Pressure-Promoted Triplet-Pair Separation in Singlet-Fission TIPS-Pentacene Nanofilms Revealed by Ultrafast Spectroscopy

Singlet fission (SF), as an effective way to break through the Shockley-Queisser limit, can dramatically improve energy conversion efficiency in solar cell areas. The formation, separation, and relaxation of triplet-pair excitons directly affect the triplet yield, especially triplet-pair separation; thus, how to enhance the triplet-pair separation rate becomes one of the key points to improve SF efficiency; the decay mechanism where the singlet state is converted into two triplet states is significant for the study of the SF mechanism. Herein, we employ ultrafast transient absorption spectroscopy to study the singlet-fission process of nano-amorphous 6, 13-bis(triisopropylsilylethynyl)-Pentacene (TIPS-pentacene) films in a diamond anvil cell (DAC). A kinetics model related to the structural geometric details, as well as an evaluation of the pressure manipulation impacts, is demonstrated based on the experimental results. The results indicate that pressure manipulation enhanced the triplet-pair separation rates of SF-based materials according to their structural micro-environmental improvement when compressed in DAC, while the triplet-exciton transportation lifetime is prolonged. This work shows that pressure may effectively optimize the structural disorder of SF materials, which were found to improve triplet-pair separation efficiency and potentially offer an effective way to further improve SF efficiency.

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Publication Details

Journal
Nanomaterials
Published
2024-09-13
DOI
https://doi.org/10.3390/nano14181487
Citations
2
Primary Topic
Advanced Chemical Physics Studies
Type
article
Field-Weighted Citation Impact
0.68

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article

Pressure-Promoted Triplet-Pair Separation in Singlet-Fission TIPS-Pentacene Nanofilms Revealed by Ultrafast Spectroscopy

Ruihua Pu, Ruixue Zhu, Lu Wang, Weimin Liu et al.
2 citations
Nanomaterials
Advanced Chemical Physics Studies
0.68
article

Pressure-Promoted Triplet-Pair Separation in Singlet-Fission TIPS-Pentacene Nanofilms Revealed by Ultrafast Spectroscopy

Ruihua Pu, Ruixue Zhu, Lu Wang, Weimin Liu, Yang Lu, Tsu-Chieu Weng
article en
2 citations

Abstract

Singlet fission (SF), as an effective way to break through the Shockley-Queisser limit, can dramatically improve energy conversion efficiency in solar cell areas. The formation, separation, and relaxation of triplet-pair excitons directly affect the triplet yield, especially triplet-pair separation; thus, how to enhance the triplet-pair separation rate becomes one of the key points to improve SF efficiency; the decay mechanism where the singlet state is converted into two triplet states is significant for the study of the SF mechanism. Herein, we employ ultrafast transient absorption spectroscopy to study the singlet-fission process of nano-amorphous 6, 13-bis(triisopropylsilylethynyl)-Pentacene (TIPS-pentacene) films in a diamond anvil cell (DAC). A kinetics model related to the structural geometric details, as well as an evaluation of the pressure manipulation impacts, is demonstrated based on the experimental results. The results indicate that pressure manipulation enhanced the triplet-pair separation rates of SF-based materials according to their structural micro-environmental improvement when compressed in DAC, while the triplet-exciton transportation lifetime is prolonged. This work shows that pressure may effectively optimize the structural disorder of SF materials, which were found to improve triplet-pair separation efficiency and potentially offer an effective way to further improve SF efficiency.

NanomaterialsVol. 14(18)
ShanghaiTech University (CN), Shanghai Advanced Research Institute (CN), Center for High Pressure Science & Technology Advanced Research (CN)
National Natural Science Foundation of China, Science and Technology Commission of Shanghai Municipality, ShanghaiTech University, National Key Research and Development Program of China
Affordable and clean energy
Openalex Percentile: Top 31%
Advanced Chemical Physics Studies
0.68
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