TY - JOUR
T1 - Passivation of Deep-Level Defects by Cesium Fluoride Post-Deposition Treatment for Improved Device Performance of Cu(In,Ga)Se2 Solar Cells
AU - Lee, Hojin
AU - Jang, Yuseong
AU - Nam, Sung Wook
AU - Jung, Chanwon
AU - Choi, Pyuck Pa
AU - Gwak, Jihye
AU - Yun, Jae Ho
AU - Kim, Kihwan
AU - Shin, Byungha
N1 - Publisher Copyright:
Copyright © 2019 American Chemical Society.
PY - 2019/10/2
Y1 - 2019/10/2
N2 - Heavy-alkali post-deposition treatments (PDTs) utilizing Cs or Rb has become an indispensable step in producing high-performance Cu(In,Ga)Se2 (CIGS) solar cells. However, full understanding of the mechanism behind the improvements of device performance by heavy-alkali treatments, particularly in terms of potential modification of defect characteristics, has not been reached yet. Here, we present an extensive study on the effects of CsF-PDT on material properties of CIGS absorbers and the performance of the final solar devices. Incorporation of an optimized concentration of Cs into CIGS resulted in a significant improvement of the device efficiency from 15.9 to 18.4% mainly due to an increase in the open-circuit voltage by 50 mV. Strong segregation of Cs at the front and rear interfaces as well as along grain boundaries of CIGS was observed via high-resolution chemical analysis such as atomic probe tomography. The study of defect chemistry using photoluminescence and capacitance-based measurements revealed that both deep-level donor-like defects such as VSe and InCu and deep-level acceptor-like defects such as VIn or CuIn are passivated by CsF-PDT, which contribute to an increased hole concentration. Additionally, it was found that CsF-PDT induces a slight change in the energetics of VCu, the most dominant point defect that is responsible for the p-type conductivity of CIGS.
AB - Heavy-alkali post-deposition treatments (PDTs) utilizing Cs or Rb has become an indispensable step in producing high-performance Cu(In,Ga)Se2 (CIGS) solar cells. However, full understanding of the mechanism behind the improvements of device performance by heavy-alkali treatments, particularly in terms of potential modification of defect characteristics, has not been reached yet. Here, we present an extensive study on the effects of CsF-PDT on material properties of CIGS absorbers and the performance of the final solar devices. Incorporation of an optimized concentration of Cs into CIGS resulted in a significant improvement of the device efficiency from 15.9 to 18.4% mainly due to an increase in the open-circuit voltage by 50 mV. Strong segregation of Cs at the front and rear interfaces as well as along grain boundaries of CIGS was observed via high-resolution chemical analysis such as atomic probe tomography. The study of defect chemistry using photoluminescence and capacitance-based measurements revealed that both deep-level donor-like defects such as VSe and InCu and deep-level acceptor-like defects such as VIn or CuIn are passivated by CsF-PDT, which contribute to an increased hole concentration. Additionally, it was found that CsF-PDT induces a slight change in the energetics of VCu, the most dominant point defect that is responsible for the p-type conductivity of CIGS.
KW - Cu(In,Ga)Se solar cells
KW - defect passivation
KW - heavy-alkali incorporation
KW - inorganic thin-film material
KW - post-deposition treatment
UR - http://www.scopus.com/inward/record.url?scp=85072848748&partnerID=8YFLogxK
U2 - 10.1021/acsami.9b08316
DO - 10.1021/acsami.9b08316
M3 - Article
C2 - 31525944
AN - SCOPUS:85072848748
SN - 1944-8244
VL - 11
SP - 35653
EP - 35660
JO - ACS applied materials & interfaces
JF - ACS applied materials & interfaces
IS - 39
ER -