Truong Minh Anh, Funasaki Tsukasa, Ueberricke Lucas, Nojo Wataru, Murdey Richard, Yamada Takumi, Hu Shuaifeng, Akatsuka Aruto, Sekiguchi Naomu, Hira Shota, Xie Lingling, Nakamura Tomoya, Shioya Nobutaka, Kan Daisuke, Tsuji Yuta, Iikubo Satoshi, Yoshida Hiroyuki, Shimakawa Yuichi, Hasegawa Takeshi, Kanemitsu Yoshihiko, Suzuki Takanori, Wakamiya Atsushi
Institute for Chemical Research, Kyoto University, Gokasho, Uji, Kyoto 611-0011, Japan.
Department of Chemistry, Faculty of Science, Hokkaido University, Sapporo 060-0810, Japan.
J Am Chem Soc. 2023 Apr 5;145(13):7528-7539. doi: 10.1021/jacs.3c00805. Epub 2023 Mar 22.
Hole-collecting monolayers have drawn attention in perovskite solar cell research due to their ease of processing, high performance, and good durability. Since molecules in the hole-collecting monolayer are typically composed of functionalized π-conjugated structures, hole extraction is expected to be more efficient when the π-cores are oriented face-on with respect to the adjacent surfaces. However, strategies for reliably controlling the molecular orientation in monolayers remain elusive. In this work, multiple phosphonic acid anchoring groups were used to control the molecular orientation of a series of triazatruxene derivatives chemisorbed on a transparent conducting oxide electrode surface. Using infrared reflection absorption spectroscopy and metastable atom electron spectroscopy, we found that multipodal derivatives align face-on to the electrode surface, while the monopodal counterpart adopts a more tilted configuration. The face-on orientation was found to facilitate hole extraction, leading to inverted perovskite solar cells with enhanced stability and high-power conversion efficiencies up to 23.0%.
空穴收集单层由于其易于加工、高性能和良好的耐久性,在钙钛矿太阳能电池研究中受到了关注。由于空穴收集单层中的分子通常由功能化的π共轭结构组成,当π核相对于相邻表面面对面取向时,预计空穴提取会更有效。然而,可靠控制单层中分子取向的策略仍然难以捉摸。在这项工作中,使用多个膦酸锚定基团来控制一系列化学吸附在透明导电氧化物电极表面的三氮杂蒽衍生物的分子取向。通过红外反射吸收光谱和亚稳态原子电子光谱,我们发现多足衍生物与电极表面面对面排列,而单足对应物则采用更倾斜的构型。发现面对面取向有利于空穴提取,从而导致具有增强稳定性和高达23.0%的高功率转换效率的倒置钙钛矿太阳能电池。