X射线光电子能谱
堆积
材料科学
能量转换效率
结晶
紫外光电子能谱
化学工程
热稳定性
有机太阳能电池
光电子学
纳米技术
化学
复合材料
聚合物
有机化学
工程类
作者
Andrés‐Felipe Castro‐Mendez,Jamie P. Wooding,Selma Fairach,Carlo A. R. Perini,Emily K. McGuinness,Jacob N. Vagott,Ruipeng Li,Sanggyun Kim,Vivek Brahmatewari,Lucille V. Dentice,Mark D. Losego,Juan‐Pablo Correa‐Baena
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-01-03
卷期号:8 (1): 844-852
被引量:12
标识
DOI:10.1021/acsenergylett.2c02272
摘要
Despite the rapid increase in power conversion efficiency (PCE) of perovskite solar cells (PSCs) over the past decade, stability remains a major roadblock to commercialization. Here, this work shows vapor phase infiltration (VPI) as a tool to create hybrid organic–inorganic layers that improve the stability of organic charge transport layers, such as hole-selective spiro-OMeTAD in PSCs and in other organic electronic devices. Using X-ray photoelectron spectroscopy (XPS), ultraviolet photoelectron spectroscopy (UPS), and grazing incident wide-angle X-ray scattering (GIWAXS), we identify that infiltration of TiO<sub>x</sub> via VPI hinders the crystallization of the spiro-OMeTAD layer by likely preventing the π–π stacking of the molecules. Infiltrated PSCs retained more than 80% of their original efficiency after an operando stability test of 200 h at 75 °C, double the efficiency retained by devices without infiltration, in which the efficiency rapidly decreases in the first 50 h. This work provides a blueprint for using VPI to stabilize organic charge transport layers via prevention of π–π stacking leading to deleterious crystallization that shortens device lifetimes.
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