Jing Haoyu, Magdaong Nikki Cecil M, Diers James R, Kirmaier Christine, Bocian David F, Holten Dewey, Lindsey Jonathan S
Department of Chemistry, North Carolina State University, Raleigh, North Carolina 27695-8204, USA.
Department of Chemistry, Washington University, St. Louis, Missouri 63130-4889, USA.
Phys Chem Chem Phys. 2023 Jan 18;25(3):1781-1798. doi: 10.1039/d2cp05400k.
A new pentad array designed to exhibit panchromatic absorption and charge separation has been synthesized and characterized. The array is composed of a triad panchromatic absorber (a bis(perylene-monoimide)-porphyrin) to which are appended an electron acceptor (perylene-diimide) and an electron donor/hole acceptor (bacteriochlorin) in a crossbar arrangement. The motivation for incorporation of the bacteriochlorin a free-base or zinc chlorin utilized in prior constructs was to facilitate hole transfer to this terminal unit and thereby achieve a higher yield of charge separation across the array. The intense S → S (Q) band of the bacteriochlorin also enhances absorption in the near-infrared spectral region. Due to synthetic constraints, a phenylethyne linker was used to join the bacteriochlorin to the core porphyrin of the panchromatic triad rather than the diphenylethyne linker employed for the prior chlorin-containing pentads. Static and time-resolved photophysical studies reveal enhanced excited-state quenching for the pentad in benzonitrile and dimethyl sulfoxide compared to the prior chlorin-containing analogues. Success was only partial, however, as a long-lived charge separated state was not observed despite the improved energetics for the final ground-state hole/electron-shift reaction. The apparent reason is more facile competing charge-recombination due to the shorter bacteriochlorin - porphyrin linker that increases electronic coupling for this process. The studies highlight design criteria for balancing panchromatic absorption and long-lived charge separation in molecular architectures for solar-energy conversion.
一种旨在实现全色吸收和电荷分离的新型五元阵列已被合成并表征。该阵列由一个三元全色吸收体(双(苝-单酰亚胺)-卟啉)组成,在其横杆排列中连接有一个电子受体(苝二酰亚胺)和一个电子供体/空穴受体(细菌叶绿素)。在之前的构建体中使用的游离碱或二价锌细菌叶绿素被纳入的动机是促进空穴转移到这个末端单元,从而在整个阵列中实现更高的电荷分离产率。细菌叶绿素强烈的S→S(Q)带也增强了近红外光谱区域的吸收。由于合成限制,使用苯乙炔连接体将细菌叶绿素连接到全色三元体的核心卟啉上,而不是用于之前含二氢卟吩的五元体的二苯乙炔连接体。静态和时间分辨光物理研究表明,与之前含二氢卟吩的类似物相比,该五元体在苯甲腈和二甲基亚砜中的激发态猝灭增强。然而,成功只是部分的,因为尽管最终基态空穴/电子转移反应的能量学有所改善,但未观察到长寿命的电荷分离态。明显的原因是由于细菌叶绿素-卟啉连接体较短,增加了该过程的电子耦合,导致更容易发生竞争性电荷复合。这些研究突出了在太阳能转换的分子结构中平衡全色吸收和长寿命电荷分离的设计标准。