钝化
材料科学
钙钛矿(结构)
光致发光
量子产额
二极管
傅里叶变换红外光谱
发光二极管
光电子学
卤化物
X射线光电子能谱
光谱学
量子效率
光化学
无机化学
化学工程
纳米技术
结晶学
化学
光学
图层(电子)
物理
工程类
量子力学
荧光
作者
Jayanta Kumar Mishra,Natalia Yantara,Anil Kanwat,Tomoki Furuhashi,Sivarajan Ramesh,Teddy Salim,Nur Fadilah Jamaludin,Benny Febriansyah,Zi En Ooi,Subodh Mhaisalkar,Tze Chien Sum,Kedar Hippalgaonkar,Nripan Mathews
标识
DOI:10.1021/acsami.2c00899
摘要
Defect management strategies are vital for enhancing the performance of perovskite-based optoelectronic devices, such as perovskite-based light-emitting diodes (PeLEDs). As additives can fucntion both as acrystallization modifier and/or defect passivator, a thorough study on the roles of additives is essential, especially for blue emissive Pe-LEDs, where the emission is strictly controlled by the n-domain distribution of the Ruddlesden–Popper (RP, L2An–1PbnX3n+1, where L refers to a bulky cation, while A and X are monovalent cation, and halide anion, respectively) perovskite films. Of the various additives that are available, octyl phosphonic acid (OPA) is of immense interest because of its ability to bind with uncoordinated Pb2+ ( notorious for nonradiative recombination) and therefore passivates them. Here, with the help of various spectroscopic techniques, such as X-ray photon-spectroscopy (XPS), Fourier-transform infrared spectroscopy (FTIR), and photoluminescence quantum yield (PLQY) measurements, we demonstrate the capability of OPA to bind and passivate unpaired Pb2+ defect sites. Modification to crystallization promoting higher n-domain formation is also observed from steady-state and transient absorption (TA) measurements. With OPA treatment, both the PLQY and EQE of the corresponding PeLED showed improvements up to 53% and 3.7% at peak emission wavelength of 485 nm, respectively.
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