Vapor Depositionand Optical Properties of Cs<sub>2</sub>AgBiCl<sub>6</sub> Thin Films

Halide perovskites, particularly those containing lead, have revolutionized the field of optoelectronics. However, lead toxicity necessitates the pursuit of environmentally friendly, lead-free alternatives. Bismuth and silver-based halide double perovskites, such as Cs<sub>2</sub>AgBiCl<sub>6</sub>, have emerged as promising candidates. Previous studies on Cs<sub>2</sub>AgBiCl<sub>6</sub> have yielded inconsistencies regarding the bandgap of the material and the origin of its characteristic visible orange emission. We address these disparities by thoroughly characterizing Cs<sub>2</sub>AgBiCl<sub>6</sub> thin films deposited via evaporation and subsequent reaction of the constituent metal halides in a high-vacuum physical vapor deposition chamber. Rigorous optical characterization reveals an indirect bandgap of 2.68 eV and a direct transition at 2.9 eV. From transient PL lifetime measurements, fitted using a physically based kinetic mathematical model of exciton decay channels, we propose that the oft-observed orange emission comprises self-trapped exciton and radiative defect emissions, with fractional contributions depending on the material synthesis conditions. These clarifications bridge knowledge gaps and open avenues for fine-tuning Cs<sub>2</sub>AgBiCl<sub>6</sub> films with potential optical, electronic, and optoelectronic applications.

Publication Details

Journal
Figshare
Published
2025-03-11
DOI
https://doi.org/10.1021/acs.jpcc.4c06622.s001
Primary Topic
Mycorrhizal Fungi and Plant Interactions
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article
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Vapor Depositionand Optical Properties of Cs2AgBiCl6 Thin Films

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Mycorrhizal Fungi and Plant Interactions
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Vapor Depositionand Optical Properties of Cs2AgBiCl6 Thin Films

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Abstract

Halide perovskites, particularly those containing lead, have revolutionized the field of optoelectronics. However, lead toxicity necessitates the pursuit of environmentally friendly, lead-free alternatives. Bismuth and silver-based halide double perovskites, such as Cs<sub>2</sub>AgBiCl<sub>6</sub>, have emerged as promising candidates. Previous studies on Cs<sub>2</sub>AgBiCl<sub>6</sub> have yielded inconsistencies regarding the bandgap of the material and the origin of its characteristic visible orange emission. We address these disparities by thoroughly characterizing Cs<sub>2</sub>AgBiCl<sub>6</sub> thin films deposited via evaporation and subsequent reaction of the constituent metal halides in a high-vacuum physical vapor deposition chamber. Rigorous optical characterization reveals an indirect bandgap of 2.68 eV and a direct transition at 2.9 eV. From transient PL lifetime measurements, fitted using a physically based kinetic mathematical model of exciton decay channels, we propose that the oft-observed orange emission comprises self-trapped exciton and radiative defect emissions, with fractional contributions depending on the material synthesis conditions. These clarifications bridge knowledge gaps and open avenues for fine-tuning Cs<sub>2</sub>AgBiCl<sub>6</sub> films with potential optical, electronic, and optoelectronic applications.

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