To make polymer: Quantum dot hybrid solar cells NIR-active by increasing diameter of PbS nanoparticles

被引:75
作者
Guchhait, Asim [1 ]
Rath, Arup K. [1 ]
Pal, Amlan J. [1 ]
机构
[1] Indian Assoc Cultivat Sci, Dept Solid State Phys, Kolkata 700032, India
关键词
NIR-Active photovoltaic devices; Polymer: PbS nanoparticle hybrid solar cells; Electron-transfer from PbS to TiO2; MULTIPLE EXCITON GENERATION; PHOTOVOLTAIC CELLS; ELECTRON INJECTION; CHARGE SEPARATION; CARBON NANOTUBES; TIO2; SIZE; DEVICES; PERFORMANCE; COMPOSITES;
D O I
10.1016/j.solmat.2010.09.034
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 fabricate NIR-active solar cells based on PbS quantum dots and a conventional conjugated polymer. These devices act as solar cells under exclusively NIR wavelengths above 650 nm. Here PbS nanoparticles absorb photons in the NIR range that in turn generate excitons. We show that with an assistance from a strong electron-acceptor (TiO2), these excitons can be dissociated to electrons and holes to yield a photocurrent in the external circuit. We then aim to extend the spectral window of the solar cells to higher wavelength region by increasing the diameter of PbS nanoparticles to make the cells further NIR-active. We observe that the short-circuit current (J(SC)) shows a peak when the diameter of PbS nanoparticles increases. Here, the spectral window can be extended till conduction band-edge of PbS quantum dots falls below that of TiO2 nanostructures cutting off the electron-transfer pathway. The NIR-active photovoltaic solar cells yield a short-circuit current (J(SC)) of 1.0 mA/cm(2), open-circuit voltage (V-OC) of 0.42 V. and power conversion efficiency (eta) of 0.16% and remain operative till 1200 nm. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:651 / 656
页数:6
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