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Reaction Pathway for Efficient CZTSe Solar Cells from Alloyed Cu-Sn Precursor via a Cu-Rich Selenization Stage

DOI:10.1002/solr.202000124 期刊:Solar RRL 出版年份:2020 更新时间:2025-09-23 15:19:57
摘要: A detailed reaction pathway for efficient CZTSe solar cells from alloyed Cu-Sn precursor via a Cu-rich selenization stage is presented. The study focuses on the selenization of stacked elemental metallic layers (Cu-Sn-Zn), a commonly reported approach in kesterite Cu2ZnSnSe4 (CZTSe) processing. The high volatility of binary selenides, such as SnSe2-x, at necessary annealing temperatures (500 – 550 °C) makes this reaction pathway prone to Sn loss, which challenges the control of the composition and quality of the grown material. The present work reports an approach based on stacked elemental and alloyed precursors, discussing the benefits of using a Zn/Cu-Sn/Zn configuration. The absence of non-alloyed elemental Sn helps in suppressing the formation and subsequent evaporation of SnSe2-x phases, preventing Sn loss from the film during selenization. This reaction pathway involves a process scheme which i) starts with the growth of CZTSe in a Cu-rich environment, ii) includes a shift of the composition by supply of SnSe2-x vapor, and iii) terminates in the Cu-poor regime, leading to device efficiencies above 10%. This composition shift in the presented process appears similar to the final stage of the commonly known CIGSe three-stage co-evaporation.
作者: Devendra Pareek,Teoman Taskesen,José A. Márquez,Helena Stange,Sergiu Levcenco,Ibrahim Simsek,David Nowak,Timo Pfeiffelmann,Wenjian Chen,Christiane Stroth,Mohamed H. Sayed,Ulf Mikolajczak,Jürgen Parisi,Thomas Unold,Roland Mainz,Levent Gütay
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Investigating the reaction pathway for efficient CZTSe solar cells from alloyed Cu-Sn precursor via a Cu-rich selenization stage to prevent Sn loss and control the composition and quality of the grown material.

The study concludes that starting with the SEAL precursor and selenization without alloy segregation provides a route of kesterite CZTSe formation without XRF-detectable Sn-loss. The formation and subsequent evaporation of SnSe2-x phases in the reaction is significantly reduced, preventing Sn loss from the layer during the selenization process. Providing extra SnSe2-x supply during the high temperature stage of the selenization process leads to an in-process composition shift in the sample from initially Cu-rich to a Cu-poor. This allows for the design of a defined reaction and composition pathway throughout the process, which could be a novel approach for reaching higher solar cell efficiencies.

The technical and application constraints include the high volatility of binary selenides at necessary annealing temperatures, which challenges the control of the composition and quality of the grown material. Potential areas for optimization include the variation in initial and final composition, and the investigation of the in-process compositional shift from Cu-rich to Cu-poor and its impact on the resulting material properties.

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