Truong Minh Anh, Ueberricke Lucas, Funasaki Tsukasa, Adachi Yuta, Hira Shota, Hu Shuaifeng, Yamada Takumi, Sekiguchi Naomu, Nakamura Tomoya, Murdey Richard, Iikubo Satoshi, Kanemitsu Yoshihiko, Wakamiya Atsushi
Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto, 611-0011, Japan.
Department of Advanced Materials Science and Engineering, Faculty of Engineering Sciences, Kyushu University, Kasuga, Fukuoka, 816-8580, Japan.
Angew Chem Int Ed Engl. 2024 Nov 11;63(46):e202412939. doi: 10.1002/anie.202412939. Epub 2024 Sep 23.
Hole-collecting monolayers have greatly advanced the development of positive-intrinsic-negative perovskite solar cells (p-i-n PSCs). To date, however, most of the anchoring groups in the reported monolayer materials are designed to bind to the transparent conductive oxide (TCO) surface, resulting in less availability for other functions such as tuning the wettability of the monolayer surface. In this work, we developed two anchorable molecules, 4PATTI-C3 and 4PATTI-C4, by employing a saddle-like indole-fused cyclooctatetraene as a π-core with four phosphonic acid anchoring groups linked through propyl or butyl chains. Both molecules form monolayers on TCO substrates. Thanks to the saddle shape of a cyclooctatetraene skeleton, two of the four phosphonic acid anchoring groups were found to point upward, resulting in hydrophilic surfaces. Compared to the devices using 4PATTI-C4 as the hole-collecting monolayer, 4PATTI-C3-based devices exhibit a faster hole-collection process, leading to higher power conversion efficiencies of up to 21.7 % and 21.4 % for a mini-cell (0.1 cm) and a mini-module (1.62 cm), respectively, together with good operational stability. This work represents how structural modification of multipodal molecules could substantially modulate the functions of the hole-collecting monolayers after being adsorbed onto TCO substrates.
空穴收集单层极大地推动了正-本征-负型钙钛矿太阳能电池(p-i-n PSCs)的发展。然而,迄今为止,报道的单层材料中的大多数锚定基团设计用于与透明导电氧化物(TCO)表面结合,导致用于其他功能(如调节单层表面润湿性)的可用性较低。在这项工作中,我们通过使用鞍状吲哚稠合环辛四烯作为π核,开发了两种可锚定分子4PATTI-C3和4PATTI-C4,其具有通过丙基或丁基链连接的四个膦酸锚定基团。这两种分子都在TCO衬底上形成单层。由于环辛四烯骨架的鞍形结构,发现四个膦酸锚定基团中的两个向上指向,从而形成亲水性表面。与使用4PATTI-C4作为空穴收集单层的器件相比,基于4PATTI-C3的器件表现出更快的空穴收集过程,对于微型电池(0.1 cm)和微型模块(1.62 cm),分别实现了高达21.7%和21.4%的更高功率转换效率,同时具有良好的操作稳定性。这项工作展示了多官能团分子的结构修饰如何在吸附到TCO衬底后显著调节空穴收集单层的功能。