Passivation of Deep-Level Defects by Cesium Fluoride Post-Deposition Treatment for Improved Device Performance of Cu(In,Ga)Se2 Solar Cells

硒化铜铟镓太阳电池 材料科学 钝化 晶界 光电子学 光致发光 接受者 开路电压 太阳能电池 纳米技术 冶金 电压 微观结构 量子力学 凝聚态物理 图层(电子) 物理
作者
Ho‐Jin Lee,Yuseong Jang,Sung‐Wook Nam,Chanwon Jung,Pyuck‐Pa Choi,Jihye Gwak,Jae Ho Yun,Kihwan Kim,Byungha Shin
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:11 (39): 35653-35660 被引量:53
标识
DOI:10.1021/acsami.9b08316
摘要

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.
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