Studies of the molecular switching of azobenzene-functionalized platform adlayers on Au(111) by chronoamperometry

被引:7
|
作者
Jung, Ulrich [1 ]
Kubitschke, Jens [2 ]
Herges, Rainer [2 ]
Magnussen, Olaf [1 ]
机构
[1] Univ Kiel, Inst Expt & Angew Phys, D-24118 Kiel, Germany
[2] Univ Kiel, Otto Diels Inst Organ Chem, D-24098 Kiel, Germany
关键词
Self-assembled monolayers; Azobenzene; Photoswitching; Functional electrode surfaces; Cyclic voltammetry; Chronoamperometry; SELF-ASSEMBLED MONOLAYERS; ATOMIC-FORCE MICROSCOPY; RAMAN-SCATTERING SERS; SINGLE-CRYSTAL PLANES; PHOTOISOMERIZATION REACTION; ELECTROCHEMICAL PROPERTIES; PHOTOSWITCHING BEHAVIOR; ELEMENTARY STEPS; GOLD; SURFACE;
D O I
10.1016/j.electacta.2013.06.123
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Photochronoamperometry is introduced as a new approach to study isomerization reactions in photoswitchable molecular adsorbate layers on metal electrodes. Using highly ordered self-assembled monolayers of molecular platforms with freestanding vertical azobenzene functionalities on single-crystalline Au(1 1 1) as an example, the photoinduced current response was measured as a function of potential and irradiation intensity and compared to complementary cyclic voltammetry studies. The observed behavior is discussed within a kinetical model that qualitatively describes the experimental findings. In order to describe the intensity dependence, the isomerization reactions, in particular, the thermal relaxation, have to occur distinctively faster than the electrochemical processes, which is in good agreement with previous results for these photoswitchable adlayers. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:869 / 880
页数:12
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