利用二氧化锡对铯铅卤化钙钛矿中激子解离追踪和提取载流子

IF 3.2 3区 化学 Q2 CHEMISTRY, PHYSICAL
Noor A. Merdad*, 
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引用次数: 0

摘要

卤化铅钙钛矿由于其优越的光物理性质而成为光电子学研究的热点。器件的性能取决于电荷载流子的提取和激子的分离程度;然而,由于器件架构的复杂性,对电荷载体的实时监测具有挑战性。本文采用稳态和时间分辨的光学吸收和光致发光(PL)测量技术,以二氧化锡(SnO2)作为电子传输层,探索和破译了从溴化铯铅(CsPbBr3)钙钛矿中提取光激发载流子的过程。采用热蒸发法,在掺杂铟氧化锡(ITO)衬底上制备了均匀的质量控制约15 nm厚的CsPbBr3。稳态PL意味着在SnO2存在下CsPbBr3发光猝灭,这进一步得到了时间相关单光子计数测量中更快衰减的支持。通过飞秒时间分辨率的泵浦探针测量,监测不同侧面激励下的基态漂白剂动力学,直接探测载流子的跟踪。动力学符合指数函数,GSB的早期上升归因于热载流子冷却时间。以下时间常数表示电荷提取(用SnO2测量CsPbBr3时)和复合。寿命值中较快的时间常数表明,当从提取层侧进行激励时,电荷提取较快。利用密度泛函理论(DFT)的第一性原理计算揭示了CsPbBr3/SnO2界面上显著的电荷重排,形成了驱动载流子提取的内部电场。我们的研究强调了在薄膜钙钛矿和电子传输层界面中实现激子解离和载流子实时跟踪的最简单方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Tracking and Extraction of Charge Carriers through Dissociation of Excitons in Cesium Lead Halide Perovskite Using Tin Dioxide

Tracking and Extraction of Charge Carriers through Dissociation of Excitons in Cesium Lead Halide Perovskite Using Tin Dioxide

Lead halide perovskites are governing interest in optoelectronics owing to their superior photophysical properties. The performances in the device depend on the extent of charge carrier extraction and separation of excitons; however, because of the complicacy of the device architect, the real-time monitoring of the charge carrier is challenging. In this work, by employing the steady-state and time-resolved techniques in terms of optical absorption and photoluminescence (PL) measurements, the exploration and deciphering of the photoexcited charge carrier extraction from cesium lead bromide (CsPbBr3) perovskite using tin dioxide (SnO2) as an electron transporting layer is reported. Adopting the thermal evaporation method, a homogeneous qualitatively controlled ∼15 nm-thick CsPbBr3 is fabricated on a previously made SnO2 on an indium-doped tin oxide (ITO) substrate. Steady-state PL implies quenching of CsPbBr3 luminescence in the presence of SnO2, which is further supported by the faster decay in time-correlated single photon counting measurements. The tracking of the charge carrier is directly probed by monitoring the ground-state bleach (GSB) dynamics in different side excitations through pump–probe measurement in femtosecond time resolution. The dynamics are fitted with exponential function, and the early rise in GSB is attributed to hot carrier cooling time. The following time constants represent charge extraction (when CsPbBr3 is measured with SnO2) and recombination. A faster time constant in lifetime values indicates fast charge extraction when the excitation is performed from the extracting layer side. The first-principles calculations using density functional theory (DFT) reveal significant charge rearrangement at the CsPbBr3/SnO2 interface, forming an internal electric field that drives carrier extraction. Our investigation highlights the simplest approaches to dissociation of the excitons and real-time tracking of charge carriers in thin-film perovskite and electron transporting layer interfaces.

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来源期刊
The Journal of Physical Chemistry C
The Journal of Physical Chemistry C 化学-材料科学:综合
CiteScore
6.50
自引率
8.10%
发文量
2047
审稿时长
1.8 months
期刊介绍: The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.
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