Cu2O/g-C3N4微球的合成及性质研究摘要本文采用使用煅烧法制备了g-C3N4纳米材料,并使用超声分散法和回流法制备了Cu2O/g-C3N4纳米复合材料。采用X射线衍射分析(XRD)研究了g-C3N4和Cu2O/g-C3N4的晶体结构,使用扫描电子显微镜(SEM)研究了g-C3N4和Cu2O/g-C3N4的形貌,采用傅里叶红外光谱(FTIR)和紫外光谱(UV)研究了g-C3N4和Cu2O/g-C3N4的的化学结构。使用循环伏安研究了g-C3N4和Cu2O/g-C3N4的循环稳定性。实验和表征结果表明:Cu2O与g-C3N4面面接触,两相间化学作用强烈;Cu2O/g-C3N4催化剂能有效利用太阳光,电子-空穴得到有效分离;当n(Cu2O)∶n(g-C3N4)=5∶1时,Cu2O/g-C3N4催化剂的活性最佳,在可见光下反应30min时,甲基橙降解率达84.1%;Cu2O/g-C3N4具有较好的活性稳定性,重复使用6次,甲基橙降解率降至64.7%;电子-空穴是Cu2O/g-C3N4光催化降解甲基橙的主要活性物种。关键词:Cu2O;g-C3N4;纳米复合;光催化AbstractInthispaper,g-C3N4nanomaterialswerepreparedbycalcinationmethod,andCu2O/g-C3N4nanocompositeswerepreparedbyultrasonicdispersionmethodandrefluxmethod.Thecrystalstructuresofg-C3N4andCu2O/g-C3N4werestudiedbyX-raydiffraction(XRD).Themorphologyofg-C3N4andCu2O/g-C3N4wasstudiedbyscanningelectronmicroscopy(SEM).Fourierinfraredwasused.Thechemicalstructuresofg-C3N4andCu2O/g-C3N4wereinvestigatedbyFTIRandUV.Thecyclicstabilityofg-C3N4andCu2O/g-C3N4wasinvestigatedusingcyclicvoltammetry.TheexperimentalandcharacterizationresultsshowthatCu2Oisincontactwithg-C3N4,andthechemicalinteractionbetweenthetwophasesisstrong.TheCu2O/g-C3N4catalystcaneffectivelyutilizesunlight,andtheelectron-holeiseffectivelyseparated.Whenn(Cu2O):n(g-C3N4)=5:1,theactivityofCu2O/g-C3N4catalystisthebest.Whenreactedfor30minundervisiblelight,thedegradationrateofmethylorangeis84.1%;Cu2O/g-C3N4hasgoodactivitystability.Afterrepeatedusefor6times,thedegradationrateofmethylorangedecreasedto64.7%;electron-holewasthemainactivespeciesofphotocatalyticdegradationofmethylorangebyCu2O/g-C3N4.Keywords:Cu2O;g-C3N4;Nanocomposite;Photocatalytic目录摘要............................................................................................................................1Abstract..........................................................................................................................1..............................................................................................................................................7.....................................................................................................................7............................................7...............................................7..........................................8.........................................8...................................................8..........................................10....................................................10.....................................................10.............................................10..........................................................11............................................11..................................................11........................................................................................................................................14..................................................14..................................................14..................................................14............................................