期刊文献+

碳量子点修饰石墨相氮化碳光催化降解罗丹明B的研究 被引量:10

Photocatalytic degradation of rhodamine B by carbon quantum dot modified graphite phase carbon nitride
下载PDF
导出
摘要 利用抗坏血酸(AA)对石墨相氮化碳(g-C3N4)进行改性,制备出表面含有碳量子点(CQDs)的催化剂CQDs/g-C3N4.通过X射线衍射(XRD)、紫外可见光漫反射(UV-Vis DRS)、透射电镜(TEM)、光致发光光谱(PL)、X射线光电子能谱(XPS)对催化剂进行结构、形貌、光学性能测试.发现CQDs很好的负载到了g-C3N4表面,增加了催化剂表面活性位点.UV-Vis DRS表明碳量子点能够使催化剂的吸收光谱发生红移,同时缩小了催化剂的带隙宽度,增强了对光的吸收能力.光致发光光谱则显示了碳量子点的修饰能够有效的抑制光生电子空穴对的复合,从而提高光催化性能.通过光降解实验表明0.01g CQDs/g-C3N4催化剂在80℃下,3h对罗丹明B(RhB)的降解率为57.2%.捕获剂实验则说明了超氧自由基(·O2^-)在光降解体系中起到了促进反应速率的作用. In this study,CQDs/g-C3N4 was prepared by using ascorbic acid and urea as precursors.The characterizations of CQDs/g-C3N4 were carried out by X-ray diffraction(XRD),ultraviolet visible light diffuse reflection(UV-vis),transmission electron microscopy(TEM),fluorescence spectrum(PL),X-ray photoelectron spectroscopy(XPS).The results showed that carbon quantum dots were well loaded onto the surface of graphite phase carbon nitride bringring about the active sites of g-C3N4 increase.The CQDs modification could effectively improve the visible light absorbance of g-C3N4,as well as decrease its band gap.At the same time,the addition of carbon quantum dots could inhibit the recombination of photogenerated electron-hole pair in catalyst.Under simulated light irradiation,the RhB photodegradation ability of CQDs/g-C3N4 was significantly higher than that of single g-C3N4.56.7% of RhB could be degraded over 0.01g of CQDs/g-C3N4 at 80℃ in 3h.Capture agent experiment result showed that superoxide radical played a major role in the photodegradation reaction system.
作者 刘帅 李学雷 王烁天 王彦娟 苑兴洲 张健 梁飞雪 胡绍争 LIU Shuai;LI Xue-lei;WANG Shuo-tian;WANG Yan-juan;YUAN Xing-zhou;ZHANG Jian;LIANG Fei-xue;HU Shao-zheng(Liaoning Shihua University,Fushun 113001,China;Yingkou Institute of Tecnology,Yingkou 115014,China)
出处 《中国环境科学》 EI CAS CSCD 北大核心 2020年第7期2909-2916,共8页 China Environmental Science
基金 辽宁省自然科学基金资助项目(20170540475)。
关键词 碳量子点 光生电子空穴对 超氧自由基 carbon quantum dots photogenic electron hole pair superoxide radical
  • 相关文献

参考文献6

二级参考文献43

共引文献51

同被引文献106

引证文献10

二级引证文献32

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部