scholarly journals Investigation of the current of P3HT:PCBM based organic solar cell extracting the spatial recombination coefficient of the active layer

IEEE Access ◽  
2021 ◽  
pp. 1-1
Author(s):  
Md. Shofiqul Islam
RSC Advances ◽  
2020 ◽  
Vol 10 (42) ◽  
pp. 24882-24892 ◽  
Author(s):  
Anjusree S. ◽  
Arya K. R. ◽  
Bikas C. Das

Current imaging by C-AFM is demonstrated as a very effective tool to probe the defects in the organic solar cell active layer.


2012 ◽  
Vol 51 (8R) ◽  
pp. 088003 ◽  
Author(s):  
Kyu-Jin Kim ◽  
Jin-Ju Bae ◽  
Yoon-Sik Seo ◽  
Byoung-Ho Kang ◽  
Se-Hyuk Yeom ◽  
...  

2016 ◽  
Vol 4 (4) ◽  
pp. 275-284 ◽  
Author(s):  
Shanmugam Saravanan ◽  
Yasser A.M. Ismail ◽  
Murugesan Silambarasan ◽  
Naoki Kishi ◽  
Tetsuo Soga

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Paik-Kyun Shin ◽  
Palanisamy Kumar ◽  
Abhirami Kumar ◽  
Santhakumar Kannappan ◽  
Shizuyasu Ochiai

Bulk heterojunction (BHJ) structure based active layers of PCDTBT/PC71BM were prepared by using different organic solvents for fabrication of organic solar cell (OSC) devices. Mixture of precursor solutions of PCDTBT/PC71BM in three different organic solvents was prepared to fabricate composite active layers by spin-coating process: chloroform; chlorobenzene; o-dichlorobenzene. Four different blend ratios (1 : 3–1 : 6) of PCDTBT: PC71BM were adopted for each organic solvent to clarify the effect on the resulting OSC device characteristics. Surface morphology of the active layers was distinctively affected by the blend ratio of PCDTBT/PC71BM in organic solvents. Influence of the blend ratio of PCDTBT/PC71BM on the OSC device parameters was discussed. Performance parameters of the resulting OSC devices with different composite active layers were comparatively investigated. Appropriate blend ratio and organic solvent to achieve better OSC device performance were proposed. Furthermore, from the UV-Vis spectrum of each active layer prepared using the PCDTBT/PC71BM mixed solution dissolved with different organic solvents, a possibility that the nanophase separation structure inside their active layer could appear was suggested.


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