Donor End‐Capped Alkyl Chain Length Dependent Non‐Radiative Energy Loss in All‐Small‐Molecule Organic Solar Cells
Abstract
Abstract A critical bottleneck for further efficiency breakthroughs in organic solar cells (OSCs) is to minimize the non‐radiative energy loss ( e Δ V nr ) while maximizing the charge generation. With the development of highly emissive low‐bandgap non‐fullerene acceptors, the design of high‐performance donors becomes critical to enable the blend with the electroluminescence quantum efficiency to approach or surpass the pristine acceptor. Herein, by shortening the end‐capped alkyl chains of the small‐molecular donors from hexyl (MPhS‐C6) to ethyl (MPhS‐C2), the material obtained aggregation that was insensitive to thermal annealing (TA) along with condensed packing simultaneously. The former leads to small phase separation and suppressed upshifts of the highest occupied molecular orbital energy level during TA, and the latter facilitates its efficient charge‐transport at aggregation‐less packing. Hence, the Δ V nr decreases from 0.242 to 0.182 V, from MPhS‐C6 to MPhS‐C2 based OSCs. An excellent PCE of 17.11% is obtained by 1,8‐diiodoctane addition due to almost unchanged high J sc (26.6 mA cm −2 ) and V oc (0.888 V) with improved fill factor, which is the record efficiency with the smallest energy loss (0.497 eV) and Δ V nr (0.192 V) in all‐small‐molecule OSCs. These results emphasize the potential material design direction of obtaining concurrent TA‐insensitivemore »
- Authors:
-
- CAS Key Laboratory of Nanosystem and Hierarchical Fabrication CAS Center for Excellence in Nanoscience National Center for Nanoscience and Technology Beijing 100190 P. R. China, Sino‐Danish Center for Education and Research Sino‐Danish College University of Chinese Academy of Sciences Beijing 100049 P. R. China
- The Institute for Advanced Studies Wuhan University Wuhan 430072 P. R. China
- CAS Key Laboratory of Nanosystem and Hierarchical Fabrication CAS Center for Excellence in Nanoscience National Center for Nanoscience and Technology Beijing 100190 P. R. China
- State Key Laboratory for Mechanical Behavior of Materials Xi'an Jiaotong University Xi'an 710049 P. R. China
- Publication Date:
- Sponsoring Org.:
- USDOE
- OSTI Identifier:
- 1896940
- Grant/Contract Number:
- DE‐AC02‐05CH11231
- Resource Type:
- Publisher's Accepted Manuscript
- Journal Name:
- Advanced Materials
- Additional Journal Information:
- Journal Name: Advanced Materials Journal Volume: 34 Journal Issue: 50; Journal ID: ISSN 0935-9648
- Publisher:
- Wiley Blackwell (John Wiley & Sons)
- Country of Publication:
- Germany
- Language:
- English
Citation Formats
Zhang, Lili, Sun, Rui, Zhang, Ziqi, Zhang, Jianqi, Zhu, Qinglian, Ma, Wei, Min, Jie, Wei, Zhixiang, and Deng, Dan. Donor End‐Capped Alkyl Chain Length Dependent Non‐Radiative Energy Loss in All‐Small‐Molecule Organic Solar Cells. Germany: N. p., 2022.
Web. doi:10.1002/adma.202207020.
Zhang, Lili, Sun, Rui, Zhang, Ziqi, Zhang, Jianqi, Zhu, Qinglian, Ma, Wei, Min, Jie, Wei, Zhixiang, & Deng, Dan. Donor End‐Capped Alkyl Chain Length Dependent Non‐Radiative Energy Loss in All‐Small‐Molecule Organic Solar Cells. Germany. https://doi.org/10.1002/adma.202207020
Zhang, Lili, Sun, Rui, Zhang, Ziqi, Zhang, Jianqi, Zhu, Qinglian, Ma, Wei, Min, Jie, Wei, Zhixiang, and Deng, Dan. Thu .
"Donor End‐Capped Alkyl Chain Length Dependent Non‐Radiative Energy Loss in All‐Small‐Molecule Organic Solar Cells". Germany. https://doi.org/10.1002/adma.202207020.
@article{osti_1896940,
title = {Donor End‐Capped Alkyl Chain Length Dependent Non‐Radiative Energy Loss in All‐Small‐Molecule Organic Solar Cells},
author = {Zhang, Lili and Sun, Rui and Zhang, Ziqi and Zhang, Jianqi and Zhu, Qinglian and Ma, Wei and Min, Jie and Wei, Zhixiang and Deng, Dan},
abstractNote = {Abstract A critical bottleneck for further efficiency breakthroughs in organic solar cells (OSCs) is to minimize the non‐radiative energy loss ( e Δ V nr ) while maximizing the charge generation. With the development of highly emissive low‐bandgap non‐fullerene acceptors, the design of high‐performance donors becomes critical to enable the blend with the electroluminescence quantum efficiency to approach or surpass the pristine acceptor. Herein, by shortening the end‐capped alkyl chains of the small‐molecular donors from hexyl (MPhS‐C6) to ethyl (MPhS‐C2), the material obtained aggregation that was insensitive to thermal annealing (TA) along with condensed packing simultaneously. The former leads to small phase separation and suppressed upshifts of the highest occupied molecular orbital energy level during TA, and the latter facilitates its efficient charge‐transport at aggregation‐less packing. Hence, the Δ V nr decreases from 0.242 to 0.182 V, from MPhS‐C6 to MPhS‐C2 based OSCs. An excellent PCE of 17.11% is obtained by 1,8‐diiodoctane addition due to almost unchanged high J sc (26.6 mA cm −2 ) and V oc (0.888 V) with improved fill factor, which is the record efficiency with the smallest energy loss (0.497 eV) and Δ V nr (0.192 V) in all‐small‐molecule OSCs. These results emphasize the potential material design direction of obtaining concurrent TA‐insensitive aggregation and condensed packing to maximize the device performances with a super low Δ V nr .},
doi = {10.1002/adma.202207020},
journal = {Advanced Materials},
number = 50,
volume = 34,
place = {Germany},
year = {Thu Nov 03 00:00:00 EDT 2022},
month = {Thu Nov 03 00:00:00 EDT 2022}
}
https://doi.org/10.1002/adma.202207020
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