Issue 51, 2025

Extending lead-free organic–inorganic semiconducting materials to new polymeric structures: 2,2′-bipyridinium iodoantimonate and quinoxalinium iodobismuthate

Abstract

We report on the synthesis, crystal structures and optoelectronic properties of two novel organic–inorganic group V iodometalates – (bpy-H)SbI4 (1) and (Qx-H)2[BiI4]2·CH3OH (2) (bpy-H: 2,2′-bipyridinium; Qx-H: quinoxalinium). Crystals of both compounds were grown solvothermally using as starting reagents antimony(III) iodide and 2,2′-bipyridine, for 1, and bismuth(III) iodide and quinoxaline, for 2. Both compounds were structurally analyzed by single crystal X-ray diffraction at 100 K and their structures feature one-dimensional edge-sharing anionic chains of MI6-octahedra, with short interchain I⋯I contacts giving rise to the possibility of three-dimensional charge transport capability. The cavities between the one-dimensional [MI4]n chains are occupied by the rigid N-protonated organic amines – 2,2′-bipyridinium (bpy-H), for 1, and quinoxalinium (Qx-H), for 2 – to balance the charge and stabilize the structures. The study of their supramolecular 3D structures assisted by a Hirshfeld surface analysis revealed that the latter are due to several types of intermolecular interactions, such as intermolecular hydrogen-bonding (H⋯I and H⋯O) and additional π⋯π and I⋯I contacts. Solid-state optical studies performed on powders and thin films were carried out and revealed that the materials display semiconductive optical band gap energies of around 2.17 eV, for 1, and 2.03 eV, for 2, which is encouraging for optoelectronic applications. The bulk crystals of 1 exhibit a broad dual-band emission which originates from both free excitons (FE) and self-trapped excitons (STE), as proven by its long lifetime (146.32 ns) and the temperature dependences of broadband emission. In contrast, bulk crystals of 2 exhibit broadband emission centred at 454 nm, common to the salt (Qx-H)Cl, originating from ligand-centered transition. These are proven by their short lifetimes (3.86 ns for 2 and 1.07 ns for (Qx-H)Cl).

Graphical abstract: Extending lead-free organic–inorganic semiconducting materials to new polymeric structures: 2,2′-bipyridinium iodoantimonate and quinoxalinium iodobismuthate

Supplementary files

Transparent peer review

To support increased transparency, we offer authors the option to publish the peer review history alongside their article.

View this article’s peer review history

Article information

Article type
Paper
Submitted
20 Aug 2025
Accepted
31 Oct 2025
First published
07 Nov 2025
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2025,15, 43523-43541

Extending lead-free organic–inorganic semiconducting materials to new polymeric structures: 2,2′-bipyridinium iodoantimonate and quinoxalinium iodobismuthate

C. Hrizi, M. Hamdouni, M. Essid, M. Nouiri, A. Khatyr, M. Knorr, L. Viau, A. Schmidt, C. Strohmann and S. Chaabouni, RSC Adv., 2025, 15, 43523 DOI: 10.1039/D5RA06189J

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements