...
首页> 外文期刊>Zeitschrift fur Physikalische Chemie: International Journal of Research in Physical Chemistry and Chemical Physics >Gold Nanoparticles in Novel Green Deep Eutectic Solvents: Self-Limited Growth, Self-Assembly & Catalytic Implications
【24h】

Gold Nanoparticles in Novel Green Deep Eutectic Solvents: Self-Limited Growth, Self-Assembly & Catalytic Implications

机译:新型绿色深共晶溶剂中的金纳米颗粒:自我限制的增长,自我组装和催化意义。

获取原文
获取原文并翻译 | 示例
           

摘要

In this article, we are reporting the catalytic activity of gold nanoparticles (AuNPs) dispersed in a novel eco-friendly Deep Eutectic Solvent (DES; choline chloride and urea) at room temperature. A low energy sputter deposition method is employed to synthesize AuNPs on the DES surface. This is a simple, economical and clean method for producing monodisperse gold nanoparticles by a self-limited growth mechanism. Detailed Small Angle X-ray Scattering (SAXS), UV-Vis and Transmission Electron Microscopy (TEM) investigations show the formation of spherical AuNPs of 5 nm in diameter. Moreover, these particles have a strong tendency to self-assemble at the DES surface as well as into the bulk. This is a new addition to a novel generation of gold based catalysts. The catalytic activity of Au nanoparticles in DES is revealed quantitatively by analyzing the apparent conversion reaction rate constant k(app) of para-nitrophenol to para-aminophenol in the presence of sodium borohydride. Catalytic activity reported in the present article is much faster (k(app) = 0.34 s(-1)) than the rate reported earlier (k(app) = 0.030 min(-1)) by Chirea et al. for gold nanowire networks [Langmuir, 2011, 27, 3906]. In agreement with the literature, we explain the higher catalytic activity in terms of a larger surface area of AuNPs in a non-self-assembled state.
机译:在本文中,我们报告了室温下分散在新型生态友好型深共晶溶剂(DES;氯化胆碱和尿素)中的金纳米颗粒(AuNPs)的催化活性。采用低能溅射沉积方法在DES表面合成AuNPs。这是一种通过自限生长机制生产单分散金纳米颗粒的简单,经济,清洁的方法。详细的小角X射线散射(SAXS),UV-Vis和透射电子显微镜(TEM)研究表明,形成了直径为5 nm的球形AuNP。而且,这些颗粒具有很强的自组装性,可以在DES表面以及散装成块。这是新一代金基催化剂的新成员。通过分析在硼氢化钠存在下对硝基苯酚向对氨基苯酚的表观转化反应速率常数k(app),定量地揭示了Au纳米粒子在DES中的催化活性。与Chirea等人先前报道的催化活性(k(app)= 0.030 min(-1))相比,本文报道的催化活性要快得多(k(app)= 0.34 s(-1))。用于金纳米线网络[Langmuir,2011,27,3906]。与文献一致,我们以非自组装状态下较大的AuNPs表面积解释了较高的催化活性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号