Room Temperature Size Tuning of CsPbI <sub>3</sub> Quantum Dots

Size quantization in halide perovskite nanocrystals provides a versatile strategy to tune their optical and electronic properties. We have now synthesized CsPbI3 quantum dots (QDs, 5–13.5 nm) by first preparing CsPbBr3 QDs at room temperature, followed by postsynthetic halide exchange with iodide ions. As the QD size decreases from 13.5 to 5 nm, we observe a pronounced blue shift in both excitonic and emission peaks, accompanied by an increase in the Stokes shift. The reduction in the excited-state lifetime with decreasing QD size is attributed to enhanced intrinsic exciton recombination and a higher density of surface defects. Photoinduced electron transfer between quantized CsPbI3 and methyl viologen revealed an ultrafast process occurring within a few picoseconds. These size-dependent excited-state dynamics and charge-transfer properties highlight the potential of CsPbI3 QDs for photocatalytic solar fuel generation and optoelectronic applications.

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Publication Details

Journal
ACS Materials Letters
Published
2026-02-13
DOI
https://doi.org/10.1021/acsmaterialslett.5c01605
Citations
1
Primary Topic
Perovskite Materials and Applications
Type
article
Field-Weighted Citation Impact
21.93
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article

Room Temperature Size Tuning of CsPbI 3 Quantum Dots

Manish Mukherjee, Prashant V. Kamat
1 citations
ACS Materials Letters
Perovskite Materials and Applications
21.93
article

Room Temperature Size Tuning of CsPbI 3 Quantum Dots

Manish Mukherjee, Prashant V. Kamat
article en
1 citations

Abstract

Size quantization in halide perovskite nanocrystals provides a versatile strategy to tune their optical and electronic properties. We have now synthesized CsPbI3 quantum dots (QDs, 5–13.5 nm) by first preparing CsPbBr3 QDs at room temperature, followed by postsynthetic halide exchange with iodide ions. As the QD size decreases from 13.5 to 5 nm, we observe a pronounced blue shift in both excitonic and emission peaks, accompanied by an increase in the Stokes shift. The reduction in the excited-state lifetime with decreasing QD size is attributed to enhanced intrinsic exciton recombination and a higher density of surface defects. Photoinduced electron transfer between quantized CsPbI3 and methyl viologen revealed an ultrafast process occurring within a few picoseconds. These size-dependent excited-state dynamics and charge-transfer properties highlight the potential of CsPbI3 QDs for photocatalytic solar fuel generation and optoelectronic applications.

ACS Materials LettersVol. 8(3)
University of Notre Dame (US)
Affordable and clean energy
Openalex Percentile: Top 1%
Perovskite Materials and Applications
21.93
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