Effects of particle morphology of ZnO buffer layer on the performance of organic solar cell devices

Authors
Mbule, P. S.Kim, T. H.Kim, B. S.Swart, H. C.Ntwaeaborwa, O. M.
Issue Date
2013-05
Publisher
ELSEVIER SCIENCE BV
Citation
SOLAR ENERGY MATERIALS AND SOLAR CELLS, v.112, pp.6 - 12
Abstract
The performance of poly(3-hexyltheopene):[6,6]-phenyl C61-butyric acid methyl ester or P3HT:PCBM based organic solar cell (OSC) devices can be improved by adding an electron extraction layer of a wide band gap semiconducting material such as ZnO or TiO2 that facilitates the electron transport from the photo-active layer (P3HT:PCBM blend) to the top metal electrode (e.g. Al) and, at the same time, blocks holes from reaching the top electrode. Other factors that determine performance of the OSC devices include morphology, thickness and donor-acceptor ratio. In this study we investigated the effects of concentration and particle morphology (nanoparticle versus nanoflake) of ZnO electron extraction layer on the performance of the OSC devices with configuration ITO/PEDOT:PSS/P3HT:PCBM/ ZnO/Al. The concentration of ZnO nanoparticle or nanoflake solutions was varied from 0.5 to 20 mg/ml. A power conversion efficiency (PCE) of 3.08% was recorded from devices incorporating ZnO nanoflake electron extraction layer, whereas PCE of 2.37% was recorded from devices with ZnO nanoparticles as the electron extraction layer. The maximum PCE was obtained from a concentration of 0.5 mg/ml ZnO for both devices. The influence of the particle morphology and the concentration of the ZnO electron extraction layer on the general performance of the OSC devices is discussed in detail. (C) 2013 Elsevier B.V. All rights reserved.
Keywords
TO-ROLL FABRICATION; POLY(3-HEXYLTHIOPHENE); PHOTOLUMINESCENCE; TO-ROLL FABRICATION; POLY(3-HEXYLTHIOPHENE); PHOTOLUMINESCENCE; Photovoltaic; Photoactive; P3HT:PCBM; ZnO nanoparticles/nanoflakes
ISSN
0927-0248
URI
https://pubs.kist.re.kr/handle/201004/128088
DOI
10.1016/j.solmat.2013.01.010
Appears in Collections:
KIST Article > 2013
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