113Cd Solid-State NMR at 21.1 T Reveals the Local Structure and Passivation Mechanism of Cadmium in Hybrid and All-Inorganic Halide Perovskites

被引:15
|
作者
Kubicki, Dominik J. [1 ]
Prochowicz, Daniel [2 ]
Hofstetter, Albert [1 ]
Walder, Brennan J. [1 ]
Emsley, Lyndon [1 ]
机构
[1] Ecole Polytech Fed Lausanne EPFL, Inst Chem Sci & Engn, Lab Magnet Resonance, CH-1015 Lausanne, Switzerland
[2] Polish Acad Sci, Inst Phys Chem, PL-01224 Warsaw, Poland
基金
瑞士国家科学基金会;
关键词
LIGHT-EMITTING-DIODES; PHASE SEGREGATION; MECHANOCHEMICAL SYNTHESIS; HIGHLY EFFICIENT; CHEMICAL-SHIFTS; IODIDE; PERFORMANCE; METHYLAMMONIUM; OPPORTUNITIES; NANOCRYSTALS;
D O I
10.1021/acsenergylett.0c01420
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Cadmium doping has recently emerged as an efficacious strategy for defect suppression and band gap tuning in hybrid as well as all-inorganic halide perovskites. However, the cadmium speciation in these materials is unknown. Here, we use high-field cadmium-113 NMR spectroscopy in conjunction with chemical shift calculations by fully relativistic density functional theory to establish the phase composition of cadmium-doped lead halide perovskites. We find that cadmium does not incorporate into the 3D perovskite lattice of MA- and FA-based lead halide perovskites (MAPbI(3) and the gold-standard triple cation mixedhalide composition). Instead, it forms separate, cadmium-rich nonperovskite phases for as little as 1 mol % Cd2+ doping. Conversely, we find that cadmium can incorporate into the 3D perovskite lattice of CsPbBr 3 via homovalent Pb2+ substitution up to around 10 mol %. Our results thus reveal the atomic-level mechanism of this recently developed defect passivation strategy.
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页码:2964 / 2971
页数:8
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