DocumentCode :
392648
Title :
Molecular level pathway to CIS deposition without post treatments
Author :
Menezes, Shalini
Author_Institution :
InterPhases Res., Thousand Oaks, CA, USA
fYear :
2002
fDate :
19-24 May 2002
Firstpage :
660
Lastpage :
663
Abstract :
CuInSe2 (CIS) based thin-film devices could potentially provide high specific power for terrestrial or space power if they were fabricated at low temperatures on low-density polymer substrates. This paper presents a molecular level electrochemical approach that may permit direct deposition of morphologically homogenous, stoichiometric CIS-alloy absorber layers without high temperature post treatments. The paper investigates the effects of deposition parameters by monitoring voltammetric characteristics, pulsed flow/deposition waveforms and film composition with different deposition system configurations. It distinguishes the CIS formation reaction mechanisms in bulk and thin layer electrolytes and identifies two new deposition parameters to increase the content of difficult-to-electrodeposit metals like In and Ga. The results provide directions for low-temperature synthesis of device quality absorber layers for efficient, inexpensive PV modules.
Keywords :
copper compounds; electrodeposition; electrodeposits; indium compounds; semiconductor growth; semiconductor thin films; ternary semiconductors; CIS based thin-film devices; CIS deposition; CIS-alloy absorber layers; CuInSe2; deposition parameters; film composition; low-temperature synthesis; molecular level electrochemical approach; voltammetric characteristics; Chemicals; Computational Intelligence Society; Condition monitoring; Epitaxial growth; Maximum likelihood estimation; Polymer films; Production; Substrates; Temperature; Thin film devices;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Photovoltaic Specialists Conference, 2002. Conference Record of the Twenty-Ninth IEEE
ISSN :
1060-8371
Print_ISBN :
0-7803-7471-1
Type :
conf
DOI :
10.1109/PVSC.2002.1190651
Filename :
1190651
Link To Document :
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