首页 | 本学科首页   官方微博 | 高级检索  
     检索      

镶嵌Pt的二氧化钛纳米管的合成及其光催化性能研究
引用本文:李海龙,罗武林,田文宇,陈涛,黎春,孙茂,朱地,刘冉冉,赵宇亮,刘春立.镶嵌Pt的二氧化钛纳米管的合成及其光催化性能研究[J].光谱学与光谱分析,2009,29(6):1623-1626.
作者姓名:李海龙  罗武林  田文宇  陈涛  黎春  孙茂  朱地  刘冉冉  赵宇亮  刘春立
作者单位:1. 北京分子科学国家实验室,北京大学化学与分子工程学院,北京,100871
2. 中国科学院高能物理研究所,核分析技术开放重点实验室及国家纳米中心-高能物理研究所纳米生物效应联合实验室,北京,100049
基金项目:国家自然科学基金,教育部高等学校博士学科点专项科研基金,国防科工委军工遗留专项基金,国家大学生创新训练计划项目 
摘    要:以金红石相二氧化钛(TiO2)粉体为原料,采用水热法合成了二氧化钛纳米管(Titania nanotubes,简写为TNTs),然后把H2PtCl6的无水乙醇溶液引入到TNTs中,得到镶嵌Pt的二氧化钛纳米管(Pt/TNTs).利用透射电镜(TEM)、X射线衍射(XRI))和紫外-可见光谱(UV-Vis)对产物进行了表征,并重点研究了Pt/TNTs的光催化性能.结果表明,有直径约为3 nm的Pt纳米粒子插入到了TNTs中,且Pt粒子以Pt单质的形式存在.Pt/TNTs在可见光区域表现出较强的吸收,并且其起始吸收带边发牛明显红移.紫外光催化降解甲基橙实验结果表明,金红石相TiO2,TNTs和Pt/TNTs对甲基橙溶液的降解率分别达到46.8%,57.2%和84.6%,Pt/TNTs的光催化活性较金红石相二氧化钛粉体和纯TNTs有显著的提高.

关 键 词:纳米管  二氧化钛  水热法  光催化
收稿时间:2008/3/28

Fabrication and Photocatalytic Activity of Pt-Inserted Titania Nanotubes
LI Hai-long,LUO Wu-lin,TIAN Wen-yu,CHEN Tao,LI Chun,SUN Mao,ZHU Di,LIU Ran-ran,ZHAO Yu-liang,LIU Chun-li.Fabrication and Photocatalytic Activity of Pt-Inserted Titania Nanotubes[J].Spectroscopy and Spectral Analysis,2009,29(6):1623-1626.
Authors:LI Hai-long  LUO Wu-lin  TIAN Wen-yu  CHEN Tao  LI Chun  SUN Mao  ZHU Di  LIU Ran-ran  ZHAO Yu-liang  LIU Chun-li
Institution:LI Hai-long1,LUO Wu-lin1,TIAN Wen-yu1,CHEN Tao1,LI Chun1,SUN Mao1,ZHU Di1,LIU Ran-ran1,ZHAO Yu-liang2,LIU Chun-li11.Beijing National Laboratory for Molecular Science,College of Chemistry , Molecular Engineering,Peking University,Beijing 100871,China2.Laboratory for Bio-Environmental Health Sciences of Nanoscale Materials , Nanosafety , Key Laboratory of Nuclear Analytical Techniques,Institute of High Energy Physics,Chinese Academy of Sciences,Beijing 100049,China
Abstract:Titania nanotubes (TNTs) were synthesized by hydrothermal treatment of rutile-phase TiO2 nanoparticals in NaOH solution at 110 ℃ for 24 hours. After drying in aceton for 36 h, the TNTs were under vacuum drying for 24 h at room temperature. The Pt-inserted titania nanotubes (Pt/TNTs) were obtained by filling H2PtCl6 ethanol solution into the TNTs after vacuum drying. The characterizations of the as-synthesized samples were confirmed by TEM, XRD, and UV-Vis. The photocatalytic activity of the Pt/TNTs was investigated by photo-induced decomposition of methyl orange(MO)under the main 365 nm UV-light. In order to comparison, the photocatalytic activity of both the rutile-phase TiO2 nanoparticles and pure TNTs were also investigated at the same time under the same experimental conditions. The TEM images show that the TNTs are hollow, a few hundred nanometers long, and the inner/outer diameter is about 6/10 nm. The crystal structure of TNTs is H2Ti2O5·H2O with a little Na. Both the shape and the crystalline of the TNTs are not changed after the modification. The oval or round Pt0 nanoparticals, about 3 nm in diameter, are found only in the nanotubes. Pt/TNTs exhibit enhanced absorption at the visible range in the UV-Vis spectra and its start absorption band edge(λ0≈457 nm)is obviously redshifted compared to the rutile-phase TiO2 nanoparticals and pure TNTs. The Pt nanoparticles are found to significantly enhance the photocatalytic activity of TNTs. Pt/TNTs are demonstrated to be highly efficient for the UV-light induced photocatalytic decomposition of MO compared to both the rutile-phase TiO2 nanoparticals and pure TNTs. After irradiation for 60 min, the photocatalysis decomposition rate of MO in rutile-phase TiO2 nanoparticals, TNTs and Pt/TNTs are 46.8%, 57.2% and 84.6% respectively.
Keywords:Pt
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号