JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, v.145, no.21, pp.11650 - 11658
Abstract
Blue-emitting Cs3Cu2I5 has attracted attention owing to its near-unity PL quantum yield and applications in DUV photodetectors and scintillators. Its PL properties originate from the unique local structure around the luminescent center, the [Cu2I5]3– polyhedron iodocuprate anion consisting of the edge-shared CuI3 triangle and the CuI4 tetrahedron dimer, which is isolated by Cs+ ions. We found that solid-state reactions between CsI and CuI occur near room temperature (RT) to form Cs3Cu2I5 and/or CsCu2I3 phases. High-quality thin films of these phases were obtained by the sequential deposition of CuI and CsI by thermal evaporation. We elucidated that the formation of interstitial Cu+ and the antisite of I– at the Cs+ site in the CsI crystal through Cu+ and I– diffusion results in the RT synthesis of Cs3Cu2I5. The unique structure formation of the luminescent center was revealed using a model based on the low packing density of the CsCl-type crystal structure, similar sizes of Cs+ and I– ions, and the high diffusivity of Cu+. The self-aligned patterning of the luminous regions on thin films was demonstrated.