The effect of dielectric spacer thickness on surface plasmon enhanced solar cells for front and rear side depositions

被引:114
作者
Pillai, S. [1 ]
Beck, F. J. [2 ]
Catchpole, K. R. [2 ]
Ouyang, Z. [1 ]
Green, M. A. [1 ]
机构
[1] Univ New S Wales, ARC Photovolta Ctr Excellence, Sydney, NSW 2052, Australia
[2] Australian Natl Univ, Coll Engn & Comp Sci, Ctr Sustainable Energy Syst, Canberra, ACT 0200, Australia
基金
澳大利亚研究理事会;
关键词
METAL-ISLAND FILMS; ABSORPTION; SILICON; SUBSTRATE;
D O I
10.1063/1.3567299
中图分类号
O59 [应用物理学];
学科分类号
摘要
The excitation of surface plasmons on metallic nanoparticles has the potential to significantly improve the performance of solar cells, in particular thin-film structures. In this article, we investigate the effect of the dielectric spacer layer thickness on the photocurrent enhancement of 2 mu m thick, thin-film poly-Si on glass solar cells, due to random arrays of self-assembled Ag nanoparticles deposited on the front or the rear of the cells. We report a strong asymmetry in the external quantum efficiency (EQE) of the cell for front and rear located particles for different spacer thicknesses, which is attributed to differences in the scattering behavior of the nanoparticles. We find that for random arrays, with spectrally broad scattering resonances, the strength of the driving field and the coupling efficiency are more important for light trapping than the resonance wavelength. For particles located on the front of the cells it is desirable to have a thin dielectric spacer layer to enhance the scattering from the Ag nanoparticles. Additionally, light trapping provided by the random sized particles on the front can overcome suppression of light transmitted in the visible wavelength regions for thin layers of Si, to result in overall EQE enhancements. However, for particles deposited on the rear it is more beneficial to have the particles as close to the Si substrate as possible to increase both the scattering and the coupling efficiency. (C) 2011 American Institute of Physics. [doi:10.1063/1.3567299]
引用
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页数:8
相关论文
共 26 条
[11]   ABSORPTION-EDGE OF SILICON FROM SOLAR-CELL SPECTRAL RESPONSE MEASUREMENTS [J].
KEEVERS, MJ ;
GREEN, MA .
APPLIED PHYSICS LETTERS, 1995, 66 (02) :174-176
[12]   Advances in Evaporated Solid-Phase-Crystallized Poly-Si Thin-Film Solar Cells on Glass (EVA) [J].
Kunz, O. ;
Ouyang, Z. ;
Wong, J. ;
Aberle, A. G. .
ADVANCES IN OPTOELECTRONICS, 2008, 2008
[13]   Photocurrent spectroscopy of optical absorption enhancement in silicon photodiodes via scattering from surface plasmon polaritons in gold nanoparticles [J].
Lim, S. H. ;
Mar, W. ;
Matheu, P. ;
Derkacs, D. ;
Yu, E. T. .
JOURNAL OF APPLIED PHYSICS, 2007, 101 (10)
[14]   Nanosphere lithography: Effect of substrate on the localized surface plasmon resonance spectrum of silver nanoparticles [J].
Malinsky, Michelle Duval ;
Kelly, K. Lance ;
Schatz, George C. ;
Van Duyne, Richard P. .
Journal of Physical Chemistry B, 2001, 105 (12) :2343-2350
[15]   Metal and dielectric nanoparticle scattering for improved optical absorption in photovoltaic devices [J].
Matheu, P. ;
Lim, S. H. ;
Derkacs, D. ;
McPheeters, C. ;
Yu, E. T. .
APPLIED PHYSICS LETTERS, 2008, 93 (11)
[16]   Radiative absorption, fluorescence, and scattering of a classical dipole near a lossless interface: a unified description [J].
Mertz, J .
JOURNAL OF THE OPTICAL SOCIETY OF AMERICA B-OPTICAL PHYSICS, 2000, 17 (11) :1906-1913
[17]   Designing periodic arrays of metal nanoparticles for light-trapping applications in solar cells [J].
Mokkapati, S. ;
Beck, F. J. ;
Polman, A. ;
Catchpole, K. R. .
APPLIED PHYSICS LETTERS, 2009, 95 (05)
[18]   Plasmon-enhanced solar energy conversion in organic bulk heterojunction photovoltaics [J].
Morfa, Anthony J. ;
Rowlen, Kathy L. ;
Reilly, Thomas H., III ;
Romero, Manuel J. ;
van de lagemaat, Jao .
APPLIED PHYSICS LETTERS, 2008, 92 (01)
[19]   Plasmonic nanoparticle enhanced light absorption in GaAs solar cells [J].
Nakayama, Keisuke ;
Tanabe, Katsuaki ;
Atwater, Harry A. .
APPLIED PHYSICS LETTERS, 2008, 93 (12)
[20]  
Ouyang Z., 2010, APPL PHYS LETT, V96, DOI DOI 10.1063/1.3460288