4.8 Article

The Role Silver Nanoparticles Plays in Silver-Based Double-Perovskite Nanocrystals

期刊

CHEMISTRY OF MATERIALS
卷 33, 期 7, 页码 2370-2377

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.chemmater.0c04536

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资金

  1. Nancy and Stephen Grand Technion energy program
  2. Alon Fellowship Program
  3. Israel Science Foundation [890015]
  4. Israeli Innovation Authority [67963]
  5. European Union [798409-HMST-PC]

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Lead-free double perovskites are being studied as alternatives to lead halide perovskites in optoelectronic applications, with a focus on the role of metallic silver nanoparticles in crystal growth. The nucleation of perovskite nanocrystals is shown to occur on preexisting silver seeds, with evidence of charge transfer between the perovskite and silver nanoparticles leading to modified optical properties. Understanding and controlling the reduction of Ag+ at all synthetic stages is critical for achieving stability and functionality in silver-based lead-free perovskite nanocrystals.
Lead-free double perovskites are studied as an optional replacement to lead halide perovskites in optoelectronic applications. Recently, double-perovskite materials in which two divalent lead cations are replaced with an Ag+ and a trivalent cation have been demonstrated. The presence of a reactive silver cation and observations of metallic silver nanodecorations raised concerns regarding the stability and applicability of these materials. To better understand the nucleation and crystal growth of lead-free double perovskites, we explore the origin and role that metallic silver nanoparticles (NPs) play in the Ag-based Pb-free double-perovskite nanocrystal (NC) systems such as Cs2AgInCl6, Cs2AgSbCl6, Cs2AgBiCl6, and Cs2AgBiBr6. With major focus on Cs2AgInCl6NCs, we show evidence supporting growth of the NCs through heterogeneous nucleation on preexisting metallic silver seeds. The silver seeds nucleate prior to injection of halide through reduction of the Ag+ ion by the aminic ligand. The presence of preexisting silver NPs is supported by a localized surface plasmon resonance (LSPR). The injection of halide precursor into the reaction mixture step initiates a fast nucleation and growth of the perovskite NC on the silver seed. The change in the dielectric medium at the interface of the silver NP results in a quantifiable red shift of the LSPR peak. In addition, we demonstrate charge transfer from the perovskite to the silver NP through photoinduced electrochemical Ostwald ripening of the silver NPs via UV irradiation. The ripened perovskite-metal hybrid nanocrystal exhibits modified optical properties in the form of quenched emission and enhanced plasmonic absorption. Future development of Ag-based double-perovskite NC applications depends on the ability to control Ag+ reduction at all synthetic stages. This understanding is critical for delivering stability and functionality for silver-based lead-free perovskite nanocrystals.

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