scholarly journals Activating intramolecular singlet exciton fission by altering π-bridge flexibility in perylene diimide trimers for organic solar cells

2020 ◽  
Vol 11 (33) ◽  
pp. 8757-8770
Author(s):  
Benedetta Carlotti ◽  
Ifeanyi K. Madu ◽  
Hyungjun Kim ◽  
Zhengxu. Cai ◽  
Hanjie Jiang ◽  
...  

We show via time resolved spectroscopy that triplet formation proceeds via intersystem crossing in a rigid-bridged perylene diimide trimer and via efficient and fast intramolecular singlet exciton fission in the analogous flexible-bridged trimer.

2015 ◽  
Author(s):  
Marina Gerhard ◽  
Andreas Arndt ◽  
Aina Quintilla ◽  
Arash Rahimi-Iman ◽  
Uli Lemmer ◽  
...  

Nano Letters ◽  
2011 ◽  
Vol 11 (4) ◽  
pp. 1495-1498 ◽  
Author(s):  
Priya J. Jadhav ◽  
Aseema Mohanty ◽  
Jason Sussman ◽  
Jiye Lee ◽  
Marc A. Baldo

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Wenjun Ni ◽  
Licheng Sun ◽  
Gagik G. Gurzadyan

AbstractSinglet exciton fission (SF) is a spin-allowed process whereby two triplet excitons are created from one singlet exciton. This phenomenon can offset UV photon energy losses and enhance the overall efficiency in photovoltaic devices. For this purpose, it requires photostable commercially available SF materials. Excited state dynamics in pure perylene film, ease of commercial production, is studied by time-resolved fluorescence and femtosecond transient absorption techniques under different photoexcitation energies. In film, polycrystalline regions contain perylene in H-type aggregate form. SF takes place from higher excited states of these aggregates in ultrafast time scale < 30 fs, reaching a triplet formation quantum yield of 108%. Moreover, at λex = 450 nm singlet fission was detected as a result of two-quantum absorption. Other competing relaxation channels are excimer (1 ps) and dimer radical cation formation (< 30 fs). Excimer radiatively relaxes within 19 ns and radical cation recombines in 3.2 ns. Besides, exciton self-trapping by crystal lattice distortions occurs within hundreds of picosecond. Our results highlight potential of simple-fabricated perylene films with similar properties as high-cost single crystal in SF based photovoltaic applications.


2016 ◽  
Author(s):  
Marina Gerhard ◽  
Dominik Gehrig ◽  
Ian A. Howard ◽  
Andreas P. Arndt ◽  
Mühenad Bilal ◽  
...  

1996 ◽  
Vol 100 (25) ◽  
pp. 10518-10522 ◽  
Author(s):  
Akira Watanabe ◽  
Osamu Ito ◽  
Motoyuki Watanabe ◽  
Haruhisa Saito ◽  
Musubu Koishi

2013 ◽  
Vol 103 (26) ◽  
pp. 263302 ◽  
Author(s):  
Nicholas J. Thompson ◽  
Daniel N. Congreve ◽  
David Goldberg ◽  
Vinod M. Menon ◽  
Marc A. Baldo

CCS Chemistry ◽  
2020 ◽  
pp. 1-18
Author(s):  
Shangshang Chen ◽  
Dong Meng ◽  
Jiachen Huang ◽  
Ningning Liang ◽  
Yan Li ◽  
...  

2021 ◽  
Vol 01 ◽  
Author(s):  
Min Deng ◽  
Zhenkai Ji ◽  
Xiaopeng Xu ◽  
Liyang Yu ◽  
Qiang Peng

Background: Perylene diimide (PDI) is among the most investigated non-fullerene electron acceptor for organic solar cells (OSCs). Constructing PDI derivatives into three-dimensional propeller-like molecular structures is not only one of the viable routes to suppress the over aggregation tendency of the PDI chromophores, but also raises possibilities to tune and optimize the optoelectronic property of the molecules. Objective: In this work, we reported the design, synthesis, and characterization of three electron-accepting materials, namely BOZ-PDI, BTZ-PDI, and BIZ-PDI, each with three PDI arms linked to benzotrioxazole, benzotrithiazole, and benzotriimidazole based center cores, respectively. Method: The introduction of electron-withdrawing center cores with heteroatoms does not significantly complicate the synthesis of the acceptor molecules but drastically influences the energy levels of the propeller-like PDI derivatives. Result: The highest power conversion efficiency was obtained with benzoxazole-based BOZ-PDI reaching 7.70% for its higher photon absorption and charge transport ability. Conclusion: This work explores the utilization of electron-withdrawing cores with heteroatoms in the propeller-like PDI derivatives, which provides a handy tool to construct high-performance non-fullerene acceptor materials.


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