Recently,
copper(I) halides have been gaining increased attention
as highly luminescent nontoxic alternatives to lead halide perovskites
for optoelectronic applications. Here, we report preparation of blue
emitting, lead free, all-inorganic halides K2CuX3 (X = Cl, Br) through five synthetic methods including traditional
solid-state and solution methods. The photoluminescence (PL) emission
spectra of K2CuCl3 and K2CuBr3 exhibit narrow peaks centered at 392 and 388 nm with full
widths at half-maximum (fwhm) values of ∼54 nm. The visible
bright blue emission is corroborated by the remarkably high photoluminescence
quantum yield (PLQY) values up to ∼97%. Furthermore, radioluminescence
measurements on K2CuCl3 yield a bright peak
at 404 nm under irradiation with X-rays at 200 kVp and 20 mA, which
is optimal for use with PMTs and Si photomultipliers, suggesting a
strong potential of this family for radiation detection applications.
Based on our combined experimental and computational investigations,
the origin of the efficient luminescence in K2CuX3 is attributed to the high stability self-trapped excitons (STE)
formed in the one-dimensional anionic ∞
1[CuX3]2– chains. Advantageously, K2CuX3 demonstrate
improved air- and photostability compared to the previously reported
copper(I) halides. The discovery of highly efficient and high stability
light emitters based on earth-abundant copper(I) halides paves the
way for their potential practical applications.