Solvent-Free Transfer of Freestanding Large-Area Conjugated Polymer Films for Optoelectronic Applications

被引:8
作者
Esparza, Guillermo L. [1 ,2 ]
Kodur, Moses [1 ]
Chen, Alexander X. [1 ]
Wang, Benjamin [1 ]
Bunch, Jordan A. [1 ]
Cramlet, Jaden [1 ]
Runser, Rory [1 ]
Fenning, David P. [1 ,2 ]
Lipomi, Darren J. [1 ,2 ]
机构
[1] Univ Calif San Diego, Dept Nano & Chem Engn, 9500 Gilman Dr,Mail Code 0448, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Mat Sci & Engn Program, 500 Gilman Dr,Mail Code 0418, La Jolla, CA 92093 USA
基金
美国国家科学基金会;
关键词
conjugated polymers; flexible electronics; microfabrication; roll-to-roll processing; thin films; VAPOR-DEPOSITION; THIN;
D O I
10.1002/adma.202207798
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Conventional processes for depositing thin films of conjugated polymers are restricted to those based on vapor, liquid, and solution-phase precursors. Each of these methods bear some limitations. For example, low-bandgap polymers with alternating donor-acceptor structures cannot be deposited from the vapor phase, and solution-phase deposition is always subject to issues related to the incompatibility of the substrate with the solvent. Here, a technique to enable deposition of large-area, ultra-thin films (approximate to 20 nm or more), which are transferred from the surface of water, is demonstrated. From the water, these pre-solidified films can then be transferred to a desired substrate, circumventing limitations such as solvent orthogonality. The quality of these films is characterized by a variety of imaging and electrochemical measurements. Mechanical toughness is identified as a limiting property of polymer compatibility, along with some strategies to address this limitation. As a demonstration, the films are used as the hole-transport layer in perovskite solar cells, in which their performance is shown to be comparable to controls formed by spin-coating.
引用
收藏
页数:7
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