期刊文献+

氟氮共掺杂二氧化钛/还原氧化石墨稀复合光催化剂的制备及其可见光催化性能 被引量:13

Synthesis of F, N Co-doped TiO_2 Decorated Reduced Graphene Oxide and Its Visible Light Photocatalytic Properties
原文传递
导出
摘要 以氧化石墨烯(GO)、TiO2、尿素、NH4F 和 Vc 为原料,采用水热法制备氟氮共掺杂二氧化钛/还原氧化石墨烯复合光催化剂(F-N-TiO2/rGO)。对制备的 F-N-TiO2/rGO 样品的相组成、结构、形貌和光谱性质进行分析表征。结果表明:F、N共掺杂的 TiO2仍为锐钛矿晶型,呈纳米颗粒状均匀分布在片状还原氧化石墨烯表面;增强了对400~800 nm 可见光的吸收,且吸收边发生明显的红移;同时 C—Ti 共价键的形成使石墨烯与 TiO2紧密结合,提高了界面电荷传输效率使光生电子有效分离,使得 F-N-TiO2/rGO 的催化活性大大增强,可见光下对甲基橙(MO)的降解速率达1.17 mg/(h·g),是商品 P25的2.8倍。 F and N co-doped TiO2 decorated graphene oxide composite photocatalysts (F-N-TiO2/rGO) were prepared with the graphene oxide (GO), TiO2, urea, NH4F and Vc as precursors by a one-step hydrothermal method. The composition, structure, morphology and spectral properties of the composite photocatalyst were investigated. The results show that F and N co-doped TiO2 particles with anatase phase are well-dispersed on the surface of the reduced graphene oxide (rGO) sheets. The absorption edge of F-N-TiO2/rGO shifts to the visible light range and the optical absorption shows an enhancement in the visible light region from 400 nm to 800 nm. The degradation rate of methyl orange on F-N-TiO2/rGO composite is 1.17 mg/(h·g) under visible light, which increases 2.8 times greater than that on commercial P25. This is attributed to the interaction between TiO2 and graphene via C-Ti covalent bonds, which promotes the efficient separation of photogenerated charges resulting from the improved electrical conductivity of the rGO sheets.
出处 《硅酸盐学报》 EI CAS CSCD 北大核心 2015年第7期919-925,共7页 Journal of The Chinese Ceramic Society
基金 国家自然科学基金项目(51372062)
关键词 二氧化钛 氧化石墨烯 氟氮共掺杂 甲基橙 可见光 titanium dioxide graphene oxide fluorine and nitrogen co-doped methyl orange visible light
  • 相关文献

参考文献3

二级参考文献30

  • 1汤心虎,韦朝海,梁洁容,王伯光.硼掺杂CeO_2/TiO_2光催化剂的制备及其活性研究[J].环境科学,2006,27(7):1329-1333. 被引量:3
  • 2李立清,刘宗耀,唐新村,唐琳,郭三霞,李海龙,何益波.B/Fe_2O_3共掺杂纳米TiO_2可见光下的催化性能[J].中国有色金属学报,2006,16(12):2098-2103. 被引量:17
  • 3Asahi R, Morikawa T, Ohwaki T, Aoki K, Taga Y. Science, 2001, 293(5528): 269
  • 4Ohno T, Akiyoshi M, Umebayashi T, Asai K, Mitsui T, Matsumur M. Appl Catal A, 2004, 265:115
  • 5Chen D M, Yang D, Wang Q, Jiang Z Y. Ind Eng Chem, Res, 2006, 45(12): 4110
  • 6Yu J G, Zhou M H, Cheng B, Zhao X J. J Mol Catal A, 2006, 246(9): 176
  • 7Li D, Ohashi N, Hishita S, Kolodiazhnyi T, Haneda H. J Solid State Chem, 2005, 178(11) : 3293
  • 8Zhao W, Ma W H, Chen C C, Zhao J C, Shuai Z G. J Am Chem Soc, 2004, 126(15): 4782
  • 9JungK Y, Park S B, Ihm S K. Appl Catal B, 2004, 51 : 239
  • 10Lettmann C, Hildenbrand K, Kisch H, Macyk W, Maier W F. Appl Catal B, 2001, 32(4): 215

共引文献41

同被引文献151

引证文献13

二级引证文献82

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部