Edge state engineering of nitrogen/phosphorus co-doped graphene nanoribbons towards electron-transfer-based peroxydisulfate activation
[Display omitted] •The multi-walled carbon nanotubes were unfolded to nanoribbon.•Graphene nanoribbon edges were enriched by nitrogen/phosphorus.•Edges play an important role for electron transfer-dominated pathway. The electron transfer-based nonradical advanced oxidation processes (AOPs) exhibit g...
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Veröffentlicht in: | Separation and purification technology 2024-12, Vol.350, p.127842, Article 127842 |
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Sprache: | eng |
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•The multi-walled carbon nanotubes were unfolded to nanoribbon.•Graphene nanoribbon edges were enriched by nitrogen/phosphorus.•Edges play an important role for electron transfer-dominated pathway.
The electron transfer-based nonradical advanced oxidation processes (AOPs) exhibit great potential for degrading organic pollutants. However, achieving efficient electron transfer-based nonradical AOPs remains challenging. In this study, we developed the edge-rich and nitrogen/phosphorus (N/P) co-doped graphene nanoribbons by unfolding the multi-walled carbon nanotubes (MWCNTs). The catalysts with the edge-rich structure are capable of efficiently activating the peroxydisulfate (PDS) towards the degradation of carbamazepine (CBZ), a representative pharmaceutical and personal care products (PPCPs). Through adjusting the N/P ratio, the N/P co-doped graphene nanoribbons presented the optimal degradation kinetic constant of 0.452 min−1, compared with 0.0611 min−1 for the intact MWCNTs. Electrochemical characterizations, in situ Raman, galvanic oxidation tests, and quenching experiments confirmed that the N/P co-doped graphene nanoribbons followed an electron transfer-dominated nonradical pathway for pollutant degradation. Density functional theory (DFT) demonstrated that the exposed N/P co-doped edges at the boundary of graphene nanoribbons could elongated OO bond of PDS in facilitating PDS activation. This study provides a new approach to develop the nonradical AOPs-based techniques. |
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ISSN: | 1383-5866 |
DOI: | 10.1016/j.seppur.2024.127842 |