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Updated: Jun 27, 2025

A Modular Microfluidic Technology for Systematic Studies of Colloidal Semiconductor Nanocrystals
Published on: May 10, 2018
Halide exchange mediated cation exchange facilitates room temperature co-doping of d-and f-block elements in cesium
Jomy Jose Philip1, Gouranga H Debnath1, David H Waldeck2,3
1Centre for Nano and Material Sciences, Jain University, Bangalore, Karnataka 562112, India. gouranga.debnath@jainuniversity.ac.in.
Abstract:
This study presents a halide exchange mediated cation exchange reaction to co-dope d- and f-block elements in CsPbX3 NPs at room temperature. Addition of MnCl2 and YbCl3 to CsPbBr3 NPs induces ion exchange reactions generating the corresponding CsPbBr3/MnCl2YbCl3 NPs. In addition to the perovskite emission, the NPs display sensitized Mn2+ and Yb3+ emissions in concert spanning the UV, visible, and NIR spectral region. Structural and spectroscopic characterizations indicate a substitutional displacement of Pb2+ by the Mn2+ and Yb3+. The identity of the host halide in modulating the ion exchange reactions was also tested. An effective perovskite host NP is presented that can be used to incorporate d-f or f-f dopant combinations to realize a gamut of dopant emission lines. A charge trapping based photophysical model is developed that focuses on rational energy alignments to predict dopant emissions semi-empirically and aids the design of optimal perovskite host-multi-dopant combinations.
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