n掺杂碳点†增强光催化活性的研究

IF 4.2 3区 化学 Q2 CHEMISTRY, PHYSICAL
Hector Daniel Almeida Gonzalez , Gabriel Rafael Guerrero Porras , Hervé Vezin , Lisandra Morales Alvarez , Angel Luis Corcho Valdés , L. Julieth Bravo Martínez , Alicia M. Díaz-García , David González-Martínez , Jose M. Moran-Mirabal , Clarissa Murru , Johnny Deschamps , Claudia Iriarte-Mesa , Qixiang Jiang , Freddy Kleitz , Luis Felipe Desdin-Garcia , Manuel Antuch
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引用次数: 0

摘要

碳纳米结构(点)已经成为光催化降解水污染物的一种新的和可持续的替代方案。本文介绍了微波辅助合成多掺杂碳纳米材料(CNs)的方法。总体而言,获得了四种碳纳米结构:(i)氮掺杂CNs (N- cds), (ii)氮与硫共掺杂CNs (N,S-CNs), (iii)氮与磷共掺杂CNs (N,P-CNs), (iv)氮、硫和磷多掺杂CNs (N,S,P-CNs)。通过傅里叶变换红外光谱(FTIR)和x射线光电子能谱(XPS)对这些纳米颗粒进行表征,确定了CO、C-N和N-H官能团对应的拉伸模式。此外,紫外可见光谱和荧光光谱允许在~ 325和400 nm处检测n -π *和π -π *吸收带,以及在438 nm处的光发射。高分辨率透射电子显微镜(TEM)表征证实了纳米材料之间的结构和形态差异,其尺寸从1到100 nm不等,这取决于起始前驱体的化学成分。最后,考虑形态、组成、催化剂和染料浓度对甲苯胺蓝降解的影响,评估了CNs的光催化活性。这种催化过程遵循伪一级动力学,其中N-CDs表现出最高的甲苯胺蓝降解潜力。我们的研究结果强调了碳纳米材料的光催化活性是一个多因素的过程,本质上是由OH自由基的形成驱动的,其中掺杂和颗粒形态也在光催化中起着共同的作用。这项工作为理解光催化纳米碳的化学成分和结构及其在水中有机污染物降解中的应用开辟了一条途径,从而为废水处理提供了一种可持续的替代方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

On the enhanced photocatalytic activity of N-doped carbon dots†

On the enhanced photocatalytic activity of N-doped carbon dots†
Carbon nanostructures (dots) have emerged as a novel and sustainable alternative for the photocatalytic degradation of water pollutants. This work presents the synthesis of multidoped carbon nanomaterials (CNs) using a microwave-assisted method. Overall, four types of carbon nanostructures were obtained: (i) nitrogen-doped CNs (N-CDs), (ii) nitrogen and sulfur co-doped CNs (N,S-CNs), (iii) nitrogen and phosphorus co-doped CNs (N,P-CNs), and (iv) nitrogen, sulfur, and phosphorus multi-doped CNs (N,S,P-CNs). The characterization of these nanoparticles was performed via Fourier-transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS), enabling the identification of stretching modes corresponding to CO, C–N, and N–H functional groups. Additionally, UV-vis and fluorescence spectroscopies allowed the detection of n–π* and π–π* absorption bands at ∼325 and 400 nm, along with light emission at 438 nm. High-resolution transmission electron microscopy (TEM) characterization confirmed structural and morphological differences between the nanomaterials, which exhibited sizes ranging from 1 to 100 nm, depending on the chemical composition of the starting precursors. Finally, the photocatalytic activity of the CNs towards the degradation of toluidine blue was assessed, considering the effects of morphology, composition, and both catalyst and dye concentration on photodegradation. Such a catalytic process followed pseudo-first-order kinetics, where N-CDs exhibited the highest potential for toluidine blue degradation. Our results highlight that the photocatalytic activity of carbon nanomaterials is a multifactorial process essentially driven by the formation of OH radicals, where doping and particle morphology also play a combined role in photocatalysis. This work opens a route for understanding the chemical composition and structure of photocatalytic nanocarbons and their application to the degradation of organic pollutants in water, thus offering a sustainable alternative for wastewater treatment.
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来源期刊
Catalysis Science & Technology
Catalysis Science & Technology CHEMISTRY, PHYSICAL-
CiteScore
8.70
自引率
6.00%
发文量
587
审稿时长
1.5 months
期刊介绍: A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis. Editor-in-chief: Bert Weckhuysen Impact factor: 5.0 Time to first decision (peer reviewed only): 31 days
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