TY - JOUR
T1 - Tailoring CsPbBr3Growth via Non-Polar Solvent Choice and Heating Methods
AU - Zamani, Hediyeh
AU - Chiang, Tsung Hsing
AU - Klotz, Kaylie R.
AU - Hsu, Annie J.
AU - Maye, Mathew M.
N1 - Publisher Copyright:
© 2022 American Chemical Society. All rights reserved.
PY - 2022/8/2
Y1 - 2022/8/2
N2 - This study describes an investigation of the role of non-polar solvents on the growth of cesium lead halide (CsPbX3X = Br and I) nanoplatelets. We employed two solvents, benzyl ether (BE) and 1-octadecene (ODE), as well as two nucleation and growth mechanisms, one-pot, facilitated by microwave irradiation (MWI)-based heating, and hot-injection, using convection. Using BE and MWI, large mesoscale CsPbBr3nanoplatelets were produced, whereas use of ODE produced small crystallites. Differences between the products were observed by optical spectroscopies, which showed first band edge absorptions consistent with thicknesses of ∼9 nm [∼15 monolayer (ML)] for the BE-CsPbBr3and ∼5 nm (∼9 ML) for ODE-CsPbBr3. Both products had orthorhombic crystal structures, with the BE-CsPbBr3revealing significant preferred orientation diffraction signals consistent with the asymmetric and two-dimensional platelet morphology. The differences in the final morphology were also observed for products formed via hot injection, with BE-CsPbBr3showing thinner square platelets with thicknesses of ∼2 ML and ODE-CsPbBr3showing similar morphologies and small crystallite sizes. To understand the role solvent plays in crystal growth, we studied lead plumbate precursor (PbBrn2-n) formation in both solvents, as well as solvent plus ligand solutions. The findings suggest that BE dissolves PbBr2salts to a higher degree than ODE, and that this BE to precursor affinity persists during growth.
AB - This study describes an investigation of the role of non-polar solvents on the growth of cesium lead halide (CsPbX3X = Br and I) nanoplatelets. We employed two solvents, benzyl ether (BE) and 1-octadecene (ODE), as well as two nucleation and growth mechanisms, one-pot, facilitated by microwave irradiation (MWI)-based heating, and hot-injection, using convection. Using BE and MWI, large mesoscale CsPbBr3nanoplatelets were produced, whereas use of ODE produced small crystallites. Differences between the products were observed by optical spectroscopies, which showed first band edge absorptions consistent with thicknesses of ∼9 nm [∼15 monolayer (ML)] for the BE-CsPbBr3and ∼5 nm (∼9 ML) for ODE-CsPbBr3. Both products had orthorhombic crystal structures, with the BE-CsPbBr3revealing significant preferred orientation diffraction signals consistent with the asymmetric and two-dimensional platelet morphology. The differences in the final morphology were also observed for products formed via hot injection, with BE-CsPbBr3showing thinner square platelets with thicknesses of ∼2 ML and ODE-CsPbBr3showing similar morphologies and small crystallite sizes. To understand the role solvent plays in crystal growth, we studied lead plumbate precursor (PbBrn2-n) formation in both solvents, as well as solvent plus ligand solutions. The findings suggest that BE dissolves PbBr2salts to a higher degree than ODE, and that this BE to precursor affinity persists during growth.
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U2 - 10.1021/acs.langmuir.2c01214
DO - 10.1021/acs.langmuir.2c01214
M3 - Article
C2 - 35862294
AN - SCOPUS:85135501390
SN - 0743-7463
VL - 38
SP - 9363
EP - 9371
JO - Langmuir
JF - Langmuir
IS - 30
ER -