quantum dots and activated carbon from pulp black liquor for photocatalytic hydrogen evolution and supercapacitor

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DOI: 10.1007/s42114-023-00714-4

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Black liquor; Carbon quantum dots; Activated carbon; Photocatalytic hydrogen evolution; Supercapacitor

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This study reports a green and simple strategy to produce Na+-functionalized carbon quantum dots (Na+-CQDs), N and S co-doped CQDs (N/S-CQDs), and N and S co-doped KOH-activated carbon (N/S-KAC) from black liquor (BL) using dialysis, hydrothermal carbonization, and activation-carbonization. The resulting materials showed excellent photoluminescence and up-conversion luminescence, leading to improved hydrogen evolution efficiency and supercapacitor performance. This study provides a versatile and scalable approach for the construction and co-production of nanostructured materials, photocatalysts, and energy storage devices.
Black liquor (BL) is a by-product of the chemical pulping industry and is mainly used as a low-value fuel; however, its potential to produce high-value products has not been fully exploited. In this study, a green and simple strategy is reported for the gradient production of Na+-functionalized carbon quantum dots (Na+-CQDs) for the first time, N and S co-doped CQDs (N/S-CQDs), and N and S co-doped KOH-activated carbon (N/S-KAC) from BL by dialysis, hydrothermal carbonization and activation-carbonization, respectively. Due to the good electron trapping ability, photoluminescence and promising up-conversion luminescence of CQDs, the hydrogen evolution efficiency of Na+-CQDs/TiO2 and N/S-CQDs/TiO2 photocatalysts was improved by 2.45 and 1.46 times, respectively, compared with pure TiO2. N/S-KAC with a high specific surface area of 2294 m(2) g(- 1) provides an excellent specific capacitance of 253 F g(- 1) at 0.5 A g(- 1) and a promising energy density of 26.92 Wh kg(- 1) under a power density of 566 W kg(- 1) for the fabricated symmetrical supercapacitor. Moreover, the electrode material has good cycling stability with a capacitance retention of similar to 93.91% after 5000 cycles. This pathway provides a versatile and scalable approach for the construction and co-production of nanostructured materials, photocatalysts and energy storage devices.

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