Structural regulation and optical behavior of zero-dimensional Cu(I)-based organometallic halides under pressure

Abstract Low-dimensional hybrid metal halides exhibit broadband emission and high photoluminescence quantum yield (PLQY), making them promising candidates for next-generation luminescent materials in lighting applications. Here, the emission intensity of (C 12 H 24 O 6 ) 2 Na 2 (H 2 O) 3 Cu 4 I 6 was strengthened between 9.3-17.2 GPa, accompanied by the redshift of emission wavelength. The photoluminescence (PL) of Cu(I)-based organometallic halides originate from multiple emission states, which are a metal-to-ligand charge transfer or a halide-to-ligand charge transfer (MLCT/HLCT) excited state and a cluster-centered (CC) excited state. MLCT/HLCT-related emission wavelength red shifts while CC-related emission wavelength remains unchanged, indicating that the rearrangement of different emission states play a critical role in the changes of luminescence wavelength. This study not only deepens the understanding of the influence of high pressure on (C 12 H 24 O 6 ) 2 Na 2 (H 2 O) 3 Cu 4 I 6 , but also provides valuable insights into the structure-property relationship of zero-dimensional Cu(I)-based organometallic halides.