Enhanced charge transport and photovoltaic performance of PBDTTT-C-T/PC70BM solar cells via UV-ozone treatment

被引:49
|
作者
Adhikary, Prajwal [1 ]
Venkatesan, Swaminathan [1 ]
Adhikari, Nirmal [1 ]
Maharjan, Purna P. [1 ]
Adebanjo, Olusegun [1 ]
Chen, Jihua [2 ]
Qiao, Qiquan [1 ]
机构
[1] S Dakota State Univ, Dept Elect Engn & Comp Sci, Ctr Adv Photovolta, Brookings, SD 57007 USA
[2] Oak Ridge Natl Lab, Ctr Nanophase Mat Sci, Oak Ridge, TN 37831 USA
基金
美国国家科学基金会;
关键词
ZNO; OXIDE; NANOSTRUCTURES; DEPOSITION; DEVICES; GROWTH;
D O I
10.1039/c3nr03355d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this work, the electron transport layer of PBDTTT-C-T/PC70BM polymer solar cells were subjected to UV-ozone treatment, leading to improved cell performances from 6.46% to 8.34%. The solar cell efficiency reached a maximum of 8.34% after an optimal 5 minute UV-ozone treatment, and then decreased if treated for a longer time. To the best of our knowledge, the mechanism behind the effects of UV-ozone treatment on the improvement of charge transport and cell performance is not fully understood. We have developed a fundamental understanding of the UV-ozone treatment mechanism, which explains both the enhancements in charge transport and photovoltaic performance at an optimal treatment time, and also the phenomenon whereby further treatment time leads to a drop in cell efficiency. Transient photocurrent measurements indicated that the cell charge transport times were 1370 ns, 770 ns, 832 ns, 867 ns, and 1150 ns for the 0 min, 5 min, 10 min, 15 min, and 20 min UV-ozone treatment times, respectively. Therefore the 5 min UV-ozone treatment time led to the shortest transport time and the most efficient charge transport in the cells. The 5 min UV-ozone treated sample exhibited the highest peak intensity (E-2) in the Raman spectra of the treated films, at about 437 cm(-1), indicating that it possessed the best wurtzite phase crystallinity of the ZnO films. Further increasing the UV-ozone treatment time from 5 to 20 min induced the formation of p-type defects (e. g. interstitial oxygen atoms), pushing the ZnO Fermi-level further away from the vacuum level, and decreasing the wurtzite crystallinity.
引用
收藏
页码:10007 / 10013
页数:7
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