Little Christopher A, Batchelor-McAuley Christopher, Ngamchuea Kamonwad, Lin Chuhong, Young Neil P, Compton Richard G
Physical and Theoretical Chemistry Laboratory Oxford University South Parks Road Oxford OX1 3QZ United Kingdom.
ChemistryOpen. 2018 May 23;7(5):370-380. doi: 10.1002/open.201800048. eCollection 2018 May.
The oxidation of silver nanoparticles is induced to occur near to, but not at, an electrode surface. This reaction at a distance from the electrode is studied through the use of dark-field microscopy, allowing individual nanoparticles and their reaction with the electrode product to be visualized. The oxidation product diffuses away from the electrode and oxidizes the nanoparticles in a reaction layer, resulting in their destruction. The kinetics of the silver nanoparticle solution-phase reaction is shown to control the length scale over which the nanoparticles react. In general, the new methodology offers a route by which nanoparticle reactivity can be studied close to an electrode surface.
银纳米颗粒的氧化在靠近但并非在电极表面处被诱导发生。通过使用暗场显微镜研究电极一定距离处的该反应,从而能够观察到单个纳米颗粒及其与电极产物的反应。氧化产物从电极扩散开来,并在反应层中氧化纳米颗粒,导致其被破坏。结果表明,银纳米颗粒溶液相反应的动力学控制着纳米颗粒发生反应的长度尺度。总体而言,这种新方法提供了一条能够在靠近电极表面处研究纳米颗粒反应活性的途径。