Hart Stephanie M, Silva W Ruchira, Frontiera Renee R
Department of Chemistry , University of Minnesota , Minneapolis , MN 55455 , USA . Email:
Chem Sci. 2017 Dec 20;9(5):1242-1250. doi: 10.1039/c7sc03496b. eCollection 2018 Feb 7.
Singlet fission is a spin-allowed process in which an excited singlet state evolves into two triplet states. We use femtosecond stimulated Raman spectroscopy, an ultrafast vibrational technique, to follow the molecular structural evolution during singlet fission in order to determine the mechanism of this process. In crystalline pentacene, we observe the formation of an intermediate characterized by pairs of excited state peaks that are red- and blue-shifted relative to the ground state features. We hypothesize that these features arise from the formation of cationic and anionic species due to partial transfer of electron density from one pentacene molecule to a neighboring molecule. These observations provide experimental evidence for the role of states with significant charge-transfer character which facilitate the singlet fission process in pentacene. Our work both provides new insight into the singlet fission mechanism in pentacene and demonstrates the utility of structurally-sensitive time-resolved spectroscopic techniques in monitoring ultrafast processes.
单重态裂变是一个自旋允许的过程,其中一个激发单重态演变成两个三重态。我们使用飞秒受激拉曼光谱(一种超快振动技术)来跟踪单重态裂变过程中的分子结构演变,以确定该过程的机制。在结晶并五苯中,我们观察到形成了一种中间体,其特征是相对于基态特征出现了红移和蓝移的激发态峰对。我们推测这些特征源于由于电子密度从一个并五苯分子部分转移到相邻分子而形成的阳离子和阴离子物种。这些观察结果为具有显著电荷转移特征的态在促进并五苯中单重态裂变过程中所起的作用提供了实验证据。我们的工作既为并五苯中的单重态裂变机制提供了新的见解,又证明了结构敏感的时间分辨光谱技术在监测超快过程中的实用性。