Direct Writing of Aligned Conjugated Polymer Micro-Ribbons for High-Performance Organic Electronics
Source abstract
Abstract
Organic semiconductors (OSCs) and relevant devices have presented their great potential in flexible and wearable electronics. Controlled solution deposition of organic semiconductors at a limited local region is highly expected because it can realize feasible and low-cost fabrication of highly integrated devices with low current leakage and free crosstalk between adjacent devices. Here, we reported a feasible microscale meniscus-guided direct writing method to purposely deposit conjugated polymer poly[2,5-(2-octyldodecyl)-3,6-diketopyrrolopyrrole-alt-5,5-(2,5-di(thien-2-yl)thieno[3,2- b ]thiophene)] micro-ribbons at preset local regions. The direct writing of OSCs was carried out on a microscale with the width of written micro-ribbons down to 5 μm, which was seldomly reported before. Direct writing operation induced anisotropic crystallization of organic semiconducting micro-ribbons, which further enhanced the electrical performance of organic transistors with a device on/off ratio of 5.1 × 10 4 and carrier mobility of 1.05 cm 2 V –1 s –1 . Small-angle X-ray diffraction analysis further proved the existence of anisotropic crystallization behavior. This technique shed light on the feasible and convenient fabrication of future high-performance organic electronics.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Organic Electronics and Photovoltaics · Advanced Sensor and Energy Harvesting Materials · Conducting polymers and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials Science, Fudan University, Shanghai200433, China
Department of Materials Science and Engineering, National University of Singapore, 9 Engineering Drive 1, Singapore117576, Singapore
Funding
Science and Technology Commission of Shanghai Municipality · National Natural Science Foundation of China
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