热分解制备CeO2-还原氧化石墨烯及其光催化性能
Preparation and photocatalytic performance of CeO2-reduced graphene oxide by thermal decomposition
作者单位E-mail
王卓 贵州大学材料与冶金学院, 贵阳 550025  
张俊山 贵州大学材料与冶金学院, 贵阳 550025
贵州省冶金工程与过程节能重点实验室, 贵阳 550025 
 
杨绍艳 贵州大学材料与冶金学院, 贵阳 550025
贵州省冶金工程与过程节能重点实验室, 贵阳 550025 
 
周玲艳 贵州大学材料与冶金学院, 贵阳 550025  
李叶迪 贵州大学材料与冶金学院, 贵阳 550025  
兰苑培 贵州大学材料与冶金学院, 贵阳 550025
贵州省冶金工程与过程节能重点实验室, 贵阳 550025 
yplan@gzu.edu.cn 
摘要: 通过一步水热法制备了CeCO3OH-rGO (还原氧化石墨烯),并在氩气(Ar)气氛下焙烧制备得到CeO2-rGO复合材料。采用X射线衍射、扫描电子显微镜、X射线光电子能谱以及紫外可见漫反射光谱(UV-Vis DRS)等研究了复合材料的物相组成、微观形貌、空位缺陷和光电化学特性等。对比研究了不同GO (氧化石墨烯)负载量和NH4HCO3添加量下所制备材料的光催化性能,发现GO负载量为10 mg、NH4HCO3添加量为15 mmol的样品(CeO2-10rGO-15)具有最窄的禁带宽度(3.17 eV),对亚甲蓝(MB)的光催化降解率达80.66%。适宜的rGO负载量有利于促进CeO2空位缺陷的形成,也有利于光生载流子的分离,进而促进光催化性能。
关键词: 二氧化铈  氧化石墨烯  热分解  复合材料  光催化
基金项目: 国家自然科学基金(No.52164025)、贵大培育[2019]30号、贵大SRT字(2022)012号资助。
Abstract: CeCO3OH-rGO (reduced graphene oxide) was prepared by a one-step hydrothermal method, and CeO2-rGO composites were prepared by roasting under argon (Ar) atmosphere. The phase composition, microstructure, vacancy defects, and photoelectrochemical properties of the composites were studied by X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy, UV visible diffuse reflectance spectroscopy (UV-Vis DRS), etc. The photocatalytic performance of the composites with different GO (graphene oxide) and NH4HCO3 addition amounts respectively were comparatively studied. It was found that the CeO2-10rGO-15 with GO and NH4HCO3 addition amounts of 10 mg and 15 mmol respectively had the narrowest band-gap width (3.17 eV), and the photocatalytic degradation ratio of methylene blue (MB) could reach 80.66%. It is beneficial to the formation vacancy defect of CeO2 and the separation of photogenic carriers for rGO loading suitably, thus promoting photocatalytic performance.
Keywords: CeO2  graphene oxide  thermal decomposition  composite  photocatalysis
投稿时间:2024-02-27 修订日期:2024-07-11
摘要点击次数:  1002
全文下载次数:  1103
王卓,张俊山,杨绍艳,周玲艳,李叶迪,兰苑培.热分解制备CeO2-还原氧化石墨烯及其光催化性能[J].无机化学学报,2024,40(9):1708-1718.
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