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铁离子掺杂TiO_(2)的制备及其光催化性能 被引量:5

Preparation and Photocatalytic Property of Iron-doped Titanium Dioxide Nanomaterials
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摘要 将Bola型两亲性短肽KI_(3)E在水溶液中组装成稳定的纤维状结构,以其自组装体作为有机模板并使用氨丙基三乙氧基硅烷为结构导向剂,利用其对TiO_(2)前驱体-二(2-羟基丙酸)二氢氧化二铵合钛的水解催化作用以及肽模板与铁离子之间的分子识别作用在TiO_(2)矿化沉积的同时引入铁离子,在温和的水溶液中制备出铁离子掺杂TiO_(2)纳米材料。使用TEM、BET、UV-vis DRS、XPS、XRD等手段对其结构和性能进行了表征。结果表明,铁元素以Fe2+/Fe3+的形式存在于TiO_(2)晶格中,抑制了晶体生长并使晶粒尺寸变小。同时,铁离子的掺杂减小了TiO_(2)的禁带宽度,提高了对可见光的响应和催化性质。铁离子掺杂量为0.5%TiO_(2),其光催化性能最好。 Iron-doped titanium dioxide(Fe-TiO_(2))nanomaterials were prepared with the stable fibrous nanostructure of self-assembled bola-type amphiphilic short peptide KI_(3)E as organic template and aminopropyl triethoxysilane as structure-directing agent via sol-gel process to ensure the simultaneous deposition of the titanium dioxide precursor and iron ions on the surface of the peptide templates.The Fe doped-TiO_(2)nanomaterials were fully characterized by Transmission electron microscope,UV-vis diffuse reflection spectroscopy,X-ray photoelectron spectroscopy,X-ray diffractometer.The results show that iron ions instead of partial titanium ions in the crystal lattice of titanium dioxide,which narrows the band gap of TiO_(2)and results in enhanced visible light responses.The test results of photocatalytic degradation of rhodamine B and methylene blue indicated that the Fe doped-TiO_(2)possessed significantly enhanced photocatalytic performance,compared to the commercial TiO_(2)(P25),while reached a maximum when the doping content of iron ions was 0.5%.
作者 荆倩 曹晗 刘方园 郗会娟 李超祥 邵韵航 曹美文 夏永清 王生杰 JING Qian;CAO Han;LIU Fangyuan;XI Huijuan;LI Chaoxiang;SHAO Yunhang;CAO Meiwen;XIAYongqing;WANG Shengjie(College of Chemical Engineering,China University of Petroleum,Qingdao 266580,China)
出处 《材料研究学报》 EI CAS CSCD 北大核心 2022年第11期862-870,共9页 Chinese Journal of Materials Research
基金 国家自然科学基金(21773310) 山东省重点科技研发计划(2019GGX103047) 山东省自然科学基金(ZR2020MB076)。
关键词 无机非金属材料 TiO_(2) 离子掺杂 Bola型两亲性短肽 光催化 inorganic non-metallic materials titanium dioxide iron-doping bola amphiphilic short-peptide photocatalysis
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