TY - JOUR
T1 - New Pb-Free Stable Sn-Ge Solid Solution Halide Perovskites Fabricated by Spray Deposition
AU - Kama, Adi
AU - Tirosh, Shay
AU - Itzhak, Anat
AU - Ejgenberg, Michal
AU - Cahen, David
N1 - Publisher Copyright:
© 2022 The Authors. Published by American Chemical Society
PY - 2022/3/28
Y1 - 2022/3/28
N2 - Considering the toxicity of lead ions, substituting Pb with nontoxic elements in halide perovskites, HaPs, has become one of the most significant challenges associated with these materials. Here, we report on replacing Pb with Sn and Ge, focusing on an all-inorganic HaP, CsSnxGe1-xBr3, and using a multihead spray deposition setup for thin-film formation to overcome the low solubility of the precursors and improve film coverage. We find that, in this way, we can form CsSnxGe1-xBr3 films up to high x values as homogeneous solid solutions; i.e., we obtain a range of compositions with one crystal structure (rather than clusters of two phases). The cubic structure of pure CsSnBr3 is maintained up to 77 atom % Ge, with the lattice spacing decreasing with increasing Ge concentration. The optical band gap is tunable between 1.8 and 2.5 eV, from pure Sn to pure Ge HaP. Most importantly, the perovskite structural stability increases with increasing concentration of Ge, with less oxidation of both Ge and Sn to the +4 state, which can be ascribed to less octahedral tilting and stronger bonding. Electrical and electronic transport measurements show the potential of these materials as Pb-free absorbers for solar cells, particularly, given their band gap range as the top cell of a tandem photovoltaic device.
AB - Considering the toxicity of lead ions, substituting Pb with nontoxic elements in halide perovskites, HaPs, has become one of the most significant challenges associated with these materials. Here, we report on replacing Pb with Sn and Ge, focusing on an all-inorganic HaP, CsSnxGe1-xBr3, and using a multihead spray deposition setup for thin-film formation to overcome the low solubility of the precursors and improve film coverage. We find that, in this way, we can form CsSnxGe1-xBr3 films up to high x values as homogeneous solid solutions; i.e., we obtain a range of compositions with one crystal structure (rather than clusters of two phases). The cubic structure of pure CsSnBr3 is maintained up to 77 atom % Ge, with the lattice spacing decreasing with increasing Ge concentration. The optical band gap is tunable between 1.8 and 2.5 eV, from pure Sn to pure Ge HaP. Most importantly, the perovskite structural stability increases with increasing concentration of Ge, with less oxidation of both Ge and Sn to the +4 state, which can be ascribed to less octahedral tilting and stronger bonding. Electrical and electronic transport measurements show the potential of these materials as Pb-free absorbers for solar cells, particularly, given their band gap range as the top cell of a tandem photovoltaic device.
KW - Halide perovskite
KW - Pb-free
KW - Sn-ge
KW - Solar cell
KW - Spray deposition
KW - Stability
UR - http://www.scopus.com/inward/record.url?scp=85127320134&partnerID=8YFLogxK
U2 - 10.1021/acsaem.1c04115
DO - 10.1021/acsaem.1c04115
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AN - SCOPUS:85127320134
SN - 2574-0962
VL - 5
SP - 3638
EP - 3646
JO - ACS Applied Energy Materials
JF - ACS Applied Energy Materials
IS - 3
ER -