首页> 外文期刊>Applied Surface Science >Nano-dot formation using self-assembled 3-mercaptopropionic acid thin films prepared by facile atmospheric-vapor-adsorption method on Au(111)
【24h】

Nano-dot formation using self-assembled 3-mercaptopropionic acid thin films prepared by facile atmospheric-vapor-adsorption method on Au(111)

机译:利用自组装的3-巯基丙酸薄膜通过简便的大气蒸气吸附法在Au(111)上形成纳米点

获取原文
获取原文并翻译 | 示例

摘要

Nanometer scale structures of self-assembled films consisting of 3-mercaptopropionic acid (MPA) were formed by using electric stimuli between scanning tunneling microscope (STM) Au tips and gold surfaces. The obtained structures were compared with those using bare gold surfaces and hexanethiol films on Au(111) under the same conditions. X-ray photoelectron spectroscopy measurements revealed that self-assembled ultrathin films of the corresponding thiol molecules were fabricated on Au(111) by a facile atmospheric-vapor-adsorption (AVA) method without solvent. Comparison of nano-structure formation suggested that the self-assembled thin films of 3-mercatopropionic acid molecules gave nano-dots below the height of voltage pulses where gold atom emission from Au tips and surface evaporation of Au(111) take place. It was found that 3-mercaptopropionic acid films easily produced much better nano-dots on Au(111) than hexanethiol films probably due to the formation of hydrogen bonding networks and/or the reactions of 3-mercaptopropionic acid when electric pulses were applied to the films. (C) 2002 Elsevier Science B.V. All rights reserved. [References: 50]
机译:通过在扫描隧道显微镜(STM)Au尖端和金表面之间施加电刺激,形成了由3-巯基丙酸(MPA)组成的自组装膜的纳米级结构。将获得的结构与在相同条件下在Au(111)上使用裸金表面和己硫醇膜的结构进行比较。 X射线光电子能谱测量表明,相应的硫醇分子的自组装超薄膜是在不使用溶剂的情况下通过简便的大气蒸气吸附(AVA)方法在Au(111)上制备的。纳米结构形成的比较表明,3-巯基丙酸分子的自组装薄膜在低于电压脉冲高度的纳米点上产生了纳米点,在该电压脉冲处发生了来自Au尖端的金原子发射和Au(111)表面蒸发。发现3-巯基丙酸薄膜在Au(111)上比己硫醇薄膜更容易产生更好的纳米点,这可能是由于氢键网络的形成和/或在施加电脉冲时3-巯基丙酸的反应所致。电影。 (C)2002 Elsevier Science B.V.保留所有权利。 [参考:50]

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