Colloidal Nanocrystals of Lead-Free Double-Perovskite (Elpasolite) Semiconductors: Synthesis and Anion Exchange To Access New Materials

被引:432
|
作者
Creutz, Sidney E. [1 ]
Crites, Evan N. [1 ]
De Siena, Michael C. [1 ]
Gamelin, Daniel R. [1 ]
机构
[1] Univ Washington, Dept Chem, Seattle, WA 98195 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Lead-free perovskites; colloidal semiconductor nanocrystals; anion exchange; elpasolites; HALIDE DOUBLE PEROVSKITE; SOLAR-CELLS; OPTICAL-PROPERTIES; RATIONAL DESIGN; CATION-EXCHANGE; QUANTUM DOTS; BR; CS2AGBIBR6; STABILITY; CRYSTAL;
D O I
10.1021/acs.nanolett.7b04659
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Concerns, about the toxicity and instability of lead-halide perovskites have driven a recent surge in research toward alternative lead-free perovskite materials, including lead-free double perovskites with the elpasolite structure and visible bandgaps. Synthetic approaches to this class of materials remain limited, however, and no examples of heterometallic elpasolites as nanomaterials have been reported. Here, we report the synthesis and characterization of colloidal nano crystals of Cs2AgBiX6 (X = Cl, Br) elpasolites using a hot injection approach. We further show that postsynthetic modification through anion exchange and cation extraction can be used to convert these nanocrystals to new materials including Cs2AgBiI6, which was previously unknown experimentally. Nanocrystals of Cs2AgBiI6, synthesized via a novel anion-exchange. protocol using trimethylsilyl iodide, have strong absorption throughout the visible region, confirming theoretical predictions that this material could be a promising photovoltaic absorber. The synthetic methodologies presented here are expected to be broadly generalizable. This work demonstrates that nanocrystal ion-exchange reactivity can be used to discover and develop new lead-free halide perovskite materials that may be difficult or impossible to access through direct synthesis.
引用
收藏
页码:1118 / 1123
页数:6
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