4.8 Article

Evolution of Morphological and Chemical Properties at p-n Junction of Cu(In,Ga)Se2 Solar Cells with Zn(O,S) Buffer Layer as a Function of KF Postdeposition Treatment Time

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 13, Issue 41, Pages 48611-48621

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c12636

Keywords

KF postdeposition treatment; Cu(In,Ga)Se-2 solar cell; chemical bath deposition Zn(O,S) buffer layer; chemical reaction; K-In-Se phase; optical-pump-THz-probe spectroscopy

Funding

  1. Technology Development Program to Solve Climate Changes of the National Research Foundation (NRF) - Ministry of Science, ICT & Future Planning [2016M1A2A2936754]
  2. New & Renewable Energy program of the Korea Institute of Energy Technology Evaluation and Planning (KETEP) - Ministry of Trade, Industry Energy [20183010014310]
  3. Electronics and Telecommunications Research Institute (ETRI) - Korean government [21YB2200]

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The highest efficiency of CIGS solar cells was achieved at a KF PDT process time of 50s, where the K-In-Se phase formed is beneficial for solar cell performance. Additionally, photocarrier transport is more effective at low barrier heights.
We carried out KF postdeposition treatment (PDT) on a Cu(In,Ga)Se-2 (CIGS) layer with a process time varying from 50 to 200 s. The highest CIGS solar-cell efficiency was achieved at a KF PDT process time of 50 s; in this condition, we observed the highest level of K element at the near-surface of the CIGS layer and the perfectly passivated pinholes on the CIGS surface. At process times above 150 s, the oversupplied KF agglomerated into large islands and was subsequently eliminated during the deposition of the chemical bath deposition (CBD)-Zn(O,S) buffer layer owing to the islands' water-soluble characteristics. As a result, the growth mechanism of the CBD-Zn(O,S) layer varied as a function of KF PDT process time. X-ray photoemission spectroscopy (XPS) measurements were used to examine the dependency of the chemical state on the KF PDT process time, and from the results, we formulated a chemical reaction model based on the shift in the elemental binding energy following deposition of the CBD-Zn(O,S) buffer layer. The chemical states of the K-In-Se phase, which have a beneficial effect on the solar-cell performance owing to the formation of durable and improved p-n junctions, are formed only at a KF PDT process time of 50 s. We derived band alignments from the XPS depth profiles by extracting the conduction- and valence-band offsets, and we used optical-pump-THz-probe spectroscopy to measure the ultrafast photocarrier lifetimes related to the defect states following KF PDT. Our key findings can be summarized as follows: (i) photocarrier transport is beneficial at a low barrier height, and (ii) the photocarrier lifetime increases when the K-In-Se phases are formed on the CIGS surface, which allows K+ ions to be effectively substituted into Cu vacancies.

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