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

被引:35
作者
Fischer, Sean A. [1 ]
Cramer, Christopher J. [2 ,3 ]
Govind, Niranjan [1 ]
机构
[1] Pacific NW Natl Lab, William R Wiley Environm Mol Sci Lab, POB 999, Richland, WA 99352 USA
[2] Univ Minnesota, Dept Chem, Supercomp Inst, 207 Pleasant St SE, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Chem Theory Ctr, Minneapolis, MN 55455 USA
关键词
EXCITATION-ENERGIES; MOLECULES; EXCHANGE; THERMOCHEMISTRY; FULLERENES; PORPHYRINS; DYNAMICS;
D O I
10.1021/acs.jpclett.6b00282
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
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.
引用
收藏
页码:1387 / 1391
页数:5
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