Synergistic effect of side-chain and backbone engineering in thieno[2,3-f]benzofuran-based conjugated polymers for high performance non-fullerene organic solar cells

2019 ◽  
Vol 7 (3) ◽  
pp. 958-964 ◽  
Author(s):  
Keke Dou ◽  
Xunchang Wang ◽  
Zurong Du ◽  
Huanxiang Jiang ◽  
Feng Li ◽  
...  

A series of copolymers containing thieno[2,3-f]benzofuran unit with different alkyl side chains are synthesized. The best photovoltaic performance with power conversion efficiency over 11% have been realized.

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Zhenrong Jia ◽  
Shucheng Qin ◽  
Lei Meng ◽  
Qing Ma ◽  
Indunil Angunawela ◽  
...  

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.


2020 ◽  
Vol 8 (44) ◽  
pp. 23239-23247
Author(s):  
Andy Man Hong Cheung ◽  
Han Yu ◽  
Siwei Luo ◽  
Zhen Wang ◽  
Zhenyu Qi ◽  
...  

This is the first time alkylthio chains are employed on Y6-like NFAs to achieve organic solar cells of power conversion efficiency higher than 16%.


2017 ◽  
Vol 4 (5) ◽  
pp. 755-766 ◽  
Author(s):  
Ibrahim Ata ◽  
Duško Popovic ◽  
Mika Lindén ◽  
Amaresh Mishra ◽  
Peter Bäuerle

A series of A–D–A–D–A co-oligomers was developed and implemented as donor materials in solution-processable organic solar cells showing the dependence of molecular structures on the power conversion efficiency upon solvent vapor annealing.


Author(s):  
Chuang Yao ◽  
Yezi Yang ◽  
Lei Li ◽  
Maolin Bo ◽  
Cheng Peng ◽  
...  

Cyano-group (−C≡N) is an electron-withdrawing group, which has been widely used to construct high-performance fused-ring electron acceptors (FREAs). Benefiting from these FREAs, the power conversion efficiency of organic solar cells...


2020 ◽  
Vol 8 (18) ◽  
pp. 6293-6298
Author(s):  
Cancan Jiao ◽  
Ziqi Guo ◽  
Binqiao Sun ◽  
Yuan-qiu-qiang Yi ◽  
Lingxian Meng ◽  
...  

An acceptor molecule with an asymmetric backbone, CC10, has been designed, which achieved a power conversion efficiency of 11.78%.


RSC Advances ◽  
2014 ◽  
Vol 4 (32) ◽  
pp. 16681-16685 ◽  
Author(s):  
O. Synooka ◽  
K.-R. Eberhardt ◽  
H. Hoppe

In this work, we demonstrate the successful replacement of a chlorinated solvent system based on a 1 : 1 mixture of chlorobenzene and ortho-dichlorobenzene with the chlorine-free solvent xylene, resulting in chlorine-free processing with a small amount of diiodooctane additive. In fact, the overall power conversion efficiency is improved from 6.71% for the chlorinated solvents to 7.15% for the chlorine-free solvent m-xylene.


2016 ◽  
Vol 12 ◽  
pp. 1788-1797 ◽  
Author(s):  
Ni Yin ◽  
Lilei Wang ◽  
Yi Lin ◽  
Jinduo Yi ◽  
Lingpeng Yan ◽  
...  

Benzo[1,2-b:4,5-b′]dithiophene (BDT) is an excellent building block for constructing π-conjugated molecules for the use in organic solar cells. In this paper, four 4,8-bis(5-alkyl-2-thienyl)benzo[1,2-b:4,5-b′]dithiophene (TBDT)-containing A–π–D–π–A-type small molecules (COOP-nHT-TBDT, n = 1, 2, 3, 4), having 2-cyano-3-octyloxy-3-oxo-1-propenyl (COOP) as terminal group and regioregular oligo(3-hexylthiophene) (nHT) as the π-conjugated bridge unit were synthesized. The optical and electrochemical properties of these compounds were systematically investigated. All these four compounds displayed broad absorption bands over 350–600 nm. The optical band gap becomes narrower (from 1.94 to 1.82 eV) and the HOMO energy levels increased (from −5.68 to −5.34 eV) with the increase of the length of the π-conjugated bridge. Organic solar cells using the synthesized compounds as the electron donor and PC61BM as the electron acceptor were fabricated and tested. Results showed that compounds with longer oligothiophene π-bridges have better power conversion efficiency and higher device stability. The device based on the quaterthiophene-bridged compound 4 gave a highest power conversion efficiency of 5.62% with a V OC of 0.93 V, J SC of 9.60 mA·cm−2, and a FF of 0.63.


2021 ◽  
Author(s):  
Jakob Hofinger ◽  
Christoph Putz ◽  
Felix Mayr ◽  
Katarina Gugujonovic ◽  
Dominik Wielend ◽  
...  

Despite the rapid increase in power conversion efficiency (PCE) of non-fullerene acceptor (NFA) based solar cells in recent years, organic photovoltaic (OPV) devices exhibit considerably larger voltage losses compared to...


RSC Advances ◽  
2017 ◽  
Vol 7 (33) ◽  
pp. 20084-20092 ◽  
Author(s):  
Lijie Zhu ◽  
Qipeng Lu ◽  
Longfeng Lv ◽  
Yue Wang ◽  
Yufeng Hu ◽  
...  

Ligand-free rutile and anatase TiO2nanocrystals were synthesizedviaa hydrolytic sol–gel method. The improved power conversion efficiency was achieved by using anatase TiO2nanocrystals as electron extraction layer in the organic solar cells.


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