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Multifunctional applications enabled by tunable multi-emission and ultra-broadband VIS-NIR luminescence energy transfer in Sn/Mn-doped lead-free Zn-based metal halides.

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School of Physical Science and Technology, School of Chemistry and Chemical Engineering, State Key Laboratory of Featured Metal Materials and Life-cycle Safety for Composite Structures, and School of Resources, Environment and Materials, Guangxi University, Nanning 530004, China.

Metal halides are widely applied in solid-state lighting (SSL), optoelectronic devices, information encryption, and near-infrared (NIR) detection due to their superior photoelectric properties and tunable emission. However, single-component phosphors that can be efficiently excited by light-emitting diode (LED) chips and cover both the visible (VIS) and NIR emission regions are still very rare. To address this issue, (TPA)ZnBr:Sn/Mn (TPA = [(CHCHCH)N]) phosphors were synthesized by using the solvent evaporation method.

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Broadband blue emission in zero-dimensional perovskites has received considerable attention, which is very important for the realization of stable blue-light emitters; however, the underlying formation mechanism remains unclear. Based on first-principles calculations, we have systematically studied the self-trapped excitons (STEs) behavior and luminescence properties in 0D-(DMA)4PbI6 perovskite. Our calculations show that there is a significant difference between the intrinsic STE luminescence mechanism (∼2.

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Low dimensional organic-inorganic hybrid metal halide materials have attracted extensive attention due to their superior optoelectronic properties. However, low photoluminescence quantum yields (PLQYs) caused by parity-forbidden transition hinder their further application in optoelectronic devices. Herein, a novel yellow-emitting PMANa(In,Sb)Cl (CHN, PMA) low-dimensional OIMHs single crystal with a PLQY as high as 88 % was successfully designed and synthesized, originating from the fact that the doping of Sb effectively relaxes the parity-forbidden transition by strong spin-orbit (SO) coupling and Jahn-Teller (JT) interaction.

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Chiral multiferroicity in two-dimensional hybrid organic-inorganic perovskites.

Nat Commun

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Joint School of National University of Singapore and Tianjin University, International Campus of Tianjin University, Binhai New City, Fuzhou, 350207, China.

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Four new coordination polymers, including 1D, 2D and 3D structures, were synthesized via a hydrothermal method using Cd/Zn/Cu metal salts as nodes. These polymers were formed through self-assembly of four different dicarboxylic acid ligands, namely adamantane-1,3-dicarboxylic acid (Hadc), glutaric acid (Hglu), 5-hydroxyisophthalic acid (Hhip) and fumaric acid (Hfum), in conjunction with the auxiliary ligand [1,4-bis(pyridin-4-ylmethyl)piperazine (bpmp). The corresponding formulae are [Cd(adc)(bpmp)Cl(HO)] (1), {[Cd(glu)(bpmp)(HO)]·8HO·2CHOH} (2), [Zn(hip)(bpmp)(HO)] (3) and [Cu(fum)(bpmp)(HO)] (4).

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