Tailoring Substitutional Sites for Efficient Lanthanide Doping in Lead-Free Perovskite Nanocrystals with Enhanced Near-Infrared Photoluminescence

The incorporation of rare earth lanthanide ions (Ln<sup>3+</sup>) into lead-free halide perovskite nanocrystals (NCs) is an effective and promising strategy to expand their optical, magnetic, and electrochemical properties. Herein, we designed and synthesized various Ln<sup>3+</sup> (including Yb<sup>3+</sup>, Er<sup>3+</sup>, and Nd<sup>3+</sup>), doped Sb<sup>3+</sup>- or Bi<sup>3+</sup>-based and Sb<sup>3+</sup>/Bi<sup>3+</sup> alloyed lead-free perovskite NCs, including vacancy-induced perovskite (A<sub>3</sub>B(III)<sub>2</sub>X<sub>9</sub>), double perovskite (A<sub>2</sub>B(I)B (III)X<sub>6</sub>), and layered-double perovskite (A<sub>4</sub>B(II)B(III)<sub>2</sub>X<sub>12</sub>) NCs with different energy transfer pathways to study the Ln<sup>3+</sup> dopant photoluminescence (PL). While a small size mismatch between dopant ions and host substitutional sites are critical for efficient doping of many first-row transitional metal ion doped metal chalcogenides, surprisingly, the Ln<sup>3+</sup> ions, including the large Nd<sup>3+</sup> ions (112 pm), prefer smaller isovalent Sb(III) octahedral (O<sub>h</sub>) sites (90 pm) instead of Bi(III) O<sub>h</sub> sites (117 pm) in these lead-free perovskite NCs. Significantly, similar substitutional site-dependent Ln<sup>3+</sup> doping efficiencies were obtained across all three different perovskite host lattices, despite differences in host-to-dopant energy transfer mechanisms, which can provide strong evidence of the preferred Sb<sup>3+</sup> substitutional sites for lanthanide dopants in these lead-free perovskite lattices. The efficient Ln<sup>3+</sup> doping in Sb<sup>3+</sup>-rich perovskite NCs leads to enhanced Ln<sup>3+</sup> ion PL of the doped NCs. The preference of smaller Sb (III) over Bi(III) substitutional sites for Ln<sup>3+</sup> dopants is attributed to the relatively high polarizabilities of lanthanide ions and the smaller cationic sites inside [SbX<sub>6</sub>]<sup>3-</sup> compared with [BiX<sub>6</sub>]<sup>3-</sup> octahedra. This study provides a fundamental understanding of Ln<sup>3+</sup> doping behavior in lead-free perovskite NCs and opportunities for designing efficient Ln<sup>3+</sup>-doped functional materials by tuning the microenvironment of the host lattice for enhanced properties.

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Journal
ACS Nano
Published
2025-04-11
DOI
https://doi.org/10.1021/acsnano.5c00487
Citations
21
Primary Topic
Perovskite Materials and Applications
Type
article
Field-Weighted Citation Impact
15.34

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article

Tailoring Substitutional Sites for Efficient Lanthanide Doping in Lead-Free Perovskite Nanocrystals with Enhanced Near-Infrared Photoluminescence

Sara Talebi, Weiwei Zheng, Arindam Chakraborty, Hanjie Lin et al.
21 citations
ACS Nano
Perovskite Materials and Applications
15.34
article

Tailoring Substitutional Sites for Efficient Lanthanide Doping in Lead-Free Perovskite Nanocrystals with Enhanced Near-Infrared Photoluminescence

Sara Talebi, Weiwei Zheng, Arindam Chakraborty, Hanjie Lin, Walker MacSwain, Vanshika Vanshika
article en
21 citations

Abstract

The incorporation of rare earth lanthanide ions (Ln<sup>3+</sup>) into lead-free halide perovskite nanocrystals (NCs) is an effective and promising strategy to expand their optical, magnetic, and electrochemical properties. Herein, we designed and synthesized various Ln<sup>3+</sup> (including Yb<sup>3+</sup>, Er<sup>3+</sup>, and Nd<sup>3+</sup>), doped Sb<sup>3+</sup>- or Bi<sup>3+</sup>-based and Sb<sup>3+</sup>/Bi<sup>3+</sup> alloyed lead-free perovskite NCs, including vacancy-induced perovskite (A<sub>3</sub>B(III)<sub>2</sub>X<sub>9</sub>), double perovskite (A<sub>2</sub>B(I)B (III)X<sub>6</sub>), and layered-double perovskite (A<sub>4</sub>B(II)B(III)<sub>2</sub>X<sub>12</sub>) NCs with different energy transfer pathways to study the Ln<sup>3+</sup> dopant photoluminescence (PL). While a small size mismatch between dopant ions and host substitutional sites are critical for efficient doping of many first-row transitional metal ion doped metal chalcogenides, surprisingly, the Ln<sup>3+</sup> ions, including the large Nd<sup>3+</sup> ions (112 pm), prefer smaller isovalent Sb(III) octahedral (O<sub>h</sub>) sites (90 pm) instead of Bi(III) O<sub>h</sub> sites (117 pm) in these lead-free perovskite NCs. Significantly, similar substitutional site-dependent Ln<sup>3+</sup> doping efficiencies were obtained across all three different perovskite host lattices, despite differences in host-to-dopant energy transfer mechanisms, which can provide strong evidence of the preferred Sb<sup>3+</sup> substitutional sites for lanthanide dopants in these lead-free perovskite lattices. The efficient Ln<sup>3+</sup> doping in Sb<sup>3+</sup>-rich perovskite NCs leads to enhanced Ln<sup>3+</sup> ion PL of the doped NCs. The preference of smaller Sb (III) over Bi(III) substitutional sites for Ln<sup>3+</sup> dopants is attributed to the relatively high polarizabilities of lanthanide ions and the smaller cationic sites inside [SbX<sub>6</sub>]<sup>3-</sup> compared with [BiX<sub>6</sub>]<sup>3-</sup> octahedra. This study provides a fundamental understanding of Ln<sup>3+</sup> doping behavior in lead-free perovskite NCs and opportunities for designing efficient Ln<sup>3+</sup>-doped functional materials by tuning the microenvironment of the host lattice for enhanced properties.

ACS NanoVol. 19(15)
Syracuse University (US)
National Science Foundation
Openalex Percentile: Top 1%
Perovskite Materials and Applications
15.34
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