| Recent years,the distinctive semiconductor chracteristics and excellent photoelectric performance of lead halide perovskite quantum dots(QDs)have made a significant enhancement in optoelectronic devices.However,the toxicity and instability of lead–based perovskites are ineligible issues,which are major limitations to the commercialization.Inorder to address the toxicity and instability of lead halide perovskite,scientists obtained the metal halide double perovskite by replacing two bivalent cations in B site with a pair of monovalent and trivalent cations,providing more alternative candidates for perovskites.Cs2AgInCl6 is a new lead–free double perovskite with a direct band gap,which has attracted great attentions due to their good stability and highly efficient luminescence.However,the parity forbidden transition limites theri photoelectric performance,the quantum yield of Cs2AgInCl6 double perovskite at nanocale still hold an unsatisfactory value.So,the synthesis,photoelectric characteristics and photoluminescence enhancement of Cs2AgInCl6 double perovskite QDs are explored and researched in this work.Firstly,Cs2AgInCl6 QDs are synthesized by injecting trimethyl chlorosilane(TMS–Cl)into the dissolved precursor at 180℃.The as–synthesized Cs2AgInCl6 QDs exhibit a weak orange emission peak at 570 nm with a photoluminescence quantum yield(PLQY)of 1.5%,which is derived from the radiative recombination of self trapped excitons(STEs).Then,in order to break the parity forbidden transition of STE,Cs2Nax Ag1–xInCl6(x=0,0.2,0.4,0.6,0.8,and 1)QDs are obtained by alloying various amounts of Na into Cs2AgInCl6 QDs via the same hot injection method,resulting a peak PLQY of 13.4%in Cs2Na0.6Ag0.4InCl6QDs.At last,a serise of Mn2+doped Cs2NaxAg1–xInCl6 QDs are synthesized by varying the Mn amount and x value systematically,which enhances the PLQY of Cs2NaxAg1–xInCl6 QDs up to 36%as the highest value.As a result,a red photoluminescence emission peak at 625 nm is observed in Mn2+doped Cs2NaxAg1–xInCl6 QDs,which derives from the 4T1→6A1 transition of Mn2+that is related to the ultrafast energy transfer from STE to Mn2+. |