An isomerized alkyl side chain enables efficient nonfullerene organic photovoltaics with good tolerance to pre/post-treatments

2021 ◽  
Vol 5 (7) ◽  
pp. 3050-3060 ◽  
Author(s):  
Chenyu Han ◽  
Huanxiang Jiang ◽  
Pengchao Wang ◽  
Lu Yu ◽  
Jianxiao Wang ◽  
...  

An alkyl isomerization strategy is reported to finely modulate the crystallinity of nonfullerene acceptors as well as their photovoltaic responses to post-treatments.

2018 ◽  
Vol 61 ◽  
pp. 185-196 ◽  
Author(s):  
Jhao-Lin Wu ◽  
Chiao-Wen Lin ◽  
Jan Golder ◽  
Tsu-Wei Lin ◽  
Chin-Ti Chen ◽  
...  

2021 ◽  
Author(s):  
Zichun Zhou ◽  
Shengjie Xu ◽  
Xiaozhang Zhu

Hierarchical morphology has been clearly demonstrated to improve all performance parameters in ternary organic photovoltaics but shows strong dependence on the molecular structures. Here we develop four small molecule electron acceptors with different alkyl chain length to find the optimal solution of alkyl chain towards the defined hierarchical morphology and carry out a clear and comprehensive investigation of the alkyl chain length effects on the structure-morphology-device performance relationships in ternary blend. There is a positive correlation between the power conversion efficiencies of the four ternary systems and their short-circuit current density parameters, manifesting the significance of distinguishing optimal alkyl side chain length of small molecule electron acceptors for defined hierarchical morphology to afford efficient carrier generation. The non-optimal side chains would retard the BTR crystalline and make the PC<sub>71</sub>BM domain sizes incontrollable, leading to a morphology without a defined hierarchy. Such a detailed mapping of the alkyl side chain length of small molecule electron acceptors provide a new insight into the materials combinations for the next-step high performance multi-component organic photovoltaics


2021 ◽  
Vol 22 (12) ◽  
pp. 6400
Author(s):  
Joseph Breheny ◽  
Cian Kingston ◽  
Robert Doran ◽  
Joao Anes ◽  
Marta Martins ◽  
...  

Herein, we report antibacterial and antifungal evaluation of a series of previously prepared (+)-tanikolide analogues. One analogue, (4S,6S)-4-methyltanikolide, displayed promising anti-methicillin-resistant Staphylococcus aureus activity with a MIC of 12.5 µg/mL. Based on the antimicrobial properties of the structurally related (−)-malyngolide, two further analogues (4S,6S)-4-methylmalyngolide and (4R,6S)-4-methylmalyngolide bearing a shortened n-nonyl alkyl side chain were prepared in the present study using a ZrCl4-catalysed deprotection/cyclisation as the key step in their asymmetric synthesis. When these were tested for activity against anti-methicillin-resistant Staphylococcus aureus, the MIC increased to 50 µg/mL.


2019 ◽  
Vol 43 (8) ◽  
pp. 3556-3564 ◽  
Author(s):  
Vinay S. Sharma ◽  
Akshara P. Shah ◽  
Anuj S. Sharma

A new class of bowl-shaped supramolecular liquid crystals (LCs) is described derived from calix[4]arene substituted with 1,3,4-thiadiazole derivatives, inbuilt with Schiff base and ester on the lower rim and with an azo group on the upper rim with an alkyl side chain (–OC3H7, –OC8H17).


2015 ◽  
Vol 210 ◽  
pp. 264-271 ◽  
Author(s):  
Kiki A. Kurnia ◽  
Catarina M.S.S. Neves ◽  
Mara G. Freire ◽  
Luís M.N.B.F. Santos ◽  
João A.P. Coutinho

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