Effects of 1-(2-amino-5-bromophenyl)ethenone modification on CsPbI2Br films and perovskite solar cells

IF 2.7 Q2 PHYSICS, CONDENSED MATTER
Ruzhe Gong, Min Zhong, Lei He
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Abstract

Despite the remarkable thermal stability of inorganic CsPbI2Br perovskites solar cells, their practical deployment is plagued by severe interfacial non-radiative recombination and black phase instability at room temperature. To address these challenges, we designed a novel multifunctional interfacial modifier 1-(2-Amino-5-bromophenyl)ethenone(2A5B). In this study, the interface of CsPbI2Br perovskite/Spiro-OMeTAD hole transport layer was modified by 2A5B. The effects of 2A5B modification on the morphology, structure, optical absorption properties, defect density, carrier lifetime, hydrophobicity and energy level of CsPbI2Br perovskite film, optoelectronic performance of the devices, and their mechanism were systematically studied, which were rarely reported. The oxygen atoms in the CO groups of 2A5B form coordination bonds with uncoordinated Cs+ ions, while the nitrogen atoms in the –NH2 groups coordinate with Pb2+ ions on the surface of CsPbI2Br, passivating interface defects, modulating interface energy levels matching, and thus inhibiting interface non-radiative recombination. Simultaneously, the hydrogen atoms in the –NH2 groups interact with surface free I/Br ions of CsPbI2Br via hydrogen bonding, suppressing halide migration and stabilizing the perovskite structure. The efficiency of the device modified with 4 mg/mL of 2A5B prepared in an air environment with relative humidity of 50 % increased by 51.08 % compared with that of the unmodified device. And 4 mg/mL 2A5B modified device could maintain an initial efficiency of 70 % after 40 days of storage at RH 50 %, whereas the unmodified device only keeps 20 % of the initial efficiency. This study provides valuable insights of designing interfacial modifiers between the perovskite layer and the hole transport layer, and the photovoltaic conversion efficiency and stability of the all-inorganic perovskite solar cells were improved in a highly humid air environment.

Abstract Image

1-(2-氨基-5-溴苯基)乙烯酮改性对CsPbI2Br薄膜和钙钛矿太阳能电池的影响
尽管无机CsPbI2Br钙钛矿太阳能电池具有显著的热稳定性,但其实际部署受到室温下严重的界面非辐射复合和黑相不稳定性的困扰。为了解决这些问题,我们设计了一种新的多功能界面改性剂1-(2-氨基-5-溴苯基)乙烯酮(2A5B)。本研究采用2A5B修饰CsPbI2Br钙钛矿/Spiro-OMeTAD空穴传输层的界面。本文系统地研究了2A5B改性对CsPbI2Br钙钛矿膜的形貌、结构、光吸收性能、缺陷密度、载流子寿命、疏水性和能级以及器件光电性能的影响,并对其机理进行了研究。2A5B的CO基团中的氧原子与不配位的Cs+离子形成配位键,而-NH2基团中的氮原子与CsPbI2Br表面的Pb2+离子形成配位键,钝化界面缺陷,调节界面能级匹配,从而抑制界面非辐射复合。同时,-NH2基团中的氢原子通过氢键与CsPbI2Br表面自由的I - /Br -离子相互作用,抑制卤化物迁移,稳定钙钛矿结构。在相对湿度为50%的空气环境中,用4 mg/mL的2A5B修饰装置的效率比未修饰装置提高了51.08%。4 mg/mL 2A5B改良装置在RH为50%的条件下保存40 d后可保持70%的初始效率,而未经改良的装置仅保持20%的初始效率。该研究为设计钙钛矿层与空穴传输层之间的界面改性剂提供了有价值的见解,并提高了全无机钙钛矿太阳能电池在高湿度空气环境下的光伏转换效率和稳定性。
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CiteScore
6.50
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