Electronic Structure at the Perovskite/Rubrene Interface: The Effect of Surface Termination

IF 3.3 3区 化学 Q2 CHEMISTRY, PHYSICAL The Journal of Physical Chemistry C Pub Date : 2024-12-16 DOI:10.1021/acs.jpcc.4c07074
Nicholas P. Sloane, Christopher G. Bailey, Jared H. Cole, Timothy W. Schmidt, Dane R. McCamey, Mykhailo V. Klymenko
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Abstract

Perovskite films have rapidly emerged as leading active materials in optoelectronic devices due to their strong optical absorption, high carrier mobility, and ease of fabrication. While proving to be promising materials for solar cells and light-emitting diodes, another application of perovskites, which makes effective use of their unique properties, is sensitization for photon upconversion. Consisting of a bulk perovskite sensitizer alongside an adjacent organic semiconductor film, the upconverting system can absorb multiple low-energy photons to emit high-energy photons. In this work, density functional theory, in conjunction with GW theory, is utilized to investigate the electronic structure at the MAPbI3/rubrene interface for different surface terminations of MAPbI3. From this investigation, we reveal that the surface termination of the perovskite layer greatly affects the charge density at the interface and within the rubrene layer, driven by the formation of interfacial dipole layers. The formation of a strong interfacial dipole for the lead-iodide-terminated perovskite alters the band alignment of the heterojunction and is expected to facilitate more efficient hole transfer, which should enhance triplet generation in rubrene through sequential charge transfer from the perovskite layer. The formation of this dipole layer is explained by the slight ionization of rubrene molecules due to the passivation of surface states and orbital hybridization. For the perovskite surface terminated with the methylammonium iodide layer, the highest occupied molecular orbital of the adjacent rubrene layer lies deep within the perovskite band gap. This termination type is further characterized by a lower density of states near the band edges and lower electron density, thereby acting as a spacer, which is anticipated to decrease the probability of charge transfer across the interface. Thus, based on our results, PbI2-terminated perovskite surfaces are predicted to be favorable for applications where hole transfer to a rubrene layer is ideal, highlighting the significance of surface termination not only for upconverting systems but for all systems where the electronic environment at the interface is crucial to performance.

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由于具有强光学吸收、高载流子迁移率和易于制造等特点,透镜薄膜已迅速成为光电设备中的主要活性材料。在被证明是太阳能电池和发光二极管的理想材料的同时,包晶体的另一个应用是光子上转换敏化剂,它有效地利用了包晶体的独特特性。光子上转换系统由块状透辉石敏化剂和相邻的有机半导体薄膜组成,可以吸收多个低能光子,从而发射高能光子。在这项研究中,我们利用密度泛函理论结合 GW 理论,研究了 MAPbI3 不同表面端接时 MAPbI3/鲁宾界面的电子结构。通过这项研究,我们发现,在界面偶极层形成的驱动下,包晶层的表面端接极大地影响了界面和红柱石层内的电荷密度。以碘化铅为端部的包晶形成的强界面偶极层改变了异质结的带排列,预计将促进更有效的空穴传输,从而通过包晶层的顺序电荷转移增强红戊二烯中三重态的生成。这种偶极层的形成可以用表面钝化和轨道杂化导致的红柱石分子轻微电离来解释。对于以碘化甲铵层终止的包晶表面,相邻红柱石层的最高占据分子轨道位于包晶带隙深处。这种终止类型的另一个特点是带边附近的状态密度较低,电子密度也较低,从而起到了间隔物的作用,预计这将降低电荷跨界面转移的概率。因此,根据我们的研究结果,预测 PbI2 端接的包晶表面有利于空穴传输到红柱石层的应用,这突出了表面端接不仅对上转换系统,而且对界面电子环境对性能至关重要的所有系统的重要性。
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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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