Key Laboratory of the Three Gorges Reservoir Region's Eco-Environment of Ministry of Education, Chongqing University, Chongqing 400044, PR China.
The Key Laboratory of Water and Sediment Sciences, Ministry of Education, College of Environmental Sciences and Engineering, Peking University, Beijing 100871, PR China; The Beijing Innovation Center for Engineering Science and Advanced Technology (BIC-ESAT), Peking University, Beijing, 100871, PR China.
J Hazard Mater. 2020 Jan 5;381:120957. doi: 10.1016/j.jhazmat.2019.120957. Epub 2019 Aug 7.
A novel tubular graphitic carbon nitride (g-CN) modified with carbon quantum dots (CQDs) was fabricated and employed for the elimination of carbamazepine (CBZ) under visible light irradiation. The as-fabricated metal-free catalysts exhibited tubular morphologies due to the preforming of tubular protonated melamine with CQDs surface adsorption as the polymerization precursors. The surface bonded CQDs did not alter the band gap structure of g-CN, but greatly inhibited the charge recombination. Therefore, the CBZ degradation kinetics of tubular g-CN were increased by over 5 times by the incorporation of CQDs. The main active species for CBZ degradation were found to be superoxide radical (O) and photo-generated holes (h), which were further confirmed by electron spin resonance (ESR) analysis. In addition, the degradation pathways of CBZ were clarified via intermediates identification and quantum chemical computation using density functional theory (DFT) and wave function analysis. The olefinic double bond with the highest condensed Fukui index (f = 0.108) in CBZ molecule was found to be the most preferable sites for radical attack. Moreover, good stability of the as-prepared photocatalysts was observed in the consecutive recycling cycles, while the slight decline of photocatalytic activity was attributed to the minimal surface oxidation.
一种新型管状石墨相氮化碳(g-CN)被制备出来,并被用于在可见光照射下消除卡马西平(CBZ)。由于管状质子化三聚氰胺的形成以及碳量子点(CQDs)表面吸附作为聚合前体,所制备的无金属催化剂呈现管状形态。表面结合的 CQDs 并没有改变 g-CN 的能带结构,但大大抑制了电荷复合。因此,通过引入 CQDs,管状 g-CN 的 CBZ 降解动力学提高了 5 倍以上。通过电子顺磁共振(ESR)分析进一步证实,CBZ 降解的主要活性物质是超氧自由基(O)和光生空穴(h)。此外,通过使用密度泛函理论(DFT)和波函数分析进行中间产物鉴定和量子化学计算,阐明了 CBZ 的降解途径。在 CBZ 分子中具有最高凝聚 Fukui 指数(f=0.108)的烯键被发现是自由基攻击的最优选定位置。此外,所制备的光催化剂在连续的循环回收中表现出良好的稳定性,而光催化活性的轻微下降归因于最小的表面氧化。