期刊文献+

疏水石墨烯水相分散液的制备及电化学性能 被引量:1

Preparation Hydrophobic Graphene Aqueous Dispersion and Electrochemical Properties
在线阅读 下载PDF
导出
摘要 通过未添加表面活性剂和稳定剂而得到均匀的石墨烯水相分散液的方法,近来来成为研究的一大热点.本工作通过提高水合肼的用量,来替代表面活性剂或者其它稳定剂的作用,得到了良好的均匀的水相石墨烯分散液,可长期稳定存放,6个月内未发生团聚现象.其Zeta电位低于-32.5mV(pH值为5.89),原子力显微镜和透射电子显微镜图像表明产物为具有褶皱结构的、六方晶系的单层石墨烯结构,厚度为0.38nm.XPS分析显示这种方法对于除去羟基和环氧基团起到了有效的作用.利用这种分散液所制备的石墨烯-玻碳电极(GE-GCE)在检测抗坏血酸(AA)和尿酸(UA)时,比普通玻碳电极(GCE)显示出更良好的电化学响应. The direct dispersion of hydrophobic graphene sheets in water without the assistant of surfactant stabilizers has recently been recognized as an important task for production of individual graphene sheets. We developed a facial method to disperse hydrophobic graphene sheets in aqueous medium through enlarging the amount of hydrazine-hydrate in the absence of surfactant or any other foreign electrostatic stabilization agents. Homogeneous aqueous graphene dispersion had produced lower zeta potential of more negative than -32. 5 mV at solution pH of 5. 89 and was stable for six months without any precipitate. The folded individual single-layer graphene sheets with 0. 38 nm layer thick and the formation of a hexagonal crystalline graphene structure were observed from AFM and TEM images, respectively. XPS analysis showed the efficient reduction of graphene oxide. As-prepared graphene-glassy carbon electrode (GE-GCE) showed a relatively sensitive electrochemical response toward the detection of AA and UA than glassy carbon electrode (GCE).
出处 《影像科学与光化学》 CAS CSCD 北大核心 2012年第4期280-288,共9页 Imaging Science and Photochemistry
基金 国家自然科学基金资助项目(21175144) 中国留学基金委的资助
关键词 石墨烯 分散液 水合肼 电化学响应 graphene dispersion hydrazine-hydrate electrochemical response
  • 相关文献

参考文献27

  • 1Novoselov K S, Jiang Z, Zhang Y, et al. Room-temperature quantum hall effect in graphene[J]. Science, 2007, 135(5817): 1379.
  • 2Ozyilmaz B, Herrero P J, Efetov D, et al. Electronic transport in locally gated graphene nanoconstrictions[J]. Appl. Ptys. Lett., 2007, 91(192107): 1-3.
  • 3Tung V C, Allen M J, Yang Y, et al. High throughput solution processing of large-scale graphene[J]. Nature Nanotechnology, 2009, 4.- 25-29.
  • 4Eda G, Fanchini G, Chhowalla M. Large-area ultrathin films of reduced graphene oxide as a transparent and flexible electronic rnaterial[J].Nature Nanotechnology, 2008, 3: 270-274.
  • 5I.iao K H, Mittal A, Bose S, et al. Aqueous only route toward graphene from graphite oxide[J]. ACS NAN(), 2011, 5(2): 1253-1258.
  • 6l.i S S, Tu K H, Lin C C, et al. Solution-processable graphene oxide as an efficient hole transport layer in polymer solar cells[J]. ACS NANO, 2010, 4(6) : 3169 -3174.
  • 7Chen G L, Shau S M, Juang T Y, et al. Single-layered graphene oxide nanosheet/polyaniline hybrids fabricated through direct molecular ex{oliation[J]. Langmuir, 2011, 27(23) : 14563-14569.
  • 8Hou S F, Kasner M L, Su S J, et al. Highly sensitive and selective dopamine biosensor fabricated with silanized graphene[J]. J. Phys. Chem. C, 2010, 114(35): 14915-14921.
  • 9Dey R S, Raj C R. Development o an amperometric cholesterol biosensor based on graphene Pt nanoparticle hybrid material[J]. J. Phys. Chem. C, 2010, 114(49): 21427-21433.
  • 10Artiles M S, Rout C S, Fisher T S. Graphene-based hybrid materials and devices for bio,;ensing[J]. Adv. Drug Deliv. Rev, 2011, 63(14-15) : 1352-1360.

同被引文献14

  • 1朱耕宇,陈雪萍,翁志学.PTFE胶乳粒子与Fe_2O_3粒子共凝聚过程的研究[J].化工生产与技术,2004,11(3):1-3. 被引量:5
  • 2杨仁春,袁毅桦,高永辉.MBS胶乳凝聚方法研究进展[J].化工生产与技术,2006,13(2):42-45. 被引量:3
  • 3Kim H, Abdala A A, Macosko C W.Graphene/Polymer Nano- composites[J].Macromolecules, 2010,43 (16) : 6515-6530.
  • 4Cai D Y, Song M. Recent Advance in Flinctionalized Graphene/ Polymer Nanocomposites[J]. Journal of Materials Chemistry, 2010, 20(37) :7906-7915.
  • 5Jeffrey R P, Christopher W B, Rodney S R. Graphene-Based Polymer Nanocomposites[J]. Polymer, 2011,52 (1) : 5-25.
  • 6Verdejo R, Bemal M M, Romasanta L J, et al. Graphene Filled Polymer Nanocomposites[J]. Journal of Materials Chemistry, 2011, 21 (10) :3301-3310.
  • 7Furusawa K, Velev O D. Electro-Kinetic Behavior in Synthetic Process of Composite Particles[J]. Colloid and Surfaces A: Physicochemieal and Engineering Aspects, 1999, 159 (2-3) : 359- 371.
  • 8Furusawa K, Anzai C. Preparation of Composite Fine Particles by Heterocoagulation[J]. Colloid and Polymer Science, 1987,265 (10) : 882-888.
  • 9Furusawa K, Anzai C. Hetero-Coagulation Behavior of Polymer Latices with Spherical Silica[J].Colloid and Surface, 1992,63 (1-2): 103-111.
  • 10Okubo M, Miyachi N, Lu Y. Variation of Surface Unevenness of Anomalous Composite Polymer Particle Produced by the Stepwise Heterocoagulation of Small Particles[J]. Colloid and Polymer Science, 1994,272 (3) : 270-275.

引证文献1

二级引证文献6

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