A novel ternary MQDs/NCDs/TiO2 nanocomposite that collaborates with activated persulfate for efficient RhB degradation under visible light irradiation†

IF 2.5 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Qian Zhang, Han Zhao, Yuming Dong, Xiangmiao Zhu, Xiang Liu and Hexing Li
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引用次数: 11

Abstract

Novel TiO2 nanosheets co-modified with MoS2 quantum dots (MQDs) and N-doped carbon dots (NCDs), designated MQDs/NCDs/TiO2, were synthesized through a simple and mild process. The MQDs/NCDs/TiO2 nanocomposites exhibited significantly improved efficiency in the photocatalytic degradation of RhB compared to pure TiO2, mainly attributed to the synergy of excellent photoconversion by NCDs and efficient separation and transfer of photogenerated electron–hole pairs induced by the two heterojunctions formed in MQDs/NCDs/TiO2. More interestingly, the degradation rate was further promoted by 2.15 times after adding 2 mmol persulfate to the MQDs/NCDs/TiO2 photocatalytic system. This result is due to the excellent collaboration between the photocatalysis and persulfate activation, in which the persulfate was effectively activated by photogenerated electrons to generate abundant sulfate radicals (SO4˙?) and hydroxyl radicals (˙OH); meanwhile, the electron consumption caused by the persulfate effectually restrained surface electron–hole recombination, inducing more holes (h+) to participate in pollutant degradation. Radical quenching experiments and electron spin resonance spectra show that SO4˙?, ˙OH, ˙O2? and h+ were all in charge of RhB elimination in the MQDs/NCDs/TiO2–PS system. This work may provide guidance for employing dual quantum dots as co-catalysts, cooperating with activated persulfate, to enhance photocatalytic performance in contaminant degradation.

Abstract Image

一种新型三元MQDs/NCDs/TiO2纳米复合材料与活化过硫酸盐协同作用,在可见光照射下有效降解RhB
以二硫化钼量子点(MQDs)和n掺杂碳点(NCDs)为共聚物,通过简单、温和的工艺合成了新型二氧化钛纳米片,命名为MQDs/NCDs/TiO2。与纯TiO2相比,MQDs/NCDs/TiO2纳米复合材料光催化降解RhB的效率显著提高,这主要是由于MQDs/NCDs/TiO2形成的两种异质结诱导光生电子空穴对高效分离和转移的协同作用。更有趣的是,在MQDs/NCDs/TiO2光催化体系中加入2 mmol过硫酸盐后,降解率提高了2.15倍。这一结果是由于光催化和过硫酸盐活化之间的良好协同作用,其中过硫酸盐被光生电子有效活化,生成丰富的硫酸盐自由基(SO4˙?)和羟基自由基(˙OH);同时,过硫酸盐引起的电子消耗有效地抑制了表面电子-空穴复合,诱导更多空穴(h+)参与污染物降解。自由基猝灭实验和电子自旋共振谱表明,SO4˙?˙哦,˙o2 ?和h+在MQDs/NCDs/ TiO2-PS体系中均负责RhB的消除。本研究为利用双量子点作为助催化剂,与活化过硫酸盐协同作用,提高光催化降解污染物的性能提供了指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
New Journal of Chemistry
New Journal of Chemistry 化学-化学综合
CiteScore
5.30
自引率
6.10%
发文量
1832
审稿时长
2 months
期刊介绍: A journal for new directions in chemistry
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