Vacancy-Ordered Quadruple Halide Perovskites: All-Inorganic Noble-Metal Semiconductors with Infrared Absorption

A unique family of inorganic halide perovskites based on noble metals was successfully synthesized, using the “stick & square” approach, where the octahedral units of the perovskite framework can be substituted with 4-coordinate square and 2-coordinate dumbbell units, orthogonally assembled to generate a perovskite-like network. The compounds have a general formula of A4Au2Pd□X12 (A = Cs, Rb; X = Cl, Br, I; □ = ordered-vacancy site), crystallizing in a pseudocubic unit cell with 4 × 4 × 4 enlargement with respect to the perovskite aristotype, AMX3. The compounds consist of square planar complexes of [AuIIIX4]2– and [PdIIX4]2– ions, randomly distributed across the crystallographic sites of the unit cell. The high symmetry of the compounds is revealed by the isolation of euhedral crystals with a rare deltoidal icositetrahedral morphology. X-ray photoelectron spectroscopy (XPS) was employed to validate the oxidation states of the elements and demonstrate the changes in the spectral response as a function of the electronegativity changes in the halide ion. All compounds are black in color, with sharp absorption edges in the near-infrared range, with an experimentally determined bandgap in the 0.8–1.55 eV range. Density functional theory (DFT) calculations based on a metal-site-ordered model reveal an indirect bandgap between the halide-p orbital-dominated valence band maximum (VBM) and the gold-dz2-dominated conduction band minimum (CBM) in the iodide analogue, changing to a palladium-d orbital-dominated VBM for the bromide and chloride analogues. The present work demonstrates the rich complexity of the late transition metal halide chemistry and illustrates that the “stick & square” approach is a viable route to access complex perovskite derivatives. A4Au2Pd□X12 compounds hold special merits in the fact that they possess a suitable bandgap for photovoltaic applications and potentially infrared electronics, while at the same time being stable against air and water, the major enemies of typical p-block halide perovskites.

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Publication Details

Journal
Chemistry of Materials
Published
2026-04-27
DOI
https://doi.org/10.1021/acs.chemmater.5c02950
Primary Topic
Perovskite Materials and Applications
Type
article
Field-Weighted Citation Impact
0.00

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article

Vacancy-Ordered Quadruple Halide Perovskites: All-Inorganic Noble-Metal Semiconductors with Infrared Absorption

Giannis G. Gkikas, Rafaela Maria Giappa, George Volonakis, Constantinos C. Stoumpos et al.
Chemistry of Materials
Perovskite Materials and Applications
article

Vacancy-Ordered Quadruple Halide Perovskites: All-Inorganic Noble-Metal Semiconductors with Infrared Absorption

Giannis G. Gkikas, Rafaela Maria Giappa, George Volonakis, Constantinos C. Stoumpos, Emmanouil G. Manidakis, Myung‐Gil Kim, A. Barakat
article en

Abstract

A unique family of inorganic halide perovskites based on noble metals was successfully synthesized, using the “stick & square” approach, where the octahedral units of the perovskite framework can be substituted with 4-coordinate square and 2-coordinate dumbbell units, orthogonally assembled to generate a perovskite-like network. The compounds have a general formula of A4Au2Pd□X12 (A = Cs, Rb; X = Cl, Br, I; □ = ordered-vacancy site), crystallizing in a pseudocubic unit cell with 4 × 4 × 4 enlargement with respect to the perovskite aristotype, AMX3. The compounds consist of square planar complexes of [AuIIIX4]2– and [PdIIX4]2– ions, randomly distributed across the crystallographic sites of the unit cell. The high symmetry of the compounds is revealed by the isolation of euhedral crystals with a rare deltoidal icositetrahedral morphology. X-ray photoelectron spectroscopy (XPS) was employed to validate the oxidation states of the elements and demonstrate the changes in the spectral response as a function of the electronegativity changes in the halide ion. All compounds are black in color, with sharp absorption edges in the near-infrared range, with an experimentally determined bandgap in the 0.8–1.55 eV range. Density functional theory (DFT) calculations based on a metal-site-ordered model reveal an indirect bandgap between the halide-p orbital-dominated valence band maximum (VBM) and the gold-dz2-dominated conduction band minimum (CBM) in the iodide analogue, changing to a palladium-d orbital-dominated VBM for the bromide and chloride analogues. The present work demonstrates the rich complexity of the late transition metal halide chemistry and illustrates that the “stick & square” approach is a viable route to access complex perovskite derivatives. A4Au2Pd□X12 compounds hold special merits in the fact that they possess a suitable bandgap for photovoltaic applications and potentially infrared electronics, while at the same time being stable against air and water, the major enemies of typical p-block halide perovskites.

Chemistry of Materials
Centre National de la Recherche Scientifique (FR), University of Crete (GR), St Petersburg University (RU), Mediterranean University (ME), Hellenic Mediterranean University (GR), Institut des Sciences Chimiques de Rennes (FR), Advanced Engineering (Czechia) (CZ), Université de Rennes (FR), Sungkyunkwan University (KR)
Saint Petersburg State University, University of Crete
Openalex Percentile: Top 17%
Perovskite Materials and Applications
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