Title of article
Stoichiometry controlled conversion efficiency in nanostructured heterojunction solar cell of CdS/CuInSXSe2 X grown by chemical ion exchange method at room temperature
Author/Authors
Rajesh A. Joshi a، نويسنده , , Vidya S. Taur a، نويسنده , , Anil V. Ghule b، نويسنده , , Ramphal Sharma a، نويسنده , , b، نويسنده , , ?، نويسنده ,
Issue Information
ماهنامه با شماره پیاپی سال 2011
Pages
6
From page
1316
To page
1321
Abstract
Here in the present paper, we report on growth of stoichiometric and nonstoichiometric nanostructured heterojunction solar cell of
CdS/CuInSXSe2–X varying X from 0 to 2 in the interval of 0.5 using cost effective, simple, chemical ion exchange method at room temperature
on ITO glass substrate. The as-grown varying composition solar cells annealed at 200 C in air and characterized for structural,
compositional, optical and illumination studies. The X-ray diffraction pattern obtained from CdS/CuInSXSe2–X solar cell confirms the
formation of CuInSe2, CuInS0.5Se1.5, CuInS1Se1, CuInS1.5Se0.5 and CuInS2 phases having tetragonal structure with varying crystallite
size from 19, 19.37, 28, 33 and 20 nm respectively. The energy dispersive X-ray analysis (EDAX) confirms the expected elemental composition
in the heterojunction solar cell. Optical absorbance analysis confirms composition controlled electronic transitions in the thin
films while energy band gap observed to be red shifted with increase the value of X. The solar energy conversion efficiency achieved upon
illuminating to 100 mW/cm2 observed to be 0.27%, 0.06%, 0.17%, 0.02% and 0.23% for CuInSe2, CuInS0.5Se1.5, CuInS1Se1, CuInS1.5Se0.5
and CuInS2 respectively, which correspond for stoichiometric dependent electron–hole pair generation and separation phenomenon.
2011 Elsevier Ltd. All rights reserved.
Keywords
CdS/CuInSXSe2–X solar cell , Nanostructured heterojunction , Electron–hole pair generation , Chemical ion exchange route
Journal title
Solar Energy
Serial Year
2011
Journal title
Solar Energy
Record number
940685
Link To Document