Energy Frontier Research Center, ¶Department of Chemistry, and §Departments of Physics and Electrical Engineering, Columbia University , New York, New York 10027, United States.
J Am Chem Soc. 2014 Jul 30;136(30):10654-60. doi: 10.1021/ja503980c. Epub 2014 Jul 17.
Singlet fission, the conversion of a singlet excitation into two triplet excitations, is a viable route to improved solar-cell efficiency. Despite active efforts to understand the singlet fission mechanism, which would aid in the rational design of new materials, a comprehensive understanding of mechanistic principles is still lacking. Here, we present the first study of singlet fission in crystalline hexacene which, together with tetracene and pentacene, enables the elucidation of mechanistic trends. We characterize the static and transient optical absorption and combine our findings with a theoretical analysis of the relevant electronic couplings and rates. We find a singlet fission time scale of 530 fs, which is orders of magnitude faster than tetracene (10-100 ps) but significantly slower than pentacene (80-110 fs). We interpret this increased time scale as a multiphonon relaxation effect originating from a large exothermicity and present a microscopic theory that quantitatively reproduces the rates in the acene family.
单线态裂变,即将单线态激发转化为两个三线态激发的过程,是提高太阳能电池效率的可行途径。尽管人们积极努力理解单线态裂变机制,这将有助于合理设计新材料,但对机械原理的全面理解仍然缺乏。在这里,我们首次研究了晶体六并苯中的单线态裂变,它与并四苯和并五苯一起,可以阐明机械趋势。我们描述了静态和瞬态光吸收,并将我们的发现与相关电子耦合和速率的理论分析结合起来。我们发现单线态裂变的时间尺度为 530fs,比并四苯(10-100ps)快几个数量级,但比并五苯(80-110fs)慢得多。我们将这个增加的时间尺度解释为源自大的放热的多声子弛豫效应,并提出了一个微观理论,该理论定量地再现了并苯家族中的速率。