TY - JOUR
T1 - Electronic effects of point defects in Cu(InxGa1-x)Se2
AU - Rockett, A.
N1 - Funding Information:
The collaboration of many colleagues and many useful discussions are gratefully appreciated. In particular the comments of Lars Stolt are appreciated. The author gratefully acknowledges the Electric Power Research Institute, the National Renewable Energy Laboratory, and the US Department of Energy contract DEFG02-91ER45439. The microanalysis was carried out in the Center for Microanalysis of Materials at the University of Illinois, which is supported by the US Department of Energy.
PY - 2000/2/21
Y1 - 2000/2/21
N2 - An overview of data accumulated on defects in CIGS is presented. From this the following conclusions are drawn. (1) The primary defects, which accommodate changes in film composition in group III rich p-type CIGS, are normally found in large superclusters on (001) planes. This is due to electrostatic interactions of the individual defect cluster dipoles. Such superclustering explains why the defects are electrically inactive, why the hole mobility does not depend upon defect concentration or composition, and why the hole concentration in CIGS depends so little on composition. One form of these superclusters may explain the CuPt ordering observed in some cases. (2) As group III rich CIGS becomes n-type (the Fermi energy rises above midgap), either by the effect of electric fields in the material or continuing addition of group III elements beyond a critical level (which depends upon Ga content and process conditions), the clusters partially or fully decompose, pinning the Fermi energy at the InCu2+ defect level. This is why sufficiently group III rich material remains only weakly n-type over a wide composition range. It may also mean that the Fermi energy is pinned at this level near the surface of some devices. (3) Na acts to improve CIGS devices at grain boundaries. This may be by increasing atomic mobility there, by electrical passivation of the grain boundaries, through increasing grain size, or through some other effect. (4) Oxygen has no beneficial effect on devices through its interaction with the CIGS either within the grains or at grain boundaries.
AB - An overview of data accumulated on defects in CIGS is presented. From this the following conclusions are drawn. (1) The primary defects, which accommodate changes in film composition in group III rich p-type CIGS, are normally found in large superclusters on (001) planes. This is due to electrostatic interactions of the individual defect cluster dipoles. Such superclustering explains why the defects are electrically inactive, why the hole mobility does not depend upon defect concentration or composition, and why the hole concentration in CIGS depends so little on composition. One form of these superclusters may explain the CuPt ordering observed in some cases. (2) As group III rich CIGS becomes n-type (the Fermi energy rises above midgap), either by the effect of electric fields in the material or continuing addition of group III elements beyond a critical level (which depends upon Ga content and process conditions), the clusters partially or fully decompose, pinning the Fermi energy at the InCu2+ defect level. This is why sufficiently group III rich material remains only weakly n-type over a wide composition range. It may also mean that the Fermi energy is pinned at this level near the surface of some devices. (3) Na acts to improve CIGS devices at grain boundaries. This may be by increasing atomic mobility there, by electrical passivation of the grain boundaries, through increasing grain size, or through some other effect. (4) Oxygen has no beneficial effect on devices through its interaction with the CIGS either within the grains or at grain boundaries.
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U2 - 10.1016/S0040-6090(99)00766-X
DO - 10.1016/S0040-6090(99)00766-X
M3 - Conference article
AN - SCOPUS:0033908150
SN - 0040-6090
VL - 361
SP - 330
EP - 337
JO - Thin Solid Films
JF - Thin Solid Films
T2 - The 1999 E-MRS Spring Conference, Symposium O: Chalcogenide Semicondutors for Photovoltaics
Y2 - 1 June 1999 through 4 June 1999
ER -