TY - JOUR
T1 - Chemical structure of a carbon-rich layer at the wet-chemical processed Cu2ZnSn(S,Se)4/Mo interface
AU - Hauschild, D.
AU - Wachs, S. J.
AU - Kogler, W.
AU - Seitz, L.
AU - Carter, J.
AU - Schnabel, T.
AU - Krause, B.
AU - Blum, M.
AU - Yang, W.
AU - Ahlswede, E.
AU - Heske, C.
AU - Weinhardt, L.
N1 - Funding Information:
This research uses resources of the Advanced Light Source, which is a DOE Office of Science User Facility under Contract DE-AC02-05CH11231.
Funding Information:
Manuscript received November 16, 2020; revised January 13, 2021; accepted February 6, 2021. Date of publication March 24, 2021; date of current version April 21, 2021. This work was supported in part by the German Federal Ministry of Education and Research (Free-InCa) under Grant 03SF0530B and Grant 03SF0530C. The work of L. Seitz was supported by the German Helmholtz-Association in the framework of the Helmholtz postdoctoral fellowship pro-
Funding Information:
The work of L. Seitz was supported by the German Helmholtz-Association in the framework of the Helmholtz postdoctoral fellowship program under Grant PD-326.
Publisher Copyright:
© 2011-2012 IEEE.
PY - 2021/5
Y1 - 2021/5
N2 - The carbon-rich layer at the back-contact interface of a solution-processed Cu2ZnSn(S,Se)4 (CZTSSe) absorber is investigated with a combination of surface-sensitive X-ray photoelectron and bulk-sensitive X-ray emission spectroscopy. For absorber deposition, an aqueous ammonium-thioglycolate (ATGL) solution was used, and the 'buried' back-contact interface was accessed by cleaving in a liquid nitrogen environment. In the pertinent literature, it is reported that such a carbon layer at the absorber/back-contact interface could have beneficial effects, e.g., to reduce series resistance or increase the short circuit current. Here, a detailed picture of the chemical structure of this carbon-rich layer at the back contact is derived, which consists of carbon (74 ± 7%), selenium (19 ± 4%), and sulfur (7 ± 3%). The selenium in this layer is found as elemental inclusions, possibly from not fully reacted selenium during the absorber production. The sulfur content in this carbon-rich layer is twice that of sulfur in the absorber. A detailed analysis of the chemical environment suggests that residuals from the aqueous ATGL solution are the origin of sulfur in this carbon-rich layer. Furthermore, underneath the carbon-rich layer, S-Mo bonds are found at the Mo back contact.
AB - The carbon-rich layer at the back-contact interface of a solution-processed Cu2ZnSn(S,Se)4 (CZTSSe) absorber is investigated with a combination of surface-sensitive X-ray photoelectron and bulk-sensitive X-ray emission spectroscopy. For absorber deposition, an aqueous ammonium-thioglycolate (ATGL) solution was used, and the 'buried' back-contact interface was accessed by cleaving in a liquid nitrogen environment. In the pertinent literature, it is reported that such a carbon layer at the absorber/back-contact interface could have beneficial effects, e.g., to reduce series resistance or increase the short circuit current. Here, a detailed picture of the chemical structure of this carbon-rich layer at the back contact is derived, which consists of carbon (74 ± 7%), selenium (19 ± 4%), and sulfur (7 ± 3%). The selenium in this layer is found as elemental inclusions, possibly from not fully reacted selenium during the absorber production. The sulfur content in this carbon-rich layer is twice that of sulfur in the absorber. A detailed analysis of the chemical environment suggests that residuals from the aqueous ATGL solution are the origin of sulfur in this carbon-rich layer. Furthermore, underneath the carbon-rich layer, S-Mo bonds are found at the Mo back contact.
KW - Back contact
KW - Chemical structure
KW - Kesterite
KW - Photoelectron spectroscopy
KW - Thin-film solar cell
KW - Wet-chemical processing
KW - X-ray emission spectroscopy (XES)
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U2 - 10.1109/JPHOTOV.2021.3059423
DO - 10.1109/JPHOTOV.2021.3059423
M3 - Article
AN - SCOPUS:85103285292
SN - 2156-3381
VL - 11
SP - 658
EP - 663
JO - IEEE Journal of Photovoltaics
JF - IEEE Journal of Photovoltaics
IS - 3
M1 - 9384891
ER -