Interface configuration effects on excitation, exciton dissociation, and charge recombination in organic photovoltaic heterojunction. Issue 4 (14th November 2019)

• Record Type: Journal Article
• Authors: Bai, Rui‐Rong; Zhang, Cai‐Rong; Wu, You‐Zhi; Yuan, Li‐Hua; Zhang, Mei‐Ling; Chen, Yu‐Hong; Liu, Zi‐Jiang; Chen, Hong‐Shan
• Is Part Of: International journal of quantum chemistry. Volume 120:Issue 4(2020)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2019-11-14
• Subjects: charge recombination -- charge transfer -- electronic structure -- organic heterojunction interface; Quantum chemistry -- Periodicals; 541.28
• DOI: 10.1002/qua.26103
• Languages: English
• ISSNs: 0020-7608

Abstract

Abstract: The morphology of donor‐acceptor heterojunction interface significantly affects the electron/hole processes in organic solar cells, including charge transfer (CT), exciton dissociation (ED), and charge recombination (CR). Here, to investigate interface molecular configuration effects, the donor‐acceptor complexes with face‐on, edge‐on, and end‐on configurations were constructed as model systems for the p‐SIDT(FBTTh2 )2 /C60 heterojunction. The geometries, electronic structures, and excitation properties of monomers and the complexes with three configurations were studied based on density functional theory (DFT) and time‐dependent DFT calculations with optimally tuned range separation parameters and solid polarization effects. In terms of Marcus theory, the rate constants of ED and CR processes were analyzed. The results show that most of the excited states for p‐SIDT(FBTTh2 )2 exhibit an intramolecular CT character, and the similarity of the excitation characters (CT and local excitation) and energies among three complexes with different configurations indicate that the electronic structure and excitation properties are insensitive to the interfacial molecular configurations. However, the rates of ED and CR processes heavily depend on it. These results underline the importance of controlling molecular configuration and then the morphology at the heterojunction interface in organic solar cells. Abstract : Based on density functional theory (DFT) and time‐dependent DFT calculations with optimally tuned range separation parameters and solid polarization effects, the exciton dissociation and charge recombination rates of p‐SIDT(FBTTh2 )2 /C60 complexes calculated using Marcus theory show that they strongly depend on the molecular configurations in an organic heterojunction interface.