Band-like Transport of Charge Carriers in Oriented Two-Dimensional Conjugated Covalent Organic Frameworks

被引:59
作者
Ghosh, Samrat [1 ,4 ]
Tsutsui, Yusuke [1 ]
Kawaguchi, Takahiro [1 ]
Matsuda, Wakana [1 ]
Nagano, Shusaku [2 ]
Suzuki, Katsuaki [3 ]
Kaji, Hironori [3 ]
Seki, Shu [1 ]
机构
[1] Kyoto Univ, Grad Sch Engn, Dept Mol Engn, Nishikyo Ku, Kyoto 6158510, Japan
[2] Rikkyo Univ, Coll Sci, Dept Chem, Toshima Ku, Tokyo 1718501, Japan
[3] Kyoto Univ, Inst Chem Res, Uji, Kyoto 6110011, Japan
[4] CSIR Cent Leather Res Inst, Inorgan & Phys Chem Lab, Chennai 600020, Tamil Nadu, India
基金
日本学术振兴会;
关键词
MOBILITY; GRAPHENE; CRYSTALLINE; IMPACT; LAYER;
D O I
10.1021/acs.chemmater.1c03533
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A tunable topology and a porous network make pi-conjugated covalent organic frameworks (COFs) a new class of organic semiconductors for optoelectronic, smart sensing, and catalytic applications. Although some of the COFs exhibit enhanced electric conductivity with a high charge carrier mobility, the nature and pathways of charge transport still remain elusive. In order to unveil the transport mechanism, herein, we have developed crystalline pi-conjugated COFs using planar building blocks, and a wafer-scale self-supporting thin film was grown, which could be transferred onto any of the desired substrates. The COF film was found to be highly oriented and exhibited a high in-plane electronic conductivity. The conductivity was almost independent of temperature with an ultra-low activation energy of 14.3 meV, approaching a band-like transport of charge carriers within the crystalline domains. The COF films also showed a high photoresponsivity in electronic conduction against a complete visible range, demonstrated as a flexible photodetector device. This work represents a thorough investigation of the mechanism and direction of charge transport in crystalline pi-conjugated COF semiconductors, which suggests their feasibility as key active materials in multifunctional organic electronics.
引用
收藏
页码:736 / 745
页数:10
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