光催化
降级(电信)
电子顺磁共振
X射线光电子能谱
光致发光
扫描电子显微镜
化学工程
傅里叶变换红外光谱
介电谱
猝灭(荧光)
漫反射红外傅里叶变换
材料科学
光谱学
化学
光化学
电化学
计算机科学
有机化学
催化作用
复合材料
光电子学
工程类
荧光
核磁共振
物理化学
物理
电信
量子力学
电极
作者
Zhongzheng Hu,Xiaoyun Xie,Shan Li,Mengxi Song,Guiwei Liang,Jing Zhao,Zhaowei Wang
标识
DOI:10.1016/j.cej.2020.126541
摘要
Abstract The novel heterojunction photocatalysts also known as carbon quantum dots-decorated BiOCOOH/ultrathin g-C3N4 nanosheets (CQDs/BiOCOOH/uCN) were designed, where carbon quantum dots (CQDs) acted as mediators to shuttle electrons between BiOCOOH and ultrathin g-C3N4 nanosheets (uCN). The physicochemical properties of as-obtained composites were systematically characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffractometry, Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. The 4-CQDs/BiOCOOH/uCN consisting of 50 wt% ultrathin g-C3N4 nanosheets (uCN) and 4 mL CQDs solution manifested the optimal photoactivity. After 90 min of LED lamp irradiation, the STZ degradation efficiency by 4-CQDs/BiOCOOH/uCN reached 99.28% ± 1.04, and the corresponding degree of mineralization was 49.58% ± 1.36. The enhanced photocatalytic performance of 4-CQDs/BiOCOOH/uCN was owing to the fast photogenerated charges transfer and separation revealed by photoluminescence (PL), transient photocurrent responses and electrochemical impedance spectra (EIS) measurements. By means of the radicals quenching experiments and electron spin resonance spectroscopy (ESR) analysis, it was demonstrated that •O2– and •OH were the dominant reactive species of STZ degradation. Besides, the effects of catalyst dosage (0.2–1.2 g/L), pH value (3.0–11.0), natural organic matter and different anions (Cl−, SO42−, NO3−) on the photocatalytic activity of 4-CQDs/BiOCOOH/uCN composite were systematically explored. 17 main intermediates were found based on high-resolution mass spectrometry (HRMS) detection. Eventually, the 4-CQDs/BiOCOOH/uCN composite showed favorable reusability in recycling experiments, and displayed satisfactory degradation abilities for STZ in deionized water (99.28% ± 1.04), tap water (97.15% ± 1.16), river water (96.44% ± 0.76), and wastewater treatment plant effluent (96.19% ± 1.20).
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