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Two-dimensional MXene enabled carbon quantum dots@Ag with enhanced catalytic activity towards the reduction of p-nitrophenol

A composite of cuttlefish ink-based carbon quantum dots@Ag/MXene (CQD@Ag/MXene) was firstly synthesized by solvothermal method as a catalyst for reduction of p-nitrophenol (PNP) to p-aminophenol (PAP). CQD@Ag/MXene was characterized by scanning electron microscopy (SEM), field emission transmission...

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Detalles Bibliográficos
Autores principales: Chen, Yingxin, Yang, Chunli, Huang, Xiaotong, Li, Lu, Yu, Na, Xie, Huan, Zhu, Zebin, Yuan, Yong, Zhou, Lihua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8981249/
https://www.ncbi.nlm.nih.gov/pubmed/35425493
http://dx.doi.org/10.1039/d1ra09177h
Descripción
Sumario:A composite of cuttlefish ink-based carbon quantum dots@Ag/MXene (CQD@Ag/MXene) was firstly synthesized by solvothermal method as a catalyst for reduction of p-nitrophenol (PNP) to p-aminophenol (PAP). CQD@Ag/MXene was characterized by scanning electron microscopy (SEM), field emission transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and Raman. The results show that loading on 2D material MXene can prevent the aggregation of CQD@Ag and expose more active sites, which contributes to a superior catalytic activity with a pseudo-first-order rate constant k (2.28 × 10(−2) s(−1)) and mass-normalized rate constant k(m) (5700 s(−1) g(−1)), nearly 2 times higher than CQD@Ag without MXene (k = 1.09 × 10(−2) s(−1) and k(m) = 2725 s(−1) g(−1)). Besides, CQD@Ag/MXene showed excellent reusability which even retained about 65% activity in successive 10 cycles. The high adsorption rate to PNP and the promotion of forming H radicals may be the reason for the outstanding catalytic activity of CQD@Ag/MXene. CQD@Ag/MXene can be a potential candidate in the removal of environmental pollutants due to its facile synthesis and high catalytic efficiency.