Towards an understanding of light activation processes in titanium oxide based inverted organic solar cells

被引:29
作者
Chambon, S. [1 ,2 ]
Destouesse, E. [1 ,2 ]
Pavageau, B. [3 ,4 ,5 ]
Hirsch, L. [1 ,2 ]
Wantz, G. [1 ,2 ]
机构
[1] Univ Bordeaux, IMS, UMR 5218, F-33400 Talence, France
[2] CNRS, IMS, UMR 5218, F-33400 Talence, France
[3] Univ Bordeaux, LOF, UMR 5258, F-33600 Pessac, France
[4] CNRS, LOF, UMR 5258, F-33600 Pessac, France
[5] RHODIA, LOF, UMR 5258, F-33600 Pessac, France
关键词
PERSISTENT PHOTOCONDUCTIVITY; TRANSIENT PHOTOCONDUCTIVITY; THIN-FILMS; LAYER; POLY(3-HEXYLTHIOPHENE); PHOTOVOLTAICS; GAN; ITO;
D O I
10.1063/1.4764026
中图分类号
O59 [应用物理学];
学科分类号
摘要
The light activation phenomenon in inverted P3HT:PCBM bulk heterojunction organic solar cells based on titanium oxide sublayer (TiOx) is characterized by fast acquisition of current-voltage (J-V) curves under light bias as function of time. TiOx layers were thermally treated under inert atmosphere at different temperatures prior active layer deposition and for every device an activation time was extracted. It is shown that the higher the TiOx annealing temperature, the faster the activation. The improvement of the overall device performances is also observed for devices with TiOx layers baked above 100 degrees C. The evolution of the characteristic of the organic semiconductors (OSC) device, from dielectric to diode, is attributed to the increase of TiOx conductivity by three orders of magnitude upon white light illumination. Additionally, devices based on baked TiOx present higher conductivity than those based on unbaked TiOx which would explain the gain in performances and the short activation time of the OSC. In order to understand the origin of the phenomenon, deactivation experiments were also performed under different conditions on OSC. The deactivation process was shown to be thermally dependent and fully reversible under inert atmosphere, which suggest that deep traps are responsible for the activation phenomenon. An optimal annealing temperature was found at 120 degrees C and gives a reasonable short activation time of approximately 1 min and photo conversion efficiency up to 4%. (C) 2012 American Institute of Physics. [http://dx.doi.org/10.1063/1.4764026]
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