Influence of molecular structure on the performance of low Voc loss polymer solar cells

2016 ◽  
Vol 4 (39) ◽  
pp. 15232-15239 ◽  
Author(s):  
Ming Wang ◽  
Hengbin Wang ◽  
Michael Ford ◽  
Jianyu Yuan ◽  
Cheng-Kang Mai ◽  
...  

Two regioregular narrow bandgap conjugated polymers (PM1 and PM2) are prepared and their devices exhibit low Voc loss and high short circuit current Jsc, but, most significantly, display improved fill factors compared to previously reported PIPCP.

2013 ◽  
Vol 136 (2) ◽  
Author(s):  
Nidal Abu-Zahra ◽  
Mahmoud Algazzar

In this research, n-dodecylthiol was added to P3HT/PC70BM polymer solar cells (PSCs) to improve the crystallinity of P3HT and enhance the phase separation of P3HT/PC70BM. Crystallinity of P3HT:PC70BM doped with 0–5% by volume of n-dodecylthiol was measured using X-ray diffraction (XRD) and differential scanning calorimetry (DSC) techniques. Both methods showed improvement in crystallinity, which resulted in improving the power conversion efficiency (PCE) of polymer solar cells by 33%. In addition, annealing at 150 °C for 30 min showed further improvement in crystallinity with n-dodecylthiol concentration up to 2%. The highest power conversion efficiency of 3.21% was achieved with polymer crystallites size L of 11.2 nm, after annealing at 150 °C for 30 min under a vacuum atmosphere. The smaller crystallite size suggests a shorter path of the charge carriers between P3HT backbones, which could be beneficial to getting a higher short circuit current in the devices made with the additive. Kinetics study of P3HT:PC70BM crystallinity using Avrami model showed a faster crystallization rate (1/t0.5) at higher temperatures.


2016 ◽  
Vol 49 (1) ◽  
pp. 177-187 ◽  
Author(s):  
Tae Ho Lee ◽  
Min Hee Choi ◽  
Sung Jae Jeon ◽  
Seung Jun Nam ◽  
Yong Won Han ◽  
...  

Polymers ◽  
2017 ◽  
Vol 9 (12) ◽  
pp. 39 ◽  
Author(s):  
Yueyue Gao ◽  
Ming Liu ◽  
Yong Zhang ◽  
Zhitian Liu ◽  
Yulin Yang ◽  
...  

2017 ◽  
Vol 17 (1) ◽  
pp. 13
Author(s):  
Shobih Shobih ◽  
Rizky Abdillah ◽  
Erlyta Septa Rosa

Hybrid polymer solar cell has privilege than its conventional structure, where it usually has structure of (ITO/PEDOT:PSS/Active Layer/Al). In humid environment the PEDOT:PSS will absorb water and hence can easily etch the ITO. Therefore it is necessary to use an alternative method to avoid this drawback and obtain more stable polymer solar cells, namely by using hybrid polymer solar cells structure with an inverted device architecture from the conventional, by reversing the nature of charge collection. In this paper we report the results of the fabrication of inverted bulk heterojunction polymer solar cells based on P3HT:PCBM as active layer, utilizing ZnO interlayer as buffer layer between the ITO and active layer with a stacked structure of ITO/ZnO/P3HT:PCBM/PEDOT:PSS/Ag. The ZnO interlayer is formed through short route, i.e. by dissolving ZnO nanoparticles powder in chloroform-methanol solvent blend rather than by sol-gel process. Based on the measurement results on electrical characteristics of inverted polymer solar cells under 500 W/m2 illumination and AM 1.5 direct filter at room temperature, cell with annealing process of active layer at 110 °C for 10 minutes results in higher cell performance than without annealing, with an open-circuit voltage of 0.21 volt, a short-circuit current density of 1.33 mA/cm2 , a fill factor of 43.1%, and a power conversion efficiency of 0.22%. The low cell’s performance is caused by very rough surface of ZnO interlayer.


