Morphology, molecular stacking, dynamics and device performance correlations of vacuum-deposited small-molecule organic solar cells

2014 ◽  
Vol 16 (19) ◽  
pp. 8852-8864 ◽  
Author(s):  
Chang-Wen Chen ◽  
Zheng-Yu Huang ◽  
Yi-Min Lin ◽  
Wei-Ching Huang ◽  
Yi-Hong Chen ◽  
...  

The “all carbon” organic solar cells based on the homocyclic molecule DBP as a donor and C60as an acceptor were comprehensively characterized.

2014 ◽  
Vol 2014 ◽  
pp. 1-6 ◽  
Author(s):  
Michal Radziwon ◽  
André Luis Fernandes Cauduro ◽  
Morten Madsen ◽  
Horst-Günter Rubahn

Recent efforts in research and development of small molecule based organic solar cells have led to power conversion efficiencies exceeding 10%. Understanding the incorporated interfaces in these devices is an utterly important parameter for their improvement. Here we investigate the influence ofα-sexithiophene (α-6T) nanostructures on the performance parameters ofα-6T/C60inverted bilayer solar cells. Byin situcontrolled growth, crystallineα-6T nanostructures are formed in the devices and a correlation between the morphology of the structures and the device performance is presented. Under certain, well-defined circumstances, we observe an efficiency increase of around 100% when implementing crystalline nanostructures.


2019 ◽  
Vol 7 (26) ◽  
pp. 7947-7952 ◽  
Author(s):  
Xuebin Chen ◽  
Bei Zhu ◽  
Bin Kan ◽  
Ke Gao ◽  
Xiaobin Peng ◽  
...  

Solvent treatment was used to simplify the device structure and enhance the device performance of porphyrin-based small molecule solar cells.


2019 ◽  
Vol 01 (01) ◽  
pp. 088-094 ◽  
Author(s):  
Junhui Miao ◽  
Bin Meng ◽  
Jun Liu ◽  
Lixiang Wang

Small-molecule donor/polymer acceptor type (MD/PA-type) organic solar cells (OSCs) have the great advantage of superior thermal stability. However, very few small molecular donors can match polymer acceptors, leading to low power conversion efficiency (PCE) of MD/PA-type OSCs. In this work, we studied the effect of terminal groups of small molecular donors on the optoelectronic properties and OSC device performance of MD/PA-type OSCs. We select a benzodithiophene unit bearing carbazolyl substituents as the core, terthiophene as the bridging unit, and electron-withdrawing methyl 2-cyanoacetate, 3-ethylrhodanine, and 2H-indene-1,3-dione as the terminal groups to develop three small-molecule donors. With the increase of the electron-withdrawing capability of the terminal groups, the small molecular donors exhibit redshifted absorption spectra and downshifted LUMO levels. Among the three small-molecule donors, the one with 3-ethylrhodanine terminal group exhibits the best photovoltaic performance with the PCE of 8.0% in MD/PA-type OSCs. This work provides important guidelines for the design of small-molecule donors for MD/PA-type OSC applications.


Energies ◽  
2021 ◽  
Vol 14 (9) ◽  
pp. 2505
Author(s):  
Haiyan Chen ◽  
Hua Tang ◽  
Dingqin Hu ◽  
Yiqun Xiao ◽  
Jiehao Fu ◽  
...  

Morphology is crucial to determining the photovoltaic performance of organic solar cells (OSCs). However, manipulating morphology involving only small-molecule donors and acceptors is extremely challenging. Herein, a simple terminal alkyl chain engineering process is introduced to fine-tune the morphology towards high-performance all-small-molecule (ASM) OSCs. We successfully chose a chlorinated two-dimension benzo[1,2-b:4,5-b′]dithiophene (BDT) central unit and two isomeric alkyl cyanoacetate as the end-capped moieties to conveniently synthesize two isomeric small-molecule donors, namely, BT-RO-Cl and BT-REH-Cl, each bearing linear n-octyl (O) as the terminal alkyl chain and another branched 2-ethylhexyl (EH) as the terminal alkyl chain. The terminal alkyl chain engineering process provided BT-RO-Cl with 13.35% efficiency and BT-REH-Cl with 13.90% efficiency ASM OSCs, both with Y6 as the electron acceptor. The successful performance resulted from uniform phase separation and the favorable combination of face-on and edge-on molecular stacking of blended small-molecule donors and acceptors, which formed a fluent 3D transport channel and thus delivered high and balanced carrier mobilities. These findings demonstrate that alkyl chain engineering can finely control the morphology of ASM OSCs, and provides an alternative for the optimal design of small-molecule materials towards high-performance ASM OSCs.


2017 ◽  
Vol 141 ◽  
pp. 262-268 ◽  
Author(s):  
Yamin Zhang ◽  
Miaomiao Li ◽  
Huanran Feng ◽  
Wang Ni ◽  
Hongtao Zhang ◽  
...  

2016 ◽  
Vol 4 (6) ◽  
pp. 2252-2262 ◽  
Author(s):  
Jin-Liang Wang ◽  
Fei Xiao ◽  
Jun Yan ◽  
Kai-Kai Liu ◽  
Zheng-Feng Chang ◽  
...  

Here we report the synthesis of a pair of D1–A-bridge–D2-bridge–A–D1 type small molecules, which have different π-conjugated bridges and investigated the effects on their photovoltaic properties.


2019 ◽  
Vol 16 (3) ◽  
pp. 236-243 ◽  
Author(s):  
Hui Zhang ◽  
Yibing Ma ◽  
Youyi Sun ◽  
Jialei Liu ◽  
Yaqing Liu ◽  
...  

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.


2021 ◽  
Vol 13 (5) ◽  
pp. 6461-6469
Author(s):  
María Privado ◽  
Fernando G. Guijarro ◽  
Pilar de la Cruz ◽  
Rahul Singhal ◽  
Fernando Langa ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document