Metastable Oxygen-Induced Light-Enhanced Doping in Mixed Sn–Pb Halide Perovskites

IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Jasmeen Nespoli, Matthijs Mugge, Lara M. van der Poll, Snigdha Lal, Bahiya Ibrahim, Bart Boshuizen, Valentina M. Caselli, Arjan J. Houtepen, Lars J. Bannenberg and Tom J. Savenije*, 
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Abstract

Mixed Sn–Pb halide perovskites are promising absorber materials for solar cells due to the possibility of tuning the bandgap energy down to 1.2–1.3 eV. However, tin-containing perovskites are susceptible to oxidation affecting the optoelectronic properties. In this work, we investigated qualitatively and quantitatively metastable oxygen-induced doping in isolated ASnxPb1–xI3 (where A is methylammonium or a mixture of formamidinium and cesium) perovskite thin films by means of microwave conductivity, structural and optical characterization techniques. We observe that longer oxygen exposure times lead to progressively higher dark conductivities, which slowly decay back to their original levels over days. Here oxygen acts as an electron acceptor, leading to tin oxidation from Sn2+ to Sn4+ and creation of free holes. The metastable oxygen-induced doping is enhanced by exposing the perovskite simultaneously to oxygen and light. Next, we show that doping not only leads to the reduction in the photoconductivity signal but also induces long-term effects even after loss of doping, which is thought to derive from consecutive oxidation reactions leading to the formation of defect states. On prolonged exposure to oxygen and light, optical and structural changes can be observed and related to the formation of SnOx and loss of iodide near the surface. Our work highlights that even a short-term exposure to oxygen immediately impairs the charge carrier dynamics of the perovskite, while structural perovskite degradation is only noticeable upon long-term exposure and accumulation of oxidation products. Hence, for efficient solar cells, exposure of mixed Sn–Pb perovskites to oxygen during production and operation should be rigorously blocked.

混合锡铅卤化物包晶石中可迁移的氧诱导光增强掺杂
由于可以将带隙能调低到 1.2-1.3 eV,锡铅混合卤化物过氧化物是一种很有前途的太阳能电池吸收材料。然而,含锡的过氧化物容易被氧化,从而影响其光电特性。在这项工作中,我们通过微波传导、结构和光学表征技术,定性和定量研究了分离的 ASnxPb1-xI3(其中 A 为甲基铵或甲脒和铯的混合物)包晶薄膜中掺杂的可蜕变氧。我们观察到,氧气暴露时间越长,暗电导率就越高,并在数天后慢慢衰减回原来的水平。在这里,氧气充当电子受体,导致锡从 Sn2+ 氧化成 Sn4+,并产生自由空穴。将过氧化物同时暴露在氧气和光下,可增强由氧气引起的掺杂。接下来,我们展示了掺杂不仅会导致光电导信号的降低,而且在失去掺杂后仍会诱发长期效应,这被认为是源于导致缺陷态形成的连续氧化反应。在长时间暴露于氧气和光的情况下,可以观察到光学和结构的变化,这些变化与氧化锡的形成和表面附近碘化物的流失有关。我们的研究突出表明,即使短期暴露在氧气中,也会立即损害包晶的电荷载流子动力学,而只有在长期暴露和氧化产物积累的情况下,包晶的结构降解才会明显。因此,为了实现高效太阳能电池,在生产和运行过程中应严格阻止锡铅混合包晶石与氧气接触。
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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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