Abstract

Metal halide perovskites have emerged as promising candidates for solution-processed blue light-emitting diodes (LEDs). However, halide phase segregation – and the resultant spectral shift – at LED operating voltages hinders their application. Here we report true-blue LEDs employing quasi-two-dimensional cesium lead bromide with a narrow size distribution of quantum wells, achieved through the incorporation of a chelating additive. Ultrafast transient absorption spectroscopy measurements reveal that the chelating agent helps to control the quantum well thickness distribution. Density functional theory calculations show that the chelating molecule destabilizes the lead species on the quantum well surface and that this in turn suppresses the growth of thicker quantum wells. Treatment with γ-aminobutyric acid passivates electronic traps and enables films to withstand 100 °C for 24 h without changes to their emission spectrum. LEDs incorporating γ-aminobutyric acid-treated perovskites exhibit blue emission with Commission Internationale de l'Éclairage coordinates of (0.12, 0.14) at an external quantum efficiency of 6.3%.

Highlights

  • Metal halide perovskites have emerged as promising candidates for solution-processed blue light-emitting diodes (LEDs)

  • In conclusion, we have demonstrated the use of chelating agents to increase PLQY and to control CsPbBr3 quantum well (QW) distribution

  • We further investigated materials and emission stability under heat/acid/base conditions of groups with a bidentate small molecule (GABA)-treated CsPbBr3 films and control films

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Summary

Introduction

Metal halide perovskites have emerged as promising candidates for solution-processed blue light-emitting diodes (LEDs). We report true-blue LEDs employing quasi-two-dimensional cesium lead bromide with a narrow size distribution of quantum wells, achieved through the incorporation of a chelating additive. LEDs incorporating γ-aminobutyric acid-treated perovskites exhibit blue emission with Commission Internationale de l'Éclairage coordinates of (0.12, 0.14) at an external quantum efficiency of 6.3%. Extra ligands (e.g., IPABr or PEABr) have been applied to achieve blue emission, but limited control over the distribution of quantum well (QW) widths results in skyblue emission (longer than 490 nm) and low device performance (EQE below 1.5%). We reasoned that a chemical strategy that controls the dynamics of CsPbBr3 QW growth—both limiting the n values formed during processing, and stabilizing them—could produce blue emission from reduced-dimensional perovskites that is both efficient and stable. GABA, a zwitterion, should passivate undercoordinated Pb sites that are otherwise susceptible to a reaction with oxygen

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