杂原子
光催化
催化作用
兴奋剂
光化学
化学
电子转移
碳纤维
降级(电信)
材料科学
反应性(心理学)
有机化学
戒指(化学)
复合材料
病理
复合数
电信
替代医学
医学
光电子学
计算机科学
作者
Ziqi Zhu,Xinghui Li,Min Luo,Minzhi Chen,Weimin Chen,Pei Yang,Xiaoyan Zhou
标识
DOI:10.1016/j.jcis.2021.07.016
摘要
The photocatalytic degradation of organic pollutant by carbon-based materials is still a challenge. Herein, xylose-derived carbon dots (X-CDs) and chitosan-derived CDs (C-CDs) were synthesized by heteroatoms-doping strategy. Although there is almost no difference in fluorescence emission behaviors, the two types of CDs demonstrated different advantages in photocatalysis and peroxymonosulfate (PMS) activation. Comparative research revealed that the X-CDs with doping of heteroatom S was superior in the separation of electron-hole pairs, resulting in a higher catalytic performance, while the S, N co-doped C-CDs can only exhibit high photocatalytic reactivity when they were coupled with PMS. The underlying reason is that the N-related functional groups with strong electron-donating property weakened the electron-trapping capacity of S-related energy level, but surface state resulting from this doping structures were conducive to promoting photo-generated electron transfer from C-CDs to PMS and played the primary role in organic oxidation. Thanks to the doping effect, both the X-CDs and C-CDs/PMS system displayed high photocatalytic performance for methylene blue removal under sunlight irradiation, showing almost 100% degradation efficiency in a 30 min period. The present study provides a valuable insight for the synthesis of CDs-based catalysts but also establishes a very promising catalytic oxidation system.
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