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A Rational Design of Isoindigo-Based Conjugated Microporous N-Type Semiconductors for High Electron Mobility and Conductivity

Abstract

The development of n-type organic semiconductors has evolved significantly slower in comparison to that of p-type organic semiconductors mainly due to the lack of electron-deficient building blocks with stability and processability. However, to realize a variety of organic optoelectronic devices, high-performance n-type polymer semiconductors are essential. Herein, conjugated microporous polymers (CMPs) comprising isoindigo acceptor units linked to benzene or pyrene donor units (BI and PI) showing n-type semiconducting behavior are reported. In addition, considering the challenges of deposition of a continuous and homogeneous thin film of CMPs for accurate Hall measurements, a plasma-assisted fabrication technique is developed to yield uniform thin films. The fully conjugated 2D networks in PI- and BI-CMP films display high electron mobility of 6.6 and 3.5 cm V s , respectively. The higher carrier concentration in PI results in high conductivity (5.3 mS cm ). Both experimental and computational studies are adequately combined to investigate structure-property relations for this intriguing class of materials in the context of organic electronics.

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A Rational Design of Isoindigo-Based Conjugated Microporous n-Type Semiconductors for High Electron Mobility and Conductivity.

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References
1.
Hiroto S, Miyake Y, Shinokubo H . Synthesis and Functionalization of Porphyrins through Organometallic Methodologies. Chem Rev. 2016; 117(4):2910-3043. DOI: 10.1021/acs.chemrev.6b00427. View

2.
Lee J, Cooper A . Advances in Conjugated Microporous Polymers. Chem Rev. 2020; 120(4):2171-2214. PMC: 7145355. DOI: 10.1021/acs.chemrev.9b00399. View

3.
Scaccabarozzi A, Basu A, Anies F, Liu J, Zapata-Arteaga O, Warren R . Doping Approaches for Organic Semiconductors. Chem Rev. 2021; 122(4):4420-4492. DOI: 10.1021/acs.chemrev.1c00581. View

4.
Griggs S, Marks A, Bristow H, McCulloch I . n-Type organic semiconducting polymers: stability limitations, design considerations and applications. J Mater Chem C Mater. 2021; 9(26):8099-8128. PMC: 8264852. DOI: 10.1039/d1tc02048j. View

5.
Zhang W, Lai W, Cao R . Energy-Related Small Molecule Activation Reactions: Oxygen Reduction and Hydrogen and Oxygen Evolution Reactions Catalyzed by Porphyrin- and Corrole-Based Systems. Chem Rev. 2017; 117(4):3717-3797. DOI: 10.1021/acs.chemrev.6b00299. View