橡胶
单重态裂变
裂变
正交晶系
单重态
材料科学
Crystal(编程语言)
化学物理
晶体结构
结晶学
化学
光电子学
物理
原子物理学
核物理学
激发态
计算机科学
中子
程序设计语言
作者
Tanner S. Volek,Zachary T. Armstrong,Jakub K. Sowa,Kelly S. Wilson,Miriam Bohlmann Kunz,Kajari Bera,MaKenna Koble,Renee R. Frontiera,Peter J. Rossky,Martin T. Zanni,Sean T. Roberts
标识
DOI:10.1021/acs.jpclett.3c02845
摘要
Materials that undergo singlet fission are of interest for their use in light-harvesting, photocatalysis, and quantum information science, but their ability to undergo fission can be sensitive to local variations in molecular packing. Herein we employ transient absorption microscopy, molecular dynamics simulations, and electronic structure calculations to interrogate how structures found at the edges of orthorhombic rubrene crystals impact singlet fission. Within a micrometer-scale spatial region at the edges of rubrene crystals, we find that the rate of singlet fission increases nearly 4-fold. This observation is consistent with formation of a region at crystal edges with reduced order that accelerates singlet fission by disrupting the symmetry found in rubrene’s orthorhombic crystal structure. Our work demonstrates that structural distortions of singlet fission materials can be used to control fission in time and in space, potentially offering a means of controlling this process in light harvesting and quantum information applications.
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