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Lead-Halide Scalar Couplings in 207Pb NMR of APbX3 Perovskites (A=Cs, Methylammonium, Formamidinium; X=Cl, Br, I)
被引:54
|作者:
Aebli, Marcel
[1
,2
]
Piveteau, Laura
[1
,2
,3
]
Nazarenko, Olga
[1
,2
]
Benin, Bogdan M.
[1
,2
]
Krieg, Franziska
[1
,2
]
Verel, Rene
[1
]
Kovalenko, Maksym V.
[1
,2
]
机构:
[1] Swiss Fed Inst Technol, Dept Chem & Appl Biosci, Vladimir Prelog Weg 1-5, CH-8093 Zurich, Switzerland
[2] Empa Swiss Fed Labs Mat Sci & Technol, Uberlandstr 129, CH-8600 Dubendorf, Switzerland
[3] Univ Orleans, CNRS, CEMHTi, UPR 3079, 1D Ave Rech Scientifique, F-45071 Orleans, France
关键词:
DEFECT-TOLERANT SEMICONDUCTORS;
LIGHT-EMITTING-DIODES;
HYBRID PEROVSKITES;
PHASE-TRANSITIONS;
MAGNETIC-RESONANCE;
CRYSTAL-STRUCTURE;
CATION DYNAMICS;
SINGLE-CRYSTALS;
CESIUM;
NANOCRYSTALS;
D O I:
10.1038/s41598-020-65071-4
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Understanding the structure and dynamics of newcomer optoelectronic materials - lead halide perovskites APbX(3) [A=Cs, methylammonium (CH3NH3+, MA), formamidinium (CH(NH2)(2)(+), FA); X=Cl, Br, I] - has been a major research thrust. In this work, new insights could be gained by using Pb-207 solid-state nuclear magnetic resonance (NMR) spectroscopy at variable temperatures between 100 and 300K. The existence of scalar couplings (1)J(Pb-Cl) of ca. 400Hz and (1)J(Pb-Br) of ca. 2.3kHz could be confirmed for MAPbX(3) and CsPbX3. Diverse and fast structure dynamics, including rotations of A-cations, harmonic and anharmonic vibrations of the lead-halide framework and ionic mobility, affect the resolution of the coupling pattern. Pb-207 NMR can therefore be used to detect the structural disorder and phase transitions. Furthermore, by comparing bulk and nanocrystalline CsPbBr3 a greater structural disorder of the PbBr6-octahedra had been confirmed in a nanoscale counterpart, not readily captured by diffraction-based techniques.
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页数:9
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