Post-Synthetic Doping and Ligand Engineering of Cs2AgInCl6 Double Perovskite Nanocrystals

被引:5
作者
Dube, Lacie [1 ]
Saghy, Peter [1 ]
Chen, Ou [1 ]
机构
[1] Brown Univ, Dept Chem, Providence, RI 02912 USA
基金
美国国家科学基金会;
关键词
HALIDE DOUBLE PEROVSKITE; NEAR-INFRARED EMISSION; LEAD-FREE; QUANTUM DOTS; DESIGN; BR; CL; TRANSFORMATION; STABILITY; EXCHANGE;
D O I
10.1021/acs.jpcc.3c05901
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
Lead-free double perovskite (DP) nanocrystals (NCs) have emerged as a promising class of perovskite nanomaterials with potential applications in various optical and optoelectronic domains. Meanwhile, doping impurity ions into perovskite structures represents a unique and effective means to tailor and optimize the properties of perovskite materials. Herein, we introduce a postsynthetic doping approach to the fabrication of Mn2+-doped Cs2AgInCl6 DP NCs with enhanced optical characteristics. We demonstrate that, in the postsynthetic reaction, the initial surface-doped Mn2+ ions undergo a gradual inward migration process within the NCs, resulting in homogeneous Mn2+ doping with a maximum photoluminescence (PL) quantum yield (QY) of 5.2%. This PL QY value can be further improved to 8.2% through codoping with Na+ ions and careful engineering of the NC surface state. In-depth studies involving conventional one-dimensional proton and two-dimensional NMR spectroscopic techniques unveil the pivotal role played by the surface ligands and their states. Based on our findings, we propose a comprehensive postsynthetic doping mechanism. Our study not only presents an accessible doping technique for lead-free perovskite NCs but also offers valuable insights into the dopant dynamics and ligand engineering for perovskite-type nanomaterials in a broader context.
引用
收藏
页码:21849 / 21859
页数:11
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