Abstract

AbstractNowadays, most of the best efficiencies of Cu2ZnSn(S,Se)4 (CZTSSe) solar cells are obtained from absorber layers fabricated using sequential processes, including the deposition of metallic stack precursors, typically by sputtering, and followed by reactive annealing under chalcogen atmosphere. The sputtering technique is widely known for the easy growth of metallic layers, although the deposition rates, growth morphology and nucleation, or the roughness can sometimes be an issue leading to inhomogeneities in the final layers. Nevertheless, MBE (molecular beam epitaxy) technique could have some advantages to obtain high‐quality metallic layers, with accurate control of the growth due to ultra‐high vacuum conditions and high purity. In this work, we study the use of advanced MBE systems to grow metallic stack precursors, alternatively to sputtering or thermal evaporation techniques, to obtain high‐quality CZTSe:Ge absorbers. Due to differences in the nature of each type of precursor, thermal annealing optimizations are presented by modifying some critical selenization parameters, such as the temperature or the selenium amount in order to obtain well‐crystallized absorbers. Detailed morphological, compositional, and structural characterizations show relevant features of each precursor, mainly related to the formation of MoSe2 at the back interface, and Se and Sn composition after selenization in different conditions. Regarding the solar cell devices, main efficiency limitations come from VOC and FF, which could be tentatively related to a noncontrolled selenization; different precursor reactivity, porosity, or composition; and different alkali diffusion during the reactive annealing. Finally, in the first optimization, a 9.2% efficiency device has been achieved with promising perspectives for future improvements.

Highlights

  • Cu2ZnSn(S,Se)[4] (CZTSSe) semiconductor materials have attracted considerable attention in the last years, being one of the most promising thin film photovoltaic absorbers, primarily through the use of earth abundant elements and low toxicity.[1,2,3] This makes kesterites CZTSSe an interesting mid‐ to long‐term alternative to the widely known CuIn1‐xGaxSe2 (CIGSe), allowing reducing the use of scarce elements like In and Ga.[4]

  • Apart from that, kesterite has several advantageous properties to be a very suitable material for photovoltaic applications: kesterite has p‐type conductivity naturally due to intrinsic point defects; it is direct band gap semiconductor with a high absorption coefficient (~104 cm−1)[5]; its band gap can be tuned with the ratio S/Se, from 1.0 eV, for the pure selenium Cu2ZnSnSe4 (CZTSe) compound, to 1.5 eV, for the pure sulfur Cu2ZnSnS4 (CZTS)[6,7]; and it is highly compatible with CIGS technology, sharing several processing steps and techniques

  • We study the use of advanced MBE systems to grow metallic precursors stacks, alternatively to the sputtering or the conventional thermal evaporation techniques, in combination with the commonly used conventional tubular furnace selenization in order to obtain high quality CZTSe absorbers

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Summary

Introduction

Cu2ZnSn(S,Se)[4] (CZTSSe) semiconductor materials have attracted considerable attention in the last years, being one of the most promising thin film photovoltaic absorbers, primarily through the use of earth abundant elements and low toxicity.[1,2,3] This makes kesterites CZTSSe an interesting mid‐ to long‐term alternative to the widely known CuIn1‐xGaxSe2 (CIGSe), allowing reducing the use of scarce elements like In and Ga.[4]. We study the use of advanced MBE (molecular beam epitaxy) systems to grow metallic precursors stacks, alternatively to the sputtering or the conventional thermal evaporation techniques, in combination with the commonly used conventional tubular furnace selenization in order to obtain high quality CZTSe absorbers.

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