Polymers ◽  
2019 ◽  
Vol 11 (5) ◽  
pp. 746 ◽  
Author(s):  
Mun Ho Yang ◽  
Ho Cheol Jin ◽  
Joo Hyun Kim ◽  
Dong Wook Chang

Three conjugated polymers, in which the electron-donating (D) 5-alkylthiophene-2-yl-substitued benzodithiophene was linked to three different electron-accepting (A) moieties, i.e., benzothiadiazole (BT), diphenylquinoxaline (DPQ), and dibenzophenazine (DBP) derivative via thiophene bridge, were synthesized using the Stille coupling reaction. In particular, the strong electron-withdrawing cyano (CN) group was incorporated into the A units BT, DPQ, and DBP to afford three D–A type target polymers PB–BTCN, PB–DPQCN, and PB–DBPCN, respectively. Owing to the significant contribution of the CN-substituent, these polymers exhibit not only low-lying energy levels of both the highest occupied molecular orbital and the lowest unoccupied molecular orbital, but also reduced bandgaps. Furthermore, to investigate the photovoltaic properties of polymers, inverted-type devices with the structure of ITO/ZnO/Polymer:PC71BM/MoO3/Ag were fabricated and analyzed. All the polymer solar cells based on the three cyano-substituted conjugated polymers showed high open-circuit voltages (Voc) greater than 0.89 V, and the highest power conversion efficiency of 4.59% was obtained from the device based on PB-BtCN with a Voc of 0.93 V, short-circuit current of 7.36 mA cm−2, and fill factor of 67.1%.


Molecules ◽  
2018 ◽  
Vol 24 (1) ◽  
pp. 54 ◽  
Author(s):  
Zhonglian Wu ◽  
Huanxiang Jiang ◽  
Xingzhu Wang ◽  
Lei Yan ◽  
Wei Zeng ◽  
...  

To investigate the influence of fluoride phenyl side-chains onto a quinoxaline (Qx) unit on the photovoltaic performance of the narrow bandgap (NBG) photovoltaic polymers, herein, two novel NBG copolymers, PBDTT-DTQx and PBDTT-DTmFQx, were synthesized and characterized. 2-ethylhexylthiothiophene-substituted benzodithiophene (BDTT), 2,3-diphenylquinoxaline (DQx) [or 2,3-bis(3-fluorophenyl)quinoxaline (DmFQx)] and 2-ethylhexylthiophene (T) were used as the electron donor (D) unit, electron-withdrawing acceptor (A) unit and π-bridge, respectively. Compared to non-fluorine substituted PBDTT-DTQx, fluoride PBDTT-DTmFQx exhibited a wide UV-Vis absorption spectrum and high hole mobility. An enhanced short-circuit current (Jsc) and fill factor (FF) simultaneously gave rise to favorable efficiencies in the polymer/PC71BM-based polymer solar cells (PSCs). Under the illumination of AM 1.5G (100 mW cm−2), a maximum power conversion efficiency (PCE) of 6.40% was achieved with an open-circuit voltage (Voc) of 0.87 V, a Jsc of 12.0 mA cm−2 and a FF of 61.45% in PBDTT-DTmFQx/PC71BM-based PSCs, while PBDTT-DTQx-based devices also exhibited a PCE of 5.43%. The excellent results obtained demonstrate that PBDTT-DTmFQx by fluorine atom engineering could be a promising candidate for organic photovoltaics.


2014 ◽  
Vol 116 (15) ◽  
pp. 154506 ◽  
Author(s):  
Yong Zhao ◽  
Chunjun Liang ◽  
Mengjie Sun ◽  
Qian Liu ◽  
Fujun Zhang ◽  
...  

2011 ◽  
Vol 23 (40) ◽  
pp. 4636-4643 ◽  
Author(s):  
Zhicai He ◽  
Chengmei Zhong ◽  
Xun Huang ◽  
Wai-Yeung Wong ◽  
Hongbin Wu ◽  
...  

2008 ◽  
Vol 1091 ◽  
Author(s):  
Osamu Yoshikawa ◽  
Taro Sonobe ◽  
Takashi Sagawa ◽  
Susumu Yoshikawa

AbstractThe performance of the devices of bulk heterojunction polymer-based solar cells were investigated by using poly(3-hexylthiophene) (P3HT) and (6,6)-phenyl C61 butyric acid methyl ester (PCBM) as light absorption (viz. active) layer, with TiOx as interlayer as follows: ITO/PEDOT:PSS/P3HT-PCBM/TiOx/Al [1] through the treatment of microwave irradiation (single mode of 2.45 GHz, 800 W for 1, 2.5, or 5 min). Such treatments enabled to increase the short-circuit current density Jsc (from 4.53 mA cm−2 to 7.27 mA cm−2) and fill factor FF (from 0.41 to 0.66) of the cell, though the open circuit voltage Voc was decreased (from 0.61 V to 0.57 V) along the irradiation. Absorption spectra of P3HT-PCBM blended film before and after the microwave treatment were observed. Shoulders at 550 nm and 600 nm appeared after the irradiation. This result implies that the microcrystallization of P3HT was slightly promoted through the microwave treatment.


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