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Abstract Highly sensitive stimuli‐responsive luminescent materials are crucial for applications in optical sensing, security, and anticounterfeiting. Here, we report two zero‐dimensional (0D) copper(I) halides, (TEP) 2 Cu 2 Br 4 , (TEP) 2 Cu 4 Br 6 , and 1D (TEP) 3 Ag 6 Br 9 , which are comprised of isolated Cu 2 Br 4 2− , Cu 4 Br 6 2− , and Ag 6 Br 9 3− polyanions, respectively, separated by TEP + (tetraethylphosphonium TEP) cations. (TEP) 2 Cu 2 Br 4 and (TEP) 2 Cu 4 Br 6 demonstrate greenish‐white and orange‐red emissions, respectively, with near unity photoluminescence quantum yields, while (TEP) 3 Ag 6 Br 9 is a poor light emitter. Optical spectroscopy measurements and density‐functional theory calculations reveal that photoemissions of these compounds originate from self‐trapped excitons due to the excited‐state distortions in the copper(I) halide units. Crystals of Cu(I) halides are radioluminescence active at room temperature under both X‐ and γ‐rays exposure. The light yields up to 15,800 ph/MeV under 662 keV γ‐rays of 137 Cs suggesting their potential for scintillation applications. Remarkably, (TEP) 2 Cu 2 Br 4 and (TEP) 2 Cu 4 Br 6 are interconvertible through chemical stimuli or reverse crystallization. In addition, both compounds demonstrate luminescence on‐off switching upon thermal stimuli. The sensitivity of (TEP) 2 Cu 2 Br 4 and (TEP) 2 Cu 4 Br 6 to the chemical and thermal stimuli coupled with their ultrabright emission allows their consideration for applications such as solid‐state lighting, sensing, information storage, and anticounterfeiting.
Popy et al. (Tue,) studied this question.