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- Cai, Zekai, et al.
(författare)
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Charge photogeneration dynamics in non-fullerene polymer solar cells with fluorinated and non-fluorinated acceptors
- 2024
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Ingår i: Journal of Chemical Physics. - 0021-9606. ; 160:7
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Tidskriftsartikel (refereegranskat)abstract
- In this work, charge photogeneration and recombination processes of PM6:IDIC-4F and PM6:IDIC blend films were investigated by the steady-state and time-resolved spectroscopies, as well as the time-dependent density functional theory calculations. The peaks in absorption and photoluminescence (PL) spectra of IDIC and IDIC-4F solutions were assigned by combining the experiment and the simulation of UV-vis absorption and PL spectra. For neat acceptor films, the exciton diffusion length of neat IDIC and IDIC-4F films was estimated as ∼28.9 and ∼19.9 nm, respectively. For PM6-based blend films, we find that the fluorine substitution engineering on the IDIC acceptor material can increase the phase separate size of acceptor material in blend films, resulting in the reduction of dissociation efficiencies of acceptor excitons. In addition, we find that the charge recombination in PM6:IDIC-4F is dominated by bimolecular recombination, in comparison to geminate type carrier recombination in PM6:IDIC blend films. In addition, we find that thermal annealing treatment has a weak influence on carrier recombination but slightly reduces the exciton dissociation efficiency of acceptor in PM6:IDIC blend films, leading to a slightly reduced power conversion efficiency of PM6:IDIC solar cells. These results may shed light on the design of high-performance semiconductor molecules for application in solar cells.
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| 2. |
- Feng, Junyi, et al.
(författare)
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Aggregation-Induced Emission in a Polymeric Photovoltaic Donor Material
- 2022
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Ingår i: Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 126:48, s. 20275-20283
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Tidskriftsartikel (refereegranskat)abstract
- In this work, we report the aggregation-induced emission in a polymeric donor material poly(bis(2-butyloctyl)[2,2′:5′,2″-terthiophene]-4,4″-dicarboxylate-5,5′-diyl-vinylene) (PTVT-T), which exhibits a high device performance for the application of photovoltaics. Time-dependent density functional theory calculations and steady-state and time-resolved spectroscopy have been employed to reveal the underlying emission mechanism. We find that the aggregation of the PTVT-T polymer chain in solution increases the exciton luminescence lifetime and exciton emission quantum yield, which is related to the effective torsional inhibition of carbon-carbon single bonds. Compared with the aggregates in solution, the exciton emission quantum yield of the aggregates in PTVT-T film is reduced. It is attributable to exciton delocalization caused by the improvement of molecular planarity in film. We also observe that the as-cast film and thermally annealed film show distinctly different emission behaviors. This work can shed light on designing optoelectronic polymer materials with the integration of photovoltaic and light-emitting functions.
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