物理化学学报
物理化學學報
물이화학학보
ACTA PHYSICO-CHIMICA SINICA
2010年
3期
654-662
,共9页
张琼%贺蕴秋%陈小刚%胡栋虎%李林江%尹婷%季伶俐
張瓊%賀蘊鞦%陳小剛%鬍棟虎%李林江%尹婷%季伶俐
장경%하온추%진소강%호동호%리림강%윤정%계령리
二氧化钛%氧化石墨%插层结构%复合材料%光催化性能
二氧化鈦%氧化石墨%插層結構%複閤材料%光催化性能
이양화태%양화석묵%삽층결구%복합재료%광최화성능
Titania%Graphite oxide%Intercalated structure%Composite material%Photocatalytic property
采用氧化石墨(GO)和硫酸钛作为初始反应物,在低温下(80℃)制备了纳米级的氧化钛.氧化石墨插层(TiO_2-GO)复合材料,研究了这一复合材料的紫外光催化性能.结果表明,在采用TiO_2-GO插层复合材料对甲基橙溶液进行紫外光催化降解时,其降解效率η=1.17 mg·min~(-1)·g~(-1),明显优于德固赛P25氧化钛粉.通过对TiO_2-GO插层复合材料进行x射线衍射(XRD)、傅里叶红外(FT-IR)光谱、X射线光电子能谱(XPS)和场发射扫描电子显微镜(FESEM)等测试,表征了产物的晶相结构、界面状况及其显微结构.结果表明:插层结构中的TiO_2晶粒为锐钛矿和金红石的混合相,且锐钛矿相含量大于金红石相含最;氧化石墨层间的含氧基团如C=O,基本被还原.对TiO_2-GO插层复合材料的形成机理以及该材料具有优越光催化性能的原因进行了探讨.
採用氧化石墨(GO)和硫痠鈦作為初始反應物,在低溫下(80℃)製備瞭納米級的氧化鈦.氧化石墨插層(TiO_2-GO)複閤材料,研究瞭這一複閤材料的紫外光催化性能.結果錶明,在採用TiO_2-GO插層複閤材料對甲基橙溶液進行紫外光催化降解時,其降解效率η=1.17 mg·min~(-1)·g~(-1),明顯優于德固賽P25氧化鈦粉.通過對TiO_2-GO插層複閤材料進行x射線衍射(XRD)、傅裏葉紅外(FT-IR)光譜、X射線光電子能譜(XPS)和場髮射掃描電子顯微鏡(FESEM)等測試,錶徵瞭產物的晶相結構、界麵狀況及其顯微結構.結果錶明:插層結構中的TiO_2晶粒為銳鈦礦和金紅石的混閤相,且銳鈦礦相含量大于金紅石相含最;氧化石墨層間的含氧基糰如C=O,基本被還原.對TiO_2-GO插層複閤材料的形成機理以及該材料具有優越光催化性能的原因進行瞭探討.
채용양화석묵(GO)화류산태작위초시반응물,재저온하(80℃)제비료납미급적양화태.양화석묵삽층(TiO_2-GO)복합재료,연구료저일복합재료적자외광최화성능.결과표명,재채용TiO_2-GO삽층복합재료대갑기등용액진행자외광최화강해시,기강해효솔η=1.17 mg·min~(-1)·g~(-1),명현우우덕고새P25양화태분.통과대TiO_2-GO삽층복합재료진행x사선연사(XRD)、부리협홍외(FT-IR)광보、X사선광전자능보(XPS)화장발사소묘전자현미경(FESEM)등측시,표정료산물적정상결구、계면상황급기현미결구.결과표명:삽층결구중적TiO_2정립위예태광화금홍석적혼합상,차예태광상함량대우금홍석상함최;양화석묵층간적함양기단여C=O,기본피환원.대TiO_2-GO삽층복합재료적형성궤리이급해재료구유우월광최화성능적원인진행료탐토.
TiO_2-graphite oxide (TiO_2-GO) composites were successfully prepared at low temperature (80 CC) using graphite oxide (GO) and titanium sulfate (Ti(SO_4)_2) as initial reactants. The photocatalytic properties of TiO_2-GO under UV light irradiation were also studied. Results show that the degradation rate of methyl orange is 1.17 mg·min~(-1)·g~(-1) (referring to the efficiency of the initial 15 min). Compared with Degussa P25 powders, this intercalation composite is far more efficiently. In addition, the crystalline structure, interface status and microscopic structure of TiO_2-GO were characterized by X-ray diffraction (XRD), Fourier-transform infrared (FT-IR) spectroscopy, X-ray photoelectron spectroscopy (XPS) and field emission scanning electron microscopy (FESEM). Result showed that the TiO_2 crystallites in the intercalated structure were composed of anatase and rutile phase with the former phase being enriched. The functional groups present in GO such as carboxyl (C=O) were mostly reduced in the intercalation composite. On the other hand, the synthesis mechanism and the main reasons responsible for the superior photocatalytic properties of TiO_2-GO are also discussed.