Materials Science and Technology of Polymers, Faculty of Science and Technology and MESA + Institute for Nanotechnology, University of Twente, 7500 AE Enschede, The Netherlands.
Nanotechnology. 2010 Jul 16;21(28):285703. doi: 10.1088/0957-4484/21/28/285703. Epub 2010 Jun 28.
Electrochemical properties of core-shell CdSe/ZnS quantum dots (QDs) in a non-aqueous solution are presented. Cathodic reduction and anodic oxidation processes involving the QD HOMO and LUMO levels as well as defect states were identified by cyclic voltammetry. The electrochemical bandgap was estimated from the anodic and cathodic redox peaks and found to match well with the optical bandgap estimated from the absorption spectrum. The trioctylphosphine oxide ligands on the surface of the QDs were exchanged to electroactive ferrocenyl thiols and the resulting material was characterized by NMR and optical spectroscopy. Cyclic voltammetry showed that the redox potentials of the QDs are modified due to the presence of ferrocene on the surface of the QD. The QD oxidation peak decreased and the reduction peak shifted to more negative potentials. The concurrent shift of the ferrocene redox peaks indicates that the system displays features of a 'molecular hybrid', where both the QD and the ligand influence each other.
呈现了核壳型 CdSe/ZnS 量子点(QD)在非水溶剂中的电化学性质。通过循环伏安法确定了涉及 QD HOMO 和 LUMO 能级以及缺陷态的阴极还原和阳极氧化过程。电化学带隙是根据阳极和阴极氧化还原峰估算得出的,与从吸收光谱估算出的光学带隙吻合良好。QD 表面的三辛基氧化膦配体被交换为电化学活性的二茂铁硫醇,所得材料通过 NMR 和光学光谱进行了表征。循环伏安法表明,由于 QD 表面存在二茂铁,QD 的氧化还原电位发生了修饰。QD 的氧化峰减小,还原峰向更负的电位移动。二茂铁氧化还原峰的同时移动表明该体系呈现出“分子杂化”的特征,其中 QD 和配体相互影响。