Abstract
In this work, a series of molecules decorated with Li atom and donor/acceptor have been theoretically designed based on bicorannulenyl molecule, where incorporating Li and different substitution are used as an effective strategy for enhancing nonlinear optical response. The mixed method is constructed through incorporating the Li and NO2/NH2 substitution. To ensure accuracy, results were compared with another two functionals. As expected, data from three different functional approximations indicate that these molecules have large first hyperpolarizability. The calculation proves that these molecules exhibit large first hyperpolarizability in the range of 1956–37,758 au. For Li doped systems, by analyzing NBO, charge transfer occurs in studied molecules, which helps to get large nonlinear optical response. It is revealed that when Li atom is introduced into the molecule with only NO2/NH2 substitution, the first hyperpolarizability increases significantly. Compared with Li doped and NO2 substitution, incorporating Li and NH2 substitution can be more powerful in increasing the first hyperpolarizabilities of bicorannulenyl molecule. In addition, the number of NH2 substitutions can more effectively enhance the first hyperpolarizability. We hope that this study could provide a new idea for designing nonlinear optical materials using bicorannulenyl molecule.
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Funding
The work was supported by the start-up Foundation of Fujian University of Technology (GY-Z13109), Development Foundation of Fujian University of Technology (GY-Z160127), the Education Department of Fujian Province (GY-Z17105, JAT170393), Science and Technology Major Special Project of Fujian Province (2014HZ0005-1), Industrial Technology joint Innovation Project of Fujian Province (2015-779), and Fujian Province Science and Technology Innovation Leaders (GY-Z17142).
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Song, YD., Wang, QT. & Ni, Q. Designing a novel material with considerable nonlinear optical responses based on the bicorannulenyl molecule. J Mol Model 26, 201 (2020). https://doi.org/10.1007/s00894-020-04450-0
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DOI: https://doi.org/10.1007/s00894-020-04450-0