期刊
ACS NANO
卷 16, 期 12, 页码 21216-21224出版社
AMER CHEMICAL SOC
DOI: 10.1021/acsnano.2c09192
关键词
quantum dots; charge transport; charge transfer; redox ligands; electrochemistry
类别
资金
- Swiss National Science Foundation Early Postdoc Mobility Fellowship
- [P2SKP2_191326]
This article presents a strategy to actively engineer long-range charge transport in colloidal quantum dot assemblies by introducing ligand functionalities. The use of electronically coupled redox ligands enables a self-exchange chain reaction and facilitates long-range charge transport across the film. The different modes of charge transport in these assemblies and their manipulation through modulation of the Fermi level and redox ligand coverage are identified.
We present a strategy to actively engineer long -range charge transport in colloidal quantum dot assemblies by using ligand functionalities that introduce electronic states and provide a path for carrier transfer. This is a shift away from the use of inactive spacers to modulate charge transport through the lowering of the tunneling barrier for interparticle carrier transfer. This is accomplished with the use of electronically coupled redox ligands by which a self-exchange chain reaction takes place and long-range charge transport is enabled across the film. We identified the different modes of charge transport in these quantum dot/redox ligand assemblies, their energetic position and kinetics, and explain how to rationally manipulate them through modulation of the Fermi level and redox ligand coverage.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据