Tanaka Masaki
Department of Biotechnology and Life Science, Tokyo University of Agriculture and Technology, Koganei, Tokyo, Japan.
Nat Commun. 2024 Oct 29;15(1):9297. doi: 10.1038/s41467-024-53633-3.
Polar organic molecules form spontaneous polarization in vacuum-deposited films by permanent dipole orientations in the films, originating from the molecule's potential ability to align itself on the film surface during deposition. This study focuses on developing polar molecules that exhibit spontaneous orientation polarization (SOP) and possess a high surface potential. In the proposed molecular design, a hexafluoropropane (6F) unit facilitates spontaneous molecular orientation to align the permanent dipoles, and a phthalimide unit induces strong molecular polarization. Furthermore, the introduction of phthalimides into the molecular backbone raises the glass transition temperature of the molecules, leading to the suppression of molecular mobility on the film surface during film deposition and an improvement in the dipole orientation. The resulting surface potential slope is approximately 280 mV nm without substrate temperature control. Furthermore, this work proposes a method using position isomers as a design strategy to tune the SOP polarity. The substitution position of the strong polar units influences the direction of the total molecular dipoles and affects the SOP polarity of the 6F-based molecules. The proposed molecular designs in this study provide wide tunability of the SOP intensity and polarity, which contributes to highly efficient organic optoelectronic and energy-harvesting devices.
极性有机分子通过薄膜中永久偶极的取向在真空沉积薄膜中形成自发极化,这源于分子在沉积过程中在薄膜表面自行排列的潜在能力。本研究聚焦于开发具有自发取向极化(SOP)且具有高表面电势的极性分子。在所提出的分子设计中,六氟丙烷(6F)单元有助于分子自发取向,使永久偶极排列整齐,而邻苯二甲酰亚胺单元可诱导强烈的分子极化。此外,将邻苯二甲酰亚胺引入分子主链会提高分子的玻璃化转变温度,从而在薄膜沉积过程中抑制薄膜表面分子的迁移率,并改善偶极取向。在不控制衬底温度的情况下,所得表面电势斜率约为280 mV/nm。此外,这项工作提出了一种使用位置异构体作为设计策略来调节SOP极性的方法。强极性单元取代位置会影响分子总偶极的方向,并影响基于6F分子的SOP极性。本研究中提出的分子设计提供了SOP强度和极性的广泛可调性,这有助于制造高效的有机光电器件和能量收集器件。