High-Rate Charge-Carrier Transport in Porphyrin Covalent Organic Frameworks: Switching from Hole to Electron to Ambipolar Conduction
High-Rate Charge-Carrier Transport in Porphyrin Covalent Organic Frameworks: Switching from Hole to Electron to Ambipolar Conduction
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DOI:
10.1002/anie.201106203
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发表时间:
2012-01-01
影响因子:
16.6
通讯作者:
Jiang, Donglin
中科院分区:
文献类型:
--
作者:
Feng, Xiao;Liu, Lili;Jiang, Donglin
Conducting polymers play a key role in optoelectronics, transistors, and solar cells owing to their capability in chargecarrier transport. To achieve high-rate carrier transport, the molecular design of a conjugated structure that allows the formation of organized conducting pathways is highly preferred.[1] In this context, two-dimensional covalent organic frameworks (2D COFs) offer a new class of conducting polymers with unconventional structures that feature 2D polygon sheets and eclipsed stacking architecture to provide preorganized pathways for charge-carrier transport.[2, 3] A significant feature of COFs is that the ordering of building blocks in the 2D polygon sheet is discrete and the layered alignment of 2D sheets is parallel and unidirectional. Such a well-organized architecture with precise intra-and interplane orderings is seldom available with conventional 1D and 3D conducting polymers.We have focused on the synthesis of p-electronic 2D COFs by integrating p-electronic components into the skeletons of 2D COFs.[3] Recently, we have developed a typical and large p system, that is, a porphyrin unit for the synthesis of a tetragonal 2D porphyrin COF, which shows high crystallinity and large surface area.[4] During the course of the study, we found that the porphyrin units stacked in an