Semitransparent organic solar cells exhibiting 13.02% efficiency and 20.2% average visible transmittance

2021 ◽  
Author(s):  
Zhenghao Hu ◽  
Jian Wang ◽  
Xiaoling Ma ◽  
Jinhua Gao ◽  
Chunyu Xu ◽  
...  
Keyword(s):  
Solar Cells ◽  
Small Molecule ◽  
Organic Solar Cells ◽  
Visible Transmittance ◽  
Narrow Bandgap

Semitransparent organic solar cells (OSCs) were fabricated with broad bandgap polymer D18-Cl as donor (D), narrow bandgap small molecule Y6-1O as acceptor (A) and ultra-narrow bandgap material Y6 as the...

Molecular electron acceptors for efficient fullerene-free organic solar cells

2017 ◽  
Vol 19 (5) ◽  
pp. 3440-3458 ◽  
Author(s):  
Shuixing Li ◽  
Zhongqiang Zhang ◽  
Minmin Shi ◽  
Chang-Zhi Li ◽  
Hongzheng Chen
Keyword(s):  
Solar Cells ◽  
Small Molecule ◽  
Organic Solar Cells ◽  
Wide Bandgap ◽  
Electron Acceptors ◽  
Electron Donors ◽  
Molecular Electron ◽  
Narrow Bandgap

Small molecule electron acceptors pairing with wide bandgap or narrow bandgap electron donors are reviewed and discussed for fullerene-free organic solar cells.

The Effect of Donor Molecular Structure on Power Conversion Efficiency of Small-Molecule-Based Organic Solar Cells

2019 ◽  
Vol 16 (3) ◽  
pp. 236-243 ◽  
Author(s):  
Hui Zhang ◽  
Yibing Ma ◽  
Youyi Sun ◽  
Jialei Liu ◽  
Yaqing Liu ◽  
...  
Keyword(s):  
Molecular Structure ◽  
Solar Cells ◽  
Power Conversion Efficiency ◽  
Conversion Efficiency ◽  
Small Molecule ◽  
Organic Solar Cells ◽  
Molecular Design ◽  
Power Conversion ◽  
The Relationship

In this review, small-molecule donors for application in organic solar cells reported in the last three years are highlighted. Especially, the effect of donor molecular structure on power conversion efficiency of organic solar cells is reported in detail. Furthermore, the mechanism is proposed and discussed for explaining the relationship between structure and power conversion efficiency. These results and discussions draw some rules for rational donor molecular design, which is very important for further improving the power conversion efficiency of organic solar cells based on the small-molecule donor.

scholarly journals High performance tandem organic solar cells via a strongly infrared-absorbing narrow bandgap acceptor

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Zhenrong Jia ◽  
Shucheng Qin ◽  
Lei Meng ◽  
Qing Ma ◽  
Indunil Angunawela ◽  
...  
Keyword(s):  
Solar Cells ◽  
Power Conversion Efficiency ◽  
Conversion Efficiency ◽  
Organic Solar Cells ◽  
High Performance ◽  
Short Circuit ◽  
Power Conversion ◽  
High Power Conversion Efficiency ◽  
Device Structure ◽  
Narrow Bandgap

AbstractTandem organic solar cells are based on the device structure monolithically connecting two solar cells to broaden overall absorption spectrum and utilize the photon energy more efficiently. Herein, we demonstrate a simple strategy of inserting a double bond between the central core and end groups of the small molecule acceptor Y6 to extend its conjugation length and absorption range. As a result, a new narrow bandgap acceptor BTPV-4F was synthesized with an optical bandgap of 1.21 eV. The single-junction devices based on BTPV-4F as acceptor achieved a power conversion efficiency of over 13.4% with a high short-circuit current density of 28.9 mA cm−2. With adopting BTPV-4F as the rear cell acceptor material, the resulting tandem devices reached a high power conversion efficiency of over 16.4% with good photostability. The results indicate that BTPV-4F is an efficient infrared-absorbing narrow bandgap acceptor and has great potential to be applied into tandem organic solar cells.

Fullerene/Non-fullerene Alloy for High-Performance All-Small-Molecule Organic Solar Cells

2021 ◽  
Vol 13 (5) ◽  
pp. 6461-6469
Author(s):  
María Privado ◽  
Fernando G. Guijarro ◽  
Pilar de la Cruz ◽  
Rahul Singhal ◽  
Fernando Langa ◽  
...  
Keyword(s):  
Solar Cells ◽  
Small Molecule ◽  
Organic Solar Cells ◽  
High Performance

scholarly journals Recent progress in small‐molecule donors for non‐fullerene all‐small‐molecule organic solar cells

Nano Select ◽  
2021 ◽  
Author(s):  
Ze Zhang ◽  
Yaokun Wang ◽  
Chenkai Sun ◽  
Zitong Liu ◽  
Haiqiao Wang ◽  
...  
Keyword(s):  
Solar Cells ◽  
Small Molecule ◽  
Organic Solar Cells ◽  
Recent Progress

scholarly journals The Effects of Molecular Packing Behavior of Small-Molecule Acceptors in Ternary Organic Solar Cells

2021 ◽  
Vol 11 (2) ◽  
pp. 755
Author(s):  
Eunhee Lim
Keyword(s):  
Solar Cells ◽  
Energy Level ◽  
Ternary System ◽  
Small Molecule ◽  
Organic Solar Cells ◽  
Orbital Energy ◽  
Working Mechanism ◽  
Energy Level Structure ◽  
The Third ◽  
Molecular Backbone

Herein, two diketopyrrolopyrrole (DPP)-based, small-molecule isomers, o- and p-DPP-PhCN, were introduced as acceptors in ternary organic solar cells (OSCs). The isomers have the same molecular backbone but differ in the positions of the cyanide (CN) substituents (ortho and para), which greatly affects their packing behavior. Ternary solar cells composed of poly(3-hexylthiophene) (P3HT):DPP-PhCN:phenyl-C61-butyric acid methyl ester (PCBM) were fabricated, and the effects of the different packing behaviors of the third component on the device performance and the working mechanism of the ternary cells were investigated. The addition of o-DPP-PhCN with a relatively high-lying lowest unoccupied molecular orbital energy level resulted in an increase in the open-circuit voltage (VOC) in the ternary devices, demonstrating the alloy-like structure of the two acceptors (o-DPP-PhCN and PCBM) in the ternary system. However, the p-DPP-PhCN-based ternary cells exhibited VOC values similar to that of a P3HT:PCBM binary cell, irrespective of the addition of p-DPP-PhCN, indicating a cascade energy-level structure in the ternary system and an effective charge transfer from the P3HT to the PCBM. Importantly, by increasing the addition of p-DPP-PhCN, the short-circuit current density increased substantially, resulting in pronounced shoulder peaks in the external quantum efficiency responses in the long-wavelength region, corresponding to the contribution of the photocurrent generated by the light absorption of p-DPP-PhCN. Despite sharing the same molecular backbone, the two DPP-PhCNs exhibited substantially different packing behaviors according to the position of their CN substituents, which also greatly affected the working mechanism of the ternary devices fabricated using the DPP-PhCNs as the third component.

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