Stability of deuterated amorphous silicon solar cells

被引:4
|
作者
Munyeme, G
Wells, JPR
van der Meer, LFG
Dijkhuis, JI
van der Weg, WF
Schropp, REI
机构
[1] Univ Utrecht, Debye Inst, SID, NL-3508 TA Utrecht, Netherlands
[2] Univ Utrecht, Debye Inst, NL-3508 TA Utrecht, Netherlands
[3] FOM, Inst Plasmaphys Rijnhuizen, Felix Free Electron Laser Facil, NL-3430 TA Nieuwegein, Netherlands
[4] Univ Sheffield, Dept Phys & Astron, Sheffield S3 7RH, S Yorkshire, England
关键词
D O I
10.1016/j.jnoncrysol.2004.02.089
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In order to elucidate the microscopic mechanism for the earlier observed enhanced stability of deuterated amorphous silicon solar cells we conducted a side-by-side study of fully deuterated intrinsic layers on crystalline silicon substrates using the free-electron laser facility at Nieuwegein (FELIX) to resonantly excite the Si-D stretching vibration and measure the various relaxation channels available to these modes, and of p-i-n solar cells with identical intrinsic absorber layers on glass/TCO substrates to record the degradation and stabilization of solar cell parameters under prolonged light soaking treatments. From our comparative study it is shown that a-Si:D has a superior resistance against light-induced defect creation as compared to a-Si:H and that this can now be explained in the light of the 'H collision model' since the initial step in the process, the release of H, is more likely than that of D. Thus, a natural explanation for the stability as observed in a-Si:D solar cells is provided. (C) 2004 Elsevier B.V. All rights reserved.
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页码:291 / 294
页数:4
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