Turning Self-Trapped Exciton Emission to Near-Infrared Region in Thermochromism Zero-Dimensional Hybrid Metal Halides

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Low dimensional lead-free metal halides have become the spotlight of the research on developing multifunctional optoelectronic materials as their properties show a wide range of tunability. However, most reported low dimensional metal halides only function in the ultra-violet to visible range due to their large bandgap. Moreover, the organic cation based low dimensional metal halides show limited thermal stability; on the other hand, their inorganic cation based counterparts suffer from limited solution processability. A hybrid cation approach is proposed, where a zero dimensional (0D) metal halide ((DFPD)2CsBiI6) is developed by using mixed organic–inorganic cations: 4, 4-difluoropiperidine (DFPD) and cesium (Cs+). This ensures both thermal stability and solution processability. Furthermore, [BiI6]3− octahedra are serving as active light absorption units, which ensures the bandgap to be located at the visible region. Its photoluminescence (PL) is further shifted to the near infrared (NIR) region by doping (DFPD)2CsBiI6 with antimony (Sb3+). The developed materials show multifunctional properties: thermochromic behavior, light detection, and NIR light emitting. This study expands the scope of developing multifunctional 0D metal halides.

OriginalsprogEngelsk
TidsskriftAdvanced Optical Materials
Sider (fra-til)3251–3257
Antal sider7
ISSN2195-1071
DOI
StatusUdgivet - 2023

Bibliografisk note

Funding Information:
T.B. and X.W. contributed equally to this work. J.C. acknowledges support from the Novo Nordisk Foundation (NNF22OC0073582). Y.H. acknowledges support from the China Scholarship Council (No. 202006150002).

Publisher Copyright:
© 2023 The Authors. Advanced Optical Materials published by Wiley-VCH GmbH.

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