Device performance enhancement of polymer solar cells by nanoparticle self-assembly

被引:5
|
作者
Zhang, Wenluan [1 ]
Nguyen, Ngoc A. [1 ,4 ]
Murray, Roy [2 ]
Mackay, Michael E. [1 ,3 ]
机构
[1] Univ Delaware, Dept Mat Sci & Engn, Newark, DE 19716 USA
[2] Univ Delaware, Dept Phys & Astron, Newark, DE 19716 USA
[3] Univ Delaware, Dept Chem & Biomol Engn, Newark, DE 19716 USA
[4] Oak Ridge Natl Lab, Mat Sci & Technol Div, Oak Ridge, TN 37831 USA
关键词
Polymer:fullerene solar cells; Nanoparticle self-assembly; Depletion flocculation; Spin coating; Neutron scattering; ORGANIC PHOTOVOLTAIC CELLS; POLY(3-HEXYLTHIOPHENE); MORPHOLOGY; SCATTERING; NEUTRON; BLENDS; FILMS;
D O I
10.1016/j.solmat.2016.10.030
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
We show that it is possible to assemble a sparse mono-layer of Fe3O4 nanoparticles (NPs) at cathode interface of a polymer solar cell based on poly(3-hexylthiophene): [6,6]-phenyl-C-60-butyric acid methyl ester (P3HT: PCBM) through the synergic effect of strong convective outflow, surface energy, Fe3O4 NPs concentration and active layer thickness. When the distance between those Fe3O4 NPs is smaller than the size of P3HT, the P3HT is excluded from the inter-particle space, and fullerene molecules fill in the space to build electron transport pathways improving charge transport and collection near cathode interface proved by transmission electron microscopy and X-ray photoelectron spectroscopy. The power conversion efficiency of the devices is improved up to 20%. The bulk morphology of light absorbing layers is not affected by the addition of Fe3O4 NPs as demonstrated by neutron and X-ray scattering results.
引用
收藏
页码:126 / 133
页数:8
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