4.8 Article

Excited-State Absorption from Real-Time Time-Dependent Density Functional Theory: Optical Limiting in Zinc Phthalocyanine

Journal

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 7, Issue 7, Pages 1387-1391

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.6b00282

Keywords

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Funding

  1. U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences
  2. Office of Advanced Scientific Computing Research [KC-030106062653, DE-SC0008666]
  3. Office of Biological and Environmental Research
  4. DOE [DE-AC05-76RL1830]
  5. Office of Science of the U.S. Department of Energy [DE-AC02-05CH11231]

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Optical-limiting materials are capable of attenuating light to protect delicate equipment from high-intensity light sources. Phthalocyanines have attracted a lot of attention for optical-limiting applications due to their versatility and large nonlinear absorption. With excited-state absorption (ESA) being the primary mechanism for optical limiting behavior in phthalocyanines, the ability to tune the optical absorption of ground and excited states in phthalocyanines would allow for the development of advanced optical limiters. We recently developed a method for the calculation of ESA based on real-time time-dependent density functional theory propagation of an excited-state density. In this work, we apply the approach to zinc phthalocyanine, demonstrating the ability of our method to efficiently identify the optical limiting potential of a molecular complex.

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