4.7 Article

Controlling Singlet Fission with Coordination Chemistry-Induced Assembly of Dipyridyl Pyrrole Bipentacenes

期刊

ACS CENTRAL SCIENCE
卷 6, 期 11, 页码 2088-2096

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acscentsci.0c01044

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  1. King Fahd University of Petroleum and Minerals, Dhahran, Saudi Arabia, under the KFUPM-Caltech Research Collaboration
  2. Joint Center for Artificial Photosynthesis, a DOE Energy Innovation Hub through Office of Science of the U.S. Department of Energy [DE-SC0004993]
  3. Caltech
  4. Dow Next Generation Educator Fund

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Singlet fission has the potential to surpass current efficiency limits in next-generation photovoltaics and to find use in quantum information science. Despite the demonstration of singlet fission in various materials, there is still a great need for fundamental design principles that allow for tuning of photophysical parameters, including the rate of fission and triplet lifetimes. Here, we describe the synthesis and photophysical characterization of a novel bipentacene dipyridyl pyrrole (HDPP-Pent) and its Li- and K-coordinated derivatives. HDPP-Pent undergoes singlet fission at roughly 50% efficiency (tau(SF) = 730 ps), whereas coordination in the Li complex induces significant structural changes to generate a dimer, resulting in a 7-fold rate increase (tau(SF) = 100 ps) and more efficient singlet fission with virtually no sacrifice in triplet lifetime. We thus illustrate novel design principles to produce favorable singlet fission properties, wherein through-space control can be achieved via coordination chemistry-induced multipentacene assembly.

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